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Reconstruction of the Centrosome Cycle from Cryoelectron Micrographs
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-0169(1996)33:1<1::aid-cm1>3.0.co;2-hopenalex-snapshot
Controls for centrosome reproduction in animal cells: Issues and recent observations
inferredcites →https://doi.org/10.1002/cm.970080305openalex-snapshot
Structural and chemical characterization of isolated centrosomes
inferredcites →https://doi.org/10.1002/cm.970170307openalex-snapshot
The iris diaphragm model of centriole and basal body formation
inferredcites →https://doi.org/10.1006/jsbi.1996.0029openalex-snapshot
Toward Fully Automated High-Resolution Electron Tomography
inferredcites →https://doi.org/10.1006/jsbi.1997.3922openalex-snapshot
Three-Dimensional Reconstruction of the Mammalian Centriole from Cryoelectron Micrographs: The Use of Common Lines for Orientation and Alignment
inferredcites →https://doi.org/10.1016/0012-1606(89)90259-5openalex-snapshot
Parthenogenesis in Xenopus eggs injected with centrosomes from synchronized human lymphoid cells
inferredcites →https://doi.org/10.1016/0304-3991(92)90235-copenalex-snapshot
Towards automatic electron tomography
inferredcites →https://doi.org/10.1016/0304-3991(93)90217-lopenalex-snapshot
Towards automatic electron tomography II. Implementation of autofocus and low-dose procedures
inferredcites →https://doi.org/10.1016/0962-8924(93)90174-yopenalex-snapshot
Molecular components of the centrosome
inferredcites →https://doi.org/10.1016/0962-8924(96)10033-7openalex-snapshot
Structure and function of the centriole in animal cells: progress and questions
inferredcites →https://doi.org/10.1016/1047-8477(92)90011-xopenalex-snapshot
Centrosome organization and centriole architecture: Their sensitivity to divalent cations
inferredcites →https://doi.org/10.1016/s0006-3495(97)78689-2openalex-snapshot
Energy filtered electron tomography of ice-embedded actin and vesicles
inferredcites →https://doi.org/10.1016/s0074-7696(08)61714-3openalex-snapshot
The Centrosome and Its Role in the Organization of Microtubules
inferredcites →https://doi.org/10.1016/s0960-9822(95)00276-4openalex-snapshot
The core of the mammalian centriole contains γ-tubulin
inferredcites →https://doi.org/10.1038/378638a0openalex-snapshot
Microtubule nucleation by γ-tubulin-containing rings in the centrosome
inferredcites →https://doi.org/10.1083/jcb.107.6.2669openalex-snapshot
Identification and localization of a novel, cytoskeletal, centrosome-associated protein in PtK2 cells.
inferredcites →https://doi.org/10.1083/jcb.129.5.1311openalex-snapshot
Structure of growing microtubule ends: two-dimensional sheets close into tubes at variable rates.
inferredcites →https://doi.org/10.1083/jcb.130.4.919openalex-snapshot
A molecular marker for centriole maturation in the mammalian cell cycle.
inferredcites →https://doi.org/10.1083/jcb.130.5.1149openalex-snapshot
Three-dimensional structural characterization of centrosomes from early Drosophila embryos.
inferredcites →https://doi.org/10.1083/jcb.135.1.5openalex-snapshot
Protofilaments and rings, two conformations of the tubulin family conserved from bacterial FtsZ to alpha/beta and gamma tubulin.
inferredcites →https://doi.org/10.1083/jcb.21.3.465openalex-snapshot
THE STRUCTURE AND FUNCTION OF CENTRIOLES AND THEIR SATELLITES IN THE JELLYFISH PHIALIDIUM GREGARIUM
inferredcites →https://doi.org/10.1083/jcb.36.2.329openalex-snapshot
THE CENTRIOLE CYCLE IN SYNCHRONIZED HELA CELLS
inferredcites →https://doi.org/10.1083/jcb.57.2.359openalex-snapshot
INDEPENDENCE OF CENTRIOLE FORMATION AND DNA SYNTHESIS
inferredcites →https://doi.org/10.1083/jcb.59.2.267openalex-snapshot
MICROTUBULES: EVIDENCE FOR 13 PROTOFILAMENTS
inferredcites →https://doi.org/10.1083/jcb.91.3.814openalex-snapshot
Centriole cycle in Chinese hamster ovary cells as determined by whole-mount electron microscopy.
