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The Journal of Clinical Endocrinology and Metabolism
|
July 1, 1997
Paraoxonase polymorphism (Gln192-Arg) is associated with coronary heart disease in Japanese noninsulin-dependent diabetes mellitus
M Odawara, Y Tachi, K Yamashita
Nucleic Acids Symposium Series
|
April 26, 2000
MTHFR gene variant is not associated with diabetic nephropathy in Japanese
M Odawara, K Yamashita, N Yamada
Diabetologia
|
August 1, 1995
Decreased cerebral blood perfusion in an NIDDM patient with an A-to-G mutation in the mitochondrial gene; a possible contribution to cognition deficits in diabetes
M Odawara, K Tada, K Yamashita
Journal of Medical Genetics
|
January 15, 2000
Pathogenicity of homoplasmic mitochondrial DNA mutation and nuclear gene involvement
M Odawara, H Maki, N Yamada
Lancet (London, England)
|
September 28, 1996
Beta 3-adrenergic receptor gene variant and Japanese NIDDM: a pitfall in meta-analysis
M Odawara, K Sasaki, K Yamashita
Diabetologia
|
March 1, 1995
Selection of primers for detection of A to G mutation at nucleotide 3243 of the mitochondrial gene
M Odawara, K Sasaki, Y Tachi, et al.
Horumon to Rinsho. Clinical Endocrinology
|
April 1, 1970
[Treatment of hypoglycemia in children by diazoxide and immunoreactive insulin depressive action]
M Ota, K Takeuchi, I Hibi, et al.
Diabetologia
|
April 16, 1998
Endothelial nitric oxide synthase gene polymorphism and coronary heart disease in Japanese NIDDM
M Odawara, K Sasaki, Y Tachi, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
June 1, 1972
[Serum iron and iron-binding capacity. 1. Problems in the determination of unsaturated iron-binding capacity of the serum]
K Nakane, K Iguchi, M Odawara, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
August 1, 1971
[Determination of alpha-amylase activity by chromogenic method]
M Odawara, K Iguchi, K Nakane, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 80) with videos related to
Sort By:
Page
of 8
The Journal of Clinical Endocrinology and Metabolism
|
July 1, 1997
Paraoxonase polymorphism (Gln192-Arg) is associated with coronary heart disease in Japanese noninsulin-dependent diabetes mellitus
M Odawara, Y Tachi, K Yamashita
Nucleic Acids Symposium Series
|
April 26, 2000
MTHFR gene variant is not associated with diabetic nephropathy in Japanese
M Odawara, K Yamashita, N Yamada
Diabetologia
|
August 1, 1995
Decreased cerebral blood perfusion in an NIDDM patient with an A-to-G mutation in the mitochondrial gene; a possible contribution to cognition deficits in diabetes
M Odawara, K Tada, K Yamashita
Journal of Medical Genetics
|
January 15, 2000
Pathogenicity of homoplasmic mitochondrial DNA mutation and nuclear gene involvement
M Odawara, H Maki, N Yamada
Lancet (London, England)
|
September 28, 1996
Beta 3-adrenergic receptor gene variant and Japanese NIDDM: a pitfall in meta-analysis
M Odawara, K Sasaki, K Yamashita
Diabetologia
|
March 1, 1995
Selection of primers for detection of A to G mutation at nucleotide 3243 of the mitochondrial gene
M Odawara, K Sasaki, Y Tachi, et al.
Horumon to Rinsho. Clinical Endocrinology
|
April 1, 1970
[Treatment of hypoglycemia in children by diazoxide and immunoreactive insulin depressive action]
M Ota, K Takeuchi, I Hibi, et al.
Diabetologia
|
April 16, 1998
Endothelial nitric oxide synthase gene polymorphism and coronary heart disease in Japanese NIDDM
M Odawara, K Sasaki, Y Tachi, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
June 1, 1972
[Serum iron and iron-binding capacity. 1. Problems in the determination of unsaturated iron-binding capacity of the serum]
K Nakane, K Iguchi, M Odawara, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
August 1, 1971
[Determination of alpha-amylase activity by chromogenic method]
M Odawara, K Iguchi, K Nakane, et al.
Page
of 8