Christa E Fluck
Christa E Fluck
University Children's Hospital, Bern University, 3010 Bern, Switzerland
Bestätigte E-Mail-Adresse bei dkf.unibe.ch
Titel
Zitiert von
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Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome
CE Flück, T Tajima, AV Pandey, W Arlt, K Okuhara, CF Verge, EW Jabs, ...
Nature genetics 36 (3), 228-230, 2004
4172004
Diversity and function of mutations in p450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesis
N Huang, AV Pandey, V Agrawal, W Reardon, PD Lapunzina, D Mowat, ...
The American Journal of Human Genetics 76 (5), 729-749, 2005
2862005
Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROP1 gene mutation resulting in the substitution of Arg→ Cys at codon 120 (R120C)
C Flück, J Deladoey, K Rutishauser, A Eblé, U Marti, W Wu, PE Mullis
The Journal of Clinical Endocrinology & Metabolism 83 (10), 3727-3734, 1998
2281998
“Hot spot” in the PROP1 gene responsible for combined pituitary hormone deficiency
J Deladoëy, C Flück, A Büyükgebiz, BV Kuhlmann, A Eblé, ...
The Journal of Clinical Endocrinology & Metabolism 84 (5), 1645-1650, 1999
2191999
Effect of non-esterified fatty acids on bovine granulosa cell steroidogenesis and proliferation in vitro
T Vanholder, J Leroy, A Van Soom, G Opsomer, D Maes, M Coryn, ...
Animal reproduction science 87 (1-2), 33-44, 2005
2172005
Why boys will be boys: two pathways of fetal testicular androgen biosynthesis are needed for male sexual differentiation
CE Flück, M Meyer-Böni, AV Pandey, P Kempná, WL Miller, EJ Schoenle, ...
The American Journal of Human Genetics 89 (2), 201-218, 2011
1682011
NADPH P450 oxidoreductase: structure, function, and pathology of diseases
AV Pandey, CE Flück
Pharmacology & therapeutics 138 (2), 229-254, 2013
1492013
High prevalence of vitamin D deficiency in children and adolescents with type 1 diabetes
M Janner, P Ballinari, PE Mullis, C Flück
Swiss medical weekly 140, w13091, 2010
1432010
The 17, 20-Lyase Activity of Cytochrome P450c17 from Human Fetal Testis Favors the Δ5 Steroidogenic Pathway
CE Flück, WL Miller, RJ Auchus
The Journal of Clinical Endocrinology & Metabolism 88 (8), 3762-3766, 2003
1432003
Aromatase Deficiency Caused by a Novel P450arom Gene Mutation: Impact of Absent Estrogen Production on Serum Gonadotropin Concentration in a Boy
J Deladoëy, C Flück, M Bex, N Yoshimura, N Harada, PE Mullis
The Journal of Clinical Endocrinology & Metabolism 84 (11), 4050-4054, 1999
1391999
GATA-4 and GATA-6 modulate tissue-specific transcription of the human gene for P450c17 by direct interaction with Sp1
CE Flück, WL Miller
Molecular Endocrinology 18 (5), 1144-1157, 2004
1372004
The adrenal cortex and its disorders
WL Miller
Brook's Clinical Pediatric Endocrinology, 2010
1222010
Satisfaction with genital surgery and sexual life of adults with XY disorders of sex development: results from the German clinical evaluation study
B Köhler, E Kleinemeier, A Lux, O Hiort, A Grüters, U Thyen, ...
The Journal of Clinical Endocrinology & Metabolism 97 (2), 577-588, 2012
1202012
Ten Novel Mutations in the NR5A1 Gene Cause Disordered Sex Development in 46,XY and Ovarian Insufficiency in 46,XX Individuals
N Camats, AV Pandey, M Fernandez-Cancio, P Andaluz, M Janner, ...
The Journal of Clinical Endocrinology & Metabolism 97 (7), E1294-E1306, 2012
1122012
Modulation of human CYP19A1 activity by mutant NADPH P450 oxidoreductase
AV Pandey, P Kempna, G Hofer, PE Mullis, CE Flück
Molecular Endocrinology 21 (10), 2579-2595, 2007
1092007
NADPH–cytochrome P450 oxidoreductase: roles in physiology, pharmacology, and toxicology
DS Riddick, X Ding, CR Wolf, TD Porter, AV Pandey, QY Zhang, J Gu, ...
Drug Metabolism and Disposition 41 (1), 12-23, 2013
962013
Adrenal gland development and defects
P Kempná, CE Flück
Best practice & research Clinical endocrinology & metabolism 22 (1), 77-93, 2008
902008
Caring for individuals with a difference of sex development (DSD): a consensus statement
M Cools, A Nordenström, R Robeva, J Hall, P Westerveld, C Flück, ...
Nature Reviews Endocrinology 14 (7), 415-429, 2018
872018
Short stature caused by a biologically inactive mutant growth hormone (GH-C53S)
A Besson, S Salemi, J Deladoëy, JM Vuissoz, A Eblé, M Bidlingmaier, ...
The Journal of Clinical Endocrinology & Metabolism 90 (5), 2493-2499, 2005
832005
P450 oxidoreductase deficiency–a new form of congenital adrenal hyperplasia
CE Flück, AV Pandey, N Huang, V Agrawal, WL Miller
Disorders of the Human Adrenal Cortex 13, 67-81, 2008
772008
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