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M Daimon

Showing results (31-40 of 108) with videos related to

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Frontiers in Endocrinology|April 12, 2013
BRET Biosensor Analysis of Receptor Tyrosine Kinase FunctionalitySana 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 deficiencyT 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, JapanH 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 diabeticsC Y Wang, M Daimon, S J Shen, et al.
Frontiers in Physiology|July 26, 2013
Plurigon: three dimensional visualization and classification of high-dimensionality dataBronwen Martin, Hongyu Chen, Caitlin M Daimon, et al.
Blood|December 12, 2001
Neonatal-onset hereditary coproporphyria with male pseudohermaphrodismH 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 ratsH 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 familyS 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 populationsL He, J Tuomilehto, Q Qiao, et al.
Pageof 11

Showing results (31-40 of 108) with videos related to

Sort By:
Pageof 11
Frontiers in Endocrinology|April 12, 2013
BRET Biosensor Analysis of Receptor Tyrosine Kinase FunctionalitySana 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 deficiencyT 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, JapanH 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 diabeticsC Y Wang, M Daimon, S J Shen, et al.
Frontiers in Physiology|July 26, 2013
Plurigon: three dimensional visualization and classification of high-dimensionality dataBronwen Martin, Hongyu Chen, Caitlin M Daimon, et al.
Blood|December 12, 2001
Neonatal-onset hereditary coproporphyria with male pseudohermaphrodismH 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 ratsH 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 familyS 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 populationsL He, J Tuomilehto, Q Qiao, et al.
Pageof 11