Articles with public access mandates - yves morelLearn more
Not available anywhere: 3
Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex development
S Benko, CT Gordon, D Mallet, R Sreenivasan, C Thauvin-Robinet, ...
Journal of medical genetics 48 (12), 825-830, 2011
Mandates: National Institute of Health and Medical Research, France
Exposure to glucocorticoids in the first part of fetal life is associated with insulin secretory defect in adult humans
JP Riveline, B Baz, JL Nguewa, T Vidal-Trecan, F Ibrahim, P Boudou, ...
The Journal of Clinical Endocrinology & Metabolism 105 (3), e191-e199, 2020
Mandates: National Institute of Health and Medical Research, France
Symposia du 27e congrès de la SFE
V Tardy, R Menassa, Y Morel
Annales d’Endocrinologie 71, 326-337, 2010
Mandates: US National Institutes of Health
Available somewhere: 8
Clinical features and prognostic factors of listeriosis: the MONALISA national prospective cohort study
C Charlier, É Perrodeau, A Leclercq, B Cazenave, B Pilmis, B Henry, ...
The Lancet Infectious Diseases 17 (5), 510-519, 2017
Mandates: National Institute of Health and Medical Research, France
Novel associations in disorders of sex development: findings from the I-DSD Registry
K Cox, J Bryce, J Jiang, M Rodie, R Sinnott, M Alkhawari, W Arlt, L Audi, ...
The Journal of Clinical Endocrinology & Metabolism 99 (2), E348-E355, 2014
Mandates: UK Medical Research Council
Deletion of P399_E401 in NADPH cytochrome P450 oxidoreductase results in partial mixed oxidase deficiency
CE Flück, D Mallet, G Hofer, D Samara-Boustani, J Leger, M Polak, ...
Biochemical and biophysical research communications 412 (4), 572-577, 2011
Mandates: Swiss National Science Foundation
CBP/p300-interacting transactivator, with Glu/Asp-rich C-terminal domain, 2, and pre-B-cell leukemia transcription factor 1 in human adrenal development and disease
B Ferraz-de-Souza, F Martin, D Mallet, RE Hudson-Davies, P Cogram, ...
The Journal of Clinical Endocrinology & Metabolism 94 (2), 678-683, 2009
Mandates: German Research Foundation
P450 oxidoreductase deficiency: loss of activity caused by protein instability from a novel L374H mutation
S Parween, F Roucher-Boulez, CE Flück, A Lienhardt-Roussie, D Mallet, ...
The Journal of Clinical Endocrinology & Metabolism 101 (12), 4789-4798, 2016
Mandates: Swiss National Science Foundation
Prenatal diagnosis of steroid 21-hydroxylase-deficient congenital adrenal hyperplasia: Experience from a tertiary care centre in India
S Dubey, V Tardy, MR Chowdhury, N Gupta, V Jain, D Deka, P Sharma, ...
Indian Journal of Medical Research 145 (2), 194-202, 2017
Mandates: Department of Science & Technology, India
Loss of LGR4/GPR48 causes severe neonatal salt wasting due to disrupted WNT signaling altering adrenal zonation
C Lucas, KS Sauter, M Steigert, D Mallet, J Wilmouth, J Olabe, I Plotton, ...
The journal of clinical investigation 133 (4), 2023
Mandates: Swiss National Science Foundation
Loss of human LGR4/GPR48 causes a novel syndromic form of severe neonatal saltwasting due to disrupted WNT signaling altering adrenal zonation
C Lucas, KS Sauter, M Steigert, D Mallet, J Wilmouth, J Olabe, I Plotton, ...
Journal of Clinical Investigation, 2022
Mandates: Swiss National Science Foundation, Agence Nationale de la Recherche
Publication and funding information is determined automatically by a computer program