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G I Bell

Showing results (291-300 of 317) with videos related to

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American Journal of Human Genetics|June 1, 1986
Relationships between the human pepsinogen DNA and protein polymorphismsR T Taggart, I M Samloff, L J Raffel, et al.
Genomics|November 1, 1990
Cloning of cDNAs for human phosphoribosylpyrophosphate synthetases 1 and 2 and X chromosome localization of PRPS1 and PRPS2 genesM A Becker, S A Heidler, G I Bell, et al.
The Journal of Clinical Investigation|March 21, 1998
A missense mutation in hepatocyte nuclear factor-4 alpha, resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitusE H Hani, L Suaud, P Boutin, et al.
Cytogenetics and Cell Genetics|January 1, 1987
Mapping polypeptide hormone genes in the mouse: somatostatin, glucagon, calcitonin, and parathyroid hormoneP A Lalley, A Y Sakaguchi, R L Eddy, et al.
Blood|May 1, 1997
Cloning and characterization of exodus, a novel beta-chemokineR Hromas, P W Gray, D Chantry, et al.
Diabetes|November 1, 1996
Altered insulin secretory responses to glucose in diabetic and nondiabetic subjects with mutations in the diabetes susceptibility gene MODY3 on chromosome 12M M Byrne, J Sturis, S Menzel, et al.
Diabetologia|September 1, 2005
The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese populationM C Y Ng, K Miyake, W Y So, et al.
Kidney International|March 18, 2000
Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1 betaC Bingham, S Ellard, L Allen, et al.
Endocrinology|August 2, 2013
GSK-3β function in bone regulates skeletal development, whole-body metabolism, and male life spanJ R Gillespie, J R Bush, G I Bell, et al.
American Journal of Human Genetics|December 1, 1996
Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locusE V Semina, N A Datson, N J Leysens, et al.
Pageof 32

Showing results (291-300 of 317) with videos related to

Sort By:
Pageof 32
American Journal of Human Genetics|June 1, 1986
Relationships between the human pepsinogen DNA and protein polymorphismsR T Taggart, I M Samloff, L J Raffel, et al.
Genomics|November 1, 1990
Cloning of cDNAs for human phosphoribosylpyrophosphate synthetases 1 and 2 and X chromosome localization of PRPS1 and PRPS2 genesM A Becker, S A Heidler, G I Bell, et al.
The Journal of Clinical Investigation|March 21, 1998
A missense mutation in hepatocyte nuclear factor-4 alpha, resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitusE H Hani, L Suaud, P Boutin, et al.
Cytogenetics and Cell Genetics|January 1, 1987
Mapping polypeptide hormone genes in the mouse: somatostatin, glucagon, calcitonin, and parathyroid hormoneP A Lalley, A Y Sakaguchi, R L Eddy, et al.
Blood|May 1, 1997
Cloning and characterization of exodus, a novel beta-chemokineR Hromas, P W Gray, D Chantry, et al.
Diabetes|November 1, 1996
Altered insulin secretory responses to glucose in diabetic and nondiabetic subjects with mutations in the diabetes susceptibility gene MODY3 on chromosome 12M M Byrne, J Sturis, S Menzel, et al.
Diabetologia|September 1, 2005
The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese populationM C Y Ng, K Miyake, W Y So, et al.
Kidney International|March 18, 2000
Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1 betaC Bingham, S Ellard, L Allen, et al.
Endocrinology|August 2, 2013
GSK-3β function in bone regulates skeletal development, whole-body metabolism, and male life spanJ R Gillespie, J R Bush, G I Bell, et al.
American Journal of Human Genetics|December 1, 1996
Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locusE V Semina, N A Datson, N J Leysens, et al.
Pageof 32