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DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/archpedi.1993.02160350086013openalex-snapshot
Velo-cardio-facial Syndrome
inferredcites →https://doi.org/10.1002/(sici)1097-0177(199608)206:4<379::aid-aja4>3.0.co;2-fopenalex-snapshot
Expression of the T-box family genes,Tbx1-Tbx5, during early mouse development
inferredcites →https://doi.org/10.1002/(sici)1097-0177(199710)210:2<146::aid-aja7>3.0.co;2-gopenalex-snapshot
Segmental identity can change independently in the hindbrain and rhombencephalic neural crest
inferredcites →https://doi.org/10.1002/ajmg.1320450307openalex-snapshot
Velo‐cardio‐facial syndrome: A review of 120 patients
inferredcites →https://doi.org/10.1006/geno.1997.4829openalex-snapshot
Isolation and Characterization of a Gene from the DiGeorge Chromosomal Region Homologous to the MouseTbx1Gene
inferredcites →https://doi.org/10.1016/0168-9525(86)90275-1openalex-snapshot
Manipulating the mouse embryo: A laboratory manual
inferredcites →https://doi.org/10.1038/43900openalex-snapshot
Congenital heart disease in mice deficient for the DiGeorge syndrome region
inferredcites →https://doi.org/10.1038/71634openalex-snapshot
Mutation of PAX9 is associated with oligodontia
inferredcites →https://doi.org/10.1038/74224openalex-snapshot
Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification
inferredcites →https://doi.org/10.1038/74231openalex-snapshot
Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
inferredcites →https://doi.org/10.1038/ng0794-383openalex-snapshot
An ancient family of embryonically expressed mouse genes sharing a conserved protein motif with the T locus
inferredcites →https://doi.org/10.1073/pnas.90.18.8424openalex-snapshot
Derivation of completely cell culture-derived mice from early-passage embryonic stem cells.
inferredcites →https://doi.org/10.1073/pnas.95.17.9991openalex-snapshot
Catechol- O -methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior
inferredcites →https://doi.org/10.1073/pnas.97.18.10090openalex-snapshot
Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/ DiGeorge syndrome region
inferredcites →https://doi.org/10.1089/gte.1997.1.99openalex-snapshot
The 22q11.2 Deletion: Screening, Diagnostic Workup, and Outcome of Results; Report on 181 Patients
inferredcites →https://doi.org/10.1093/hmg/6.2.237openalex-snapshot
Cloning and Developmental Expression Analysis of Chick Hira (Chira), a Candidate Gene for DiGeorge Syndrome
inferredcites →https://doi.org/10.1093/hmg/6.2.247openalex-snapshot
The Murine Homologue of HIRA, a DiGeorge Syndrome Candidate Gene, Is Expressed in Embryonic Structures Affected in Human CATCH22 Patients
inferredcites →https://doi.org/10.1093/hmg/7.12.1835openalex-snapshot
Functional analysis of Gscl in the pathogenesis of the DiGeorge and velocardiofacial syndromes
inferredcites →https://doi.org/10.1093/hmg/7.12.1841openalex-snapshot
Goosecoid-like (GSCL), a candidate gene for velocardiofacial syndrome, is not essential for normal mouse development
inferredcites →https://doi.org/10.1093/hmg/8.12.2229openalex-snapshot
Deletion of 150 kb in the Minimal Digeorge/Velocardiofacial Syndrome Critical Region in Mouse
inferredcites →https://doi.org/10.1101/gad.12.17.2735openalex-snapshot
Pax9 -deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities
inferredcites →https://doi.org/10.1126/science.283.5405.1158openalex-snapshot
A Molecular Pathway Revealing a Genetic Basis for Human Cardiac and Craniofacial Defects
inferredcites →https://doi.org/10.1136/jmg.32.9.746openalex-snapshot
Monozygotic twins with chromosome 22q11 deletion and discordant phenotype.
