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Items: 34


Hearing is normal without connexin30.

Boulay AC, del Castillo FJ, Giraudet F, Hamard G, Giaume C, Petit C, Avan P, Cohen-Salmon M.

J Neurosci. 2013 Jan 9;33(2):430-4. doi: 10.1523/JNEUROSCI.4240-12.2013.


Depressed levels of prostaglandin F2α in mice lacking Akr1b7 increase basal adiposity and predispose to diet-induced obesity.

Volat FE, Pointud JC, Pastel E, Morio B, Sion B, Hamard G, Guichardant M, Colas R, Lefrançois-Martinez AM, Martinez A.

Diabetes. 2012 Nov;61(11):2796-806. doi: 10.2337/db11-1297. Epub 2012 Jul 30.


Sumoylation by Ubc9 regulates the stem cell compartment and structure and function of the intestinal epithelium in mice.

Demarque MD, Nacerddine K, Neyret-Kahn H, Andrieux A, Danenberg E, Jouvion G, Bomme P, Hamard G, Romagnolo B, Terris B, Cumano A, Barker N, Clevers H, Dejean A.

Gastroenterology. 2011 Jan;140(1):286-96. doi: 10.1053/j.gastro.2010.10.002. Epub 2010 Oct 14.


The AMPKγ1 subunit plays an essential role in erythrocyte membrane elasticity, and its genetic inactivation induces splenomegaly and anemia.

Foretz M, Hébrard S, Guihard S, Leclerc J, Do Cruzeiro M, Hamard G, Niedergang F, Gaudry M, Viollet B.

FASEB J. 2011 Jan;25(1):337-47. doi: 10.1096/fj.10-169383. Epub 2010 Sep 29.


Cubilin is essential for albumin reabsorption in the renal proximal tubule.

Amsellem S, Gburek J, Hamard G, Nielsen R, Willnow TE, Devuyst O, Nexo E, Verroust PJ, Christensen EI, Kozyraki R.

J Am Soc Nephrol. 2010 Nov;21(11):1859-67. doi: 10.1681/ASN.2010050492. Epub 2010 Aug 26.


A murine model of Denys-Drash syndrome reveals novel transcriptional targets of WT1 in podocytes.

Ratelade J, Arrondel C, Hamard G, Garbay S, Harvey S, Biebuyck N, Schulz H, Hastie N, Pontoglio M, Gubler MC, Antignac C, Heidet L.

Hum Mol Genet. 2010 Jan 1;19(1):1-15. doi: 10.1093/hmg/ddp462.


Stereocilin-deficient mice reveal the origin of cochlear waveform distortions.

Verpy E, Weil D, Leibovici M, Goodyear RJ, Hamard G, Houdon C, Lefèvre GM, Hardelin JP, Richardson GP, Avan P, Petit C.

Nature. 2008 Nov 13;456(7219):255-8. doi: 10.1038/nature07380. Epub 2008 Oct 8.


A missense mutation in podocin leads to early and severe renal disease in mice.

Philippe A, Weber S, Esquivel EL, Houbron C, Hamard G, Ratelade J, Kriz W, Schaefer F, Gubler MC, Antignac C.

Kidney Int. 2008 May;73(9):1038-47. doi: 10.1038/ki.2008.27. Epub 2008 Feb 20.


Gain-of-function mutant of angiotensin II receptor, type 1A, causes hypertension and cardiovascular fibrosis in mice.

Billet S, Bardin S, Verp S, Baudrie V, Michaud A, Conchon S, Muffat-Joly M, Escoubet B, Souil E, Hamard G, Bernstein KE, Gasc JM, Elghozi JL, Corvol P, Clauser E.

J Clin Invest. 2007 Jul;117(7):1914-25.


Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse.

Roux I, Safieddine S, Nouvian R, Grati M, Simmler MC, Bahloul A, Perfettini I, Le Gall M, Rostaing P, Hamard G, Triller A, Avan P, Moser T, Petit C.

Cell. 2006 Oct 20;127(2):277-89.


Targeted disruption of the hepcidin 1 gene results in severe hemochromatosis.

Lesbordes-Brion JC, Viatte L, Bennoun M, Lou DQ, Ramey G, Houbron C, Hamard G, Kahn A, Vaulont S.

