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Journal Abstract Search

133 related items for PubMed ID: 26322982

  • 1. Novel Alternative Splice Variants of Mouse Cdk5rap2.
    Kraemer N, Issa-Jahns L, Neubert G, Ravindran E, Mani S, Ninnemann O, Kaindl AM.
    PLoS One; 2015; 10(8):e0136684. PubMed ID: 26322982
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  • 2. 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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  • 3. Loss of CDK5RAP2 affects neural but not non-neural mESC differentiation into cardiomyocytes.
    Kraemer N, Ravindran E, Zaqout S, Neubert G, Schindler D, Ninnemann O, Gräf R, Seiler AE, Kaindl AM.
    Cell Cycle; 2015 Apr 15; 14(13):2044-57. PubMed ID: 25942099
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  • 4. CDK5RAP2 expression during murine and human brain development correlates with pathology in primary autosomal recessive microcephaly.
    Issa L, Kraemer N, Rickert CH, Sifringer M, Ninnemann O, Stoltenburg-Didinger G, Kaindl AM.
    Cereb Cortex; 2013 Sep 15; 23(9):2245-60. PubMed ID: 22806269
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  • 5. Altered inhibition and excitation in neocortical circuits in congenital microcephaly.
    Zaqout S, Blaesius K, Wu YJ, Ott S, Kraemer N, Becker LL, Rosário M, Rosenmund C, Strauss U, Kaindl AM.
    Neurobiol Dis; 2019 Sep 15; 129():130-143. PubMed ID: 31102767
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  • 9. Proteome changes in autosomal recessive primary microcephaly.
    Zaqout S, Mannaa A, Klein O, Krajewski A, Klose J, Luise-Becker L, Elsabagh A, Ferih K, Kraemer N, Ravindran E, Makridis K, Kaindl AM.
    Ann Hum Genet; 2023 Mar 15; 87(1-2):50-62. PubMed ID: 36448252
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  • 10. Congenital microcephaly-linked CDK5RAP2 affects eye development.
    Zaqout S, Ravindran E, Stoltenburg-Didinger G, Kaindl AM.
    Ann Hum Genet; 2020 Jan 15; 84(1):87-91. PubMed ID: 31355417
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  • 11. Species-Specific Expression of Full-Length and Alternatively Spliced Variant Forms of CDK5RAP2.
    Park JS, Lee MK, Kang S, Jin Y, Fu S, Rosales JL, Lee KY.
    PLoS One; 2015 Jan 15; 10(11):e0142577. PubMed ID: 26550838
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  • 12. CDK5RAP2 primary microcephaly is associated with hypothalamic, retinal and cochlear developmental defects.
    Nasser H, Vera L, Elmaleh-Bergès M, Steindl K, Letard P, Teissier N, Ernault A, Guimiot F, Afenjar A, Moutard ML, Héron D, Alembik Y, Momtchilova M, Milani P, Kubis N, Pouvreau N, Zollino M, Guilmin Crepon S, Kaguelidou F, Gressens P, Verloes A, Rauch A, El Ghouzzi V, Drunat S, Passemard S.
    J Med Genet; 2020 Jun 15; 57(6):389-399. PubMed ID: 32015000
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  • 13. Autosomal recessive primary microcephalies (MCPH).
    Kaindl AM.
    Eur J Paediatr Neurol; 2014 Jul 15; 18(4):547-8. PubMed ID: 24780602
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  • 14. A novel splice-site mutation in the ASPM gene underlies autosomal recessive primary microcephaly.
    Hashmi JA, Al-Harbi KM, Ramzan K, Albalawi AM, Mehmood A, Samman MI, Basit S.
    Ann Saudi Med; 2016 Jul 15; 36(6):391-396. PubMed ID: 27920410
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  • 18. CDK5RAP2 interaction with components of the Hippo signaling pathway may play a role in primary microcephaly.
    Sukumaran SK, Stumpf M, Salamon S, Ahmad I, Bhattacharya K, Fischer S, Müller R, Altmüller J, Budde B, Thiele H, Tariq M, Malik NA, Nürnberg P, Baig SM, Hussain MS, Noegel AA.
    Mol Genet Genomics; 2017 Apr 15; 292(2):365-383. PubMed ID: 28004182
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