inferredcites →https://doi.org/10.1161/01.res.84.2.127openalex-snapshot
HIRA, a DiGeorge Syndrome Candidate Gene, Is Required for Cardiac Outflow Tract Septation
inferredcites →https://doi.org/10.1242/dev.127.9.1869openalex-snapshot
Migration of cardiac neural crest cells in Splotch embryos
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4122571openalex-extracted
APJ+ Cells in the SHF Contribute to Aorta and Pulmonary Trunk Through APJ and Canonical WNT Signaling Pathways
inferred← citeshttps://doi.org/10.1002/1096-8628(20011001)103:2<172::aid-ajmg1524>3.0.co;2-0openalex-snapshot
Benign idiopathic partial seizures in the velocardiofacial syndrome: Report of two cases
inferred← citeshttps://doi.org/10.1002/9780470015902.a0006074.pub2openalex-snapshot
22q11 Deletion Syndrome: A Role for Tbx1 in Pharynx and Cardiovascular Development
inferred← citeshttps://doi.org/10.1002/9780470015902.a0026850openalex-snapshot
At the Heart of a Complex Disease ‘Molecular Genetics of Congenital Heart Disease’
inferred← citeshttps://doi.org/10.1002/9780470090121.ch4openalex-snapshot
Identification and Analysis of Genes Involved in Congenital Malformation Syndromes
inferred← citeshttps://doi.org/10.1002/9780470988664.ch18openalex-snapshot
Tbx5 Specifies the Left/Right Ventricles and Ventricular Septum Position During Cardiogenesis
inferred← citeshttps://doi.org/10.1002/9780470988664.ch32openalex-snapshot
Molecular Mechanisms Regulating Tissue‐Specific Expression of Tbx1
inferred← citeshttps://doi.org/10.1002/9780470988664.ch33openalex-snapshot
Tbx1and Digeorge Syndrome: A Genetic Link between Cardiovascular and Pharyngeal Development
inferred← citeshttps://doi.org/10.1002/9780470988664.ch34openalex-snapshot
New Insights into the Role ofTbx1in the Digeorge Mouse Model
inferred← citeshttps://doi.org/10.1002/9780470988664.ch58openalex-snapshot
T‐Box Gene Family and Congenital Cardiovascular Anomalies
inferred← citeshttps://doi.org/10.1002/9780470988664.part8openalex-snapshot
Role of Neural Crest Cells in Cardiovascular Development
inferred← citeshttps://doi.org/10.1002/9781118498026.ch5openalex-snapshot
Craniofacial Muscle Development
inferred← citeshttps://doi.org/10.1002/9781119624608.ch7openalex-snapshot
Hematopoietic and Lymphoid Tissues
inferred← citeshttps://doi.org/10.1002/9781119847212.ch4openalex-snapshot
Causes of Genetic Conditions and Laboratory and Testing Approaches
inferred← citeshttps://doi.org/10.1002/9783527619689.ch23openalex-snapshot
Molecular Networks in Cardiac Development
inferred← citeshttps://doi.org/10.1002/9783527679348.ch06openalex-snapshot
Generation and Use of Transgenic Mice in Drug Discovery
inferred← citeshttps://doi.org/10.1002/ajmg.a.10914openalex-snapshot
DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion
inferred← citeshttps://doi.org/10.1002/ajmg.a.10980openalex-snapshot
Development of the pharyngeal arches
inferred← citeshttps://doi.org/10.1002/ajmg.a.30439openalex-snapshot
The genetics of tethered cord syndrome
inferred← citeshttps://doi.org/10.1002/ajmg.a.30601openalex-snapshot
Autosomal dominant inheritance of left ventricular outflow tract obstruction
inferred← citeshttps://doi.org/10.1002/ajmg.a.31250openalex-snapshot
T‐genes and limb bud development
inferred← citeshttps://doi.org/10.1002/ajmg.a.32762openalex-snapshot
Vertebral fusion in a patient with supernumerary‐der(22)t(11;22) syndrome
inferred← citeshttps://doi.org/10.1002/ajmg.a.32764openalex-snapshot
NR2F1 deletion in a patient with a de novo paracentric inversion, inv(5)(q15q33.2), and syndromic deafness
inferred← citeshttps://doi.org/10.1002/ajmg.a.34441openalex-snapshot
Chromosome 22q11.2 duplication is rare in a population‐based cohort of Danish children with cardiovascular malformations
inferred← citeshttps://doi.org/10.1002/ajmg.a.35517openalex-snapshot
Phenotypic variability of atypical 22q11.2 deletions not includingTBX1
inferred← citeshttps://doi.org/10.1002/ajmg.a.35881openalex-snapshot