inferredcites →https://doi.org/10.1083/jcb.93.3.938openalex-snapshot
Centrioles in the cell cycle. I. Epithelial cells.
inferredcites →https://doi.org/10.1146/annurev.bi.63.070194.003231openalex-snapshot
THE CENTROSOME AND CELLULAR ORGANIZATION
inferredcites →https://doi.org/10.1242/jcs.107.11.3127openalex-snapshot
Approaching microtubule structure with the scanning tunneling microscope (STM)
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.4692176openalex-extracted
Targeted Localization of the Mother Centrosome in CD8 T Cells Undergoing Asymmetric Cell Division Promotes Memory Formation
inferred← citeshttps://doi.org/10.1002/9780470015902.a0002597.pub2openalex-snapshot
Centrosomes: Methods for Preparation
inferred← citeshttps://doi.org/10.1002/9780470593042.ch2openalex-snapshot
Basal Bodies: Their Roles in Generating Asymmetry
inferred← citeshttps://doi.org/10.1002/cm.10115openalex-snapshot
Higher order structure of the PCM adjacent to the centriole
inferred← citeshttps://doi.org/10.1002/cm.10154openalex-snapshot
The centrosome: The centriole‐PCM coalition
inferred← citeshttps://doi.org/10.1002/cm.20536openalex-snapshot
Assessing the localization of centrosomal proteins by PALM/STORM nanoscopy
inferred← citeshttps://doi.org/10.1002/jemt.20637openalex-snapshot
Electron tomography study of isolated human centrioles
inferred← citeshttps://doi.org/10.1006/jmbi.2000.3696openalex-snapshot
Microtubules switch occasionally into unfavorable configurations during elongation
inferred← citeshttps://doi.org/10.1006/jsbi.1997.3922openalex-snapshot
Three-Dimensional Reconstruction of the Mammalian Centriole from Cryoelectron Micrographs: The Use of Common Lines for Orientation and Alignment
inferred← citeshttps://doi.org/10.1007/978-94-007-2004-6_9openalex-snapshot
Primary Cilia are Mechanosensory Organelles with Chemosensory Roles
inferred← citeshttps://doi.org/10.1007/978-94-007-5808-7_1openalex-snapshot
Primary and Motile Cilia: Their Ultrastructure and Ciliogenesis
inferred← citeshttps://doi.org/10.1007/s00018-026-06080-wopenalex-snapshot
The γ-TuRC: mastermind of multipurpose actions at the centrosome
inferred← citeshttps://doi.org/10.1007/s00418-005-0032-xopenalex-snapshot
Structure and microtubule-nucleation activity of isolated Drosophila embryo centrosomes characterized by whole mount scanning and transmission electron microscopy
inferred← citeshttps://doi.org/10.1007/s10059-009-0017-zopenalex-snapshot
Ab ovo or de novo? Mechanisms of Centriole Duplication
inferred← citeshttps://doi.org/10.1016/b978-0-12-370873-1.00039-3openalex-snapshot
Basal Bodies and Associated Structures
inferred← citeshttps://doi.org/10.1016/j.bbrc.2014.01.129openalex-snapshot
Asymmetric spindle pole formation in CPAP-depleted mitotic cells
inferred← citeshttps://doi.org/10.1016/j.bpj.2020.01.045openalex-snapshot
Stochastic Model of T Cell Repolarization during Target Elimination I
inferred← citeshttps://doi.org/10.1016/j.ceb.2005.12.012openalex-snapshot
Life sciences require the third dimension
inferred← citeshttps://doi.org/10.1016/j.ceb.2016.09.003openalex-snapshot
Microtubule-organizing centers: from the centrosome to non-centrosomal sites
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.115127openalex-snapshot
Targeted localization of the mother centrosome in CD8+ T cells undergoing asymmetric cell division promotes memory formation
inferred← citeshttps://doi.org/10.1016/j.crmeth.2022.100322openalex-snapshot
A high-throughput electron tomography workflow reveals over-elongated centrioles in relapsed/refractory multiple myeloma
inferred← citeshttps://doi.org/10.1016/j.cub.2004.11.055openalex-snapshot
CLIP-170/Tubulin-Curved Oligomers Coassemble at Microtubule Ends and Promote Rescues
inferred← citeshttps://doi.org/10.1016/j.cub.2023.08.075openalex-snapshot
Cep104 is a component of the centriole distal tip complex that regulates centriole growth and contributes to Drosophila spermiogenesis
