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Journal Abstract Search

270 related items for PubMed ID: 27453578

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  • 3. CIT, a gene involved in neurogenic cytokinesis, is mutated in human primary microcephaly.
    Basit S, Al-Harbi KM, Alhijji SA, Albalawi AM, Alharby E, Eldardear A, Samman MI.
    Hum Genet; 2016 Oct; 135(10):1199-207. PubMed ID: 27519304
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  • 7. PLK1-mediated phosphorylation of WDR62/MCPH2 ensures proper mitotic spindle orientation.
    Miyamoto T, Akutsu SN, Fukumitsu A, Morino H, Masatsuna Y, Hosoba K, Kawakami H, Yamamoto T, Shimizu K, Ohashi H, Matsuura S.
    Hum Mol Genet; 2017 Nov 15; 26(22):4429-4440. PubMed ID: 28973348
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  • 8. Mutations in the microtubule-associated protein MAP11 (C7orf43) cause microcephaly in humans and zebrafish.
    Perez Y, Bar-Yaacov R, Kadir R, Wormser O, Shelef I, Birk OS, Flusser H, Birnbaum RY.
    Brain; 2019 Mar 01; 142(3):574-585. PubMed ID: 30715179
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  • 9. Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutation.
    Issa L, Mueller K, Seufert K, Kraemer N, Rosenkotter H, Ninnemann O, Buob M, Kaindl AM, Morris-Rosendahl DJ.
    Orphanet J Rare Dis; 2013 Apr 15; 8():59. PubMed ID: 23587236
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  • 11. Mutations in WDR62, encoding a centrosomal and nuclear protein, in Indian primary microcephaly families with cortical malformations.
    Bhat V, Girimaji SC, Mohan G, Arvinda HR, Singhmar P, Duvvari MR, Kumar A.
    Clin Genet; 2011 Dec 15; 80(6):532-40. PubMed ID: 21496009
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  • 12. Citron kinase - renaissance of a neglected mitotic kinase.
    D'Avino PP.
    J Cell Sci; 2017 May 15; 130(10):1701-1708. PubMed ID: 28468989
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  • 13. Genetic interaction between PLK1 and downstream MCPH proteins in the control of centrosome asymmetry and cell fate during neural progenitor division.
    González-Martínez J, Cwetsch AW, Gilabert-Juan J, Gómez J, Garaulet G, Schneider P, de Cárcer G, Mulero F, Caleiras E, Megías D, Porlan E, Malumbres M.
    Cell Death Differ; 2022 Aug 15; 29(8):1474-1485. PubMed ID: 35058575
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  • 14. Angelman syndrome protein UBE3A interacts with primary microcephaly protein ASPM, localizes to centrosomes and regulates chromosome segregation.
    Singhmar P, Kumar A.
    PLoS One; 2011 Aug 15; 6(5):e20397. PubMed ID: 21633703
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  • 15. Biallelic variants in KIF14 cause intellectual disability with microcephaly.
    Makrythanasis P, Maroofian R, Stray-Pedersen A, Musaev D, Zaki MS, Mahmoud IG, Selim L, Elbadawy A, Jhangiani SN, Coban Akdemir ZH, Gambin T, Sorte HS, Heiberg A, McEvoy-Venneri J, James KN, Stanley V, Belandres D, Guipponi M, Santoni FA, Ahangari N, Tara F, Doosti M, Iwaszkiewicz J, Zoete V, Backe PH, Hamamy H, Gleeson JG, Lupski JR, Karimiani EG, Antonarakis SE.
    Eur J Hum Genet; 2018 Mar 15; 26(3):330-339. PubMed ID: 29343805
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  • 16. Cdk5rap2 exposes the centrosomal root of microcephaly syndromes.
    Megraw TL, Sharkey JT, Nowakowski RS.
    Trends Cell Biol; 2011 Aug 15; 21(8):470-80. PubMed ID: 21632253
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  • 17. Misregulation of mitotic chromosome segregation in a new type of autosomal recessive primary microcephaly.
    Marchal JA, Ghani M, Schindler D, Gavvovidis I, Winkler T, Esquitino V, Sternberg N, Busche A, Krawitz P, Hecht J, Robinson P, Mundlos S, Graul-Neumann L, Sperling K, Trimborn M, Neitzel H.
    Cell Cycle; 2011 Sep 01; 10(17):2967-77. PubMed ID: 21857152
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  • 18. Overexpression of the PLK4 Gene as a Novel Strategy for the Treatment of Autosomal Recessive Microcephaly by Improving Centrosomal Dysfunction.
    Xu YS, Su ZY, Sun L, Yang XM, Sun SY, Ji XF, Ji YZ, Zhang SQ, Tian J, Wu QC.
    J Mol Neurosci; 2021 Dec 01; 71(12):2618-2627. PubMed ID: 34272646
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  • 19. Molecular and cellular basis of autosomal recessive primary microcephaly.
    Barbelanne M, Tsang WY.
    Biomed Res Int; 2014 Dec 01; 2014():547986. PubMed ID: 25548773
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  • 20. Mutations in STIL, encoding a pericentriolar and centrosomal protein, cause primary microcephaly.
    Kumar A, Girimaji SC, Duvvari MR, Blanton SH.
    Am J Hum Genet; 2009 Feb 01; 84(2):286-90. PubMed ID: 19215732
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