Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Nils Krone

Showing results (31-40 of 94) with videos related to

Pageof 10
Sort By:
The Journal of Clinical Endocrinology and Metabolism|August 14, 2013
A diagnosis not to be missed: nonclassic steroid 11β-hydroxylase deficiency presenting with premature adrenarche and hirsutismNicole Reisch, Wolfgang Högler, Silvia Parajes, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|August 9, 2022
Adrenal Gland Function and Dysfunction During COVID-19Waldemar Kanczkowski, Waqar Haider Gaba, Nils Krone, et al.
Endocrinology|December 10, 2015
Ferredoxin 1b (Fdx1b) Is the Essential Mitochondrial Redox Partner for Cortisol Biosynthesis in ZebrafishAliesha Griffin, Silvia Parajes, Meltem Weger, et al.
Molecular Endocrinology (Baltimore, Md.)|May 17, 2007
Differential inhibition of CYP17A1 and CYP21A2 activities by the P450 oxidoreductase mutant A287PVivek Dhir, Hannah E Ivison, Nils Krone, et al.
Nature Clinical Practice. Endocrinology & Metabolism|October 24, 2007
Cushing's syndrome in women with polycystic ovaries and hyperandrogenismP Gerry Fegan, Derek D Sandeman, Nils Krone, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 2011
A missense mutation in the human cytochrome b5 gene causes 46,XY disorder of sex development due to true isolated 17,20 lyase deficiencyJan Idkowiak, Tabitha Randell, Vivek Dhir, et al.
Hormone Research in Paediatrics|April 22, 2015
Influence of 17-Hydroxyprogesterone, Progesterone and Sex Steroids on Mineralocorticoid Receptor Transactivation in Congenital Adrenal HyperplasiaChristiaan F Mooij, Silvia Parajes, Karijn J Pijnenburg-Kleizen, et al.
European Journal of Endocrinology|April 9, 2005
Early manifestation of calcinosis cutis in pseudohypoparathyroidism type Ia associated with a novel mutation in the GNAS geneFelix G Riepe, Wiebke Ahrens, Nils Krone, et al.
The Journal of Clinical Endocrinology and Metabolism|May 4, 2006
Analyzing the functional and structural consequences of two point mutations (P94L and A368D) in the CYP11B1 gene causing congenital adrenal hyperplasia resulting from 11-hydroxylase deficiencyNils Krone, Yulia Grischuk, Marina Müller, et al.
Plos Genetics|May 8, 2020
Bidirectional crosstalk between Hypoxia-Inducible Factor and glucocorticoid signalling in zebrafish larvaeDavide Marchi, Kirankumar Santhakumar, Eleanor Markham, et al.
Pageof 10

Showing results (31-40 of 94) with videos related to

Sort By:
Pageof 10
The Journal of Clinical Endocrinology and Metabolism|August 14, 2013
A diagnosis not to be missed: nonclassic steroid 11β-hydroxylase deficiency presenting with premature adrenarche and hirsutismNicole Reisch, Wolfgang Högler, Silvia Parajes, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|August 9, 2022
Adrenal Gland Function and Dysfunction During COVID-19Waldemar Kanczkowski, Waqar Haider Gaba, Nils Krone, et al.
Endocrinology|December 10, 2015
Ferredoxin 1b (Fdx1b) Is the Essential Mitochondrial Redox Partner for Cortisol Biosynthesis in ZebrafishAliesha Griffin, Silvia Parajes, Meltem Weger, et al.
Molecular Endocrinology (Baltimore, Md.)|May 17, 2007
Differential inhibition of CYP17A1 and CYP21A2 activities by the P450 oxidoreductase mutant A287PVivek Dhir, Hannah E Ivison, Nils Krone, et al.
Nature Clinical Practice. Endocrinology & Metabolism|October 24, 2007
Cushing's syndrome in women with polycystic ovaries and hyperandrogenismP Gerry Fegan, Derek D Sandeman, Nils Krone, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 2011
A missense mutation in the human cytochrome b5 gene causes 46,XY disorder of sex development due to true isolated 17,20 lyase deficiencyJan Idkowiak, Tabitha Randell, Vivek Dhir, et al.
Hormone Research in Paediatrics|April 22, 2015
Influence of 17-Hydroxyprogesterone, Progesterone and Sex Steroids on Mineralocorticoid Receptor Transactivation in Congenital Adrenal HyperplasiaChristiaan F Mooij, Silvia Parajes, Karijn J Pijnenburg-Kleizen, et al.
European Journal of Endocrinology|April 9, 2005
Early manifestation of calcinosis cutis in pseudohypoparathyroidism type Ia associated with a novel mutation in the GNAS geneFelix G Riepe, Wiebke Ahrens, Nils Krone, et al.
The Journal of Clinical Endocrinology and Metabolism|May 4, 2006
Analyzing the functional and structural consequences of two point mutations (P94L and A368D) in the CYP11B1 gene causing congenital adrenal hyperplasia resulting from 11-hydroxylase deficiencyNils Krone, Yulia Grischuk, Marina Müller, et al.
Plos Genetics|May 8, 2020
Bidirectional crosstalk between Hypoxia-Inducible Factor and glucocorticoid signalling in zebrafish larvaeDavide Marchi, Kirankumar Santhakumar, Eleanor Markham, et al.
Pageof 10