Development of the human aortic arch system captured in an interactive three‐dimensional reference model
inferred← citeshttps://doi.org/10.1002/ajmg.a.36083openalex-snapshot
Co‐occurrence of 22q11 deletion syndrome and hdr syndrome
inferred← citeshttps://doi.org/10.1002/ajmg.a.37177openalex-snapshot
SNP microarray abnormalities in a cohort of 28 infants with congenital diaphragmatic hernia
inferred← citeshttps://doi.org/10.1002/ajmg.a.37872openalex-snapshot
Malformations of the middle and inner ear on CT imaging in 22q11 deletion syndrome
inferred← citeshttps://doi.org/10.1002/ajmg.a.37980openalex-snapshot
Congenital diaphragmatic hernia in 22q11.2 deletion syndrome
inferred← citeshttps://doi.org/10.1002/ajmg.a.38597openalex-snapshot
Variable immune deficiency related to deletion size in chromosome 22q11.2 deletion syndrome
inferred← citeshttps://doi.org/10.1002/ajmg.a.38662openalex-snapshot
Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well‐established knowledge to new frontiers
inferred← citeshttps://doi.org/10.1002/ajmg.a.38851openalex-snapshot
A case of severeTBCE‐negative hypoparathyroidism‐retardation‐dysmorphism syndrome: Case report and literature review
inferred← citeshttps://doi.org/10.1002/ajmg.a.40504openalex-snapshot
Molecular genetics of 22q11.2 deletion syndrome
inferred← citeshttps://doi.org/10.1002/ajmg.a.7openalex-snapshot
Vestibular dysfunction is a manifestation of 22q11.2 deletion syndrome
inferred← citeshttps://doi.org/10.1002/ajmg.c.31435openalex-snapshot
Developmental trajectories in 22q11.2 deletion syndrome
inferred← citeshttps://doi.org/10.1002/ar.25129openalex-snapshot
Transpositions of the great arteries versus aortic dextropositions. A review of some embryogenetic and morphological aspects
inferred← citeshttps://doi.org/10.1002/bdr2.2006openalex-snapshot
Bis‐diamine administration during pregnancy induces developmental and reproductive toxicities in rats
inferred← citeshttps://doi.org/10.1002/bdra.20604openalex-snapshot
Single nucleotide polymorphism discovery in TBX1 in individuals with and without 22q11.2 deletion syndrome
inferred← citeshttps://doi.org/10.1002/bdra.20793openalex-snapshot
Xenopus: An emerging model for studying congenital heart disease
inferred← citeshttps://doi.org/10.1002/bdra.20803openalex-snapshot
Tbx1, subpulmonary myocardium and conotruncal congenital heart defects
inferred← citeshttps://doi.org/10.1002/bdrc.10001openalex-snapshot
T‐box genes and cardiac development
inferred← citeshttps://doi.org/10.1002/bdrc.20013openalex-snapshot
The neural crest: Basic biology and clinical relationships in the craniofacial and enteric nervous systems
inferred← citeshttps://doi.org/10.1002/bdrc.20017openalex-snapshot
Making the mouse embryo transparent: Identifying developmental malformations using magnetic resonance imaging
inferred← citeshttps://doi.org/10.1002/bdrc.20160openalex-snapshot
Cell fate determination during tooth development and regeneration
inferred← citeshttps://doi.org/10.1002/bdrc.21076openalex-snapshot
Evolutionary and developmental origins of the cardiac neural crest: Building a divided outflow tract
inferred← citeshttps://doi.org/10.1002/bdrc.21081openalex-snapshot
The neural crest: A versatile organ system
inferred← citeshttps://doi.org/10.1002/bdrc.21082openalex-snapshot
Connecting teratogen‐induced congenital heart defects to neural crest cells and their effect on cardiac function
inferred← citeshttps://doi.org/10.1002/bies.10288openalex-snapshot
About face: Signals and genes controlling jaw patterning and identity in vertebrates
inferred← citeshttps://doi.org/10.1002/bies.200900148openalex-snapshot
Nucleocytoplasmic functions of the PDZ‐LIM protein family: new insights into organ development
inferred← citeshttps://doi.org/10.1002/bies.20484openalex-snapshot
DiGeorge syndrome and pharyngeal apparatus development
inferred← citeshttps://doi.org/10.1002/ca.20723openalex-snapshot
Can recent insights into cardiac development improve our understanding of congenitally malformed hearts?