inferred← citeshttps://doi.org/10.1016/j.devcel.2005.08.004openalex-snapshot
Centrosome Duplication and Nematodes: Recent Insights from an Old Relationship
inferred← citeshttps://doi.org/10.1016/j.devcel.2007.07.002openalex-snapshot
Plk4-Induced Centriole Biogenesis in Human Cells
inferred← citeshttps://doi.org/10.1016/j.devcel.2007.07.004openalex-snapshot
Regulated HsSAS-6 Levels Ensure Formation of a Single Procentriole per Centriole during the Centrosome Duplication Cycle
inferred← citeshttps://doi.org/10.1016/j.devcel.2009.12.022openalex-snapshot
Ofd1, a Human Disease Gene, Regulates the Length and Distal Structure of Centrioles
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.04.024openalex-snapshot
Centriolar CPAP/SAS-4 Imparts Slow Processive Microtubule Growth
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.05.008openalex-snapshot
The Secret of Centriole Length: Keep a LID on It
inferred← citeshttps://doi.org/10.1016/j.devcel.2024.12.002openalex-snapshot
Molecular architectures of centrosomes in C. elegans embryos visualized by cryo-electron tomography
inferred← citeshttps://doi.org/10.1016/j.febslet.2007.02.069openalex-snapshot
Clockwise or anticlockwise? Turning the centriole triplets in the right direction!
inferred← citeshttps://doi.org/10.1016/j.semcdb.2009.07.002openalex-snapshot
Centriole maturation and transformation to basal body
inferred← citeshttps://doi.org/10.1016/j.semcdb.2014.02.014openalex-snapshot
Stem cell decisions: A twist of fate or a niche market?
inferred← citeshttps://doi.org/10.1016/j.semcdb.2021.12.001openalex-snapshot
The centriolar tubulin code
inferred← citeshttps://doi.org/10.1016/j.tcb.2007.03.003openalex-snapshot
Centrosome duplication: of rules and licenses
inferred← citeshttps://doi.org/10.1016/j.tcb.2008.06.004openalex-snapshot
Mechanisms of procentriole formation
inferred← citeshttps://doi.org/10.1016/j.yexcr.2023.113751openalex-snapshot
Primary cilia in skeletal development and disease
inferred← citeshttps://doi.org/10.1016/s0002-9440(10)65513-7openalex-snapshot
Altered Centrosome Structure Is Associated with Abnormal Mitoses in Human Breast Tumors
inferred← citeshttps://doi.org/10.1016/s0014-5793(99)00534-7openalex-snapshot
Protein kinases in control of the centrosome cycle
inferred← citeshttps://doi.org/10.1016/s0070-2153(99)49008-8openalex-snapshot
Comparative structural, molecular, and functional aspects of the Dictyostelium discoideum centrosome
inferred← citeshttps://doi.org/10.1016/s0070-2153(99)49010-6openalex-snapshot
Basal bodies and centrioles: Their function and structure
inferred← citeshttps://doi.org/10.1016/s0070-2153(99)49011-8openalex-snapshot
Centriole duplication and maturation in animal cells
inferred← citeshttps://doi.org/10.1016/s0070-2153(99)49020-9openalex-snapshot
The centrosome in early drosophila embryogenesis
inferred← citeshttps://doi.org/10.1016/s0074-7696(08)62416-xopenalex-snapshot
Molecular Characteristics of the Centrosome
inferred← citeshttps://doi.org/10.1016/s0091-679x(06)79004-5openalex-snapshot
Correlative Light and Electron Microscopy of Early Caenorhabditis elegans Embryos in Mitosis
inferred← citeshttps://doi.org/10.1016/s0248-4900(99)80097-5openalex-snapshot
Polarities of the centriolar structure: Morphogenetic consequences
inferred← citeshttps://doi.org/10.1016/s0955-0674(00)00173-3openalex-snapshot
The tubulin fraternity: alpha to eta
inferred← citeshttps://doi.org/10.1016/s0960-9822(01)00289-5openalex-snapshot
Centrioles take center stage
inferred← citeshttps://doi.org/10.1038/10054openalex-snapshot
Centrosome duplication in mammalian somatic cells requires E2F and Cdk2–Cyclin A
inferred← citeshttps://doi.org/10.1038/emboj.2010.45openalex-snapshot
Procentriole assembly revealed by cryo‐electron tomography
inferred← citeshttps://doi.org/10.1038/nature08435openalex-snapshot
Asymmetric centrosome inheritance maintains neural progenitors in the neocortex
