Search Results - "Bronshteyn, Illya G."

L-cycloserine slows the clinical and pathological course in mice with globoid cell leukodystrophy (twitcher mice) by LeVine, Steven M., Pedchenko, Tetyana V., Bronshteyn, Illya G., Pinson, David M.

“…Globoid cell leukodystrophy (Krabbe's disease) is an autosomal recessive disease that affects the lysosomal enzyme galactosylceramidase. Galactosylceramidase…”
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Corrigendum to “TNF-receptor 1 deficiency fails to alter the clinical and pathological course in mice with globoid cell leukodystrophy (twitcher mice) but affords protection following LPS challenge” [J. Neuroimmunol. 110 (2000) 186–194] by Pedchenko, Tetyana V., Bronshteyn, Illya G., LeVine, Steven M.

“…Twitcher mice have an autosomal recessive mutation in the gene for the lysosomal enzyme galactosylceramidase, which is the same gene that is affected in human…”
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TNF-receptor 1 deficiency fails to alter the clinical and pathological course in mice with globoid cell leukodystrophy (twitcher mice) but affords protection following LPS challenge by Pedchenko, Tetyana V., Bronshteyn, Illya G., LeVine, Steven M.

“…Twitcher mice have an autosomal recessive mutation in the gene for the lysosomal enzyme galactosylceramidase, which is the same gene that is affected in human…”
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IL-6 deficiency allows for enhanced therapeutic value after bone marrow transplantation across a minor histocompatibility barrier in the twitcher (globoid cell leukodystrophy) mouse by Biswas, Sangita, Pinson, David M., Bronshteyn, Illya G., LeVine, Steven M.

“…Bone marrow transplantation (BMT) has therapeutic value for twitcher (globoid cell leukodystrophy) mice, which suffer from a genetic deficiency of the…”
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