inferred← citeshttps://doi.org/10.1002/cne.20418openalex-snapshot
Dlx gene expression during chick inner ear development
inferred← citeshttps://doi.org/10.1002/ddrr.4openalex-snapshot
Genetic modifiers of the physical malformations in velo‐cardio‐facial syndrome/DiGeorge syndrome
inferred← citeshttps://doi.org/10.1002/dvdy.10154openalex-snapshot
Isolation and developmental expression analysis of Tbx22, the mouse homolog of the human X‐linked cleft palate gene
inferred← citeshttps://doi.org/10.1002/dvdy.10208openalex-snapshot
T‐box gene products are required for mesenchymal induction of epithelial branching in the embryonic mouse lung
inferred← citeshttps://doi.org/10.1002/dvdy.10358openalex-snapshot
Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis
inferred← citeshttps://doi.org/10.1002/dvdy.144openalex-snapshot
Molecular and cellular mechanisms of the organogenesis and development of the mammalian carotid body
inferred← citeshttps://doi.org/10.1002/dvdy.20122openalex-snapshot
The Tbx‐files: The truth is out there
inferred← citeshttps://doi.org/10.1002/dvdy.20201openalex-snapshot
T‐box genes and heart development: Putting the “T” in heart
inferred← citeshttps://doi.org/10.1002/dvdy.20268openalex-snapshot
Retinoic acid down‐regulates Tbx1 expression in vivo and in vitro
inferred← citeshttps://doi.org/10.1002/dvdy.20274openalex-snapshot
The MLC1v gene provides a transgenic marker of myocardium formation within developing chambers of the Xenopus heart
inferred← citeshttps://doi.org/10.1002/dvdy.20276openalex-snapshot
XTbx1 is a transcriptional activator involved in head and pharyngeal arch development in Xenopus laevis
inferred← citeshttps://doi.org/10.1002/dvdy.20686openalex-snapshot
Tbx1 is regulated by forkhead proteins in the secondary heart field†
inferred← citeshttps://doi.org/10.1002/dvdy.20714openalex-snapshot
Developmental expression patterns of Tbx1, Tbx2, Tbx5, and Tbx20 in Xenopus tropicalis
inferred← citeshttps://doi.org/10.1002/dvdy.20833openalex-snapshot
Recent advances in craniofacial morphogenesis
inferred← citeshttps://doi.org/10.1002/dvdy.20905openalex-snapshot
Retinoic acid is required for endodermal pouch morphogenesis and not for pharyngeal endoderm specification
inferred← citeshttps://doi.org/10.1002/dvdy.21010openalex-snapshot
Tbx1 regulation of myogenic differentiation in the limb and cranial mesoderm
inferred← citeshttps://doi.org/10.1002/dvdy.21063openalex-snapshot
Visualization of outflow tract development in the absence of Tbx1 using an FgF10 enhancer trap transgene
inferred← citeshttps://doi.org/10.1002/dvdy.21287openalex-snapshot
Abnormal venous and arterial patterning in chordin mutants
inferred← citeshttps://doi.org/10.1002/dvdy.21715openalex-snapshot
Retinoic acid down‐regulates Tbx1 expression and induces abnormal differentiation of tongue muscles in fetal mice
inferred← citeshttps://doi.org/10.1002/dvdy.21718openalex-snapshot
Properties of branchiomeric and somite‐derived muscle development in Tbx1 mutant embryos
inferred← citeshttps://doi.org/10.1002/dvdy.21772openalex-snapshot
Expression of Islet1 in thyroid development related to budding, migration, and fusion of primordia
inferred← citeshttps://doi.org/10.1002/dvdy.22156openalex-snapshot
WNT5A mutations in patients with autosomal dominant Robinow syndrome
inferred← citeshttps://doi.org/10.1002/dvdy.22334openalex-snapshot
A novel role for transcription factor Lmo4 in thymus development through genetic interaction with Cited2
inferred← citeshttps://doi.org/10.1002/dvdy.22765openalex-snapshot
ARVCF depletion cooperates with Tbx1 deficiency in the development of 22q11.2DS‐like phenotypes in Xenopus
inferred← citeshttps://doi.org/10.1002/dvdy.23812openalex-snapshot
Biallelic expression of Tbx1 protects the embryo from developmental defects caused by increased receptor tyrosine kinase signaling
inferred← citeshttps://doi.org/10.1002/dvdy.23862openalex-snapshot
The regulation of endogenous retinoic acid level through CYP26B1 is required for elevation of palatal shelves
inferred← citeshttps://doi.org/10.1002/dvdy.23918openalex-snapshot
During Embryogenesis, Esrp1 Expression Is Restricted to a Subset of Epithelial Cells and Is Associated With Splicing of a Number of Developmentally Important Genes
