Soubrier F - Search Results

1

Hereditary hemorrhagic telangiectasia: evidence for regional founder effects of ACVRL1 mutations in French and Italian patients.

Lesca G, Genin E, Blachier C, Olivieri C, Coulet F, Brunet G, Dupuis-Girod S, Buscarini E, Soubrier F, Calender A, Danesino C, Giraud S, Plauchu H; French-Italian HHT Network. Lesca G, et al. Among authors: soubrier f. Eur J Hum Genet. 2008 Jun;16(6):742-9. doi: 10.1038/ejhg.2008.3. Epub 2008 Feb 20. Eur J Hum Genet. 2008. PMID: 18285823

2

[Mutation in the MSH2 gene in Muir-Torre syndrome].

Godard V, Coulet F, Bernaudin JF, Housset M, Soubrier F. Godard V, et al. Among authors: soubrier f. Ann Dermatol Venereol. 1999 Aug-Sep;126(8-9):600-3. Ann Dermatol Venereol. 1999. PMID: 10530347 Free article. French.

3

[Molecular analysis of genetic predispositions to breast cancer].

Coulet F, Godard V, Dumont C, Soubrier F. Coulet F, et al. Among authors: soubrier f. Bull Acad Natl Med. 1999;183(8):1627-39; discussion 1639-41. Bull Acad Natl Med. 1999. PMID: 10987054 French.

4

No evidence for point mutations of the calcium-sensing receptor in familial idiopathic hypercalciuria.

Lerolle N, Coulet F, Lantz B, Paillard F, Houillier P, Soubrier F, Gattegno B, Jeunemaitre X, Ronco P, Rondeau E. Lerolle N, et al. Among authors: soubrier f. Nephrol Dial Transplant. 2001 Dec;16(12):2317-22. doi: 10.1093/ndt/16.12.2317. Nephrol Dial Transplant. 2001. PMID: 11733622

5

Identification of hypoxia-response element in the human endothelial nitric-oxide synthase gene promoter.

Coulet F, Nadaud S, Agrapart M, Soubrier F. Coulet F, et al. Among authors: soubrier f. J Biol Chem. 2003 Nov 21;278(47):46230-40. doi: 10.1074/jbc.M305420200. Epub 2003 Sep 8. J Biol Chem. 2003. PMID: 12963737 Free article.

6

Molecular screening of ALK1/ACVRL1 and ENG genes in hereditary hemorrhagic telangiectasia in France.

Lesca G, Plauchu H, Coulet F, Lefebvre S, Plessis G, Odent S, Rivière S, Leheup B, Goizet C, Carette MF, Cordier JF, Pinson S, Soubrier F, Calender A, Giraud S; French Rendu-Osler Network. Lesca G, et al. Among authors: soubrier f. Hum Mutat. 2004 Apr;23(4):289-99. doi: 10.1002/humu.20017. Hum Mutat. 2004. PMID: 15024723

7

Endoglin germline mutation in a patient with hereditary haemorrhagic telangiectasia and dexfenfluramine associated pulmonary arterial hypertension.

Chaouat A, Coulet F, Favre C, Simonneau G, Weitzenblum E, Soubrier F, Humbert M. Chaouat A, et al. Among authors: soubrier f. Thorax. 2004 May;59(5):446-8. doi: 10.1136/thx.2003.11890. Thorax. 2004. PMID: 15115879 Free PMC article.

8

Altered endothelial gene expression associated with hereditary haemorrhagic telangiectasia.

Thomas B, Eyries M, Montagne K, Martin S, Agrapart M, Simerman-François R, Letarte M, Soubrier F. Thomas B, et al. Among authors: soubrier f. Eur J Clin Invest. 2007 Jul;37(7):580-8. doi: 10.1111/j.1365-2362.2007.01824.x. Eur J Clin Invest. 2007. PMID: 17576210

9

Clinical outcomes of pulmonary arterial hypertension in carriers of BMPR2 mutation.

Sztrymf B, Coulet F, Girerd B, Yaici A, Jais X, Sitbon O, Montani D, Souza R, Simonneau G, Soubrier F, Humbert M. Sztrymf B, et al. Among authors: soubrier f. Am J Respir Crit Care Med. 2008 Jun 15;177(12):1377-83. doi: 10.1164/rccm.200712-1807OC. Epub 2008 Mar 20. Am J Respir Crit Care Med. 2008. PMID: 18356561

10

First genetic analysis in Tunisian familial adenomatous polyposis probands.

Bougatef K, Marrakchi R, Moussa A, Blondeau-Lahely Y, Najjar T, Coulet F, Colas C, Ben Ayed F, Ben Ammar Elgaaied A, Soubrier F. Bougatef K, et al. Among authors: soubrier f. Oncol Rep. 2008 May;19(5):1213-8. Oncol Rep. 2008. PMID: 18425378

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