Coulet F - Search Results

1

[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: coulet f. Ann Dermatol Venereol. 1999 Aug-Sep;126(8-9):600-3. Ann Dermatol Venereol. 1999. PMID: 10530347 Free article. French.

2

Comparative evaluation by semiquantitative reverse transcriptase polymerase chain reaction of MDR1, MRP and GSTp gene expression in breast carcinomas.

Lacave R, Coulet F, Ricci S, Touboul E, Flahault A, Rateau JG, Cesari D, Lefranc JP, Bernaudin JF. Lacave R, et al. Among authors: coulet f. Br J Cancer. 1998 Mar;77(5):694-702. doi: 10.1038/bjc.1998.115. Br J Cancer. 1998. PMID: 9514046 Free PMC article.

3

p53 gene status as a predictor of tumor response to induction chemotherapy of patients with locoregionally advanced squamous cell carcinomas of the head and neck.

Temam S, Flahault A, Périé S, Monceaux G, Coulet F, Callard P, Bernaudin JF, St Guily JL, Fouret P. Temam S, et al. Among authors: coulet f. J Clin Oncol. 2000 Jan;18(2):385-94. doi: 10.1200/JCO.2000.18.2.385. J Clin Oncol. 2000. PMID: 10637254

4

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. Thromb Haemost. 2000 May;83(5):796-7. Thromb Haemost. 2000. PMID: 10823287 No abstract available.

5

[Molecular analysis of genetic predispositions to breast cancer].

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

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: coulet 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: coulet f. Nephrol Dial Transplant. 2001 Dec;16(12):2317-22. doi: 10.1093/ndt/16.12.2317. Nephrol Dial Transplant. 2001. PMID: 11733622

8

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. 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.

9

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: coulet f. Hum Mutat. 2004 Apr;23(4):289-99. doi: 10.1002/humu.20017. Hum Mutat. 2004. PMID: 15024723

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: coulet 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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