Christa E Fluck
Christa E Fluck
University Children's Hospital, Bern University, 3010 Bern, Switzerland
Verified email at
Cited by
Cited by
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
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
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
“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
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
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
NADPH P450 oxidoreductase: structure, function, and pathology of diseases
AV Pandey, CE Flück
Pharmacology & therapeutics 138 (2), 229-254, 2013
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
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
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
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
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
The adrenal cortex and its disorders
WL Miller, CE Flück, DT Breault, BJ Feldman
Sperling Pediatric Endocrinology, 425-490, 2014
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
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
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
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
Adrenal gland development and defects
P Kempná, CE Flück
Best practice & research Clinical endocrinology & metabolism 22 (1), 77-93, 2008
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
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
The system can't perform the operation now. Try again later.
Articles 1–20