Soubrier F - Search Results

1

Unexplained polyposis: a challenge for geneticists, pathologists and gastroenterologists.

Mongin C, Coulet F, Lefevre JH, Colas C, Svrcek M, Eyries M, Lahely Y, Fléjou JF, Soubrier F, Parc Y. Mongin C, et al. Among authors: soubrier f. Clin Genet. 2012 Jan;81(1):38-46. doi: 10.1111/j.1399-0004.2011.01676.x. Epub 2011 May 4. Clin Genet. 2012. PMID: 21476993

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

Lack of association of the prothrombin gene variant G20210A with myocardial infarction in Caucasian males.

Coulet F, Godard V, Verdy E, Soubrier F. Coulet F, et al. Among authors: soubrier f. Thromb Haemost. 2000 May;83(5):796-7. Thromb Haemost. 2000. PMID: 10823287 No abstract available.

4

[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.

5

Increased shedding of angiotensin-converting enzyme by a mutation identified in the stalk region.

Eyries M, Michaud A, Deinum J, Agrapart M, Chomilier J, Kramers C, Soubrier F. Eyries M, et al. Among authors: soubrier f. J Biol Chem. 2001 Feb 23;276(8):5525-32. doi: 10.1074/jbc.M007706200. Epub 2000 Nov 13. J Biol Chem. 2001. PMID: 11076943 Free article.

6

Deep vein thrombosis during enoxaparin prophylactic treatment in a young pregnant woman homozygous for factor V Leiden and heterozygous for the G127-->a mutation in the thrombomodulin gene.

Magdelaine A, Verdy E, Coulet F, Berkane N, Girot R, Uzan S, Soubrier F. Magdelaine A, et al. Among authors: soubrier f. Blood Coagul Fibrinolysis. 2000 Dec;11(8):761-5. doi: 10.1097/00001721-200012000-00010. Blood Coagul Fibrinolysis. 2000. PMID: 11132655

7

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

8

Phorbol ester induction of angiotensin-converting enzyme transcription is mediated by Egr-1 and AP-1 in human endothelial cells via ERK1/2 pathway.

Eyries M, Agrapart M, Alonso A, Soubrier F. Eyries M, et al. Among authors: soubrier f. Circ Res. 2002 Nov 15;91(10):899-906. doi: 10.1161/01.res.0000042703.39845.b4. Circ Res. 2002. PMID: 12433834

9

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.

10

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.

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