inferred← citeshttps://doi.org/10.1002/dvdy.23928openalex-snapshot
Tbx1 is required for second heart field proliferation in zebrafish
inferred← citeshttps://doi.org/10.1002/dvdy.24147openalex-snapshot
Endoderm‐specific deletion of Tbx1 reveals an FGF‐independent role for Tbx1 in pharyngeal apparatus morphogenesis
inferred← citeshttps://doi.org/10.1002/dvdy.24186openalex-snapshot
The role of Zic genes in inner ear development in the mouse: Exploring mutant mouse phenotypes
inferred← citeshttps://doi.org/10.1002/dvdy.24289openalex-snapshot
Pharyngeal arch deficiencies affect taste bud development in the circumvallate papilla with aberrant glossopharyngeal nerve formation
inferred← citeshttps://doi.org/10.1002/dvdy.24380openalex-snapshot
Coronary stem development in wild‐type and Tbx1 null mouse hearts
inferred← citeshttps://doi.org/10.1002/dvdy.24664openalex-snapshot
Sculpting the skull through neurosensory epithelial–mesenchymal signaling
inferred← citeshttps://doi.org/10.1002/dvg.20476openalex-snapshot
Gain of function of Tbx1 affects pharyngeal and heart development in the mouse
inferred← citeshttps://doi.org/10.1002/dvg.23278openalex-snapshot
Insights into retinoic acid deficiency and the induction of craniofacial malformations and microcephaly in fetal alcohol spectrum disorder
inferred← citeshttps://doi.org/10.1002/dvg.23300openalex-snapshot
Retinoic acid signaling in heart development
inferred← citeshttps://doi.org/10.1002/dvg.23326openalex-snapshot
Reduced maternal vitamin A status increases the incidence of normal aortic arch variants
inferred← citeshttps://doi.org/10.1002/dvg.23421openalex-snapshot
Setd5 is required in cardiopharyngeal mesoderm for heart development and its haploinsufficiency is associated with outflow tract defects in mouse
inferred← citeshttps://doi.org/10.1002/eji.200324294openalex-snapshot
T cell development and function in CrkL‐deficient mice
inferred← citeshttps://doi.org/10.1002/eji.201545814openalex-snapshot
FOXN1 in thymus organogenesis and development
inferred← citeshttps://doi.org/10.1002/gene.20114openalex-snapshot
Fgf15 is required for proper morphogenesis of the mouse cardiac outflow tract
inferred← citeshttps://doi.org/10.1002/humu.21568openalex-snapshot
Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/digeorge/22q11.2 deletion syndrome patients
inferred← citeshttps://doi.org/10.1002/humu.22354openalex-snapshot
Chimeric Negative Regulation ofp14ARFandTBX1by a t(9;22) Translocation Associated with Melanoma, Deafness, and DNA Repair Deficiency
inferred← citeshttps://doi.org/10.1002/humu.22814openalex-snapshot
Whole-Genome Sequencing and Integrative Genomic Analysis Approach on Two 22q11.2 Deletion Syndrome Family Trios for Genotype to Phenotype Correlations
inferred← citeshttps://doi.org/10.1002/jcb.21315openalex-snapshot
A role for Tbx2 in the regulation of the α2(1) collagen gene in human fibroblasts
inferred← citeshttps://doi.org/10.1002/jcp.26168openalex-snapshot
RNA binding protein Musashi‐2 regulates PIWIL1 and TBX1 in mouse spermatogenesis
inferred← citeshttps://doi.org/10.1002/jcu.21992openalex-snapshot
Prenatal diagnosis of 22q11.2 deletion syndrome in twin pregnancy: A case report
inferred← citeshttps://doi.org/10.1002/jez.b.21055openalex-snapshot
Evolutionary origins of vertebrate placodes: insights from developmental studies and from comparisons with other deuterostomes
inferred← citeshttps://doi.org/10.1002/jez.b.21182openalex-snapshot
Deconstructing the pharyngeal metamere
inferred← citeshttps://doi.org/10.1002/jez.b.21215openalex-snapshot
Mandibular arch muscle identity is regulated by a conserved molecular process during vertebrate development
inferred← citeshttps://doi.org/10.1002/lio2.214openalex-snapshot
Cellular and molecular mechanisms of cleft palate development
inferred← citeshttps://doi.org/10.1002/mc.20768openalex-snapshot
A novel role for the T‐box transcription factor Tbx1 as a negative regulator of tumor cell growth in mice
inferred← citeshttps://doi.org/10.1002/mgg3.1057openalex-snapshot
Candidate modifier genes for immune function in 22q11.2 deletion syndrome
