Dalloz C - Search Results

1

Deletion of 5' sequences of the CSB gene provides insight into the pathophysiology of Cockayne syndrome.

Laugel V, Dalloz C, Stary A, Cormier-Daire V, Desguerre I, Renouil M, Fourmaintraux A, Velez-Cruz R, Egly JM, Sarasin A, Dollfus H. Laugel V, et al. Among authors: dalloz c. Eur J Hum Genet. 2008 Mar;16(3):320-7. doi: 10.1038/sj.ejhg.5201991. Epub 2008 Jan 9. Eur J Hum Genet. 2008. PMID: 18183039

2

Cerebro-oculo-facio-skeletal syndrome: three additional cases with CSB mutations, new diagnostic criteria and an approach to investigation.

Laugel V, Dalloz C, Tobias ES, Tolmie JL, Martin-Coignard D, Drouin-Garraud V, Valayannopoulos V, Sarasin A, Dollfus H. Laugel V, et al. Among authors: dalloz c. J Med Genet. 2008 Sep;45(9):564-71. doi: 10.1136/jmg.2007.057141. Epub 2008 Jul 15. J Med Genet. 2008. PMID: 18628313

3

Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome.

Laugel V, Dalloz C, Durand M, Sauvanaud F, Kristensen U, Vincent MC, Pasquier L, Odent S, Cormier-Daire V, Gener B, Tobias ES, Tolmie JL, Martin-Coignard D, Drouin-Garraud V, Heron D, Journel H, Raffo E, Vigneron J, Lyonnet S, Murday V, Gubser-Mercati D, Funalot B, Brueton L, Sanchez Del Pozo J, Muñoz E, Gennery AR, Salih M, Noruzinia M, Prescott K, Ramos L, Stark Z, Fieggen K, Chabrol B, Sarda P, Edery P, Bloch-Zupan A, Fawcett H, Pham D, Egly JM, Lehmann AR, Sarasin A, Dollfus H. Laugel V, et al. Among authors: dalloz c. Hum Mutat. 2010 Feb;31(2):113-26. doi: 10.1002/humu.21154. Hum Mutat. 2010. PMID: 19894250

4

Neuroimaging in Cockayne syndrome.

Koob M, Laugel V, Durand M, Fothergill H, Dalloz C, Sauvanaud F, Dollfus H, Namer IJ, Dietemann JL. Koob M, et al. Among authors: dalloz c. AJNR Am J Neuroradiol. 2010 Oct;31(9):1623-30. doi: 10.3174/ajnr.A2135. Epub 2010 Jun 3. AJNR Am J Neuroradiol. 2010. PMID: 20522568 Free PMC article.

5

[Clinical and social statistics on the remote results of 22 systematically followed up pneumonectomies].

MEYER L, de ROUGEMONT, DALLOZ C, DURAND M, ALAUX P. MEYER L, et al. Among authors: dalloz c. Mars Med. 1962;99:844-52. Mars Med. 1962. PMID: 13935293 French. No abstract available.

6

Targeted inactivation of dystrophin gene product Dp71: phenotypic impact in mouse retina.

Dalloz C, Sarig R, Fort P, Yaffe D, Bordais A, Pannicke T, Grosche J, Mornet D, Reichenbach A, Sahel J, Nudel U, Rendon A. Dalloz C, et al. Hum Mol Genet. 2003 Jul 1;12(13):1543-54. doi: 10.1093/hmg/ddg170. Hum Mol Genet. 2003. PMID: 12812982

7

Differential distribution of the members of the dystrophin glycoprotein complex in mouse retina: effect of the mdx(3Cv) mutation.

Dalloz C, Claudepierre T, Rodius F, Mornet D, Sahel J, Rendon A. Dalloz C, et al. Mol Cell Neurosci. 2001 May;17(5):908-20. doi: 10.1006/mcne.2001.0978. Mol Cell Neurosci. 2001. PMID: 11358487

8

Characterization of the intermolecular associations of the dystrophin-associated glycoprotein complex in retinal Müller glial cells.

Claudepierre T, Dalloz C, Mornet D, Matsumura K, Sahel J, Rendon A. Claudepierre T, et al. Among authors: dalloz c. J Cell Sci. 2000 Oct;113 Pt 19:3409-17. doi: 10.1242/jcs.113.19.3409. J Cell Sci. 2000. PMID: 10984432

9

Expression of Dp71 in Müller glial cells: a comparison with utrophin- and dystrophin-associated proteins.

Claudepierre T, Mornet D, Pannicke T, Forster V, Dalloz C, Bolaños F, Sahel J, Reichenbach A, Rendon A. Claudepierre T, et al. Among authors: dalloz c. Invest Ophthalmol Vis Sci. 2000 Jan;41(1):294-304. Invest Ophthalmol Vis Sci. 2000. PMID: 10634634

10

[Congenital heart diseases in the adult].

Normand J, Bozio A, Joffre B, Age C, Dalloz C. Normand J, et al. Among authors: dalloz c. Rev Prat. 1980 Apr 1;30(19):1227-33. Rev Prat. 1980. PMID: 7367794 French. No abstract available.

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