about
Investigation of salicylate hepatic responses in comparison with chemical analogues of the drugPrecision diabetes: learning from monogenic diabetes.The LKB1-salt-inducible kinase pathway functions as a key gluconeogenic suppressor in the liver.Cellular responses to the metal-binding properties of metformin.Successful transfer to sulfonylureas in KCNJ11 neonatal diabetes is determined by the mutation and duration of diabetes.Differential regulation of serum microRNA expression by HNF1β and HNF1α transcription factors.Type 1 Diabetes Genetic Risk Score: A Novel Tool to Discriminate Monogenic and Type 1 DiabetesThe Common p.R114W HNF4A Mutation Causes a Distinct Clinical Subtype of Monogenic Diabetes.Glucose-6-phosphate-mediated activation of liver glycogen synthase plays a key role in hepatic glycogen synthesis.Prospective functional classification of all possible missense variants in PPARG.A Type 1 Diabetes Genetic Risk Score Can Aid Discrimination Between Type 1 and Type 2 Diabetes in Young Adults.Hyperglycaemia-related complications at the time of diagnosis can cause permanent neurological disability in children with neonatal diabetes.Metformin selectively targets redox control of complex I energy transduction.Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetranceInterpretation of thyroid scintigraphy is inconsistent among endocrinologists.A type 1 diabetes genetic risk score can discriminate monogenic autoimmunity with diabetes from early-onset clustering of polygenic autoimmunity with diabetes.A UK nationwide prospective study of treatment change in MODY: genetic subtype and clinical characteristics predict optimal glycaemic control after discontinuing insulin and metforminThe Common Variant I27L Is a Modifier of Age at Diabetes Diagnosis in Individuals With HNF1A-MODYUtility of systematic TSHR gene testing in adults with hyperthyroidism lacking overt autoimmunity and diffuse uptake on thyroid scintigraphyZinc Transporter 8 Autoantibodies (ZnT8A) and a Type 1 Diabetes Genetic Risk Score Can Exclude Individuals With Type 1 Diabetes From Inappropriate Genetic Testing for Monogenic DiabetesPLIN1 Haploinsufficiency Is Not Associated With LipodystrophyAssessing the Pathogenicity, Penetrance, and Expressivity of Putative Disease-Causing Variants in a Population SettingType 1 diabetes genetic risk score discriminates between monogenic and Type 1 diabetes in children diagnosed at the age of <5 years in the Iranian populationPrediction algorithms: pitfalls in interpreting genetic variants of autosomal dominant monogenic diabetesPatterns of postmeal insulin secretion in individuals with sulfonylurea-treated KCNJ11 neonatal diabetes show predominance of non-KATP-channel pathwaysTrisomy 21 Is a Cause of Permanent Neonatal Diabetes That Is Autoimmune but Not HLA AssociatedTransient Neonatal Diabetes: An Etiologic Clue for the Adult Diabetologist
P50
Q28829020-50AF93EB-7E71-477A-8228-FB44D0C8DDF6Q33453490-9187B12C-C0C2-470B-A893-63ABDB131AA1Q34086454-931BB5FA-192B-4910-B87C-BB930A71C335Q35976604-74BEFEE0-5671-4BF2-A2BB-732740734046Q36908155-CFBBA3E6-5B59-483D-BB7B-515D207A45BDQ36990179-70B58FC3-3D74-4968-AED5-8495E40A0C52Q37036350-108DBE2A-8354-489A-B2A3-FD0917FAE9E7Q37281017-D57B49A8-A783-4FCB-84DB-0BFFFB36680DQ37333458-5BF92D19-D567-4FB5-8480-5257B6643E74Q37461625-99778EBB-6B52-430A-AEBE-D5A0A7D17EFEQ42250838-8F2F4825-CAB9-42EE-8952-898B4D6B3428Q42333965-35192978-C5B2-4E96-9E19-0AB732731451Q42362632-C4573375-1D65-48C4-A7CA-769B07B068C7Q42376064-961F42B6-5FE2-49B1-9CBF-4379CBACD9AFQ48184171-D64496A8-AB11-44B0-BC9E-3D3F6B182563Q50126673-E88B6396-F01B-499A-8EF6-8B295D19D5C8Q57155520-78B0DF05-35AC-4D3F-BC39-A5D210F72BB4Q57155520-D62ABD46-EF26-4FF4-855A-B032376E4C3DQ57303405-4C435FCF-DCB3-4494-9EEF-064DE3267B5AQ58101934-E096B6C9-57CC-414C-9F51-25AD88CC9B30Q58578876-93EA74ED-333C-4AAC-B2AC-7A07217BF135Q63352738-D7112284-36F8-4D09-B42B-D114306E7A3CQ64234829-6239C3F8-8A9D-4ECC-AA5D-A54AF1E01D5AQ91647835-B2C84823-5BDD-44D5-B5C2-DB07FD6F9600Q91798861-0D0D3424-3266-41DB-AED7-FB434D5C1C1EQ92463058-E6ABEBB5-8F68-40C2-8A0B-17F6519E8AD2Q92952806-471FEE79-92CE-4A68-9B96-58F92707FF38Q93128321-9AAAAB32-E1D4-4B14-A17C-6302BC711582
P50
description
researcher ORCID ID = 0000-0002-9240-8104
@en
wetenschapper
@nl
name
Kashyap A Patel
@ast
Kashyap A Patel
@en
Kashyap A Patel
@nl
type
label
Kashyap A Patel
@ast
Kashyap A Patel
@en
Kashyap A Patel
@nl
prefLabel
Kashyap A Patel
@ast
Kashyap A Patel
@en
Kashyap A Patel
@nl
P106
P31
P496
0000-0002-9240-8104