02.12.2012 Views

annuaire partie 4 pdf - Cours et travaux - Collège - Collège de France

annuaire partie 4 pdf - Cours et travaux - Collège - Collège de France

annuaire partie 4 pdf - Cours et travaux - Collège - Collège de France

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

LES ÉQUIPES ACCUEILLIES AU COLLÈGE DE FRANCE 1053<br />

6. Geller D.S., Zhang J., Zennaro M.C., Vallo-Boado A., Rodriguez-Soriano J.,<br />

Furu L., Haws R., M<strong>et</strong>zger D., Botelho B., Karaviti L., Haqq A.M., Corey H.,<br />

Janssens S., Corvol P., Lifton R.P. Autosomal dominant pseudohypoaldosteronism<br />

type 1 : mechanisms, evi<strong>de</strong>nce for neonatal l<strong>et</strong>hality, and phenotypic expression<br />

in adults. J. Am. Soc. Nephrol., 2006 May ; 17(5) : 1429-36.<br />

7. Perdu J., Boutouyrie P., Bourgain C., Stern N., LalouxB., Bozec E.,<br />

Azizi M., Bonaiti-Pellie C., Plouin P.F., Laurent S, Gimenez-Roqueplo A.P.,<br />

Jeunemaître X. Inheritance of arterial lesions in renal fibromuscular dysplasia. J.<br />

Hum. Hypertens., 2007 May ; 21 (5) : 393-400.<br />

8. Perdu J., Gimenez-Roqueplo A.P., Boutouyrie P., Beaujour S., LalouxB.,<br />

Nau V., Fiqu<strong>et</strong>-Kempf B., Emmerich J., Tich<strong>et</strong> J., Plouin P.F., Laurent S., Jeunemaître<br />

X. Alpha1-antitrypsin gene polymorphisms are not associated with renal<br />

arterial fibromuscular dysplasia. J Hypertens., 2006 Apr. ; 24 (4) : 705-10.<br />

9. Pujo L., Fagart J., Gary F., Papadimitriou D.T., Claes A., Jeunemaître X.,<br />

Zennaro M.C. Mineralocorticoid receptor mutations are the principal cause of<br />

renal type 1 pseudohypoaldosteronism. Hum Mutat., 2007 Jan ; 28 (1) : 33-40.<br />

10. Sainte Marie Y., Toulon A., Paus R., Maubec E., Cherfa A., Grossin M.,<br />

Descamps V., Clemessy M., Gasc J.M., Peuchmaur M., Glick A., Farman N.,<br />

Jaisser F. Targ<strong>et</strong>ed Skin Overexpression of the Mineralocorticoid Receptor in<br />

Mice Causes Epi<strong>de</strong>rmal Atrophy, Premature Skin Barrier Formation, Eye Abnormalities,<br />

and Alopecia. Am. J. Pathol., 2007, 171 (3) : 846-60.<br />

11. Sainte-Marie Y., Cat A.N., Perrier R, Mangin L., Soukaseum C., Peuchmaur<br />

M., Tronche F., Farman N., Escoub<strong>et</strong> B., Benitah J.P., Jaisser F. Conditional<br />

glucocorticoid receptor expression in the heart induces atrio-ventricular block.<br />

FASEB J., 2007, 21 (12) : 3133-41.<br />

12. Vargas-Poussou R., Houillier P., Le Pottier N., Strompf L., Loirat C.,<br />

Baudouin V., Macher M.A., DechauxM., Ulinski T., Nobili F., Eckart P.,<br />

Novo R., Cailliez M., Salomon R., Niv<strong>et</strong> H., Cochat P., Tack I., Fargeot A.,<br />

Bouissou F., Kesler G.R., Lorotte S, Go<strong>de</strong>froid N., Lay<strong>et</strong> V, Morin G., Jeunemaître<br />

X., Blanchard A. Gen<strong>et</strong>ic investigation of autosomal recessive distal renal<br />

tubular acidosis : evi<strong>de</strong>nce for early sensorineural hearing loss associated with<br />

mutations in the ATP6V0A4 gene. J. Am. Soc. Nephrol., 2006 May ; 17 (5) :<br />

1437-43.<br />

13. Zhu L., VranckxR., Khau Van Kien P., Lalan<strong>de</strong> A., Boiss<strong>et</strong> N.,<br />

Mathieu F., Wegman M., Glancy L., Gasc J.M., Brunotte F., Bruneval P.,<br />

Wolf J.E., Michel J.B., Jeunemaître X. Mutations in myosin heavy chain 11<br />

cause a syndrome associating thoracic aortic aneurysm/aortic dissection and<br />

patent ductus arteriosus. Nat. Gen<strong>et</strong>., 2006 Mar. ; 38 (3) : 343-9.<br />

5983$$ UNEQ 21-01-2008 17:11:20Imprimerie CHIRAT

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!