inferred← citeshttps://doi.org/10.1038/ncb1146openalex-snapshot
Centriolar SAS-5 is required for centrosome duplication in C. elegans
inferred← citeshttps://doi.org/10.1038/ncb1251openalex-snapshot
Odf2-deficient mother centrioles lack distal/subdistal appendages and the ability to generate primary cilia
inferred← citeshttps://doi.org/10.1038/ncb2617openalex-snapshot
The amorphous pericentriolar cloud takes shape
inferred← citeshttps://doi.org/10.1038/ncb3412openalex-snapshot
EB1 interacts with outwardly curved and straight regions of the microtubule lattice
inferred← citeshttps://doi.org/10.1038/nrc3995openalex-snapshot
Centrosomes and cancer: revisiting a long-standing relationship
inferred← citeshttps://doi.org/10.1038/s41467-018-03641-xopenalex-snapshot
Over-elongation of centrioles in cancer promotes centriole amplification and chromosome missegregation
inferred← citeshttps://doi.org/10.1038/s41467-018-06005-7openalex-snapshot
The mitotic spindle is chiral due to torques within microtubule bundles
inferred← citeshttps://doi.org/10.1038/s41567-019-0542-4openalex-snapshot
Lattice defects induce microtubule self-renewal
inferred← citeshttps://doi.org/10.1038/s41598-019-43338-9openalex-snapshot
Cryo-Electron Tomography and Proteomics studies of centrosomes from differentiated quiescent thymocytes
inferred← citeshttps://doi.org/10.1038/srep27075openalex-snapshot
Computational support for a scaffolding mechanism of centriole assembly
inferred← citeshttps://doi.org/10.1042/bj20071501openalex-snapshot
Cep57, a multidomain protein with unique microtubule and centrosomal localization domains
inferred← citeshttps://doi.org/10.1074/jbc.m109.096586openalex-snapshot
The 90-kDa Heat Shock Protein Hsp90 Protects Tubulin against Thermal Denaturation
inferred← citeshttps://doi.org/10.1074/jbc.m114.603423openalex-snapshot
Centrobin-mediated Regulation of the Centrosomal Protein 4.1-associated Protein (CPAP) Level Limits Centriole Length during Elongation Stage
inferred← citeshttps://doi.org/10.1080/14728222.2018.1410140openalex-snapshot
PLK4: a link between centriole biogenesis and cancer
inferred← citeshttps://doi.org/10.1083/jcb.141.3.689openalex-snapshot
Characterization of the Human Homologue of the Yeast Spc98p and Its Association with γ-Tubulin
inferred← citeshttps://doi.org/10.1083/jcb.141.7.1563openalex-snapshot
C-Nap1, a Novel Centrosomal Coiled-Coil Protein and Candidate Substrate of the Cell Cycle–regulated Protein Kinase Nek2
inferred← citeshttps://doi.org/10.1083/jcb.149.2.317openalex-snapshot
The Respective Contributions of the Mother and Daughter Centrioles to Centrosome Activity and Behavior in Vertebrate Cells
inferred← citeshttps://doi.org/10.1083/jcb.200301105openalex-snapshot
A novel human protein of the maternal centriole is required for the final stages of cytokinesis and entry into S phase
inferred← citeshttps://doi.org/10.1083/jcb.200610043openalex-snapshot
Xenopus tropicalis egg extracts provide insight into scaling of the mitotic spindle
inferred← citeshttps://doi.org/10.1083/jcb.200808082openalex-snapshot
hPOC5 is a centrin-binding protein required for assembly of full-length centrioles
inferred← citeshttps://doi.org/10.1083/jcb.201307049openalex-snapshot
Mechanisms of HsSAS-6 assembly promoting centriole formation in human cells
inferred← citeshttps://doi.org/10.1083/jcb.201601099openalex-snapshot
Divergent regulation of functionally distinct γ-tubulin complexes during differentiation
inferred← citeshttps://doi.org/10.1083/jcb.201801014openalex-snapshot
A homeostatic clock sets daughter centriole size in flies
inferred← citeshttps://doi.org/10.1083/jcb.201910019openalex-snapshot
Prolonged mitosis results in structurally aberrant and over-elongated centrioles
inferred← citeshttps://doi.org/10.1083/jcb.202305009openalex-snapshot
CCDC15 localizes to the centriole inner scaffold and controls centriole length and integrity
