D. Gomès

发表

Loss‐of‐function and residual channel activity of connexin26 mutations associated with non‐syndromic deafness

S. Marlin, R. Bruzzone, C. Petit, 2003, FEBS letters.

Immunohistochemical localization of the myelin basic protein and of the glial fibrillary acidic protein: Comparative study in normal, quaking and jimpy mice

C. Jacque, P. Dupouey, D. Gomès, 1980, Journal of neuroscience research.

Cell coupling and Cx43 expression in embryonic mouse neural progenitor cells.

P. Meda, R. Bruzzone, N. Duval, 2002, Journal of cell science.

Connexin32 Mutations Associated with X-Linked Charcot–Marie–Tooth Disease Show Two Distinct Behaviors: Loss of Function and Altered Gating Properties

D. Pham‐Dinh, R. Bruzzone, C. Ressot, 1998, The Journal of Neuroscience.

Altered gene expression in Schwann cells of connexin32 knockout animals

R. Bruzzone, B. de Néchaud, S. Nicholson, 2001, Journal of neuroscience research.

Recent evolutionary origin of the expression of the glial fibrillary acidic protein (GFAP) in lens epithelial cells. A molecular and genetic analysis of various mouse species.

J. Guénet, X. Montagutelli, P. Dupouey, 1991, Brain research. Molecular brain research.

Functional Analysis of a Dominant Mutation of Human Connexin26 Associated with Nonsyndromic Deafness

D. Weil, J. Perea, R. Bruzzone, 2001, Cell communication & adhesion.

Molecular and Functional Diversity of Neural Connexins in the Retina

R. Weiler, R. Bruzzone, D. Spray, 2000, The Journal of Neuroscience.

Localization of galactosylceramide and sulfatide at the surface of the myelin sheath: an immunofluorescence study in liquid medium.

B. Zalc, P. Dupouey, D. Gomès, 1979, Cellular and molecular biology, including cyto-enzymology.

Expression of carbonic anhydrase II gene in early brain cells as revealed by in situ hybridization and immunohistochemistry

J. Hillion, S. Dumas, A. Tixier-vidal, 1989, Journal of neuroscience research.

Connexin32 in the Peripheral Nervous System: Functional Analysis of Mutations Associated with X‐linked Charcot‐Marie‐Tooth Syndrome and Implications for the Pathophysiology of the Disease

J. Perea, R. Bruzzone, P. D'andrea, 1999, Annals of the New York Academy of Sciences.

Induction of Myelin Gene Expression in Murine Schwann Cells in Primary Culture and in a Schwann Cell Line

R. Bruzzone, A. Baron-Van Evercooren, D. Gomès, 1999, Annals of the New York Academy of Sciences.

Expression of glial fibrillary acidic protein and vimentin in mouse lens epithelial cells during development in vivo and during proliferation and differentiation in vitro: Comparison with the developmental appearance of GFAP in the mouse central nervous system

A. M. Hill, B. de Néchaud, R. Maunoury, 1990, Journal of neuroscience research.

Functional properties, developmental regulation, and chromosomal localization of murine connexin36, a gap-junctional protein expressed preferentially in retina and brain.

P. Avner, R. Bruzzone, M. Al-Ubaidi, 2000, Journal of neuroscience research.

Functional properties, developmental regulation, and chromosomal localization of murine connexin36, a gap‐junctional protein expressed preferentially in retina and brain

P. Avner, R. Bruzzone, M. Al-Ubaidi, 2000 .

Immunohistochemical demonstration of an organized cytoarchitecture of the radial glia in the CNS of the embryonic mouse.

P. Dupouey, D. Gomès, S. Benjelloun, 1985, Developmental neuroscience.

Glial fibrillary acidic protein expression in a new human glioma cell line in culture before and after xenogenic transplantation into nude mice

V. M. Neto, F. Labrousse, B. de Néchaud, 1997, Acta Neuropathologica.

Connexin32 in the peripheral nervous system. Functional analysis of mutations associated with X-linked Charcot-Marie-Tooth syndrome and implications for the pathophysiology of the disease.

J. Perea, R. Bruzzone, P. D'andrea, 1999, Annals of the New York Academy of Sciences.