inferred← citeshttps://doi.org/10.1002/mrd.21279openalex-snapshot
The duplicated rainbow trout (Oncorhynchus mykiss) T‐box transcription factors 1, tbx1a and tbx1b, are up‐regulated during testicular development
inferred← citeshttps://doi.org/10.1002/pd.320openalex-snapshot
Interrupted aortic arch type A with 22q11 deletion: prenatal detection of an unusual association
inferred← citeshttps://doi.org/10.1002/pd.4586openalex-snapshot
Why increased nuchal translucency is associated with congenital heart disease: a systematic review on genetic mechanisms
inferred← citeshttps://doi.org/10.1002/pd.4864openalex-snapshot
The benefits and limitations of cell‐free DNA screening for 22q11.2 deletion syndrome
inferred← citeshttps://doi.org/10.1002/stem.3027openalex-snapshot
Concise Review: Genetic and Epigenetic Regulation of Cardiac Differentiation from Human Pluripotent Stem Cells
inferred← citeshttps://doi.org/10.1002/uog.12550openalex-snapshot
Microdeletions/duplications involving TBX1 gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescence in‐situ hybridization
inferred← citeshttps://doi.org/10.1002/wdev.146openalex-snapshot
Developing stratified epithelia: lessons from the epidermis and thymus
inferred← citeshttps://doi.org/10.1002/wdev.147openalex-snapshot
Development and evolution of the pharyngeal apparatus
inferred← citeshttps://doi.org/10.1002/wdev.336openalex-snapshot
Choanal atresia and stenosis: Development and diseases of the nasal cavity
inferred← citeshttps://doi.org/10.1002/wdev.75openalex-snapshot
The 22q11 deletion: DiGeorge and velocardiofacial syndromes and the role of TBX1
inferred← citeshttps://doi.org/10.1002/wsbm.1537openalex-snapshot
The crucial role of model systems in understanding the complexity of cell signaling in human neurocristopathies
inferred← citeshttps://doi.org/10.1006/dbio.2002.0689openalex-snapshot
Homeobox Gene Hoxa3 Is Essential for the Formation of the Carotid Body in the Mouse Embryos
inferred← citeshttps://doi.org/10.1006/dbio.2002.0819openalex-snapshot
The Role of Neural Crest during Cardiac Development in a Mouse Model of DiGeorge Syndrome
inferred← citeshttps://doi.org/10.1006/geno.2001.6566openalex-snapshot
Isolation and Characterization of a Novel Gene from the DiGeorge Chromosomal Region That Encodes for a Mediator Subunit
inferred← citeshttps://doi.org/10.1006/geno.2002.7009openalex-snapshot
Genetic and Comparative Mapping of Genes Dysregulated in Mouse Hearts Lacking the Hand2 Transcription Factor Gene
inferred← citeshttps://doi.org/10.1007/0-387-24990-7_27openalex-snapshot
Mutations of Transcription Factors in Human with Heart Disease for Understanding the Development and Mechanisms of Congenital Cardiovascular Heart Disease
inferred← citeshttps://doi.org/10.1007/0-387-27421-9_16openalex-snapshot
RING Finger-B Box-Coiled Coil (RBCC) Proteins As Ubiquitin Ligase in the Control of Protein Degradation and Gene Regulation
inferred← citeshttps://doi.org/10.1007/0-387-27530-4_1openalex-snapshot
Development of Parathyroid Glands
inferred← citeshttps://doi.org/10.1007/0-387-27530-4_12openalex-snapshot
Genetic Causes of Hypoparathyroidism
inferred← citeshttps://doi.org/10.1007/0-387-30678-1_3openalex-snapshot
Morphogenesis of the Inner Ear
inferred← citeshttps://doi.org/10.1007/82_2013_322openalex-snapshot
Development and Function of Cortical Thymic Epithelial Cells
inferred← citeshttps://doi.org/10.1007/978-0-387-46954-6_14openalex-snapshot
Molecular Bases of Human Neurocristopathies
inferred← citeshttps://doi.org/10.1007/978-0-387-46954-6_8openalex-snapshot
Neural Crest Contribution to the Cardiovascular System
inferred← citeshttps://doi.org/10.1007/978-1-0716-2059-5_4openalex-snapshot
Whole-Mount Immunofluorescence Protocol for 3D Imaging, Reconstruction, and Quantification of Fourth Pharyngeal Arch Artery Formation
inferred← citeshttps://doi.org/10.1007/978-1-4419-7823-3_6openalex-snapshot
Autoregulatory Mechanisms Controlling the Microprocessor
inferred← citeshttps://doi.org/10.1007/978-1-4471-4881-4_3openalex-snapshot
Developmental Aspects of the Electrophysiology of the Heart: Function Follows Form
inferred← citeshttps://doi.org/10.1007/978-1-4614-5203-4_2openalex-snapshot
Molecular Mechanisms of Cardiac Development
