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Transfer RNA gene recruitment in mitochondrial DNA
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1096-8628(19990101)82:1<89::aid-ajmg18>3.0.co;2-vopenalex-snapshot
Reply to the letter to the editor by Partington and Turner??Wolf-Hirschhorn and Pitt-Rogers-Danks syndromes?
inferredcites →https://doi.org/10.1002/0471650129.dob0522openalex-snapshot
PAUP * [Phylogenetic Analysis Using Parsimony (and Other Methods)]
inferredcites →https://doi.org/10.1002/0471695998.mgs055openalex-snapshot
W olf‐ H irschhorn (4 p ‐) Syndrome
inferredcites →https://doi.org/10.1002/1096-8628(20000918)94:3<254::aid-ajmg13>3.0.co;2-7openalex-snapshot
Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome
inferredcites →https://doi.org/10.1002/1521-1878(200007)22:7<616::aid-bies4>3.0.co;2-ropenalex-snapshot
Six family genes-structure and function as transcription factors and their roles in development
inferredcites →https://doi.org/10.1002/ajmg.10160openalex-snapshot
The end of the beginning of chromosome ends†
inferredcites →https://doi.org/10.1002/ajmg.1203openalex-snapshot
First known microdeletion within the Wolf-Hirschhorn syndrome critical region refines genotype-phenotype correlation
inferredcites →https://doi.org/10.1002/ajmg.1320570415openalex-snapshot
Interstitial deletions of the short arm of chromosome 4 in patients with a similar combination of multiple minor anomalies and mental retardation
inferredcites →https://doi.org/10.1002/ajmg.a.20080openalex-snapshot
Malignant hematological disorders in children with Wolf–Hirschhorn syndrome
inferredcites →https://doi.org/10.1002/ajmg.a.20208openalex-snapshot
Inv dup del(4)(:p14 → p16.3::p16.3 → qter) with manifestations of partial duplication 4p and Wolf‐Hirschhorn syndrome
inferredcites →https://doi.org/10.1002/ajmg.a.20608openalex-snapshot
Cutaneous T‐cell lymphoma in a 21‐year‐old male with Wolf–Hirschhorn syndrome
inferredcites →https://doi.org/10.1002/dvdy.10090openalex-snapshot
Isolation of DNTNP, which encodes a potential nuclear protein that is expressed in the developing, dorsal neural tube
inferredcites →https://doi.org/10.1002/j.1460-2075.1989.tb03450.xopenalex-snapshot
Amplification enhancers and replication origins in the autosomal chorion gene cluster of Drosophila.
inferredcites →https://doi.org/10.1002/j.1460-2075.1989.tb08600.xopenalex-snapshot
The role of ACE3 in Drosophila chorion gene amplification.
inferredcites →https://doi.org/10.1002/pd.1970110209openalex-snapshot
PRENATAL DIAGNOSIS OF CYSTIC HYGROMA AND CHORIOANGIOMA IN THE WOLF‐HIRSCHHORN SYNDROME
inferredcites →https://doi.org/10.1002/pro.5560070722openalex-snapshot
Conserved sequence motifs among bacterial, eukaryotic, and archaeal phosphatases that define a new phosphohydrolase superfamily
inferredcites →https://doi.org/10.1006/dbio.1993.1287openalex-snapshot
Developmental Progression of DNA Puffs in Sciara coprophila: Amplification and Transcription
inferredcites →https://doi.org/10.1006/dbio.1997.8845openalex-snapshot
Multiple Roles of theeyes absentGene inDrosophila
inferredcites →https://doi.org/10.1006/dbio.2001.0185openalex-snapshot
The Homeobox Protein Six3 Interacts with the Groucho Corepressor and Acts as a Transcriptional Repressor in Eye and Forebrain Formation
inferredcites →https://doi.org/10.1006/dbio.2001.0325openalex-snapshot
The Caenorhabditis elegans Six/sine oculis Class Homeobox Gene ceh-32 Is Required for Head Morphogenesis
inferredcites →https://doi.org/10.1006/geno.1999.5881openalex-snapshot
LETM1, A Novel Gene Encoding a Putative EF-Hand Ca2+-Binding Protein, Flanks the Wolf–Hirschhorn Syndrome (WHS) Critical Region and Is Deleted in Most WHS Patients
inferredcites →https://doi.org/10.1006/jmbi.1994.0043openalex-snapshot
The Mitochondrial DNA of the Amoeboid Protozoon,Acanthamoeba castellanii: Complete Sequence, Gene Content and Genome Organization
inferredcites →https://doi.org/10.1006/scdb.2001.0271openalex-snapshot
Mammalian homologues of the Drosophila eye specification genes
inferredcites →https://doi.org/10.1007/bf00279124openalex-snapshot
Deletion of short arms of chromosome 4?5 in a child with defects of midline fusion
inferredcites →https://doi.org/10.1007/bf00336780openalex-snapshot
A multitude of suppressors of group II intron-splicing defects in yeast
inferredcites →https://doi.org/10.1007/bf00344233openalex-snapshot
Molecular characterization of an 18 kb segment of DNA puff C4 of Bradysia hygida (Diptera, Sciaridae)
inferredcites →https://doi.org/10.1007/bf00710035openalex-snapshot
DNA puff C4 ofBradysia hygida (Diptera: Sciaridae) contains genes unequally amplified and differentially expressed during development
inferredcites →https://doi.org/10.1007/bf00848156openalex-snapshot
Mutations affecting the pattern of the larval cuticle inDrosophila melanogaster
inferredcites →https://doi.org/10.1007/s00239-003-2494-6openalex-snapshot
The Evolution of tRNA-Leu Genes in Animal Mitochondrial Genomes
inferredcites →https://doi.org/10.1007/s003359900480openalex-snapshot
Eyes absent: A gene family found in several metazoan phyla
inferredcites →https://doi.org/10.1007/s00412-002-0194-4openalex-snapshot
A DNase I hypersensitive site flanks an origin of DNA replication and amplification in Sciara
inferredcites →https://doi.org/10.1007/s00412-004-0302-8openalex-snapshot
Schizosaccharomyces pombe replication protein Cdc45/Sna41 requires Hsk1/Cdc7 and Rad4/Cut5 for chromatin binding
inferredcites →https://doi.org/10.1007/s00412-004-0304-6openalex-snapshot
Molecular characterization of the B-2 DNA puff gene of Rhynchosciara americana
inferredcites →https://doi.org/10.1007/s00412-004-0309-1openalex-snapshot
Meiotic defects in the Arabidopsis rad50 mutant point to conservation of the MRX complex function in early stages of meiotic recombination
inferredcites →https://doi.org/10.1007/s004120050380openalex-snapshot
DNA replication during amplification of the C3 puff of Rhynchosciara americana initiates at multiple sites in a 6 kb region
inferredcites →https://doi.org/10.1007/s004120100131openalex-snapshot
The nuclear location and chromatin organization of active chorion amplification origins
inferredcites →https://doi.org/10.1007/s004380051067openalex-snapshot
Homologs of animal eyes absent (eya) genes are found in higher plants
