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Journal Abstract Search

261 related items for PubMed ID: 21529752

  • 1. The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis.
    Bakircioglu M, Carvalho OP, Khurshid M, Cox JJ, Tuysuz B, Barak T, Yilmaz S, Caglayan O, Dincer A, Nicholas AK, Quarrell O, Springell K, Karbani G, Malik S, Gannon C, Sheridan E, Crosier M, Lisgo SN, Lindsay S, Bilguvar K, Gergely F, Gunel M, Woods CG.
    Am J Hum Genet; 2011 May 13; 88(5):523-35. PubMed ID: 21529752
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  • 2. Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected].
    Alkuraya FS, Cai X, Emery C, Mochida GH, Al-Dosari MS, Felie JM, Hill RS, Barry BJ, Partlow JN, Gascon GG, Kentab A, Jan M, Shaheen R, Feng Y, Walsh CA.
    Am J Hum Genet; 2011 May 13; 88(5):536-47. PubMed ID: 21529751
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  • 3. Novel NDE1 homozygous mutation resulting in microhydranencephaly and not microlyssencephaly.
    Guven A, Gunduz A, Bozoglu TM, Yalcinkaya C, Tolun A.
    Neurogenetics; 2012 Aug 13; 13(3):189-94. PubMed ID: 22526350
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  • 5. [Microlissencephaly due to pathogenic variants of NDE1: from pathology to normal brain development].
    Cabet S, Guibaud L, Sanlaville D.
    Med Sci (Paris); 2020 Oct 13; 36(10):866-871. PubMed ID: 33026328
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  • 8. The scaffold protein Nde1 safeguards the brain genome during S phase of early neural progenitor differentiation.
    Houlihan SL, Feng Y.
    Elife; 2014 Sep 23; 3():e03297. PubMed ID: 25245017
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  • 10. Mitotic spindle regulation by Nde1 controls cerebral cortical size.
    Feng Y, Walsh CA.
    Neuron; 2004 Oct 14; 44(2):279-93. PubMed ID: 15473967
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  • 11. Severe NDE1-mediated microcephaly results from neural progenitor cell cycle arrests at multiple specific stages.
    Doobin DJ, Kemal S, Dantas TJ, Vallee RB.
    Nat Commun; 2016 Aug 24; 7():12551. PubMed ID: 27553190
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  • 20. p78/MCRS1 forms a complex with centrosomal protein Nde1 and is essential for cell viability.
    Hirohashi Y, Wang Q, Liu Q, Du X, Zhang H, Sato N, Greene MI.
    Oncogene; 2006 Aug 10; 25(35):4937-46. PubMed ID: 16547491
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