inferred← citeshttps://doi.org/10.1007/978-1-4614-5398-7_3openalex-snapshot
Trim Proteins as Ring Finger E3 Ubiquitin Ligases
inferred← citeshttps://doi.org/10.1007/978-1-4614-6435-8_888-3openalex-snapshot
CATCH 22 (Chromosome 22q11 Deletion Syndrome)
inferred← citeshttps://doi.org/10.1007/978-1-4614-7696-2_12openalex-snapshot
Generation of Anterior Foregut Derivatives from Pluripotent Stem Cells
inferred← citeshttps://doi.org/10.1007/978-1-59259-156-5_8openalex-snapshot
Genetic Control of Parathyroid Gland Development and Molecular Insights into Hypoparathyroidism
inferred← citeshttps://doi.org/10.1007/978-1-59259-353-8_8openalex-snapshot
Behavioral Phenotype in Velo-Cardio-Facial Syndrome
inferred← citeshttps://doi.org/10.1007/978-1-59259-732-1_6openalex-snapshot
Epithelial Stem/Progenitor Cells in Thymus Organogenesis
inferred← citeshttps://doi.org/10.1007/978-1-59259-878-6_10openalex-snapshot
Genetic Underpinnings of Cardiogenesis and Congenital Heart Disease
inferred← citeshttps://doi.org/10.1007/978-1-59259-878-6_6openalex-snapshot
Development of the Vertebrate Heart
inferred← citeshttps://doi.org/10.1007/978-1-59259-963-9_10openalex-snapshot
Congenital Heart Disease
inferred← citeshttps://doi.org/10.1007/978-1-59745-039-3_26openalex-snapshot
Chromosome-Engineered Mouse Models
inferred← citeshttps://doi.org/10.1007/978-1-59745-272-4_10openalex-snapshot
Stem Cell Differentiation Toward a Cardiac Myocyte Phenotype
inferred← citeshttps://doi.org/10.1007/978-1-59745-395-0_8openalex-snapshot
Thymus Organogenesis and Development of the Thymic Stroma
inferred← citeshttps://doi.org/10.1007/978-1-60327-227-8_33openalex-snapshot
Epithelial Stem Cells and the Development of the Thymus, Parathyroid, and Skin
inferred← citeshttps://doi.org/10.1007/978-1-84628-715-2_127openalex-snapshot
Genetic Aspects of Congenital Heart Disease
inferred← citeshttps://doi.org/10.1007/978-1-84628-715-2_52openalex-snapshot
Cardiac Development: Toward a Molecular Basis for Congenital Heart Disease
inferred← citeshttps://doi.org/10.1007/978-1-84628-854-8_3openalex-snapshot
Developmental Aspects of the Electrophysiology of the Heart: Function Follows Form
inferred← citeshttps://doi.org/10.1007/978-1-84800-378-1_1openalex-snapshot
Origin and Identity of the Right Heart
inferred← citeshttps://doi.org/10.1007/978-3-030-42937-9_9-1openalex-snapshot
The Role of Genetics in Development of Congenital Heart Disease
inferred← citeshttps://doi.org/10.1007/978-3-031-07418-9_2openalex-snapshot
Embryology of the Parathyroid Glands
inferred← citeshttps://doi.org/10.1007/978-3-031-07563-6_9openalex-snapshot
The Role of Genetics in Development of Congenital Heart Disease
inferred← citeshttps://doi.org/10.1007/978-3-031-44087-8_2openalex-snapshot
Human Genetics of Congenital Heart Defects
inferred← citeshttps://doi.org/10.1007/978-3-031-44087-8_46openalex-snapshot
Molecular Pathways and Animal Models of Semilunar Valve and Aortic Arch Anomalies
inferred← citeshttps://doi.org/10.1007/978-3-031-44087-8_52openalex-snapshot
Molecular Pathways and Animal Models of Truncus Arteriosus
inferred← citeshttps://doi.org/10.1007/978-3-031-77921-3_2openalex-snapshot
Thymus Ontogeny and Development
inferred← citeshttps://doi.org/10.1007/978-3-031-81813-4_39openalex-snapshot
Treatment of Hypoparathyroidism
inferred← citeshttps://doi.org/10.1007/978-3-032-14178-1_1openalex-snapshot
Anatomy and Embryology of Parathyroid Glands
inferred← citeshttps://doi.org/10.1007/978-3-319-21082-7_4openalex-snapshot
Neural Regulation of Lung Development
inferred← citeshttps://doi.org/10.1007/978-3-319-26794-4_35openalex-snapshot
Treatment of Hypoparathyroidism
inferred← citeshttps://doi.org/10.1007/978-3-319-31251-4_2openalex-snapshot
Cardiomyocytes: Function and Regeneration
inferred← citeshttps://doi.org/10.1007/978-3-319-33299-4_10openalex-snapshot
Dental Stem Cells for Tooth Regeneration
inferred← citeshttps://doi.org/10.1007/978-3-319-39562-3_9openalex-snapshot
Regulation of Megakaryocyte and Platelet Survival
inferred← citeshttps://doi.org/10.1007/978-3-319-91280-6_888openalex-snapshot
CATCH 22 (Chromosome 22q11 Deletion Syndrome)
inferred← citeshttps://doi.org/10.1007/978-3-540-76341-3_11openalex-snapshot
