Coulet F - Search Results

1

Characteristics of pulmonary arterial hypertension in affected carriers of a mutation located in the cytoplasmic tail of bone morphogenetic protein receptor type 2.

Girerd B, Coulet F, Jaïs X, Eyries M, Van Der Bruggen C, De Man F, Houweling A, Dorfmüller P, Savale L, Sitbon O, Vonk-Noordegraaf A, Soubrier F, Simonneau G, Humbert M, Montani D. Girerd B, et al. Among authors: coulet f. Chest. 2015 May;147(5):1385-1394. doi: 10.1378/chest.14-0880. Chest. 2015. PMID: 25429696

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: coulet 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. 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: coulet 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. 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

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.

7

Role of truncating mutations in MME gene in fetomaternal alloimmunisation and antenatal glomerulopathies.

Debiec H, Nauta J, Coulet F, van der Burg M, Guigonis V, Schurmans T, de Heer E, Soubrier F, Janssen F, Ronco P. Debiec H, et al. Among authors: coulet f. Lancet. 2004 Oct 2-8;364(9441):1252-9. doi: 10.1016/S0140-6736(04)17142-0. Lancet. 2004. PMID: 15464186

8

Mutations of the TGF-beta type II receptor BMPR2 in pulmonary arterial hypertension.

Machado RD, Aldred MA, James V, Harrison RE, Patel B, Schwalbe EC, Gruenig E, Janssen B, Koehler R, Seeger W, Eickelberg O, Olschewski H, Elliott CG, Glissmeyer E, Carlquist J, Kim M, Torbicki A, Fijalkowska A, Szewczyk G, Parma J, Abramowicz MJ, Galie N, Morisaki H, Kyotani S, Nakanishi N, Morisaki T, Humbert M, Simonneau G, Sitbon O, Soubrier F, Coulet F, Morrell NW, Trembath RC. Machado RD, et al. Among authors: coulet f. Hum Mutat. 2006 Feb;27(2):121-32. doi: 10.1002/humu.20285. Hum Mutat. 2006. PMID: 16429395

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: coulet 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

Quantitative PCR high-resolution melting (qPCR-HRM) curve analysis, a new approach to simultaneously screen point mutations and large rearrangements: application to MLH1 germline mutations in Lynch syndrome.

Rouleau E, Lefol C, Bourdon V, Coulet F, Noguchi T, Soubrier F, Bièche I, Olschwang S, Sobol H, Lidereau R. Rouleau E, et al. Among authors: coulet f. Hum Mutat. 2009 Jun;30(6):867-75. doi: 10.1002/humu.20947. Hum Mutat. 2009. PMID: 19224586

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