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K Muroya

Showing results (41-50 of 66) with videos related to

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Human Genetics|May 1, 1995
Refinement of the locus for X-linked recessive chondrodysplasia punctataK Muroya, T Ogata, G Rappold, et al.
Molecular and Cellular Biology|August 1, 1994
CRK protein binds to two guanine nucleotide-releasing proteins for the Ras family and modulates nerve growth factor-induced activation of Ras in PC12 cellsM Matsuda, Y Hashimoto, K Muroya, et al.
Human Genetics|September 16, 1998
Microphthalmia with linear skin defects syndrome in a mosaic female infant with monosomy for the Xp22 region: molecular analysis of the Xp22 breakpoint and the X-inactivation patternT Ogata, K Wakui, K Muroya, et al.
Journal of Biochemistry|July 1, 1995
Morphology of ras-transformed cells becomes apparently normal again with tyrosine kinase inhibitors without a decrease in the ras-GTP complexH J Kwon, M Yoshida, K Muroya, et al.
American Journal of Medical Genetics|June 8, 2000
Structural analysis of a rare rearranged Y chromosome and its bearing on genotype-phenotype correlationT Ogata, K Wakui, T Kosho, et al.
American Journal of Medical Genetics|September 6, 1996
Mental retardation in a boy with an interstitial deletion at Xp22.3 involving STS, KAL1, and OA1: implication for the MRX locusK Muroya, T Ogata, N Matsuo, et al.
AJNR. American Journal of Neuroradiology|December 30, 2008
Abnormal basiocciput development in CHARGE syndromeK Fujita, N Aida, Y Asakura, et al.
Biochemical and Biophysical Research Communications|May 5, 1995
Hepatocyte growth factor specifically expressed in microglia activated Ras in the neurons, similar to the action of neurotrophic factorsT Yamagata, K Muroya, T Mukasa, et al.
Nihon Kokyuki Gakkai Zasshi = the Journal of the Japanese Respiratory Society|March 24, 1999
[Primary racemose hemangioma of bronchial artery]N Sukoh, H Yamamoto, K Muroya, et al.
The Journal of Clinical Endocrinology and Metabolism|November 10, 2001
Turner syndrome and Xp deletions: clinical and molecular studies in 47 patientsT Ogata, K Muroya, N Matsuo, et al.
Pageof 7

Showing results (41-50 of 66) with videos related to

Sort By:
Pageof 7
Human Genetics|May 1, 1995
Refinement of the locus for X-linked recessive chondrodysplasia punctataK Muroya, T Ogata, G Rappold, et al.
Molecular and Cellular Biology|August 1, 1994
CRK protein binds to two guanine nucleotide-releasing proteins for the Ras family and modulates nerve growth factor-induced activation of Ras in PC12 cellsM Matsuda, Y Hashimoto, K Muroya, et al.
Human Genetics|September 16, 1998
Microphthalmia with linear skin defects syndrome in a mosaic female infant with monosomy for the Xp22 region: molecular analysis of the Xp22 breakpoint and the X-inactivation patternT Ogata, K Wakui, K Muroya, et al.
Journal of Biochemistry|July 1, 1995
Morphology of ras-transformed cells becomes apparently normal again with tyrosine kinase inhibitors without a decrease in the ras-GTP complexH J Kwon, M Yoshida, K Muroya, et al.
American Journal of Medical Genetics|June 8, 2000
Structural analysis of a rare rearranged Y chromosome and its bearing on genotype-phenotype correlationT Ogata, K Wakui, T Kosho, et al.
American Journal of Medical Genetics|September 6, 1996
Mental retardation in a boy with an interstitial deletion at Xp22.3 involving STS, KAL1, and OA1: implication for the MRX locusK Muroya, T Ogata, N Matsuo, et al.
AJNR. American Journal of Neuroradiology|December 30, 2008
Abnormal basiocciput development in CHARGE syndromeK Fujita, N Aida, Y Asakura, et al.
Biochemical and Biophysical Research Communications|May 5, 1995
Hepatocyte growth factor specifically expressed in microglia activated Ras in the neurons, similar to the action of neurotrophic factorsT Yamagata, K Muroya, T Mukasa, et al.
Nihon Kokyuki Gakkai Zasshi = the Journal of the Japanese Respiratory Society|March 24, 1999
[Primary racemose hemangioma of bronchial artery]N Sukoh, H Yamamoto, K Muroya, et al.
The Journal of Clinical Endocrinology and Metabolism|November 10, 2001
Turner syndrome and Xp deletions: clinical and molecular studies in 47 patientsT Ogata, K Muroya, N Matsuo, et al.
Pageof 7