Hôpital Necker-Enfants malades
Hospital
Location:
Paris,
France (FR)
ISNI: 0000000405939113
ROR: https://ror.org/05tr67282
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Whole-exome sequencing identifies mutations of TBC1D1 encoding a Rab-GTPase-activating protein in patients with congenital anomalies of the kidneys and urinary tract (CAKUT) (2016)
Kosfeld A, Kreuzer M, Daniel C, Brand F, Schaefer AK, Chadt A, Weiss AC, et al.
Journal article
The global spread of HIV-1 subtype B epidemic (2016)
Magiorkinis G, Angelis K, Mamais I, Katzourakis A, Hatzakis A, Albert J, Lawyer G, et al.
Journal article
Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome (2015)
Kreins AY, Ciancanelli MJ, Okada S, Kong XF, Ramirez-Alejo N, Kilic SS, El Baghdadi J, et al.
Journal article
Renal fibrosis is the common feature of autosomal dominant tubulointerstitial kidney diseases caused by mutations in mucin 1 or uromodulin (2014)
Ekici AB, Hackenbeck T, Moriniere V, Panness A, Büttner M, Uebe S, Janka RM, et al.
Journal article
Expression of cell-cell interacting genes distinguishes HLXB9/TEL from MLL-positive childhood acute myeloid leukemia (2010)
Wildenhain S, Ruckert C, Roettgers S, Harbott J, Ludwig WD, Schuster FR, Beldjord K, et al.
Journal article, Letter