inferredcites →https://doi.org/10.1007/s004380051126openalex-snapshot
Isolation and characterization of AtMLH1, a MutL homologue from Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/0022-2836(74)90098-9openalex-snapshot
Ribosomal RNA gene amplification by rolling circles
inferredcites →https://doi.org/10.1016/0022-2836(87)90605-xopenalex-snapshot
Amplification of a chorion gene cluster in Drosophila is subject to multiple cis-regulatory elements and to long-range position effects
inferredcites →https://doi.org/10.1016/0027-5107(75)90233-xopenalex-snapshot
Mitotic crossing-over as an important mechanism of floral sectoring in tradescantia
inferredcites →https://doi.org/10.1016/0092-8674(80)90082-3openalex-snapshot
Two clusters of genes for major chorion proteins of Drosophila melanogaster
inferredcites →https://doi.org/10.1016/0092-8674(89)90328-0openalex-snapshot
Recent progress in understanding mechanisms of mammalian DNA amplification
inferredcites →https://doi.org/10.1016/0092-8674(93)90115-7openalex-snapshot
The eyes absent gene: Genetic control of cell survival and differentiation in the developing Drosophila eye
inferredcites →https://doi.org/10.1016/0092-8674(93)90719-7openalex-snapshot
p53-dependent apoptosis modulates the cytotoxicity of anticancer agents
inferredcites →https://doi.org/10.1016/0303-2647(85)90026-7openalex-snapshot
Probing fungal mitochondrial evolution with tRNA
inferredcites →https://doi.org/10.1016/0378-1119(94)90380-8openalex-snapshot
Identification of homeobox genes expressed in human haemopoietic progenitor cells
inferredcites →https://doi.org/10.1016/j.cell.2004.05.018openalex-snapshot
Protein Tyrosine Phosphatases in the Human Genome
inferredcites →https://doi.org/10.1016/j.cell.2004.07.026openalex-snapshot
C. elegans HIM-17 Links Chromatin Modification and Competence for Initiation of Meiotic Recombination
inferredcites →https://doi.org/10.1016/j.copbio.2004.02.005openalex-snapshot
A tale of two integrations, transgene and T-DNA: gene targeting by homologous recombination in rice
inferredcites →https://doi.org/10.1016/j.cub.2003.10.055openalex-snapshot
Perp Is a Mediator of p53-Dependent Apoptosis in Diverse Cell Types
inferredcites →https://doi.org/10.1016/j.cub.2004.12.030openalex-snapshot
Identification of Thermosensory and Olfactory Neuron-Specific Genes via Expression Profiling of Single Neuron Types
inferredcites →https://doi.org/10.1016/j.dnarep.2003.12.007openalex-snapshot
SMC6 is required for MMS-induced interchromosomal and sister chromatid recombinations in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1016/j.mod.2004.05.019openalex-snapshot
The transcription factor Six2 activates expression of the Gdnf gene as well as its own promoter
inferredcites →https://doi.org/10.1016/j.molcel.2004.06.040openalex-snapshot
hMSH4-hMSH5 Recognizes Holliday Junctions and Forms a Meiosis-Specific Sliding Clamp that Embraces Homologous Chromosomes
inferredcites →https://doi.org/10.1016/j.molcel.2004.09.034openalex-snapshot
The INO80 Protein Controls Homologous Recombination in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.tig.2004.01.007openalex-snapshot
Tandem and segmental gene duplication and recombination in the evolution of plant disease resistance genes
inferredcites →https://doi.org/10.1016/j.tig.2004.07.004openalex-snapshot
Metabolic enzymes and coenzymes in transcription – a direct link between metabolism and transcription?
inferredcites →https://doi.org/10.1016/j.ydbio.2003.08.003openalex-snapshot
A transcriptional chain linking eye specification to terminal determination of cone cells in the Drosophila eye
inferredcites →https://doi.org/10.1016/j.ygeno.2003.08.013openalex-snapshot
LETM1, a gene deleted in Wolf–Hirschhorn syndrome, encodes an evolutionarily conserved mitochondrial protein
inferredcites →https://doi.org/10.1016/s0012-1606(03)00127-1openalex-snapshot
A somatic role for eyes absent (eya) and sine oculis (so) in drosophila spermatocyte development
inferredcites →https://doi.org/10.1016/s0014-5793(00)02335-8openalex-snapshot
Modulation of WHSC2 expression in human endothelial cells
inferredcites →https://doi.org/10.1016/s0021-9258(19)84789-0openalex-snapshot
Sequence-specific pausing during in vitro DNA replication on double-stranded DNA templates
inferredcites →https://doi.org/10.1016/s0021-9924(03)00037-6openalex-snapshot
Speech and language in Wolf-Hirschhorn syndrome: a case-study
inferredcites →https://doi.org/10.1016/s0092-8674(00)00073-8openalex-snapshot
p53AIP1, a Potential Mediator of p53-Dependent Apoptosis, and Its Regulation by Ser-46-Phosphorylated p53
inferredcites →https://doi.org/10.1016/s0092-8674(00)81476-2openalex-snapshot
Reduced Apoptosis and Cytochrome c–Mediated Caspase Activation in Mice Lacking Caspase 9
inferredcites →https://doi.org/10.1016/s0092-8674(00)81477-4openalex-snapshot
Differential Requirement for Caspase 9 in Apoptotic Pathways In Vivo
inferredcites →https://doi.org/10.1016/s0092-8674(00)81733-xopenalex-snapshot
Apaf1 Is Required for Mitochondrial Pathways of Apoptosis and Brain Development
inferredcites →https://doi.org/10.1016/s0092-8674(01)00334-8openalex-snapshot
Endoreplication Cell Cycles
inferredcites →https://doi.org/10.1016/s0378-1119(01)00496-6openalex-snapshot
Molecular characterization of homologues of both subunits A (SPO11) and B of the archaebacterial topoisomerase 6 in plants
inferredcites →https://doi.org/10.1016/s0378-1119(03)00552-3openalex-snapshot
Transfer RNA paralogs: evidence for genetic code-amino acid biosynthesis coevolution and an archaeal root of life
inferredcites →https://doi.org/10.1016/s0378-1119(97)00104-2openalex-snapshot
Molecular characterization of the C-3 DNA puff gene of Rhynchosciara americana
inferredcites →https://doi.org/10.1016/s0925-4773(00)00415-9openalex-snapshot
Isolation and characterization of AINT: a novel ARNT interacting protein expressed during murine embryonic development
inferredcites →https://doi.org/10.1016/s0925-4773(98)00052-5openalex-snapshot
Dual functions of the Drosophila eyes absent gene in the eye and embryo
inferredcites →https://doi.org/10.1016/s0959-437x(05)80091-7openalex-snapshot
Developmentally regulated processing and replication of the Tetrahymena rDNA minichromosome
