about
Fourteen monogenic genes account for 15% of nephrolithiasis/nephrocalcinosis.Clinical and genetic analysis of patients with cystinuria in the United Kingdom.A novel LMX1B mutation in a family with end-stage renal disease of 'unknown cause'.Clinical, biochemical, and pathophysiological analysis of SLC34A1 mutations.ARL3 Mutations Cause Joubert Syndrome by Disrupting Ciliary Protein CompositionIdentification of a novel, methylation-dependent, RUNX2 regulatory region associated with osteoarthritis riskEsomeprazole Increases Airway Surface Liquid pH in Primary Cystic Fibrosis Epithelial CellsPrioritization of PLEC and GRINA as Osteoarthritis Risk Genes Through the Identification and Characterization of Novel Methylation Quantitative Trait LociBialleleic PKD1 mutations underlie early-onset autosomal dominant polycystic kidney disease in Saudi Arabian familiesDiscovery and analysis of methylation quantitative trait loci (mQTLs) mapping to novel osteoarthritis genetic risk signals
P50
Q35124270-84F55F19-4FAC-4193-8D68-C2C702EC55B5Q35817051-57A9514B-9E51-40E9-B5E7-E81A6D6393A7Q41789233-31716E14-68BD-4AB4-AE67-834837E1CA67Q55350639-47ED0936-7C1E-4876-98A4-ABF7272F05FEQ57023929-0D7E12F3-9E85-4F1E-B037-F32DA80E69CBQ58788904-A1B33F1D-5A16-4CAD-A6B5-FDB5A786259CQ60960121-40A618B8-94B9-4B34-80D1-CD8E95E44082Q91397070-0206430C-23DD-435F-8704-C73C0AB9EEC7Q91952927-ACCF0D5E-C997-4828-A0EB-95E91250F706Q92586488-CDABD242-5893-4D2E-8585-5129037E91F3
P50
description
Forscher
@de
chercheur
@fr
hulumtuese
@sq
investigador
@es
researcher
@en
հետազոտող
@hy
研究者
@zh
name
Sarah J Rice
@ast
Sarah J Rice
@en
Sarah J Rice
@es
Sarah J Rice
@nl
type
label
Sarah J Rice
@ast
Sarah J Rice
@en
Sarah J Rice
@es
Sarah J Rice
@nl
prefLabel
Sarah J Rice
@ast
Sarah J Rice
@en
Sarah J Rice
@es
Sarah J Rice
@nl
P21
P31
P496
0000-0003-3343-5986