inferred← citeshttps://doi.org/10.1083/jcb.202406061openalex-snapshot
Centriolar cap proteins CP110 and CPAP control slow elongation of microtubule plus ends
inferred← citeshttps://doi.org/10.1083/jcb.202601174openalex-snapshot
Slow but steady: Molecular mechanisms controlling microtubule growth in centrioles and cilia
inferred← citeshttps://doi.org/10.1089/1044549041562276openalex-snapshot
The Centrosome in Normal and Transformed Cells
inferred← citeshttps://doi.org/10.1091/mbc.e04-10-0939openalex-snapshot
The Forkhead-associated Domain Protein Cep170 Interacts with Polo-like Kinase 1 and Serves as a Marker for Mature Centrioles
inferred← citeshttps://doi.org/10.1091/mbc.e09-12-1049openalex-snapshot
Daughter Centriole Elongation Is Controlled by Proteolysis
inferred← citeshttps://doi.org/10.1091/mbc.e18-02-0115openalex-snapshot
Ccdc61 controls centrosomal localization of Cep170 and is required for spindle assembly and symmetry
inferred← citeshttps://doi.org/10.1093/hmg/ddu318openalex-snapshot
A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family
inferred← citeshttps://doi.org/10.1093/jb/mvy031openalex-snapshot
Ultrastructural diversity between centrioles of eukaryotes
inferred← citeshttps://doi.org/10.1098/rsob.180062openalex-snapshot
Who are you, subdistal appendages of centriole?
inferred← citeshttps://doi.org/10.1098/rstb.2013.0452openalex-snapshot
Centrosomes back in the limelight
inferred← citeshttps://doi.org/10.1098/rstb.2013.0456openalex-snapshot
Lessons from yeast: the spindle pole body and the centrosome
inferred← citeshttps://doi.org/10.1101/2021.12.29.474442openalex-snapshot
Microtubule plus-end regulation by centriolar cap proteins
inferred← citeshttps://doi.org/10.1101/2023.02.16.528810openalex-snapshot
CCDC15 localizes to the centriole inner scaffold and regulates centriole integrity and ciliogenesis
inferred← citeshttps://doi.org/10.1101/2024.04.03.587742openalex-snapshot
Native molecular architectures of centrosomes in C. elegans embryos
inferred← citeshttps://doi.org/10.1101/sqb.2017.82.034496openalex-snapshot
The ABCs of Centriole Architecture: The Form and Function of Triplet Microtubules
inferred← citeshttps://doi.org/10.1111/j.1095-8312.2010.01507.xopenalex-snapshot
Changes in sperm tail development associated with Y chromosome meiotic drive leading to an excess of males in the medfly Ceratitis capitata (Diptera: Tephritidae)
inferred← citeshttps://doi.org/10.1128/mcb.01138-14openalex-snapshot
JAK2 Tyrosine Kinase Phosphorylates and Is Negatively Regulated by Centrosomal Protein Ninein
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-100616-060454openalex-snapshot
Centriole Biogenesis: From Identifying the Characters to Understanding the Plot
inferred← citeshttps://doi.org/10.1159/000479666openalex-snapshot
Novel STIL Compound Heterozygous Mutations Cause Severe Fetal Microcephaly and Centriolar Lengthening
inferred← citeshttps://doi.org/10.1186/1747-1028-5-25openalex-snapshot
Polo-like kinase 4: the odd one out of the family
inferred← citeshttps://doi.org/10.1186/1747-1028-6-2openalex-snapshot
The G1 phase Cdks regulate the centrosome cycle and mediate oncogene-dependent centrosome amplification
inferred← citeshttps://doi.org/10.1242/bio.20122337openalex-snapshot
3D-structured illumination microscopy provides novel insight into architecture of human centrosomes
inferred← citeshttps://doi.org/10.1242/jcs.005231openalex-snapshot
Structure and duplication of the centrosome
inferred← citeshttps://doi.org/10.1242/jcs.00859openalex-snapshot
Mutations in α-tubulin promote basal body maturation and flagellar assembly in the absence of δ-tubulin
inferred← citeshttps://doi.org/10.1242/jcs.01128openalex-snapshot
The arithmetic of centrosome biogenesis
inferred← citeshttps://doi.org/10.1242/jcs.092429openalex-snapshot
Microtubule assembly during mitosis – from distinct origins to distinct functions?
