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Journal of Molecular Endocrinology
|
August 1, 1997
Cloning of mouse islet amyloid polypeptide gene and characterization of its promoter
K Ekawa, M Nishi, S Ohagi, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 20, 1998
A case of Albright's hereditary osteodystrophy-like syndrome complicated by several endocrinopathies: normal Gs alpha gene and chromosome 2q37
H Sakaguchi, T Sanke, S Ohagi, et al.
Biochemical and Biophysical Research Communications
|
August 25, 2001
Analysis of 825C/T polymorphism of G proteinbeta3 subunit in obese/diabetic Japanese
Y Ohshiro, K Ueda, H Wakasaki, et al.
Horumon to Rinsho. Clinical Endocrinology
|
March 1, 1970
[Metastatic goiter accompanied with hyperthyroidism]
S Ito, N Hirose, K Nanjo, et al.
Metabolism: Clinical and Experimental
|
October 1, 1986
Effect of calcium antagonists on reactive hypoglycemia associated with hyperinsulinemia
T Sanke, K Nanjo, M Kondo, et al.
Neurology
|
May 29, 2001
An epidemic of arsenic neuropathy from a spiked curry
Y Kishi, H Sasaki, H Yamasaki, et al.
Diabetes
|
April 1, 1995
Association of the prohormone convertase 2 gene (PCSK2) on chromosome 20 with NIDDM in Japanese subjects
H Yoshida, S Ohagi, T Sanke, et al.
Diabetologia
|
July 14, 1998
Organization of the human carboxypeptidase E gene and molecular scanning for mutations in Japanese subjects with NIDDM or obesity
N Utsunomiya, S Ohagi, T Sanke, et al.
Diabetologia
|
August 1, 1997
A missense mutation of the muscle glycogen synthase gene (M416V) is associated with insulin resistance in the Japanese population
H Shimomura, T Sanke, K Ueda, et al.
Nihon Sanka Fujinka Gakkai Zasshi
|
May 1, 1993
[Lipoleiomyoma of the uterus: report of a case]
F Miyauchi, K Nanjo, K Otsuka, et al.
Page
of 12
Search research articles
Search
Showing results (41-50 of 117) with videos related to
Sort By:
Page
of 12
Journal of Molecular Endocrinology
|
August 1, 1997
Cloning of mouse islet amyloid polypeptide gene and characterization of its promoter
K Ekawa, M Nishi, S Ohagi, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 20, 1998
A case of Albright's hereditary osteodystrophy-like syndrome complicated by several endocrinopathies: normal Gs alpha gene and chromosome 2q37
H Sakaguchi, T Sanke, S Ohagi, et al.
Biochemical and Biophysical Research Communications
|
August 25, 2001
Analysis of 825C/T polymorphism of G proteinbeta3 subunit in obese/diabetic Japanese
Y Ohshiro, K Ueda, H Wakasaki, et al.
Horumon to Rinsho. Clinical Endocrinology
|
March 1, 1970
[Metastatic goiter accompanied with hyperthyroidism]
S Ito, N Hirose, K Nanjo, et al.
Metabolism: Clinical and Experimental
|
October 1, 1986
Effect of calcium antagonists on reactive hypoglycemia associated with hyperinsulinemia
T Sanke, K Nanjo, M Kondo, et al.
Neurology
|
May 29, 2001
An epidemic of arsenic neuropathy from a spiked curry
Y Kishi, H Sasaki, H Yamasaki, et al.
Diabetes
|
April 1, 1995
Association of the prohormone convertase 2 gene (PCSK2) on chromosome 20 with NIDDM in Japanese subjects
H Yoshida, S Ohagi, T Sanke, et al.
Diabetologia
|
July 14, 1998
Organization of the human carboxypeptidase E gene and molecular scanning for mutations in Japanese subjects with NIDDM or obesity
N Utsunomiya, S Ohagi, T Sanke, et al.
Diabetologia
|
August 1, 1997
A missense mutation of the muscle glycogen synthase gene (M416V) is associated with insulin resistance in the Japanese population
H Shimomura, T Sanke, K Ueda, et al.
Nihon Sanka Fujinka Gakkai Zasshi
|
May 1, 1993
[Lipoleiomyoma of the uterus: report of a case]
F Miyauchi, K Nanjo, K Otsuka, et al.
Page
of 12