Blood. 2006 Aug 15;108(4):1402-5. Epub 2006 Mar 30.


Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout mice.

Kappeler C, Saillour Y, Baudoin JP, Tuy FP, Alvarez C, Houbron C, Gaspar P, Hamard G, Chelly J, Métin C, Francis F.

Hum Mol Genet. 2006 May 1;15(9):1387-400. Epub 2006 Mar 28. Erratum in: Hum Mol Genet. 2006 May 1;15(9):2183.


Lactadherin promotes VEGF-dependent neovascularization.

Silvestre JS, Théry C, Hamard G, Boddaert J, Aguilar B, Delcayre A, Houbron C, Tamarat R, Blanc-Brude O, Heeneman S, Clergue M, Duriez M, Merval R, Lévy B, Tedgui A, Amigorena S, Mallat Z.

Nat Med. 2005 May;11(5):499-506. Epub 2005 Apr 17.


Six1 and Six4 homeoproteins are required for Pax3 and Mrf expression during myogenesis in the mouse embryo.

Grifone R, Demignon J, Houbron C, Souil E, Niro C, Seller MJ, Hamard G, Maire P.

Development. 2005 May;132(9):2235-49. Epub 2005 Mar 23.


Deafness and cochlear fibrocyte alterations in mice deficient for the inner ear protein otospiralin.

Delprat B, Ruel J, Guitton MJ, Hamard G, Lenoir M, Pujol R, Puel JL, Brabet P, Hamel CP.

Mol Cell Biol. 2005 Jan;25(2):847-53.


Liver-targeted disruption of Apc in mice activates beta-catenin signaling and leads to hepatocellular carcinomas.

Colnot S, Decaens T, Niwa-Kawakita M, Godard C, Hamard G, Kahn A, Giovannini M, Perret C.

Proc Natl Acad Sci U S A. 2004 Dec 7;101(49):17216-21. Epub 2004 Nov 24.


Colorectal cancers in a new mouse model of familial adenomatous polyposis: influence of genetic and environmental modifiers.

Colnot S, Niwa-Kawakita M, Hamard G, Godard C, Le Plenier S, Houbron C, Romagnolo B, Berrebi D, Giovannini M, Perret C.

Lab Invest. 2004 Dec;84(12):1619-30.


Targeted inactivation of serum response factor in the developing heart results in myocardial defects and embryonic lethality.

Parlakian A, Tuil D, Hamard G, Tavernier G, Hentzen D, Concordet JP, Paulin D, Li Z, Daegelen D.

Mol Cell Biol. 2004 Jun;24(12):5281-9.


Altered myogenesis in Six1-deficient mice.

Laclef C, Hamard G, Demignon J, Souil E, Houbron C, Maire P.

Development. 2003 May;130(10):2239-52.


Cre-mediated germline mosaicism: a new transgenic mouse for the selective removal of residual markers from tri-lox conditional alleles.

Leneuve P, Colnot S, Hamard G, Francis F, Niwa-Kawakita M, Giovannini M, Holzenberger M.

Nucleic Acids Res. 2003 Mar 1;31(5):e21.


Intralysosomal cystine accumulation in mice lacking cystinosin, the protein defective in cystinosis.

Cherqui S, Sevin C, Hamard G, Kalatzis V, Sich M, Pequignot MO, Gogat K, Abitbol M, Broyer M, Gubler MC, Antignac C.

Mol Cell Biol. 2002 Nov;22(21):7622-32.


Experimental IGF-I receptor deficiency generates a sexually dimorphic pattern of organ-specific growth deficits in mice, affecting fat tissue in particular.

Holzenberger M, Hamard G, Zaoui R, Leneuve P, Ducos B, Beccavin C, Périn L, Le Bouc Y.

Endocrinology. 2001 Oct;142(10):4469-78.


Cre-mediated germline mosaicism: a method allowing rapid generation of several alleles of a target gene.

Holzenberger M, Lenzner C, Leneuve P, Zaoui R, Hamard G, Vaulont S, Bouc YL.

Nucleic Acids Res. 2000 Nov 1;28(21):E92.