inferredcites →https://doi.org/10.1016/s0960-9822(01)00444-4openalex-snapshot
Origin recognition complex binding to a metazoan replication origin
inferredcites →https://doi.org/10.1016/s0960-9822(02)00768-6openalex-snapshot
Identification of Tah11/Sid2 as the Ortholog of the Replication Licensing Factor Cdt1 in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1016/s0960-9822(98)70089-2openalex-snapshot
Fluctuations in Cyclin E levels are required for multiple rounds of endocycle S phase in Drosophila
inferredcites →https://doi.org/10.1016/s0960-9822(98)70090-9openalex-snapshot
Continuous Cyclin E expression inhibits progression through endoreduplication cycles in Drosophila
inferredcites →https://doi.org/10.1016/s0969-2126(02)00769-4openalex-snapshot
Structure of the Retinal Determination Protein Dachshund Reveals a DNA Binding Motif
inferredcites →https://doi.org/10.1016/s1097-2765(00)00136-2openalex-snapshot
The Combined Functions of Proapoptotic Bcl-2 Family Members Bak and Bax Are Essential for Normal Development of Multiple Tissues
inferredcites →https://doi.org/10.1016/s1097-2765(00)80457-8openalex-snapshot
twin of eyeless, a Second Pax-6 Gene of Drosophila, Acts Upstream of eyeless in the Control of Eye Development
inferredcites →https://doi.org/10.1016/s1097-2765(01)00284-2openalex-snapshot
p53DINP1, a p53-Inducible Gene, Regulates p53-Dependent Apoptosis
inferredcites →https://doi.org/10.1016/s1097-2765(03)00050-9openalex-snapshot
p53 Has a Direct Apoptogenic Role at the Mitochondria
inferredcites →https://doi.org/10.1016/s1097-2765(03)00278-8openalex-snapshot
A 3′ Exonuclease that Specifically Interacts with the 3′ End of Histone mRNA
inferredcites →https://doi.org/10.1016/s1360-1385(00)01861-6openalex-snapshot
Plant meiosis: the means to 1N
inferredcites →https://doi.org/10.1016/s1360-1385(03)00002-5openalex-snapshot
Re-engineering plant gene targeting
inferredcites →https://doi.org/10.1016/s1383-5718(99)00147-3openalex-snapshot
Radiation hazard caused by the Chernobyl accident in inhabited areas of Ukraine can be monitored by transgenic plants
inferredcites →https://doi.org/10.1016/s1534-5807(01)00011-9openalex-snapshot
Eyes Absent Mediates Cross-Talk between Retinal Determination Genes and the Receptor Tyrosine Kinase Signaling Pathway
inferredcites →https://doi.org/10.1016/s1535-6108(02)00127-7openalex-snapshot
Distinct BH3 domains either sensitize or activate mitochondrial apoptosis, serving as prototype cancer therapeutics
inferredcites →https://doi.org/10.1016/s1568-7864(02)00093-9openalex-snapshot
Arabidopsis thaliana, a versatile model system for study of eukaryotic genome-maintenance functions
inferredcites →https://doi.org/10.1023/a:1016047231597openalex-snapshot
Molecular cloning and characterization of RAD51-like genes from Arabidopsis thaliana
inferredcites →https://doi.org/10.1034/j.1399-0004.2003.00126.xopenalex-snapshot
Population data suggest that deletions of 1p36 are a relatively common chromosome abnormality
inferredcites →https://doi.org/10.1038/12722openalex-snapshot
Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia
inferredcites →https://doi.org/10.1038/23730openalex-snapshot
Bid-deficient mice are resistant to Fas-induced hepatocellular apoptosis
inferredcites →https://doi.org/10.1038/329853a0openalex-snapshot
Duplication and remoulding of tRNA genes during the evolutionary rearrangement of mitochondrial genomes
inferredcites →https://doi.org/10.1038/35007110openalex-snapshot
The Cdt1 protein is required to license DNA for replication in fission yeast
inferredcites →https://doi.org/10.1038/35017595openalex-snapshot
Elevated UV-B radiation reduces genome stability in plants
inferredcites →https://doi.org/10.1038/3505openalex-snapshot
Transgenic plants are sensitive bioindicators of nuclear pollution caused by the Chernobyl accident
inferredcites →https://doi.org/10.1038/35060086openalex-snapshot
DNA replication control through interaction of E2F–RB and the origin recognition complex
inferredcites →https://doi.org/10.1038/35078527openalex-snapshot
Apaf-1 is a transcriptional target for E2F and p53
inferredcites →https://doi.org/10.1038/356215a0openalex-snapshot
Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours
inferredcites →https://doi.org/10.1038/362847a0openalex-snapshot
p53 is required for radiation-induced apoptosis in mouse thymocytes
inferredcites →https://doi.org/10.1038/366701a0openalex-snapshot
p21 is a universal inhibitor of cyclin kinases
inferredcites →https://doi.org/10.1038/370220a0openalex-snapshot
p53-Dependent apoptosis in the absence of transcriptional activation of p53-target genes
inferredcites →https://doi.org/10.1038/377052a0openalex-snapshot
Patterning of the Caenorhabditis elegans head region by the Pax-6 family member vab-3
inferredcites →https://doi.org/10.1038/377055a0openalex-snapshot
Specification of sense-organ identity by a Caenorhabditis elegans Pax-6 homologue
inferredcites →https://doi.org/10.1038/385637a0openalex-snapshot
Bax suppresses tumorigenesis and stimulates apoptosis in vivo
inferredcites →https://doi.org/10.1038/387296a0openalex-snapshot
Mdm2 promotes the rapid degradation of p53
inferredcites →https://doi.org/10.1038/71743openalex-snapshot
Molecular mechanism for duplication 17p11.2— the homologous recombination reciprocal of the Smith-Magenis microdeletion
inferredcites →https://doi.org/10.1038/79102openalex-snapshot
Pidd, a new death-domain–containing protein, is induced by p53 and promotes apoptosis
inferredcites →https://doi.org/10.1038/79152openalex-snapshot
A transactivation-deficient mouse model provides insights into Trp53 regulation and function
inferredcites →https://doi.org/10.1038/89327openalex-snapshot
A sensitive transgenic plant system to detect toxic inorganic compounds in the environment
inferredcites →https://doi.org/10.1038/nature01228openalex-snapshot
Role for a Drosophila Myb-containing protein complex in site-specific DNA replication
inferredcites →https://doi.org/10.1038/nature01683openalex-snapshot
Pathogen-induced systemic plant signal triggers DNA rearrangements
inferredcites →https://doi.org/10.1038/nature02083openalex-snapshot
Eya protein phosphatase activity regulates Six1–Dach–Eya transcriptional effects in mammalian organogenesis
inferredcites →https://doi.org/10.1038/nature02093openalex-snapshot