inferred← citeshttps://doi.org/10.1242/jcs.114.11.2095openalex-snapshot
The non-catalytic domain of the Xenopus laevis auroraA kinase localises the protein to the centrosome
inferred← citeshttps://doi.org/10.1242/jcs.114.20.3749openalex-snapshot
Centrosome cohesion is regulated by a balance of kinase and phosphatase activities
inferred← citeshttps://doi.org/10.1242/jcs.121186openalex-snapshot
Par6γ is at the mother centriole and controls centrosomal protein composition through a Par6α-dependent pathway
inferred← citeshttps://doi.org/10.1242/jcs.157008openalex-snapshot
Proteomic analysis of mammalian sperm cells identifies new components of the centrosome
inferred← citeshttps://doi.org/10.2147/btt.s87396openalex-snapshot
Centrosome – a promising anti-cancer target
inferred← citeshttps://doi.org/10.2478/s11535-009-0061-xopenalex-snapshot
CLERC and centrosomal leucine-rich repeat proteins
inferred← citeshttps://doi.org/10.3389/fcell.2020.619869openalex-snapshot
Mechanochemical Control of Symmetry Breaking in the Caenorhabditis elegans Zygote
inferred← citeshttps://doi.org/10.3389/fonc.2013.00277openalex-snapshot
Centrosome Dysfunction Contributes to Chromosome Instability, Chromoanagenesis, and Genome Reprograming in Cancer
inferred← citeshttps://doi.org/10.3389/fonc.2021.587554openalex-snapshot
Polo-Like Kinase 4’s Critical Role in Cancer Development and Strategies for Plk4-Targeted Therapy
inferred← citeshttps://doi.org/10.3390/cells14141094openalex-snapshot
Centriole Duplication at the Crossroads of Cell Cycle Control and Oncogenesis
inferred← citeshttps://doi.org/10.3390/cells9061429openalex-snapshot
With Age Comes Maturity: Biochemical and Structural Transformation of a Human Centriole in the Making
inferred← citeshttps://doi.org/10.3390/ijms20061336openalex-snapshot
Primary Cilium in Cancer Hallmarks
inferred← citeshttps://doi.org/10.3410/f.1165696.628732openalex-snapshot
Faculty Opinions recommendation of Asymmetric centrosome inheritance maintains neural progenitors in the neocortex.
inferred← citeshttps://doi.org/10.3410/f.1165696.827062openalex-snapshot
Faculty Opinions recommendation of Asymmetric centrosome inheritance maintains neural progenitors in the neocortex.
inferred← citeshttps://doi.org/10.4236/abb.2015.67045openalex-snapshot
Centrosome Functions as a Molecular Dynamo in the Living Cell
inferred← citeshttps://doi.org/10.5075/epfl-thesis-4491openalex-snapshot
Functional characterization of the SAS-4-related protein CPAP in centrosome biology of human cells
inferred← citeshttps://doi.org/10.5282/edoc.13046openalex-snapshot
Human CPAP and CP110 in centriole elongation and ciliogenesis
inferred← citeshttps://doi.org/10.5282/edoc.1962openalex-snapshot
Functional characterization of the novel centrosomal protein Nlp (ninein-like protein)
inferred← citeshttps://doi.org/10.53846/goediss-475openalex-snapshot
Function of MCPH1 in Neurogenesis
inferred← citeshttps://doi.org/10.70675/3516de18z2b10z4699z9e91z0abb28f5fcb6openalex-snapshot
Mise en évidence d'un nouveau mécanisme permettant le rajeunissement des microtubules : l'effet des moteurs moléculaires
inferred← citeshttps://doi.org/10.70675/763ca66az53efz4562zb337z755d833bb64dopenalex-snapshot
Study of Exon Junction Complex in mouse neural stem cells
inferred← citeshttps://doi.org/10.70675/7a53239dzc652z4ea4z8b95z4a71961c83b4openalex-snapshot
Role of VDAC1 hypoxic form, VDAC1-∆C, in the expression of primary cilia and tumor progression
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