About: Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2)

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scientific article (publication date: December 2002)

Attributes	Values
rdf:type	Item
description	artículu científicu espublizáu en 2002 (ast) vědecký článek publikovaný v roce 2002 (cs) наукова стаття, опублікована в грудні 2002 (uk) 2002 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած (hyw) 2002 թվականի դեկտեմբերին հրատարակված գիտական հոդված (hy) مقالة علمية (نشرت في ديسمبر 2002) (ar) vedecký článok (publikovaný 2002-12) (sk) wetenschappelijk artikel (gepubliceerd in 2002-12) (nl) article scientifique publié en 2002 (fr) scientific article (publication date: December 2002) (en) im Dezember 2002 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28215167-4272711D-6A58-4DCA-9A39-762DBC638AAE
publication date	2002-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28215167-5F7AE8C6-909B-4B3B-9091-CD3288965327
language of work or name	English
exact match	wds:Q28215167-4D358638-27A8-4AA8-A1DC-5259E5548F9D
exact match	https://scigraph.springernature.com/pub.10.1007/s00439-002-0820-5
author name string	wds:Q28215167-1EC8881E-CE56-4D78-B2CC-B21898B02299 wds:Q28215167-2DE9EC50-8114-4C23-87AD-2CE7AEEF2273 wds:Q28215167-B0CBE97C-EFE0-47CD-909B-9F302231B5AA wds:Q28215167-E0C3036C-1AE7-428F-A0C3-8E5058A1F421
OpenCitations bibliographic resource ID	wds:Q28215167-451AE6D1-4655-4E5D-9554-2C6A0BD48ADA
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/1358594
author name string	L P van den Heuvel L Monnens M Willemsen K Assink
OpenCitations bibliographic resource ID	1358594
rdfs:label	Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2) (en) Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2) (nl) Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2) (ast)
skos:prefLabel	Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2) (en) Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2) (nl) Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2) (ast)
name	Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2) (en) Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2) (nl) Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2) (ast)
title	wds:Q28215167-CAB06EF6-8CFA-458F-8F4B-7A335368F7EA
title	Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2) (en)
page(s)	wds:Q28215167-F58B8270-2B47-49EB-9595-4453FAA35E09
page(s)	544-7
instance of	wds:Q28215167-34DF84E5-BD98-44D2-8D88-5B2D96E69EFC
instance of	scholarly article
main subject	wds:Q28215167-2b74cd9c-861b-4b81-96fe-b948ca4e5839 wds:Q28215167-D6D25536-0CDC-4676-AA9B-C4E37DEB5037
main subject	glycobiology glucose
PubMed ID	wds:Q28215167-66511416-540D-4A5D-A1F5-5D29370092F4
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/12436245
PubMed ID	12436245
published in	wds:Q28215167-0D34050F-B51B-48E3-8824-07B8E4EA2C0A
published in	Human Genetics
issue	wds:Q28215167-2EB57C70-A7CC-427A-8D39-DCFC37634CBE
volume	wds:Q28215167-667FA2FB-7DA6-41EF-8221-431F13936E98
issue	6
volume	111
DOI	wds:Q28215167-361CA8EC-023D-4BD2-AF76-61A81C3EAB5E
DOI	http://dx.doi.org/10.1007/S00439-002-0820-5
DOI	10.1007/S00439-002-0820-5
Dimensions Publication ID	wds:Q28215167-8F2FEB02-AFCB-4DF2-B460-3F86E717BBD5
Dimensions Publication ID	1002363097
is owl:sameAs of	Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28215167
is cites work of	Sodium-glucose transporter-2 (SGLT2; SLC5A2) enhances cellular uptake of aminoglycosides Impaired intestinal and renal glucose transport in PDK-1 hypomorphic mice Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria Multiple-dose pharmacokinetics and pharmacodynamics of sergliflozin etabonate, a novel inhibitor of glucose reabsorption, in healthy overweight and obese subjects: a randomized double-blind study The sodium/glucose cotransport family SLC5 Active sugar transport in health and disease Sodium-glucose transport: role in diabetes mellitus and potential clinical implications. Pygo1 and Pygo2 roles in Wnt signaling in mammalian kidney development Functional properties and genomics of glucose transporters The Cellular Fate of Glucose and Its Relevance in Type 2 Diabetes Dapagliflozin for the treatment of type 2 diabetes SGLT2 inhibitors: molecular design and potential differences in effect Effects of SGLT2 inhibitors on cardiovascular outcomes Sodium-glucose cotransport inhibition with dapagliflozin in type 2 diabetes Dapagliflozin: where does it fit in the treatment of type 2 diabetes? Organization of the pronephric kidney revealed by large-scale gene expression mapping. Drug off-target effects predicted using structural analysis in the context of a metabolic network model SGLT2 inhibition--a novel strategy for diabetes treatment SGLT2 inhibitor empagliflozin reduces renal growth and albuminuria in proportion to hyperglycemia and prevents glomerular hyperfiltration in diabetic Akita mice. The iodide-transport-defect-causing mutation R124H: a δ-amino group at position 124 is critical for maturation and trafficking of the Na+/I- symporter. SGLT2 mediates glucose reabsorption in the early proximal tubule. Pathophysiology of the diabetic kidney. SGLT2 inhibitors: a promising new therapeutic option for treatment of type 2 diabetes mellitus Pharmacological profile of ipragliflozin (ASP1941), a novel selective SGLT2 inhibitor, in vitro and in vivo. Dapagliflozin: a novel sodium-glucose cotransporter type 2 inhibitor for the treatment of type 2 diabetes mellitus Renal sodium glucose cotransporter 2 inhibitors as a novel therapeutic approach to treatment of type 2 diabetes: Clinical data and mechanism of action Pharmacodynamic model of sodium-glucose transporter 2 (SGLT2) inhibition: implications for quantitative translational pharmacology Familial renal glucosuria: SLC5A2 mutation analysis and evidence of salt-wasting Abnormal expression and dysfunction of novel SGLT2 mutations identified in familial renal glucosuria patients Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletion Effect of kidney disease on glucose handling (including genetic defects). Familial renal glucosuria: a clinicogenetic study of 23 additional cases. Defective SLC5A2 does not cotransport Glc and Na+ from extracellular region to cytosol Role of genetic variation in the human sodium-glucose cotransporter 2 gene (SGLT2) in glucose homeostasis Diabetes area participation analysis: a review of companies and targets described in the 2008 - 2010 patent literature Dapagliflozin efficacy and safety: a perspective review.

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