Eyes absent represents a class of protein tyrosine phosphatases
inferredcites →https://doi.org/10.1038/nature02097openalex-snapshot
The transcription factor Eyes absent is a protein tyrosine phosphatase
inferredcites →https://doi.org/10.1038/nature02514openalex-snapshot
The ubiquitin ligase COP1 is a critical negative regulator of p53
inferredcites →https://doi.org/10.1038/nature02694openalex-snapshot
Chromatin regulates origin activity in Drosophila follicle cells
inferredcites →https://doi.org/10.1038/nbt737openalex-snapshot
Efficient gene targeting by homologous recombination in rice
inferredcites →https://doi.org/10.1038/ncb1123openalex-snapshot
Mitochondrial p53 activates Bak and causes disruption of a Bak–Mcl1 complex
inferredcites →https://doi.org/10.1038/ng0297-157openalex-snapshot
A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family
inferredcites →https://doi.org/10.1038/ng0494-348openalex-snapshot
Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development
inferredcites →https://doi.org/10.1038/ng0496-390openalex-snapshot
Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3
inferredcites →https://doi.org/10.1038/ng1093openalex-snapshot
The codon 72 polymorphic variants of p53 have markedly different apoptotic potential
inferredcites →https://doi.org/10.1038/ng846openalex-snapshot
Pathogen stress increases somatic recombination frequency in Arabidopsis
inferredcites →https://doi.org/10.1038/nrc883openalex-snapshot
The Bcl2 family: regulators of the cellular life-or-death switch
inferredcites →https://doi.org/10.1038/nrg1207openalex-snapshot
Clues to catastrophic telomere loss in mammals from yeast telomere rapid deletion
inferredcites →https://doi.org/10.1038/nrg727openalex-snapshot
The complex structure and dynamic evolution of human subtelomeres
inferredcites →https://doi.org/10.1038/nrm1202openalex-snapshot
Mechanism and regulation of human non-homologous DNA end-joining
inferredcites →https://doi.org/10.1038/sj.cdd.4401180openalex-snapshot
p53 triggers apoptosis in oncogene-expressing fibroblasts by the induction of Noxa and mitochondrial Bax translocation
inferredcites →https://doi.org/10.1038/sj.emboj.7600055openalex-snapshot
The Arabidopsis homologue of Xrcc3 plays an essential role in meiosis
inferredcites →https://doi.org/10.1038/sj.emboj.7600077openalex-snapshot
DNA topology, not DNA sequence, is a critical determinant for Drosophila ORC–DNA binding
inferredcites →https://doi.org/10.1038/sj.emboj.7600146openalex-snapshot
Brca2 is involved in meiosis in Arabidopsis thaliana as suggested by its interaction with Dmc1
inferredcites →https://doi.org/10.1038/sj.embor.7400256openalex-snapshot
SNM‐dependent recombinational repair of oxidatively induced DNA damage in Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/sj.onc.1201263openalex-snapshot
The polyproline region of p53 is required to activate apoptosis but not growth arrest
inferredcites →https://doi.org/10.1038/sj.onc.1204110openalex-snapshot
Loss of heterozygosity at 4p16.3 and mutation of FGFR3 in transitional cell carcinoma
inferredcites →https://doi.org/10.1039/b312466eopenalex-snapshot
A ‘molecular switchboard’—covalent modifications to proteins and their impact on transcription
inferredcites →https://doi.org/10.1042/0300-5127:0290684openalex-snapshot
Mechanisms of p53-dependent apoptosis
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00694.xopenalex-snapshot
AtRAD1, a plant homologue of human and yeast nucleotide excision repair endonucleases, is involved in dark repair of UV damages and recombination
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00707.xopenalex-snapshot
Repair of UV damage in plants by nucleotide excision repair: Arabidopsis UVH1 DNA repair gene is a homolog of Saccharomyces cerevisiae Rad1
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00867.xopenalex-snapshot
Elevated levels of intrachromosomal homologous recombination in Arabidopsis overexpressing the MIM gene
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00905.xopenalex-snapshot
A new hyperrecombinogenic mutant of Nicotiana tabacum
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.00928.xopenalex-snapshot
Disruption of the Arabidopsis RAD50 gene leads to plant sterility and MMS sensitivity
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01162.xopenalex-snapshot
The participation of AtXPB1, the XPB/RAD25 homologue gene from Arabidopsis thaliana, in DNA repair and plant development
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01183.xopenalex-snapshot
Gene targeting in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0336115100openalex-snapshot
Unique mitochondrial genome architecture in unicellular relatives of animals
inferredcites →https://doi.org/10.1073/pnas.0401139101openalex-snapshot
The Six1 homeoprotein stimulates tumorigenesis by reactivation of cyclin A1
inferredcites →https://doi.org/10.1073/pnas.0403286101openalex-snapshot
Suppression of tumorigenesis by the p53 target PUMA
inferredcites →https://doi.org/10.1073/pnas.040378897openalex-snapshot
Pw1/Peg3 is a potential cell death mediator and cooperates with Siah1a in p53-mediated apoptosis
inferredcites →https://doi.org/10.1073/pnas.0404110101openalex-snapshot
The Arabidopsis AtRAD51 gene is dispensable for vegetative development but required for meiosis
inferredcites →https://doi.org/10.1073/pnas.1533446100openalex-snapshot
Bad -deficient mice develop diffuse large B cell lymphoma
inferredcites →https://doi.org/10.1073/pnas.230251897openalex-snapshot
UV-damage-mediated induction of homologous recombination in Arabidopsis is dependent on photosynthetically active radiation
inferredcites →https://doi.org/10.1073/pnas.2435285100openalex-snapshot
Requirement of p53 targets in chemosensitization of colonic carcinoma to death ligand therapy
inferredcites →https://doi.org/10.1073/pnas.2535036100openalex-snapshot
Changing identities: tRNA duplication and remolding within animal mitochondrial genomes
inferredcites →https://doi.org/10.1073/pnas.2627984100openalex-snapshot
PUMA mediates the apoptotic response to p53 in colorectal cancer cells
inferredcites →https://doi.org/10.1073/pnas.60.2.553openalex-snapshot
Differential synthesis of the genes for ribosomal RNA during amphibian oögenesis.
