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Submissions from 1998

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Mammalian Mtj1, Michael W. Lassle, Bruce R. Zetter, Shannon E. Brightman, and Gregory L. Blatch

Submissions from 1997

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Connexin32 and X-linked Charcot–Marie–Tooth Disease, Linda Jo Bone, Suzanne M. Deschênes, Rita J. Balice-Gordon, Kenneth H. Fischbeck, and Steven S. Scherer

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Altered Trafficking of Mutant Connexin32, Suzanne M. Deschênes, Jessica L. Walcott, Tamara L. Wexler, Steven S. Scherer, and Kenneth H. Fischbeck

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Connexin32 and X-Linked Charcot-Marie-Tooth Disease, Kenneth H. Fischbeck, Suzanne M. Deschênes, Linda Jo Bone, and Steven S. Scherer

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Inhibition of Axonal Growth by Brefeldin A in Hippocampal Neurons in Culture, Mark Jareb and Gary Banker

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The Role of the Gap Junction Protein Connexin32 in the Myelin Sheath, Steven S. Scherer, Linda Jo Bone, Suzanne M. Deschênes, Kenneth H. Fischbeck, and Rita J. Balice-Gordon

Submissions from 1996

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Connexin32 and X-Linked Charcot-Marie-Tooth Disease, Suzanne M. Deschênes, Linda Jo Bone, Kenneth H. Fischbeck, and Steven S. Scherer

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Mutagenicity of Acridines in a Reversion Assay Based on Tetracycline Resistance in Plasmid pBR322 in Escherichia Coli, George R. Hoffman, Suzanne M. Deschênes, Teresa Manyin, and Robert P. P. Fuchs

Submissions from 1995

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Isolation of a Mouse cDNA Encoding MTJ1, a New Murine Member of the DnaJ Family of Proteins, Shannon E. Brightman, Gregory L. Blatch, and Bruce R. Zetter

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Increased Stem Cell Factor Release by Hemangioma-Derived Endothelial Cells, C. J. Meininger, Shannon Brightman, K. A. Kelly, and B. R. Zetter

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Connexin32 is a Myelin-Related Protein in the PNS and CNS, Steven S. Scherer, Suzanne M. Deschênes, Yi-Tian Xu, Judith B. Grinspan, Kenneth H. Fischbeck, and David L. Paul

Submissions from 1994

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Comparative Mapping of Canine and Human Proximal Xq and Genetic Analysis of Canine X-Linked Severe Combined Immunodeficiency, Suzanne M. Deschênes, Jennifer M. Puck, Amalia S. Dutra, Richard L. Somberg, Peter J. Felsberg, and Paula S. Henthorn

Submissions from 1993

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The Interleukin-2 Receptor γ Chain Maps to Xq13.1 and is Mutated in X-Linked Severe Combined Immunodeficiency, SCIDX1, Jennifer M. Puck, Suzanne M. Deschênes, Joanne C. Porter, Amalia S. Dutra, Carolyn J. Brown, Huntington F. Willard, and Paula S. Henthorn