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J L Clark

Showing results (181-190 of 204) with videos related to

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Molecular and Cellular Endocrinology|January 3, 2013
Familial glucocorticoid deficiency: New genes and mechanismsEirini Meimaridou, Claire R Hughes, Julia Kowalczyk, et al.
American Journal of Clinical Oncology|August 1, 1995
Phase II trial of etoposide, doxorubicin, and cisplatin combination in advanced measurable gastric cancer. An Eastern Cooperative Oncology Group studyJ L Clark, O Küçük, D S Neuberg, et al.
Clinical Endocrinology|January 17, 2007
Severe loss-of-function mutations in the adrenocorticotropin receptor (ACTHR, MC2R) can be found in patients diagnosed with salt-losing adrenal hypoplasiaLin Lin, Peter C Hindmarsh, Louise A Metherell, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 4, 2003
Gene association studies in small for gestational age infantsLinda B Johnston, Nicolette Arends, Jovanna Dahlgren, et al.
Clinical Endocrinology|December 31, 2009
d3-GHR genotype does not explain heterogeneity in GH responsiveness in hypopituitary adultsV J Moyes, D M Walker, S Owusu-Antwi, et al.
Sexually Transmitted Infections|November 26, 2008
Risk factors for the spread of HIV and other sexually transmitted infections among men who have sex with men infected with HIV in Lima, PeruJ L Clark, K A Konda, E R Segura, et al.
Clinical Endocrinology|January 28, 2009
Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiencyLi F Chan, Louise A Metherell, Heiko Krude, et al.
Endocrinology|December 29, 2007
The melanocortin 2 receptor accessory protein exists as a homodimer and is essential for the function of the melanocortin 2 receptor in the mouse y1 cell lineSadani N Cooray, Isabel Almiro Do Vale, Kit-Yi Leung, et al.
Pediatrics|February 1, 1988
Simultaneous administration of measles-mumps-rubella vaccine with booster doses of diphtheria-tetanus-pertussis and poliovirus vaccinesA Deforest, S S Long, H W Lischner, et al.
Clinical Endocrinology|May 1, 2007
Novel polymorphisms and lack of mutations in the ACD gene in patients with ACTH resistance syndromesCatherine E Keegan, Janna E Hutz, Andrea S Krause, et al.
Pageof 21

Showing results (181-190 of 204) with videos related to

Sort By:
Pageof 21
Molecular and Cellular Endocrinology|January 3, 2013
Familial glucocorticoid deficiency: New genes and mechanismsEirini Meimaridou, Claire R Hughes, Julia Kowalczyk, et al.
American Journal of Clinical Oncology|August 1, 1995
Phase II trial of etoposide, doxorubicin, and cisplatin combination in advanced measurable gastric cancer. An Eastern Cooperative Oncology Group studyJ L Clark, O Küçük, D S Neuberg, et al.
Clinical Endocrinology|January 17, 2007
Severe loss-of-function mutations in the adrenocorticotropin receptor (ACTHR, MC2R) can be found in patients diagnosed with salt-losing adrenal hypoplasiaLin Lin, Peter C Hindmarsh, Louise A Metherell, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 4, 2003
Gene association studies in small for gestational age infantsLinda B Johnston, Nicolette Arends, Jovanna Dahlgren, et al.
Clinical Endocrinology|December 31, 2009
d3-GHR genotype does not explain heterogeneity in GH responsiveness in hypopituitary adultsV J Moyes, D M Walker, S Owusu-Antwi, et al.
Sexually Transmitted Infections|November 26, 2008
Risk factors for the spread of HIV and other sexually transmitted infections among men who have sex with men infected with HIV in Lima, PeruJ L Clark, K A Konda, E R Segura, et al.
Clinical Endocrinology|January 28, 2009
Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiencyLi F Chan, Louise A Metherell, Heiko Krude, et al.
Endocrinology|December 29, 2007
The melanocortin 2 receptor accessory protein exists as a homodimer and is essential for the function of the melanocortin 2 receptor in the mouse y1 cell lineSadani N Cooray, Isabel Almiro Do Vale, Kit-Yi Leung, et al.
Pediatrics|February 1, 1988
Simultaneous administration of measles-mumps-rubella vaccine with booster doses of diphtheria-tetanus-pertussis and poliovirus vaccinesA Deforest, S S Long, H W Lischner, et al.
Clinical Endocrinology|May 1, 2007
Novel polymorphisms and lack of mutations in the ACD gene in patients with ACTH resistance syndromesCatherine E Keegan, Janna E Hutz, Andrea S Krause, et al.
Pageof 21