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Journal Abstract Search

133 related items for PubMed ID: 26322982

  • 21. Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings.
    Woods CG, Bond J, Enard W.
    Am J Hum Genet; 2005 May; 76(5):717-28. PubMed ID: 15806441
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  • 22. [Update on autosomal recessive primary microcephaly (MCPH)-associated proteins].
    Wang YJ, Zhou XK, Xu D.
    Yi Chuan; 2019 Oct 20; 41(10):905-918. PubMed ID: 31624053
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  • 23. What's the hype about CDK5RAP2?
    Kraemer N, Issa L, Hauck SC, Mani S, Ninnemann O, Kaindl AM.
    Cell Mol Life Sci; 2011 May 20; 68(10):1719-36. PubMed ID: 21327915
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  • 26. Many roads lead to primary autosomal recessive microcephaly.
    Kaindl AM, Passemard S, Kumar P, Kraemer N, Issa L, Zwirner A, Gerard B, Verloes A, Mani S, Gressens P.
    Prog Neurobiol; 2010 Mar 20; 90(3):363-83. PubMed ID: 19931588
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  • 27. CDK5RAP2 Is Required to Maintain the Germ Cell Pool during Embryonic Development.
    Zaqout S, Bessa P, Krämer N, Stoltenburg-Didinger G, Kaindl AM.
    Stem Cell Reports; 2017 Feb 14; 8(2):198-204. PubMed ID: 28162995
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  • 28. Microcephaly-associated protein WDR62 regulates neurogenesis through JNK1 in the developing neocortex.
    Xu D, Zhang F, Wang Y, Sun Y, Xu Z.
    Cell Rep; 2014 Jan 16; 6(1):104-16. PubMed ID: 24388750
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  • 31. A novel nonsense CDK5RAP2 mutation in a Somali child with primary microcephaly and sensorineural hearing loss.
    Pagnamenta AT, Murray JE, Yoon G, Sadighi Akha E, Harrison V, Bicknell LS, Ajilogba K, Stewart H, Kini U, Taylor JC, Keays DA, Jackson AP, Knight SJ.
    Am J Med Genet A; 2012 Oct 16; 158A(10):2577-82. PubMed ID: 22887808
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  • 34. Disruption of Aspm causes microcephaly with abnormal neuronal differentiation.
    Fujimori A, Itoh K, Goto S, Hirakawa H, Wang B, Kokubo T, Kito S, Tsukamoto S, Fushiki S.
    Brain Dev; 2014 Sep 16; 36(8):661-9. PubMed ID: 24220505
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  • 37. A case report: Autosomal recessive microcephaly caused by a novel mutation in MCPH1 gene.
    Ghafouri-Fard S, Fardaei M, Gholami M, Miryounesi M.
    Gene; 2015 Oct 15; 571(1):149-50. PubMed ID: 26192461
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  • 38. Cdk5rap2 interacts with pericentrin to maintain the neural progenitor pool in the developing neocortex.
    Buchman JJ, Tseng HC, Zhou Y, Frank CL, Xie Z, Tsai LH.
    Neuron; 2010 May 13; 66(3):386-402. PubMed ID: 20471352
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  • 39. What next-generation sequencing (NGS) technology has enabled us to learn about primary autosomal recessive microcephaly (MCPH).
    Morris-Rosendahl DJ, Kaindl AM.
    Mol Cell Probes; 2015 Oct 13; 29(5):271-81. PubMed ID: 26050940
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  • 40. Novel alternatively spliced variant form of human CDK5RAP2.
    Kim T, Park JS, Lee P, Jin Y, Fu SB, Rosales JL, Lee KY.
    Cell Cycle; 2011 Mar 15; 10(6):1010-2. PubMed ID: 21346412
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