inferredcites →https://doi.org/10.1073/pnas.71.5.1819openalex-snapshot
The Amplified Ribosomal DNA of Dytiscid Beetles
inferredcites →https://doi.org/10.1073/pnas.71.8.3082openalex-snapshot
A Small Number of Cistrons for Ribosomal RNA in the Germinal Nucleus of a Eukaryote, Tetrahymena pyriformis
inferredcites →https://doi.org/10.1073/pnas.72.5.1909openalex-snapshot
A Co-Evolution Theory of the Genetic Code
inferredcites →https://doi.org/10.1073/pnas.77.5.2791openalex-snapshot
Convergence and minimal mutation criteria for evaluating early events in tRNA evolution.
inferredcites →https://doi.org/10.1073/pnas.83.10.3341openalex-snapshot
Trans-acting amplification mutants and other eggshell mutants of the third chromosome in Drosophila melanogaster.
inferredcites →https://doi.org/10.1073/pnas.89.11.4913openalex-snapshot
The highest gene concentrations in the human genome are in telomeric bands of metaphase chromosomes.
inferredcites →https://doi.org/10.1073/pnas.90.12.5613openalex-snapshot
Lethality induced by a single site-specific double-strand break in a dispensable yeast plasmid.
inferredcites →https://doi.org/10.1073/pnas.93.18.9970openalex-snapshot
Environmental stress sensitivity of an ascorbic acid-deficient Arabidopsis mutant.
inferredcites →https://doi.org/10.1073/pnas.93.26.15335openalex-snapshot
Identification of a novel p53 functional domain that is necessary for efficient growth suppression
inferredcites →https://doi.org/10.1073/pnas.94.1.328openalex-snapshot
An Arabidopsis photolyase mutant is hypersensitive to ultraviolet-B radiation
inferredcites →https://doi.org/10.1073/pnas.94.6.2345openalex-snapshot
bax -deficiency promotes drug resistance and oncogenic transformation by attenuating p53-dependent apoptosis
inferredcites →https://doi.org/10.1073/pnas.94.8.3888openalex-snapshot
The k43 gene, required for chorion gene amplification and diploid cell chromosome replication, encodes the Drosophila homolog of yeast origin recognition complex subunit 2
inferredcites →https://doi.org/10.1073/pnas.95.24.14220openalex-snapshot
Expression of myogenin during embryogenesis is controlled by Six/ sine oculis homeoproteins through a conserved MEF3 binding site
inferredcites →https://doi.org/10.1073/pnas.96.18.10302openalex-snapshot
Rare germinal unequal crossing-over leading to recombinant gene formation and gene duplication in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.97.22.12050openalex-snapshot
Peg3/Pw1 promotes p53-mediated apoptosis by inducing Bax translocation from cytosol to mitochondria
inferredcites →https://doi.org/10.1073/pnas.97.7.3358openalex-snapshot
RecA stimulates sister chromatid exchange and the fidelity of double-strand break repair, but not gene targeting, in plants transformed by Agrobacterium
inferredcites →https://doi.org/10.1073/pnas.98.4.1711openalex-snapshot
RAD50 function is essential for telomere maintenance in Arabidopsis
inferredcites →https://doi.org/10.1074/jbc.274.48.33985openalex-snapshot
Mechanistic Studies of Phosphoserine Phosphatase, an Enzyme Related to P-type ATPases
inferredcites →https://doi.org/10.1074/jbc.275.10.7337openalex-snapshot
p53 Induces Apoptosis by Caspase Activation through Mitochondrial Cytochrome c Release
inferredcites →https://doi.org/10.1074/jbc.275.21.16202openalex-snapshot
Death Signal-induced Localization of p53 Protein to Mitochondria
inferredcites →https://doi.org/10.1074/jbc.c300418200openalex-snapshot
Cut5 Is Required for the Binding of Atr and DNA Polymerase α to Genotoxin-damaged Chromatin
inferredcites →https://doi.org/10.1074/jbc.m003360200openalex-snapshot
Physical and Functional Interaction between p53 Mutants and Different Isoforms of p73
inferredcites →https://doi.org/10.1074/jbc.m004577200openalex-snapshot
The α Subunits of Gz and Gi Interact with the eyes absent Transcription Cofactor Eya2, Preventing Its Interaction with the Six Class of Homeodomain-containing Proteins
inferredcites →https://doi.org/10.1074/jbc.m004714200openalex-snapshot
Essential Role for Caspase-8 in Transcription-independent Apoptosis Triggered by p53
inferredcites →https://doi.org/10.1074/jbc.m106643200openalex-snapshot
Transcriptional Repression of the Anti-apoptoticsurvivin Gene by Wild Type p53
inferredcites →https://doi.org/10.1074/jbc.m109360200openalex-snapshot
Galectin-7 (PIG1) Exhibits Pro-apoptotic Function through JNK Activation and Mitochondrial Cytochrome cRelease
inferredcites →https://doi.org/10.1074/jbc.m313987200openalex-snapshot
Transforming Acidic Coiled-coil Protein 3 (TACC3) Controls Friend of GATA-1 (FOG-1) Subcellular Localization and Regulates the Association between GATA-1 and FOG-1 during Hematopoiesis
inferredcites →https://doi.org/10.1074/jbc.m403335200openalex-snapshot
The Cytoplasmic Tyrosine Kinase Pyk2 as a Novel Effector of Fibroblast Growth Factor Receptor 3 Activation
inferredcites →https://doi.org/10.1074/jbc.m403607200openalex-snapshot
The LETM1/YOL027 Gene Family Encodes a Factor of the Mitochondrial K+ Homeostasis with a Potential Role in the Wolf-Hirschhorn Syndrome
inferredcites →https://doi.org/10.1074/jbc.m404130200openalex-snapshot
A Classic Zinc Finger from Friend of GATA Mediates an Interaction with the Coiled-coil of Transforming Acidic Coiled-coil 3
inferredcites →https://doi.org/10.1080/10635150500221044openalex-snapshot
Poriferan mtDNA and Animal Phylogeny Based on Mitochondrial Gene Arrangements
inferredcites →https://doi.org/10.1080/15227950307697openalex-snapshot
Mouse Models Orthologous to FGFR3-Related Skeletal Dysplasias
inferredcites →https://doi.org/10.1083/jcb.110.4.903openalex-snapshot
Multiple replication origins are used during Drosophila chorion gene amplification.
