L. Bone

发表

Connexin32 and X-linked Charcot-Marie-Tooth disease.

K. Fischbeck, R. Balice-Gordon, S. Scherer, 1997, Neurobiology of disease.

Connexin32‐null mice develop demyelinating peripheral neuropathy

K. Fischbeck, K. Willecke, S. Scherer, 1998, Glia.

The Role of the Gap Junction Protein Connexin32 in the Myelin Sheath

K. Fischbeck, R. Balice-Gordon, S. Scherer, 1997 .

Connexin32 and X-linked Charcot–Marie–Tooth Disease

K. Fischbeck, R. Balice-Gordon, S. Scherer, 1997, Neurobiology of Disease.

The human connexin32 gene is transcribed from two tissue-specific promoters

R. Werner, V. Ionasescu, L. Bone, 1996, Bioscience reports.

Connexin mutations in X-linked Charcot-Marie-Tooth disease.

K. Fischbeck, D. Paul, S. Scherer, 1993, Science.

Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndrome.

M. Tessier-Lavigne, K. Kvaløy, D. Patterson, 1995, American journal of human genetics.

Functional Gap Junctions in the Schwann Cell Myelin Sheath

R. Balice-Gordon, S. Scherer, L. Bone, 1998, The Journal of cell biology.

New connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease

K. Fischbeck, M. Lensch, P. Chance, 1995, Neurology.

Connexin32 and X-linked Charcot-Marie-Tooth Disease

K. Fischbeck, S. Scherer, L. Bone, 1996 .

The role of the gap junction protein connexin32 in the pathogenesis of X-linked Charcot-Marie-Tooth disease.

K. Fischbeck, R. Balice-Gordon, S. Scherer, 1999, Novartis Foundation symposium.

Studies in transgenic mice indicate a loss of connexin32 function in X-linked Charcot-Marie-Tooth disease.

K. Fischbeck, S. Scherer, A. Messing, 1999, Journal of neuropathology and experimental neurology.