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Frontiers in Endocrinology
|
April 12, 2013
BRET Biosensor Analysis of Receptor Tyrosine Kinase Functionality
Sana Siddiqui, Wei-Na Cong, Caitlin M Daimon, et al.
Biochemical and Biophysical Research Communications
|
January 3, 1997
Identification of a human cDNA homologue to the Drosophila translocation protein 1 (Dtrp1)
M Daimon, S Susa, K Suzuki, et al.
Human Pathology
|
April 1, 1997
Islet changes in hereditary ceruloplasmin deficiency
T Kato, M Daimon, T Kawanami, et al.
Journal of Clinical Epidemiology
|
October 1, 1996
Family study of acute intermittent porphyria and hereditary coproporphyria in Niigata and Akita Prefectures, Japan
H Sasaki, K Kaneko, H Tsuneyama, et al.
Molecular Endocrinology (Baltimore, Md.)
|
March 1, 1988
Insulin-like growth factor-I messenger ribonucleic acid in the developing human placenta and in term placenta of diabetics
C Y Wang, M Daimon, S J Shen, et al.
Frontiers in Physiology
|
July 26, 2013
Plurigon: three dimensional visualization and classification of high-dimensionality data
Bronwen Martin, Hongyu Chen, Caitlin M Daimon, et al.
Blood
|
December 12, 2001
Neonatal-onset hereditary coproporphyria with male pseudohermaphrodism
H Takeuchi, M Kondo, M Daimon, et al.
Physiology & Behavior
|
December 9, 2000
Impaired neural regulation of insulin secretion related to the leptin receptor gene mutation in Wistar fatty rats
H Ohnuma, K Yamatani, M Daimon, et al.
Journal of Human Genetics
|
September 25, 1998
A novel mutation of coproporphyrinogen oxidase (CPO) gene in a Japanese family
S Susa, M Daimon, I Yamamori, et al.
Diabetes & Metabolism
|
September 19, 2015
Impact of classical risk factors of type 2 diabetes among Asian Indian, Chinese and Japanese populations
L He, J Tuomilehto, Q Qiao, et al.
Page
of 11
Search research articles
Search
Showing results (31-40 of 108) with videos related to
Sort By:
Page
of 11
Frontiers in Endocrinology
|
April 12, 2013
BRET Biosensor Analysis of Receptor Tyrosine Kinase Functionality
Sana Siddiqui, Wei-Na Cong, Caitlin M Daimon, et al.
Biochemical and Biophysical Research Communications
|
January 3, 1997
Identification of a human cDNA homologue to the Drosophila translocation protein 1 (Dtrp1)
M Daimon, S Susa, K Suzuki, et al.
Human Pathology
|
April 1, 1997
Islet changes in hereditary ceruloplasmin deficiency
T Kato, M Daimon, T Kawanami, et al.
Journal of Clinical Epidemiology
|
October 1, 1996
Family study of acute intermittent porphyria and hereditary coproporphyria in Niigata and Akita Prefectures, Japan
H Sasaki, K Kaneko, H Tsuneyama, et al.
Molecular Endocrinology (Baltimore, Md.)
|
March 1, 1988
Insulin-like growth factor-I messenger ribonucleic acid in the developing human placenta and in term placenta of diabetics
C Y Wang, M Daimon, S J Shen, et al.
Frontiers in Physiology
|
July 26, 2013
Plurigon: three dimensional visualization and classification of high-dimensionality data
Bronwen Martin, Hongyu Chen, Caitlin M Daimon, et al.
Blood
|
December 12, 2001
Neonatal-onset hereditary coproporphyria with male pseudohermaphrodism
H Takeuchi, M Kondo, M Daimon, et al.
Physiology & Behavior
|
December 9, 2000
Impaired neural regulation of insulin secretion related to the leptin receptor gene mutation in Wistar fatty rats
H Ohnuma, K Yamatani, M Daimon, et al.
Journal of Human Genetics
|
September 25, 1998
A novel mutation of coproporphyrinogen oxidase (CPO) gene in a Japanese family
S Susa, M Daimon, I Yamamori, et al.
Diabetes & Metabolism
|
September 19, 2015
Impact of classical risk factors of type 2 diabetes among Asian Indian, Chinese and Japanese populations
L He, J Tuomilehto, Q Qiao, et al.
Page
of 11