Genetic Disorders of Calcium and Phosphate Homeostasis
inferred← citeshttps://doi.org/10.1007/978-3-642-27843-3_10-1openalex-snapshot
Physiology of the Developing Kidney: Disorders and Therapy of Calcium and Phosphorous Homeostasis
inferred← citeshttps://doi.org/10.1007/978-3-662-43596-0_10openalex-snapshot
Physiology of the Developing Kidney: Disorders and Therapy of Calcium and Phosphorous Homeostasis
inferred← citeshttps://doi.org/10.1007/978-3-662-46780-0_9openalex-snapshot
Basics of Developmental Disorders of Speech and Language
inferred← citeshttps://doi.org/10.1007/978-3-7091-1883-2_42openalex-snapshot
Molecular Pathways and Animal Models of Semilunar Valve and Aortic Arch Anomalies
inferred← citeshttps://doi.org/10.1007/978-3-7091-1883-2_48openalex-snapshot
Molecular Pathways and Animal Models of Truncus Arteriosus
inferred← citeshttps://doi.org/10.1007/978-4-431-54628-3openalex-snapshot
Etiology and Morphogenesis of Congenital Heart Disease
inferred← citeshttps://doi.org/10.1007/978-4-431-54628-3_26openalex-snapshot
A History and Interaction of Outflow Progenitor Cells Implicated in “Takao Syndrome”
inferred← citeshttps://doi.org/10.1007/978-4-431-54634-4_8openalex-snapshot
Tbx1/Ripply3/Retinoic Acid Signal Network That Regulates Pharyngeal Arch Development
inferred← citeshttps://doi.org/10.1007/978-88-470-5376-2_2openalex-snapshot
Embryology of the Parathyroid Glands
inferred← citeshttps://doi.org/10.1007/978-94-010-1019-1_3openalex-snapshot
Genetics of Congenital Heart Disease
inferred← citeshttps://doi.org/10.1007/978-981-10-1400-0_5openalex-snapshot
Genetics of Inner Ear Malformation and Cochlear Nerve Deficiency
inferred← citeshttps://doi.org/10.1007/s00018-005-5532-2openalex-snapshot
Insights into the genetic basis of congenital heart disease
inferred← citeshttps://doi.org/10.1007/s00018-007-6518-zopenalex-snapshot
Cardiovascular development: towards biomedical applicability
inferred← citeshttps://doi.org/10.1007/s00018-011-0842-zopenalex-snapshot
Immunological aspects of 22q11.2 deletion syndrome
inferred← citeshttps://doi.org/10.1007/s00018-013-1305-5openalex-snapshot
Regulation of organogenesis and stem cell properties by T-box transcription factors
inferred← citeshttps://doi.org/10.1007/s00018-013-1430-1openalex-snapshot
Of mice and men: molecular genetics of congenital heart disease
inferred← citeshttps://doi.org/10.1007/s00109-002-0331-9openalex-snapshot
Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10p
inferred← citeshttps://doi.org/10.1007/s00223-003-0106-5openalex-snapshot
Tbx2 Represses Expression of Connexin43 in Osteoblastic-like Cells
inferred← citeshttps://doi.org/10.1007/s00246-009-9613-0openalex-snapshot
22q11 Deletion Syndrome: A Role for TBX1 in Pharyngeal and Cardiovascular Development
inferred← citeshttps://doi.org/10.1007/s00246-013-0694-4openalex-snapshot
22q11.2 Deletions in Patients with Conotruncal Defects: Data from 1,610 Consecutive Cases
inferred← citeshttps://doi.org/10.1007/s00246-015-1173-xopenalex-snapshot
A Novel TBX1 Loss-of-Function Mutation Associated with Congenital Heart Disease
inferred← citeshttps://doi.org/10.1007/s00246-018-1860-5openalex-snapshot
Planar Cell Polarity Signaling in Mammalian Cardiac Morphogenesis
inferred← citeshttps://doi.org/10.1007/s00281-020-00826-9openalex-snapshot
Inborn errors of thymic stromal cell development and function
inferred← citeshttps://doi.org/10.1007/s00335-010-9304-4openalex-snapshot
Manipulation of endogenous regulatory elements and transgenic analyses of the Tbx1 gene
inferred← citeshttps://doi.org/10.1007/s00383-006-1641-8openalex-snapshot
FISH investigation of 22q11.2 deletion in patients with immunodeficiency and/or cardiac abnormalities
inferred← citeshttps://doi.org/10.1007/s00383-013-3455-9openalex-snapshot
Altered Tbx1 gene expression is associated with abnormal oesophageal development in the adriamycin mouse model of oesophageal atresia/tracheo-oesophageal fistula
inferred← citeshttps://doi.org/10.1007/s00415-025-13237-3openalex-snapshot
Vertigo and dizziness in genetic neurodevelopmental disorders: an international cross-sectional study
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