Cdk5rap2 exposes the centrosomal root of microcephaly syndromes
Megraw, Timothy L., Sharkey, James T., Nowakowski, Richard S.·2011·Trends in Cell Biology
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Items 101–124 of 124
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- RNA-binding protein Orb2 causes microcephaly and supports centrosome asymmetry in Drosophila neural stem cellsBeverly V. Robinson, Joseph Buehler, Taylor Hailstock, Temitope H. Adebambo, Junnan Fang, Dipen S. Mehta, Dorothy A. Lerit · 2021 · bioRxiv (Cold Spring Harbor Laboratory)
- Expanding the Clinical and Molecular Spectrum of Primary Autosomal Recessive Microcephaly: Novel CDK5RAP2 Gene Variants and Functional Insights on the Intronic VariantsBurcu Yeter, Yasemin Kendir Demirkol, Esra Usluer, İpek Görüşen Kavak, Sena Gjota Ergin, N. Elçioğlu · 2025 · Genes
- Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesisYoann Vial, Jeannette Nardelli, Adeline Alice Bonnard, Justine Rousselot, Michèle Souyri, Pierre Gressèns, Hélène Cavé, Séverine Drunat · 2024 · EMBO Reports
- The regulatory subunit phr2AB of Dictyostelium discoideum phosphatase PP2A interacts with the centrosomal protein CEP161, a CDK5RAP2 orthologRolf Müller, Maria Stumpf, Regina Wehrstedt, Salil Kalarikkal Sukumaran, Malte A. Karow, Marija Marko, Angelika Anna Noegel, Ludwig Eichinger · 2018 · Genes to Cells
- Congenital and postnatal microcephaliesYoungshin Lim, Jeffrey Alan Golden · 2020 · Elsevier eBooks
- Cerebral Organoids: A Model of Brain DevelopmentKirill K. Sukhinich, M. A. Aleksandrova · 2020 · Russian Journal of Developmental Biology
- Centrosomes in Asymmetric Cell Division and Neocortical DevelopmentFelipe Mora‐Bermúdez, Wieland Β. Huttner · 2018 · Wiley eBooks
- RNA methyltransferase SPOUT1/CENP-32 links mitotic spindle organization with the neurodevelopmental disorder SpADMiSSAvinash V. Dharmadhikari, Maria Alba Abad, Sheraz Khan, Reza Maroofian, Tristan T. Sands, Farid Ullah, Itaru Samejima, Martin A. Wear, Kiara E. Moore, Elena Kondakova et al. · 2024 · medRxiv
- In vitro reconstitution of minimal human centrosomesManolo U. Rios, Weronika E. Stachera, Nicole E. Familiari, Cláudia Brito, Thomas Surrey, Jeffrey B. Woodruff · 2025 · bioRxiv (Cold Spring Harbor Laboratory)
- Characterization of CDK5RAP2 as a novel regulator in the Hippo signaling pathwaySalil Kalarikkal Sukumaran · 2014 · Kölner Universitäts PublikationsServer (Universität zu Köln)
- A review on microcephaly genesSyed M. Shahid, Saba Irshad · 2012 · Biopolymers and Cell
- Lack of adaptation to centriolar defects leads to p53-independent microcephaly in the absence of Cep135José González‐Martínez, Andrzej W Cwetsch, Diego Martínez‐Alonso, Luis Rodrigo López-Sainz, Jorge Almagro, Diego Megı́as, Jasminka Boskovic, Javier Gilabert‐Juan, Osvaldo Graña‐Castro, Alessandra Pierani et al. · 2020 · bioRxiv (Cold Spring Harbor Laboratory)
- Brain organoids as a model system for human neurodevelopment in health and diseaseOrly Reiner, Eyal Karzbrun · 2020 · Elsevier eBooks
- Faculty Opinions recommendation of Actomyosin-Driven Tension at Compartmental Boundaries Orients Cell Division Independently of Cell Geometry In Vivo.Ronen Zaidel‐Bar, Priti Agarwal · 2018 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
- Faculty Opinions recommendation of Pericentrin-mediated SAS-6 recruitment promotes centriole assembly.Sue L. Jaspersen · 2020 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
- Faculty Opinions recommendation of Cerebral organoids model human brain development and microcephaly.David J Stephens · 2013 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
- Faculty Opinions recommendation of Actomyosin-Driven Tension at Compartmental Boundaries Orients Cell Division Independently of Cell Geometry In Vivo.Emmanuel Farge · 2020 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
- Faculty Opinions recommendation of Pericentrin-mediated SAS-6 recruitment promotes centriole assembly.Kyung Sang Lee, Jung‐Eun Park · 2019 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
- Estudo das bases genéticas da microcefalia sindrômica associada a distúrbios de neurodesenvolvimentoGiovanna Cantini Tolezano · 2023
- Identification of CDK5RAP2 as a causative gene of focal epilepsy without microcephalyLi Xiao, Hui Sun, Yang Tian, Song Lan, Kaixian Du, Xuejiao Chen, Li Lin, Jing Zhi Guan, Qiong‐Xiang Zhai, Jie Wang et al. · 2025 · Seizure
- Microcephaly-associated protein WDR62 supports purine metabolism by interacting with co-chaperone BAG2Matthew J. Morris, Yvonne Y.C. Yeap, Jonathon R Edwards, Chi Chen, Annalisa Paolino, Sebastian G. B. Furness, S. Sean Millard, Julia K. Pagan, Laura R. Fenlon, Dominic C.H. Ng · 2026 · The EMBO Journal
- Study of Exon Junction Complex in mouse neural stem cellsRahul Mishra · 2016
- Rare genetic causes of primary microcephaly in two Saudi families identified via whole-exome sequencing: Genomic and phenotypic delineation of pathogenic CDK5RAP2 and CIT variantsDaniah Albokhari, Rayya A. Almarwani, Emad Khadawardi, Muhamed Saleemi, Najlaa Abdulaziz, Kamal Matar, Mustafa Zubier · 2026 · Molecular Genetics and Metabolism Reports