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Human Genetics
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May 1, 1995
Refinement of the locus for X-linked recessive chondrodysplasia punctata
K 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 cells
M 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 pattern
T 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 complex
H 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 correlation
T 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 locus
K Muroya, T Ogata, N Matsuo, et al.
AJNR. American Journal of Neuroradiology
|
December 30, 2008
Abnormal basiocciput development in CHARGE syndrome
K 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 factors
T 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 patients
T Ogata, K Muroya, N Matsuo, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 66) with videos related to
Sort By:
Page
of 7
Human Genetics
|
May 1, 1995
Refinement of the locus for X-linked recessive chondrodysplasia punctata
K 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 cells
M 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 pattern
T 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 complex
H 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 correlation
T 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 locus
K Muroya, T Ogata, N Matsuo, et al.
AJNR. American Journal of Neuroradiology
|
December 30, 2008
Abnormal basiocciput development in CHARGE syndrome
K 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 factors
T 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 patients
T Ogata, K Muroya, N Matsuo, et al.
Page
of 7