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498 results

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Page 1
ZIKA virus elicits P53 activation and genotoxic stress in human neural progenitors similar to mutations involved in severe forms of genetic microcephaly.
Ghouzzi VE, Bianchi FT, Molineris I, Mounce BC, Berto GE, Rak M, Lebon S, Aubry L, Tocco C, Gai M, Chiotto AM, Sgrò F, Pallavicini G, Simon-Loriere E, Passemard S, Vignuzzi M, Gressens P, Di Cunto F. Ghouzzi VE, et al. Among authors: gressens p. Cell Death Dis. 2016 Oct 27;7(10):e2440. doi: 10.1038/cddis.2016.266. Cell Death Dis. 2016. PMID: 27787521 Free PMC article.
Autosomal recessive primary microcephalies (MCPH).
Kaindl AM, Passemard S, Gressens P. Kaindl AM, et al. Among authors: gressens p. Eur J Paediatr Neurol. 2009 Sep;13(5):458. doi: 10.1016/j.ejpn.2008.07.010. Epub 2008 Sep 5. Eur J Paediatr Neurol. 2009. PMID: 18774316 No abstract available.
Vulnerability of white matter towards antenatal hypoxia is linked to a species-dependent regulation of glutamate receptor subunits.
Fontaine RH, Olivier P, Massonneau V, Leroux P, Degos V, Lebon S, El Ghouzzi V, Lelièvre V, Gressens P, Baud O. Fontaine RH, et al. Among authors: gressens p. Proc Natl Acad Sci U S A. 2008 Oct 28;105(43):16779-84. doi: 10.1073/pnas.0803004105. Epub 2008 Oct 15. Proc Natl Acad Sci U S A. 2008. PMID: 18922769 Free PMC article.
Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations.
Passemard S, Titomanlio L, Elmaleh M, Afenjar A, Alessandri JL, Andria G, de Villemeur TB, Boespflug-Tanguy O, Burglen L, Del Giudice E, Guimiot F, Hyon C, Isidor B, Mégarbané A, Moog U, Odent S, Hernandez K, Pouvreau N, Scala I, Schaer M, Gressens P, Gerard B, Verloes A. Passemard S, et al. Among authors: gressens p. Neurology. 2009 Sep 22;73(12):962-9. doi: 10.1212/WNL.0b013e3181b8799a. Neurology. 2009. PMID: 19770472
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. Kaindl AM, et al. Among authors: gressens p. Prog Neurobiol. 2010 Mar;90(3):363-83. doi: 10.1016/j.pneurobio.2009.11.002. Epub 2009 Dec 2. Prog Neurobiol. 2010. PMID: 19931588 Review.
VIP-induced neuroprotection of the developing brain.
Passemard S, Sokolowska P, Schwendimann L, Gressens P. Passemard S, et al. Among authors: gressens p. Curr Pharm Des. 2011;17(10):1036-9. doi: 10.2174/138161211795589409. Curr Pharm Des. 2011. PMID: 21524251 Free PMC article. Review.
VIP blockade leads to microcephaly in mice via disruption of Mcph1-Chk1 signaling.
Passemard S, El Ghouzzi V, Nasser H, Verney C, Vodjdani G, Lacaud A, Lebon S, Laburthe M, Robberecht P, Nardelli J, Mani S, Verloes A, Gressens P, Lelièvre V. Passemard S, et al. Among authors: gressens p. J Clin Invest. 2011 Aug;121(8):3071-87. doi: 10.1172/JCI43824. J Clin Invest. 2011. PMID: 21737879 Free PMC article.
A novel RAB33B mutation in Smith-McCort dysplasia.
Dupuis N, Lebon S, Kumar M, Drunat S, Graul-Neumann LM, Gressens P, El Ghouzzi V. Dupuis N, et al. Among authors: gressens p. Hum Mutat. 2013 Feb;34(2):283-6. doi: 10.1002/humu.22235. Epub 2012 Nov 8. Hum Mutat. 2013. PMID: 23042644 Free article.
Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities.
Breuss M, Heng JI, Poirier K, Tian G, Jaglin XH, Qu Z, Braun A, Gstrein T, Ngo L, Haas M, Bahi-Buisson N, Moutard ML, Passemard S, Verloes A, Gressens P, Xie Y, Robson KJ, Rani DS, Thangaraj K, Clausen T, Chelly J, Cowan NJ, Keays DA. Breuss M, et al. Among authors: gressens p. Cell Rep. 2012 Dec 27;2(6):1554-62. doi: 10.1016/j.celrep.2012.11.017. Epub 2012 Dec 13. Cell Rep. 2012. PMID: 23246003 Free PMC article. Clinical Trial.
498 results