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Human Genetics
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September 1, 1995
Mutations of the fibroblast growth factor receptor-3 gene in one familial and six sporadic cases of achondroplasia in Japanese patients
S Ikegawa, Y Fukushima, M Isomura, et al.
Molecular Immunology
|
September 4, 1999
Gene structure of the P100 serine-protease component of the human Ra-reactive factor
Y Takayama, F Takada, M Nowatari, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
June 1, 1995
[Molecular diagnosis of a kindred with novel mutation of methylmalonyl-CoA mutase gene using non-RI SSCP]
Y Toyo-Oka, C Wada, Y Ohnuki, et al.
Advances in Second Messenger and Phosphoprotein Research
|
January 1, 1990
Importance of subunit interactions in regulation of casein kinase II
J A Traugh, W J Lin, F Takada-Axelrod, et al.
American Journal of Medical Genetics
|
March 1, 1990
Cytogenetic and molecular study of Angelman syndrome
K Imaizumi, F Takada, Y Kuroki, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
May 1, 1996
[Nucleotide sequences at intron 6 and exon 7 junction of fibroblast growth factor receptor 2 and rapid mutational analysis in Apert syndrome]
C Wada, M Ishigaki, Y Toyo-oka, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
May 1, 1996
[Frequent missense mutations of fibroblast growth factor receptor (FGFR) gene families in craniofacial syndromes in Japanese patients]
M Ishigaki, C Wada, Y Toyo-oka, et al.
Basal Facts
|
January 1, 1986
A template therapy approach for non-specific complaints
K Maehara, S Sato, F Takada, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 15, 2001
Myozenin: an alpha-actinin- and gamma-filamin-binding protein of skeletal muscle Z lines
F Takada, D L Vander Woude, H Q Tong, et al.
Neurology
|
August 28, 2002
Mutations of the slow muscle alpha-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy
D Wattanasirichaigoon, K J Swoboda, F Takada, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
Human Genetics
|
September 1, 1995
Mutations of the fibroblast growth factor receptor-3 gene in one familial and six sporadic cases of achondroplasia in Japanese patients
S Ikegawa, Y Fukushima, M Isomura, et al.
Molecular Immunology
|
September 4, 1999
Gene structure of the P100 serine-protease component of the human Ra-reactive factor
Y Takayama, F Takada, M Nowatari, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
June 1, 1995
[Molecular diagnosis of a kindred with novel mutation of methylmalonyl-CoA mutase gene using non-RI SSCP]
Y Toyo-Oka, C Wada, Y Ohnuki, et al.
Advances in Second Messenger and Phosphoprotein Research
|
January 1, 1990
Importance of subunit interactions in regulation of casein kinase II
J A Traugh, W J Lin, F Takada-Axelrod, et al.
American Journal of Medical Genetics
|
March 1, 1990
Cytogenetic and molecular study of Angelman syndrome
K Imaizumi, F Takada, Y Kuroki, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
May 1, 1996
[Nucleotide sequences at intron 6 and exon 7 junction of fibroblast growth factor receptor 2 and rapid mutational analysis in Apert syndrome]
C Wada, M Ishigaki, Y Toyo-oka, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
May 1, 1996
[Frequent missense mutations of fibroblast growth factor receptor (FGFR) gene families in craniofacial syndromes in Japanese patients]
M Ishigaki, C Wada, Y Toyo-oka, et al.
Basal Facts
|
January 1, 1986
A template therapy approach for non-specific complaints
K Maehara, S Sato, F Takada, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 15, 2001
Myozenin: an alpha-actinin- and gamma-filamin-binding protein of skeletal muscle Z lines
F Takada, D L Vander Woude, H Q Tong, et al.
Neurology
|
August 28, 2002
Mutations of the slow muscle alpha-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy
D Wattanasirichaigoon, K J Swoboda, F Takada, et al.
Page
of 3