A targeted partial invalidation of the insulin-like growth factor I receptor gene in mice causes a postnatal growth deficit.

Holzenberger M, Leneuve P, Hamard G, Ducos B, Perin L, Binoux M, Le Bouc Y.

Endocrinology. 2000 Jul;141(7):2557-66.


Ubiquitous postnatal LoxP recombination using a doxycycline auto-inducible Cre transgene (DAI-Cre).

Holzenberger M, Zaoui R, Leneuve P, Hamard G, Le Bouc Y.

Genesis. 2000 Feb;26(2):157-9. No abstract available.


Effects of repetitive strains on vertebral end plates in young rats.

Revel M, Andre-Deshays C, Roudier R, Roudier B, Hamard G, Amor B.

Clin Orthop Relat Res. 1992 Jun;(279):303-9.


Illegitimate transcription. Application to the analysis of truncated transcripts of the dystrophin gene in nonmuscle cultured cells from Duchenne and Becker patients.

Chelly J, Gilgenkrantz H, Hugnot JP, Hamard G, Lambert M, Récan D, Akli S, Cometto M, Kahn A, Kaplan JC.

J Clin Invest. 1991 Oct;88(4):1161-6.


Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophies.

Chelly J, Gilgenkrantz H, Lambert M, Hamard G, Chafey P, Récan D, Katz P, de la Chapelle A, Koenig M, Ginjaar IB, et al.

Cell. 1990 Dec 21;63(6):1239-48.


Dystrophin gene transcribed from different promoters in neuronal and glial cells.

Chelly J, Hamard G, Koulakoff A, Kaplan JC, Kahn A, Berwald-Netter Y.

Nature. 1990 Mar 1;344(6261):64-5.


Recovery of functional DNA inserts by electroendosmotic elution during gel electrophoresis.

Tan HV, Kitzis A, Berthollet T, Hamard G, Beldjord C, Benarous R.

Nucleic Acids Res. 1988 Mar 25;16(5):1921-30.


De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophy.

Chelly J, Marlhens F, Le Marec B, Jeanpierre M, Lambert M, Hamard G, Dutrillaux B, Kaplan JC.

Hum Genet. 1986 Oct;74(2):193-6.


Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.

Kunkel LM, Hejtmancik JF, Caskey CT, Speer A, Monaco AP, Middlesworth W, Colletti CA, Bertelson C, Müller U, Bresnan M, Shapiro F, Tantravahi U, Speer J, Latt SA, Bartlett R, Pericak-Vance MA, Roses AD, Thompson MW, Ray PN, Worton RG, Fischbeck KH, Gallano P, Coulon M, Duros C, Boue J, Junien C, Chelly J, Hamard G, Jeanpierre M, Lambert M, Kaplan JC, Emery A, Dorkins H, McGlade S, Davies KE, Boehm C, Arveiler B, Lemaire C, Morgan GJ, Denton MJ, Amos J, Bobrow M, Benham F, Boswinkel E, Cole C, Dubowitz V, Hart K, Hodgson S, Johnson L, Walker A, Roncuzzi L, Ferlini A, Nobile C, Romeo G, Wilcox DE, Affara NA, Ferguson-Smith MA, Lindolf M, Kaariainen H, de la Chapelle A, Ionasescu V, Searby C, Ionasescu R, Bakker E, van Ommen GJ, Pearson PL, Greenberg CR, Hamerton JL, Wrogemann K, Doherty RA, Polakowska R, Hyser C, Quirk S, Thomas N, Harper JF, Darras BT, Francke U.

Nature. 1986 Jul 3-9;322(6074):73-7.


[Prenatal diagnosis of hemophilia A by analysis of DNA].

Delpech M, Maisonneuve P, Baudis M, Deburgrave N, Hamard G, Lambert M, Bardin JM, Sultan Y, Kaplan JC.

Ann Med Interne (Paris). 1986;137(2):112-4. French.


[Should we still explore placental sulfatase deficiencies? Reflections apropos of a case report].

Giovangrandi Y, Magnin G, Sauvanet E, Soutoul JH, Cedard L, Bedin M, Moraine C, Nottin P, Hamard G.

Rev Fr Gynecol Obstet. 1984 Oct;79(10):653-7. French.


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