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Journal Abstract Search

176 related items for PubMed ID: 25942099

  • 21. A novel mutation in CDK5RAP2 gene causes primary microcephaly with speech impairment and sparse eyebrows in a consanguineous Pakistani family.
    Abdullah U, Farooq M, Mang Y, Marriam Bakhtiar S, Fatima A, Hansen L, Kjaer KW, Larsen LA, Faryal S, Tommerup N, Mahmood Baig S.
    Eur J Med Genet; 2017 Dec; 60(12):627-630. PubMed ID: 28778786
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  • 24. Generation of iPSC-derived Human Brain Organoids to Model Early Neurodevelopmental Disorders.
    Gabriel E, Gopalakrishnan J.
    J Vis Exp; 2017 Apr 14; (122):. PubMed ID: 28448044
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  • 27. Isolation and characterization of alveolar epithelial type II cells derived from mouse embryonic stem cells.
    Sun H, Quan Y, Yan Q, Peng X, Mao Z, Wetsel RA, Wang D.
    Tissue Eng Part C Methods; 2014 Jun 14; 20(6):464-72. PubMed ID: 24102479
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  • 28. Enhancement of Spontaneous Activity by HCN4 Overexpression in Mouse Embryonic Stem Cell-Derived Cardiomyocytes - A Possible Biological Pacemaker.
    Saito Y, Nakamura K, Yoshida M, Sugiyama H, Ohe T, Kurokawa J, Furukawa T, Takano M, Nagase S, Morita H, Kusano KF, Ito H.
    PLoS One; 2015 Jun 14; 10(9):e0138193. PubMed ID: 26384234
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  • 29. Comparison of two different media for maturation rate of neural progenitor cells to neuronal and glial cells emphasizing on expression of neurotrophins and their respective receptors.
    Ebadi R, Kordi-Tamandani DM, Ghaedi K, Nasr-Esfahani MH.
    Mol Biol Rep; 2018 Dec 14; 45(6):2377-2391. PubMed ID: 30306506
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  • 30. 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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  • 33. The impact of TP53 activation and apoptosis in primary hereditary microcephaly.
    Iegiani G, Ferraro A, Pallavicini G, Di Cunto F.
    Front Neurosci; 2023 Feb 14; 17():1220010. PubMed ID: 37457016
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  • 34. Resveratrol promotes differentiation of mouse embryonic stem cells to cardiomyocytes.
    Ding H, Xu X, Qin X, Yang C, Feng Q.
    Cardiovasc Ther; 2016 Aug 14; 34(4):283-9. PubMed ID: 27225714
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  • 35. The expression of calcium-sensing receptor in mouse embryonic stem cells (mESCs) and its influence on differentiation of mESC into cardiomyocytes.
    Sun J, He W, Bai SZ, Peng X, Zhang N, Li HX, Zhang WH, Wang LN, Shao XQ, He YQ, Yang GD, Wu LY, Wang R, Xu CQ.
    Differentiation; 2013 Jan 14; 85(1-2):32-40. PubMed ID: 23314289
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  • 37. [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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  • 38. Compound heterozygote CDK5RAP2 mutations in a Guatemalan/Honduran child with autosomal recessive primary microcephaly, failure to thrive and speech delay.
    Li MH, Arndt K, Das S, Weiss EM, Wu Y, Gwal K, Shekdar KV, Zackai EH.
    Am J Med Genet A; 2015 Jun 20; 167(6):1414-7. PubMed ID: 25899944
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