Le fonctionnement de la cochlée expliqué par la génétique : Voyage au coeur de l'oreillePETIT, Christine.Biofutur (Puteaux). 2012, Num 337, pp 31-37, issn 0294-3506, 7 p.Article

Hereditary sensory defects: From genes to pathogenesis : Genetics of deafnessPETIT, Christine.American journal of medical genetics. 2004, Vol 130A, Num 1, pp 3-7, issn 0148-7299, 5 p.Article

Les mécanismes de transduction du signal olfactif = Signal transduction of olfactive systemLEGOUIS, R.Annales de l'Institut Pasteur. Actualités. 1995, Vol 6, Num 4, pp 249-255, issn 0924-4204Article

Les dystrophies rétiniennes humaines héréditaires = Human hereditary retinal dystrophiesKAPLAN, J.Annales de l'Institut Pasteur. Actualités. 1995, Vol 6, Num 4, pp 292-299, issn 0924-4204Article

Transduction mécanoélectrique par les cellules ciliées de l'oreille interne = Mecanoelectric transduction by ciliated cells of the inner earDULON, D.Annales de l'Institut Pasteur. Actualités. 1995, Vol 6, Num 4, pp 263-267, issn 0924-4204Article

La cellule ciliée externe de la cochlée des mammifères : Un amplificateur aux propriétés exceptionnelles = The outer hair cell of the mammalian cochlea : an outstanding amplifierLEGENDRE, Kirian; PETIT, Christine; EL-AMRAOUI, Aziz et al.MS. Médecine sciences. 2009, Vol 25, Num 2, pp 117-120, issn 0767-0974, 4 p.Article

The Auditory Hair Cell Ribbon Synapse: From Assembly to FunctionSAFIEDDINE, Saaid; EL-AMRAOUI, Aziz; PETIT, Christine et al.Annual review of neuroscience (Print). 2012, Vol 35, pp 509-528, issn 0147-006X, 20 p.Article

Cartographie de gènes responsables de surdité chez l'homme = Mapping genes reponsible for deafness in humansChaib, Hassan; Petit, Christine.1997, 169 p.Thesis

La région pseudo-autosomique des bras courts des chromosomes sexuels humains = The pseudoautosomal region of the human sex chromosome short armsSlim, Rima; Petit, Christine.1993, 184 p.Thesis

ETABLISSEMENT D'UN MODELE ANIMAL DU SYNDROME DE KALLMANN DE MORSIER LIE AU CHROMOSOME X = ESTABLISHMENT OF AN ANIMAL MODEL OF THE X-LINKED FORM OF KALLMANN DE MORSIER SYNDROMEArdouin, Olivier; Petit, Christine.1999, 189 p.Thesis

SURDITES HEREDITAIRES HUMAINES : GENOTYPES ET PHENOTYPES EN RELATION AVEC LES MUTATIONS DU GENE SALL1 ET DU GENE CX26 = Human hereditary deafness : genotypes and phenotypes related to the mutations in SALL1 gene and in CX26 geneMarlin, Sandrine; Petit, Christine.1999, 220 p.Thesis

Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chipLEVEQUE, Marianne; MARLIN, Sandrine; FRANCANNET, Christine et al.European journal of human genetics. 2007, Vol 15, Num 11, pp 1145-1155, issn 1018-4813, 11 p.Article

Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potentialTEUBNER, Barbara; MICHEL, Vincent; PETIT, Christine et al.Human molecular genetics (Print). 2003, Vol 12, Num 1, pp 13-21, issn 0964-6906, 9 p.Article

Electrooxidation potential as a tool in the early screening for new safer clozapine-like analoguesMOUITHYS-MICKALAD, Ange; KAUFFMANN, Jean-Michel; LIEGEOIS, Jean-Francois et al.Journal of medicinal chemistry (Print). 2001, Vol 44, Num 5, pp 769-776, issn 0022-2623Article

Contribution de la génétique humaine à la compréhension des systèmes sensoriels. Discussion = Unravelling the sensory systems : contribution of human hereditary defects. DiscussionPETIT, Christine; ARTHUIS, Michel; NORDMANN, Roger et al.Bulletin de l'Académie nationale de médecine. 2000, Vol 184, Num 7, pp 1383-1392, issn 0001-4079Conference Paper

Déficits héréditaires de l'audition chez l'enfant = Hereditary hearing loss in childrenHAMMADI AYADI; ALI BELKAHIA; LEVILLIERS, J et al.Annales de l'Institut Pasteur. Actualités. 1995, Vol 6, Num 4, pp 304-309, issn 0924-4204Article

Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafnessDELMAGHANI, Sedigheh; AGHAIE, Asadollah; MICHALSKI, Nicolas et al.Human molecular genetics (Print). 2012, Vol 21, Num 17, pp 3835-3844, issn 0964-6906, 10 p.Article

Re-assigning the DFNB33 locus to chromosome 10p11.23-q21.1BELGUITH, Hanen; MASMOUDI, Saber; MEDLEJ-HASHIM, Myrna et al.European journal of human genetics. 2009, Vol 17, Num 1, pp 122-124, issn 1018-4813, 3 p.Article

Stereocilin-deficient mice reveal the origin of cochlear waveform distortionsVERPY, Elisabeth; WEIL, Dominique; PETIT, Christine et al.Nature (London). 2008, Vol 456, Num 7219, pp 255-258, issn 0028-0836, 4 p.Article

Interactions in the network of Usher syndrome type 1 proteinsADATO, Avital; MICHEL, Vincent; KIKKAWA, Yoshiaki et al.Human molecular genetics (Print). 2005, Vol 14, Num 3, pp 347-356, issn 0964-6906, 10 p.Article

Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locusVERPY, Elisabeth; MASMOUDI, Saber; MORENO, Felipe et al.Nature genetics. 2001, Vol 29, Num 3, pp 345-349, issn 1061-4036Article

A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1CVERPY, Elisabeth; LEIBOVICI, Michel; SLIM, Rima et al.Nature genetics. 2000, Vol 26, Num 1, pp 51-55, issn 1061-4036Article

Ciliary proteins link basal body polarization to planar cell polarity regulationJONES, Chonnettia; ROPER, Venus C; FOUCHER, Isabelle et al.Nature genetics. 2008, Vol 40, Num 1, pp 69-77, issn 1061-4036, 9 p.Article

The GJB2 mutation R75Q can cause nonsyndromic hearing loss DFNA3 or hereditary palmoplantar keratoderma with deafnessFELDMANN, Delphine; DENOYELLE, Francoise; MARLIN, Sandrine et al.American journal of medical genetics. 2005, Vol 137A, Num 2, pp 225-227, issn 0148-7299, 3 p.Article

GJB2 and GJB6 mutations : Genotypic and phenotypic correlations in a large cohort of hearing-impaired patientsMARLIN, Sandrine; FELDMANN, Delphine; JOANNARD, Alain et al.Archives of otolaryngology, head & neck surgery. 2005, Vol 131, Num 6, pp 481-487, issn 0886-4470, 7 p.Article