inferredcites →https://doi.org/10.1083/jcb.200207046openalex-snapshot
Visualization of replication initiation and elongation in Drosophila
inferredcites →https://doi.org/10.1083/jcb.200207090openalex-snapshot
The Xenopus Xmus101 protein is required for the recruitment of Cdc45 to origins of DNA replication
inferredcites →https://doi.org/10.1084/jem.188.11.2033openalex-snapshot
p53 Activates the CD95 (APO-1/Fas) Gene in Response to DNA Damage by Anticancer Drugs
inferredcites →https://doi.org/10.1084/jem.191.1.195openalex-snapshot
Ionizing Radiation and Chemotherapeutic Drugs Induce Apoptosis in Lymphocytes in the Absence of FAS or Fadd/Mort1 Signaling
inferredcites →https://doi.org/10.1086/341610openalex-snapshot
Heterozygous Submicroscopic Inversions Involving Olfactory Receptor–Gene Clusters Mediate the Recurrent t(4;8)(p16;p23) Translocation
inferredcites →https://doi.org/10.1086/367925openalex-snapshot
Mapping the Wolf-Hirschhorn Syndrome Phenotype Outside the Currently Accepted WHS Critical Region and Defining a New Critical Region, WHSCR-2
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Four new Scopalina from Southern California: the first Scopalinida (Porifera: Demospongiae) from the temperate Eastern Pacific
inferred← citeshttps://doi.org/10.1002/9780470015902.a0022846openalex-snapshot
Deciphering the Evolution of the Mitochondrial Genetic Code in Arthropods
inferred← citeshttps://doi.org/10.1002/wrna.103openalex-snapshot
Structure of transfer RNAs: similarity and variability
inferred← citeshttps://doi.org/10.1007/978-3-642-22380-8_17openalex-snapshot
Mitochondrial tRNA Structure, Identity, and Evolution of the Genetic Code
inferred← citeshttps://doi.org/10.1007/s00227-005-0134-yopenalex-snapshot
Low variation in partial cytochrome oxidase subunit I (COI) mitochondrial sequences in the coralline demosponge Astrosclera willeyana across the Indo-Pacific
inferred← citeshttps://doi.org/10.1007/s00239-005-0313-yopenalex-snapshot
Patterns of Group I Intron Presence in Nuclear SSU rDNA of the Lichen Family Parmeliaceae
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Mitochondrial Genome of Savalia savaglia (Cnidaria, Hexacorallia) and Early Metazoan Phylogeny
inferred← citeshttps://doi.org/10.1007/s00239-007-9037-5openalex-snapshot
Structure and Evolution of the Atypical Mitochondrial Genome of Armadillidium vulgare (Isopoda, Crustacea)
inferred← citeshttps://doi.org/10.1007/s00239-007-9042-8openalex-snapshot
The Mitochondrial Genome of the Screamer Louse Bothriometopus (Phthiraptera: Ischnocera): Effects of Extensive Gene Rearrangements on the Evolution of the Genome
inferred← citeshttps://doi.org/10.1007/s00294-009-0273-7openalex-snapshot
The complete mitochondrial genome sequence of the liverwort Pleurozia purpurea reveals extremely conservative mitochondrial genome evolution in liverworts
inferred← citeshttps://doi.org/10.1007/s10750-008-9295-2openalex-snapshot
Contrasting genetic structure of two Pacific Hymeniacidon species
inferred← citeshttps://doi.org/10.1016/j.cbd.2015.08.001openalex-snapshot
Complete mitochondrial genome of Anadara vellicata (Bivalvia: Arcidae): A unique gene order and large atypical non-coding region
inferred← citeshttps://doi.org/10.1016/j.gene.2007.12.010openalex-snapshot
Recruitment of mitochondrial tRNA genes as auxiliary variability markers for both intra- and inter-species analysis: The paradigm of brown hare (Lepus europaeus)
inferred← citeshttps://doi.org/10.1016/j.gene.2008.01.001openalex-snapshot
Mitochondrial genome of Suberites domuncula: Palindromes and inverted repeats are abundant in non-coding regions
inferred← citeshttps://doi.org/10.1016/j.gene.2010.12.009openalex-snapshot
Gene recruitment – A common mechanism in the evolution of transfer RNA gene families
inferred← citeshttps://doi.org/10.1016/j.gene.2012.05.039openalex-snapshot
Small inverted repeats drive mitochondrial genome evolution in Lake Baikal sponges
inferred← citeshttps://doi.org/10.1016/j.gene.2012.07.032openalex-snapshot
New features of Asian Crassostrea oyster mitochondrial genomes: A novel alloacceptor tRNA gene recruitment and two novel ORFs
inferred← citeshttps://doi.org/10.1016/j.gene.2012.08.037openalex-snapshot
A unique tRNA gene family and a novel, highly expressed ORF in the mitochondrial genome of the silver-lip pearl oyster, Pinctada maxima (Bivalvia: Pteriidae)
inferred← citeshttps://doi.org/10.1016/j.gene.2013.09.077openalex-snapshot
Evolution of the tRNA gene family in mitochondrial genomes of five Meretrix clams (Bivalvia, Veneridae)
inferred← citeshttps://doi.org/10.1016/j.gene.2014.09.033openalex-snapshot
Shotgun assembly of the assassin bug Brontostoma colossus mitochondrial genome (Heteroptera, Reduviidae)
inferred← citeshttps://doi.org/10.1016/j.gene.2015.01.065openalex-snapshot
Mitochondrial genome plasticity among species of the nematode genus Meloidogyne (Nematoda: Tylenchina)
inferred← citeshttps://doi.org/10.1016/j.gene.2021.146102openalex-snapshot
A novel gene order and remolded tRNAs revealed in the mitogenome of Asian gecarcinucid freshwater crabs (Brachyura, Gecarcinucidae)
inferred← citeshttps://doi.org/10.1016/j.ijpara.2005.10.010openalex-snapshot
Parasite histories and novel phylogenetic tools: Alternative approaches to inferring parasite evolution from molecular markers
inferred← citeshttps://doi.org/10.1016/j.mito.2010.01.004openalex-snapshot
MitoZoa: A curated mitochondrial genome database of metazoans for comparative genomics studies
inferred← citeshttps://doi.org/10.1016/j.ympev.2005.12.012openalex-snapshot
