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Showing results (531-540 of 1,212) with videos related to

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American Journal of Hypertension|December 1, 1998
Sympathetic nerve activity and insulin sensitivity in normotensive offspring of hypertensive parentsM Hausberg, C A Sinkey, A L Mark, et al.
American Journal of Human Genetics|July 1, 1997
Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28E Pegoraro, J Whitaker, P Mowery-Rushton, et al.
International Journal of Computational Biology and Drug Design|January 9, 2010
Identification of condition-specific regulatory modules through multi-level motif and mRNA expression analysisLi Chen, Jianhua Xuan, Yue Wang, et al.
Diabetes Care|September 1, 1988
Glucagon responses to hypoglycemia in children and adolescents with IDDMC Singer-Granick, R P Hoffman, K Kerensky, et al.
Society of General Physiologists Series|January 1, 1995
In vivo sodium channel structure/function studies: consecutive Arg1448 changes to Cys, His, and Pro at the extracellular surface of IVS4J Wang, V Dubowitz, F Lehmann-Horn, et al.
Human Genetics|May 1, 1995
Towards fully automated genotyping: use of an X linked recessive spastic paraplegia family to test alternative analysis methodsH Kobayashi, T C Matise, M W Perlin, et al.
Journal of Virology|January 1, 1992
Evidence for intracellular down-regulation of the epidermal growth factor (EGF) receptor during adenovirus infection by an EGF-independent mechanismP Hoffman, P Rajakumar, B Hoffman, et al.
Development (Cambridge, England)|July 14, 2011
Barx2 and Fgf10 regulate ocular glands branching morphogenesis by controlling extracellular matrix remodelingCindy Tsau, Masataka Ito, Anastasia Gromova, et al.
Journal of Hypertension|September 1, 1995
Dissociation of sympathoexcitatory and vasodilator actions of modestly elevated plasma insulin levelsM Hausberg, A L Mark, R P Hoffman, et al.
Journal of Pediatric and Adolescent Gynecology|August 15, 1998
17 alpha-hydroxylase/17,20-lyase dysregulation is not caused by mutations in the coding regions of CYP17S F Witchel, P A Lee, M Suda-Hartman, et al.
Pageof 122

Showing results (531-540 of 1,212) with videos related to

Sort By:
Pageof 122
American Journal of Hypertension|December 1, 1998
Sympathetic nerve activity and insulin sensitivity in normotensive offspring of hypertensive parentsM Hausberg, C A Sinkey, A L Mark, et al.
American Journal of Human Genetics|July 1, 1997
Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28E Pegoraro, J Whitaker, P Mowery-Rushton, et al.
International Journal of Computational Biology and Drug Design|January 9, 2010
Identification of condition-specific regulatory modules through multi-level motif and mRNA expression analysisLi Chen, Jianhua Xuan, Yue Wang, et al.
Diabetes Care|September 1, 1988
Glucagon responses to hypoglycemia in children and adolescents with IDDMC Singer-Granick, R P Hoffman, K Kerensky, et al.
Society of General Physiologists Series|January 1, 1995
In vivo sodium channel structure/function studies: consecutive Arg1448 changes to Cys, His, and Pro at the extracellular surface of IVS4J Wang, V Dubowitz, F Lehmann-Horn, et al.
Human Genetics|May 1, 1995
Towards fully automated genotyping: use of an X linked recessive spastic paraplegia family to test alternative analysis methodsH Kobayashi, T C Matise, M W Perlin, et al.
Journal of Virology|January 1, 1992
Evidence for intracellular down-regulation of the epidermal growth factor (EGF) receptor during adenovirus infection by an EGF-independent mechanismP Hoffman, P Rajakumar, B Hoffman, et al.
Development (Cambridge, England)|July 14, 2011
Barx2 and Fgf10 regulate ocular glands branching morphogenesis by controlling extracellular matrix remodelingCindy Tsau, Masataka Ito, Anastasia Gromova, et al.
Journal of Hypertension|September 1, 1995
Dissociation of sympathoexcitatory and vasodilator actions of modestly elevated plasma insulin levelsM Hausberg, A L Mark, R P Hoffman, et al.
Journal of Pediatric and Adolescent Gynecology|August 15, 1998
17 alpha-hydroxylase/17,20-lyase dysregulation is not caused by mutations in the coding regions of CYP17S F Witchel, P A Lee, M Suda-Hartman, et al.
Pageof 122