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Primus E Mullis

Showing results (31-40 of 97) with videos related to

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Plos One|July 23, 2013
Differential regulation of human 3β-hydroxysteroid dehydrogenase type 2 for steroid hormone biosynthesis by starvation and cyclic AMP stimulation: studies in the human adrenal NCI-H295R cell modelSameer Udhane, Petra Kempna, Gaby Hofer, et al.
The Journal of Clinical Endocrinology and Metabolism|February 12, 2002
An exon splice enhancer mutation causes autosomal dominant GH deficiencyChanda T Moseley, Primus E Mullis, Melissa A Prince, et al.
Atherosclerosis|December 22, 2014
Increased ambulatory arterial stiffness index in obese childrenChristoph Saner, Giacomo D Simonetti, Elke Wühl, et al.
Endocrinology|June 11, 2010
Impact of differential P450c17 phosphorylation by cAMP stimulation and by starvation conditions on enzyme activities and androgen production in NCI-H295R cellsPetra Kempná, Andrea Hirsch, Gaby Hofer, et al.
Molecular Endocrinology (Baltimore, Md.)|March 5, 2002
Decreased expression of the GHRH receptor gene due to a mutation in a Pit-1 binding siteRoberto Salvatori, Xiaoguang Fan, Primus E Mullis, et al.
European Journal of Pediatrics|June 1, 2016
Circadian and ultradian cardiovascular rhythmicity in obese childrenChristoph Saner, Giacomo D Simonetti, Elke Wühl, et al.
Hormone Research in Paediatrics|December 4, 2013
The role of zinc dynamics in growth hormone secretionMaria Consolata Miletta, Martin H Schöni, Kristin Kernland, et al.
Molecular Endocrinology (Baltimore, Md.)|June 28, 2007
Modulation of human CYP19A1 activity by mutant NADPH P450 oxidoreductaseAmit V Pandey, Petra Kempná, Gaby Hofer, et al.
Endocrinology|June 3, 2016
Rescue of Isolated GH Deficiency Type II (IGHD II) via Pharmacologic Modulation of GH-1 SplicingMaria Consolata Miletta, Vibor Petkovic, Andrée Eblé, et al.
Swiss Medical Weekly|August 2, 2005
Genetic testing for glucokinase mutations in clinically selected patients with MODY: a worthwhile investmentSabine Schnyder, Primus E Mullis, Sian Ellard, et al.
Pageof 10

Showing results (31-40 of 97) with videos related to

Sort By:
Pageof 10
Plos One|July 23, 2013
Differential regulation of human 3β-hydroxysteroid dehydrogenase type 2 for steroid hormone biosynthesis by starvation and cyclic AMP stimulation: studies in the human adrenal NCI-H295R cell modelSameer Udhane, Petra Kempna, Gaby Hofer, et al.
The Journal of Clinical Endocrinology and Metabolism|February 12, 2002
An exon splice enhancer mutation causes autosomal dominant GH deficiencyChanda T Moseley, Primus E Mullis, Melissa A Prince, et al.
Atherosclerosis|December 22, 2014
Increased ambulatory arterial stiffness index in obese childrenChristoph Saner, Giacomo D Simonetti, Elke Wühl, et al.
Endocrinology|June 11, 2010
Impact of differential P450c17 phosphorylation by cAMP stimulation and by starvation conditions on enzyme activities and androgen production in NCI-H295R cellsPetra Kempná, Andrea Hirsch, Gaby Hofer, et al.
Molecular Endocrinology (Baltimore, Md.)|March 5, 2002
Decreased expression of the GHRH receptor gene due to a mutation in a Pit-1 binding siteRoberto Salvatori, Xiaoguang Fan, Primus E Mullis, et al.
European Journal of Pediatrics|June 1, 2016
Circadian and ultradian cardiovascular rhythmicity in obese childrenChristoph Saner, Giacomo D Simonetti, Elke Wühl, et al.
Hormone Research in Paediatrics|December 4, 2013
The role of zinc dynamics in growth hormone secretionMaria Consolata Miletta, Martin H Schöni, Kristin Kernland, et al.
Molecular Endocrinology (Baltimore, Md.)|June 28, 2007
Modulation of human CYP19A1 activity by mutant NADPH P450 oxidoreductaseAmit V Pandey, Petra Kempná, Gaby Hofer, et al.
Endocrinology|June 3, 2016
Rescue of Isolated GH Deficiency Type II (IGHD II) via Pharmacologic Modulation of GH-1 SplicingMaria Consolata Miletta, Vibor Petkovic, Andrée Eblé, et al.
Swiss Medical Weekly|August 2, 2005
Genetic testing for glucokinase mutations in clinically selected patients with MODY: a worthwhile investmentSabine Schnyder, Primus E Mullis, Sian Ellard, et al.
Pageof 10