The complete mitochondrial genomes of Schistosoma haematobium and Schistosoma spindale and the evolutionary history of mitochondrial genome changes among parasitic flatworms
inferred← citeshttps://doi.org/10.1016/j.ympev.2007.12.004openalex-snapshot
The complete mitochondrial genome of the demosponge Negombata magnifica (Poecilosclerida)
inferred← citeshttps://doi.org/10.1016/j.ympev.2008.05.014openalex-snapshot
Reconstructing ordinal relationships in the Demospongiae using mitochondrial genomic data
inferred← citeshttps://doi.org/10.1016/j.ympev.2012.08.023openalex-snapshot
MITOS: Improved de novo metazoan mitochondrial genome annotation
inferred← citeshttps://doi.org/10.1016/j.ympev.2012.10.020openalex-snapshot
Genetic aspects of mitochondrial genome evolution
inferred← citeshttps://doi.org/10.1016/j.ympev.2019.106710openalex-snapshot
Hidden cases of tRNA gene duplication and remolding in mitochondrial genomes of amphipods
inferred← citeshttps://doi.org/10.1017/s0025315410002122openalex-snapshot
New polymorphic mitochondrial markers for sponge phylogeography
inferred← citeshttps://doi.org/10.1038/s41598-024-57736-1openalex-snapshot
The completed mitochondrial genomes of Globodera vulgaris reveals new insights into the genus Globodera phylogeny
inferred← citeshttps://doi.org/10.1038/srep25634openalex-snapshot
Mitochondrial genomes of praying mantises (Dictyoptera, Mantodea): rearrangement, duplication, and reassignment of tRNA genes
inferred← citeshttps://doi.org/10.1073/pnas.0602076103openalex-snapshot
Mitochondrial genome of Trichoplax adhaerens supports Placozoa as the basal lower metazoan phylum
inferred← citeshttps://doi.org/10.1093/gbe/evaa213openalex-snapshot
Mitochondrial Genome Evolution of Placozoans: Gene Rearrangements and Repeat Expansions
inferred← citeshttps://doi.org/10.1093/gbe/evaf020openalex-snapshot
Pervasive Mitochondrial tRNA Gene Loss in Clade B of Haplosclerid Sponges (Porifera, Demospongiae)
inferred← citeshttps://doi.org/10.1093/gbe/evt081openalex-snapshot
Deep Sequencing of Mixed Total DNA without Barcodes Allows Efficient Assembly of Highly Plastic Ascidian Mitochondrial Genomes
inferred← citeshttps://doi.org/10.1093/gbe/evv124openalex-snapshot
Cytonuclear Interactions in the Evolution of Animal Mitochondrial tRNA Metabolism
inferred← citeshttps://doi.org/10.1093/gbe/evw187openalex-snapshot
Comparative Large-Scale Mitogenomics Evidences Clade-Specific Evolutionary Trends in Mitochondrial DNAs of Bivalvia
inferred← citeshttps://doi.org/10.1093/gbe/evw195openalex-snapshot
Animal Mitochondrial DNA as We Do Not Know It: mt-Genome Organization and Evolution in Nonbilaterian Lineages
inferred← citeshttps://doi.org/10.1093/gbe/evx007openalex-snapshot
The Mitochondrial Genome of the Guanaco Louse, Microthoracius praelongiceps: Insights into the Ancestral Mitochondrial Karyotype of Sucking Lice (Anoplura, Insecta)
inferred← citeshttps://doi.org/10.1093/icb/icj056openalex-snapshot
Lophotrochozoan mitochondrial genomes
inferred← citeshttps://doi.org/10.1093/icb/icm042openalex-snapshot
Key transitions in animal evolution
inferred← citeshttps://doi.org/10.1093/icb/icm045openalex-snapshot
Key transitions in animal evolution: a mitochondrial DNA perspective
inferred← citeshttps://doi.org/10.1093/molbev/msi108openalex-snapshot
Mitochondrial Genomes of Two Demosponges Provide Insights into An Early Stage of Animal Evolution
inferred← citeshttps://doi.org/10.1093/molbev/msl154openalex-snapshot
Mitochondrial Diversity of Early-Branching Metazoa Is Revealed by the Complete mt Genome of a Haplosclerid Demosponge
inferred← citeshttps://doi.org/10.1093/molbev/msl167openalex-snapshot
Mitochondrial Genome of the Homoscleromorph Oscarella carmela (Porifera, Demospongiae) Reveals Unexpected Complexity in the Common Ancestor of Sponges and Other Animals
inferred← citeshttps://doi.org/10.1093/molbev/msm054openalex-snapshot
The Mitochondrial Genome of the Lizard Calotes versicolor and a Novel Gene Inversion in South Asian Draconine Agamids
inferred← citeshttps://doi.org/10.1093/molbev/msn173openalex-snapshot
Coevolution of Codon Usage and tRNA Genes Leads to Alternative Stable States of Biased Codon Usage
inferred← citeshttps://doi.org/10.1093/molbev/msp317openalex-snapshot
Rapid Proliferation of Repetitive Palindromic Elements in mtDNA of the Endemic Baikalian Sponge Lubomirskia baicalensis
inferred← citeshttps://doi.org/10.1093/molbev/msv029openalex-snapshot
Evolution of tRNA Repertoires in Bacillus Inferred with OrthoAlign
inferred← citeshttps://doi.org/10.1093/nar/gki757openalex-snapshot
The Rhodomonas salina mitochondrial genome: bacteria-like operons, compact gene arrangement and complex repeat region
inferred← citeshttps://doi.org/10.1093/nar/gkr073openalex-snapshot
An unusual tRNAThr derived from tRNAHis reassigns in yeast mitochondria the CUN codons to threonine
inferred← citeshttps://doi.org/10.1093/nar/gkv746openalex-snapshot
Towards a comprehensive picture of alloacceptor tRNA remolding in metazoan mitochondrial genomes
inferred← citeshttps://doi.org/10.1101/001875openalex-snapshot
How and where to look for tRNAs in Metazoan mitochondrial genomes, and what you might find when you get there
inferred← citeshttps://doi.org/10.1101/793372openalex-snapshot
Phylogenetic relationships of heteroscleromorph demosponges and the affinity of the genus Myceliospongia (Demospongiae incertae sedis )
inferred← citeshttps://doi.org/10.1111/j.1471-8286.2005.01259.xopenalex-snapshot
CO1 phylogenies in diploblasts and the ‘Barcoding of Life’— are we sequencing a suboptimal partition?
