Petit, Christine

Defective myosin VIIA gene responsible for Usher syndrome type IB

Well, D., Blanchard, S., Kaplan, J., Guilford, P., Gibson, F., Walsh, J., Mburu, P., Varela, A., Levilliers, J., Weston, M. D., et al. (1995) · Nature

Retinal Development and DisordersGenetic and Kidney Cyst Diseases

Cited by 1,068

Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2

Dodé, C., Teixeira, L., Levilliers, J., Fouveaut, C., Bouchard, P., Kottler, M.-L., Lespinasse, J., Lienhardt-Roussie, A., Mathieu, M., Moerman, A., et al. (2006) · PLoS Genetics

Hypothalamic control of reproductive hormonesOlfactory and Sensory Function Studies

Cited by 457

Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model

Akil, O., Dyka, F., Calvet, C., Emptoz, A., Lahlou, G., Nouaille, S., Boutet de Monvel, J., Hardelin, J.-P., Hauswirth, W. W., Avan, P., et al. (2019) · Proceedings of the National Academy of Sciences

Hearing, Cochlea, Tinnitus, GeneticsVirus-based gene therapy research

Cited by 300

Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome

Hardelin, J.-P., Levilliers, J., Blanchard, S., Carel, J.-C., Leutenegger, M., Pinard-Bertelletto, J.-P., Bouloux, P., & Petit, C. (1993) · Human Molecular Genetics

Hypothalamic control of reproductive hormonesGenetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Cited by 203

MyRIP, a novel Rab effector, enables myosin VIIa recruitment to retinal melanosomes

El‐Amraoui, A., Schonn, J., Küssel‐Andermann, P., Blanchard, S., Desnos, C., Henry, J., Wolfrum, U., Darchen, F., & Petit, C. (2002) · The EMBO Reports

Cellular transport and secretionRetinal Development and Disorders

Cited by 187

Involvement of the Rab27 Binding Protein Slac2c/MyRIP in Insulin Exocytosis

Waselle, L., Coppola, T., Fukuda, M., Iezzi, M., El-Amraoui, A., Petit, C., & Regazzi, R. (2003) · Molecular Biology of the Cell

Cellular transport and secretionPancreatic function and diabetes

Cited by 159

Viral transfer of mini-otoferlins partially restores the fast component of exocytosis and uncovers ultrafast endocytosis in auditory hair cells of otoferlin knock-out mice

Tertrais, M., Bouleau, Y., Emptoz, A., Belleudy, S., Sutton, R. B., Petit, C., Safieddine, S., & Dulon, D. (2019) · The Journal of Neuroscience

Hearing, Cochlea, Tinnitus, GeneticsCellular transport and secretion

Cited by 49