Nemos C - Search Results

1

A retrospective study by oligonucleotide array-CGH analysis in 50 fetuses with multiple malformations.

Valduga M, Philippe C, Bach Segura P, Thiebaugeorges O, Miton A, Beri M, Bonnet C, Nemos C, Foliguet B, Jonveaux P. Valduga M, et al. Among authors: nemos c. Prenat Diagn. 2010 Apr;30(4):333-41. doi: 10.1002/pd.2460. Prenat Diagn. 2010. PMID: 20155755

2

Screening of subtle copy number changes in Aicardi syndrome patients with a high resolution X chromosome array-CGH.

Yilmaz S, Fontaine H, Brochet K, Grégoire MJ, Devignes MD, Schaff JL, Philippe C, Nemos C, McGregor JL, Jonveaux P. Yilmaz S, et al. Among authors: nemos c. Eur J Med Genet. 2007 Sep-Oct;50(5):386-91. doi: 10.1016/j.ejmg.2007.05.006. Epub 2007 Jun 7. Eur J Med Genet. 2007. PMID: 17625997

3

[Management of the CNVs in constitutional human genetics using array CGH].

Nemos C, Bursztejn AC, Jonveaux P. Nemos C, et al. Pathol Biol (Paris). 2008 Sep;56(6):354-61. doi: 10.1016/j.patbio.2008.03.015. Epub 2008 Jun 2. Pathol Biol (Paris). 2008. PMID: 18515018 Review. French.

4

Mutational spectrum of CDKL5 in early-onset encephalopathies: a study of a large collection of French patients and review of the literature.

Nemos C, Lambert L, Giuliano F, Doray B, Roubertie A, Goldenberg A, Delobel B, Layet V, N'guyen MA, Saunier A, Verneau F, Jonveaux P, Philippe C. Nemos C, et al. Clin Genet. 2009 Oct;76(4):357-71. doi: 10.1111/j.1399-0004.2009.01194.x. Clin Genet. 2009. PMID: 19793311 Review.

5

Molecular characterization of a monosomy 1p36 presenting as an Aicardi syndrome phenocopy.

Bursztejn AC, Bronner M, Peudenier S, Grégoire MJ, Jonveaux P, Nemos C. Bursztejn AC, et al. Among authors: nemos c. Am J Med Genet A. 2009 Nov;149A(11):2493-500. doi: 10.1002/ajmg.a.33051. Am J Med Genet A. 2009. PMID: 19842196

6

Long term culture of mesenchymal stem cells in hypoxia promotes a genetic program maintaining their undifferentiated and multipotent status.

Basciano L, Nemos C, Foliguet B, de Isla N, de Carvalho M, Tran N, Dalloul A. Basciano L, et al. Among authors: nemos c. BMC Cell Biol. 2011 Mar 30;12:12. doi: 10.1186/1471-2121-12-12. BMC Cell Biol. 2011. PMID: 21450070 Free PMC article.

7

Drug delivery by polymeric nanoparticles induces autophagy in macrophages.

Eidi H, Joubert O, Némos C, Grandemange S, Mograbi B, Foliguet B, Tournebize J, Maincent P, Le Faou A, Aboukhamis I, Rihn BH. Eidi H, et al. Among authors: nemos c. Int J Pharm. 2012 Jan 17;422(1-2):495-503. doi: 10.1016/j.ijpharm.2011.11.020. Epub 2011 Nov 22. Int J Pharm. 2012. PMID: 22119964

8

14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements.

Allou L, Lambert L, Amsallem D, Bieth E, Edery P, Destrée A, Rivier F, Amor D, Thompson E, Nicholl J, Harbord M, Nemos C, Saunier A, Moustaïne A, Vigouroux A, Jonveaux P, Philippe C. Allou L, et al. Among authors: nemos c. Eur J Hum Genet. 2012 Dec;20(12):1216-23. doi: 10.1038/ejhg.2012.127. Epub 2012 Jun 27. Eur J Hum Genet. 2012. PMID: 22739344 Free PMC article.

9

Patient with a heterozygous pathogenic variant in CSNK2A1 gene: A new case to update the Okur-Chung neurodevelopmental syndrome.

Blanc A, Bonnet C, Wandzel M, Roth V, Duffourd Y, Safraou H, Leheup B, Muller F, D Colne J, Feillet F, Schmitt E, Castro M, Savatt J, Burcheri A, Nemos C, Philippe C, Lambert L. Blanc A, et al. Among authors: nemos c. Am J Med Genet A. 2024 Sep;194(9):e63642. doi: 10.1002/ajmg.a.63642. Epub 2024 May 6. Am J Med Genet A. 2024. PMID: 38711237

10

Interleukin-24 mediates apoptosis in human B-cells through early activation of cell cycle arrest followed by late induction of the mitochondrial apoptosis pathway.

Hadife N, Nemos C, Frippiat JP, Hamadé T, Perrot A, Dalloul A. Hadife N, et al. Among authors: nemos c. Leuk Lymphoma. 2013 Mar;54(3):587-97. doi: 10.3109/10428194.2012.717079. Epub 2012 Aug 30. Leuk Lymphoma. 2013. PMID: 22860893

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