inferred← citeshttps://doi.org/10.1111/jzs.12164openalex-snapshot
Characterization of the first mitochondrial genome of a catenulid flatworm:Stenostomum leucops(Platyhelminthes)
inferred← citeshttps://doi.org/10.1134/s1022795410120100openalex-snapshot
Phylogenetic position of sponges from Chagatai and Tore-Khol lakes
inferred← citeshttps://doi.org/10.1139/g2012-008openalex-snapshot
Widespread atypical mitochondrial DNA structure in isopods (Crustacea, Peracarida) related to a constitutive heteroplasmy in terrestrial species
inferred← citeshttps://doi.org/10.1139/z06-003openalex-snapshot
Systematics and evolution of Demospongiae
inferred← citeshttps://doi.org/10.11646/zootaxa.2901.1.2openalex-snapshot
A new species of Sigmaxinella Dendy, 1897 (Demospongiae, Poecilosclerida, Desmacellidae) from the Tasman Sea
inferred← citeshttps://doi.org/10.1186/1471-2148-10-288openalex-snapshot
Diversity of sponge mitochondrial introns revealed by cox 1sequences of Tetillidae
inferred← citeshttps://doi.org/10.1186/1471-2148-10-300openalex-snapshot
Mitochondrial genome evolution in fire ants (Hymenoptera: Formicidae)
inferred← citeshttps://doi.org/10.1186/1471-2148-10-309openalex-snapshot
The phylogenetic position of Acoela as revealed by the complete mitochondrial genome of Symsagittifera roscoffensis
inferred← citeshttps://doi.org/10.1186/1471-2148-6-71openalex-snapshot
Putative cross-kingdom horizontal gene transfer in sponge (Porifera) mitochondria
inferred← citeshttps://doi.org/10.1186/1471-2148-7-155openalex-snapshot
The mitochondrial genome of Phallusia mammillata and Phallusia fumigata (Tunicata, Ascidiacea): high genome plasticity at intra-genus level
inferred← citeshttps://doi.org/10.1186/1471-2164-10-591openalex-snapshot
The mitochondrial genomes of sponges provide evidence for multiple invasions by Repetitive Hairpin-forming Elements (RHE)
inferred← citeshttps://doi.org/10.1186/1471-2164-11-440openalex-snapshot
Sessile snails, dynamic genomes: gene rearrangements within the mitochondrial genome of a family of caenogastropod molluscs
inferred← citeshttps://doi.org/10.1186/1471-2164-9-33openalex-snapshot
The mitochondrial genome of the hexactinellid sponge Aphrocallistes vastus: Evidence for programmed translational frameshifting
inferred← citeshttps://doi.org/10.1186/1471-2164-9-610openalex-snapshot
Comparative and phylogenomic studies on the mitochondrial genomes of Pentatomomorpha (Insecta: Hemiptera: Heteroptera)
inferred← citeshttps://doi.org/10.1186/s12864-016-3357-zopenalex-snapshot
Evolution of mitochondrial genomes in Baikalian amphipods
inferred← citeshttps://doi.org/10.1186/s12864-020-6612-2openalex-snapshot
Operon-based approach for the inference of rRNA and tRNA evolutionary histories in bacteria
inferred← citeshttps://doi.org/10.1261/rna.041681.113openalex-snapshot
tRNA anticodon shifts in eukaryotic genomes
inferred← citeshttps://doi.org/10.1371/journal.pbio.0040127openalex-snapshot
Parallel Evolution of the Genetic Code in Arthropod Mitochondrial Genomes
inferred← citeshttps://doi.org/10.1371/journal.pgen.0030013openalex-snapshot
Comparative Genomics of Large Mitochondria in Placozoans
inferred← citeshttps://doi.org/10.1371/journal.pone.0002723openalex-snapshot
Seventeen New Complete mtDNA Sequences Reveal Extensive Mitochondrial Genome Evolution within the Demospongiae
inferred← citeshttps://doi.org/10.1371/journal.pone.0287281openalex-snapshot
Phylomitogenomics bolsters the high-level classification of Demospongiae (phylum Porifera)
inferred← citeshttps://doi.org/10.17537/2025.20.54openalex-snapshot
The Effect of Codon Reassignment on the Properties and Structure of the Mitochondrial Proteins of the Baikal Amphipods
inferred← citeshttps://doi.org/10.3109/19401736.2010.490832openalex-snapshot
The mitochondrial genome of the Japanese skeleton shrimpCaprella mutica(Amphipoda: Caprellidea) reveals a unique gene order and shared apomorphic translocations with Gammaridea
inferred← citeshttps://doi.org/10.6084/m9.figshare.12144363openalex-snapshot
Additional file 1 of Operon-based approach for the inference of rRNA and tRNA evolutionary histories in bacteria
inferred← citeshttps://doi.org/10.70675/98efd384zdb06z4edez89c2z7207630ad7aaopenalex-snapshot
Systématique, phylogénie et évolution moléculaires des Phyllostomidae (Mammalia, Chiroptera) : une approche mitogénomique comparative
inferred← citeshttps://doi.org/10.70675/ac55872az6638z4491z92f6z6a7906970c40openalex-snapshot
Biodiversité et maladies infectieuses : impact des activités humaines sur le cycle de transmission des leishmanioses en Guyane
inferred← citeshttps://doi.org/10.7717/peerj.18255openalex-snapshot
The complete mitochondrial DNA of the carnivorous sponge Lycopodina hypogea is putatively complemented by microDNAs
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