(Q36906186)

English

Ser1369Ala variant in sulfonylurea receptor gene ABCC8 is associated with antidiabetic efficacy of gliclazide in Chinese type 2 diabetic patients

scientific article published on 3 July 2008

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Ser1369Ala variant in sulfonylurea receptor gene ABCC8 is associated with antidiabetic efficacy of gliclazide in Chinese type 2 diabetic patients (English)

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

1 reference

based on heuristic

inferred from title

author name string

Yan Feng

1

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Guangyun Mao

2

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Xiaowei Ren

3

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Houxun Xing

4

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Genfu Tang

5

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Qiang Li

6

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Xueqi Li

7

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Lirong Sun

8

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Jinqui Yang

9

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Weiqing Ma

10

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Xiaobin Wang

11

1 reference

Europe PubMed Central

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17 August 2017

Xiping Xu

12

1 reference

Europe PubMed Central

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17 August 2017

language of work or name

0 references

publication date

3 July 2008

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

1 reference

Europe PubMed Central

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17 August 2017

31

1 reference

Europe PubMed Central

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17 August 2017

10

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

1939-1944

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

A rare mutation in ABCC8/SUR1 leading to altered ATP-sensitive K+ channel activity and beta-cell glucose sensing is associated with type 2 diabetes in adults

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2551631

29 September 2017

A new era for Type 2 diabetes genetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2551631

29 September 2017

Effect of genetic variation in the organic cation transporter 1 (OCT1) on metformin action

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2551631

29 September 2017

Type 2 diabetes-associated missense polymorphisms KCNJ11 E23K and ABCC8 A1369S influence progression to diabetes and response to interventions in the Diabetes Prevention Program

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2551631

29 September 2017

Glycemic durability of rosiglitazone, metformin, or glyburide monotherapy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2551631

29 September 2017

Activating mutations in the ABCC8 gene in neonatal diabetes mellitus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2551631

29 September 2017

Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2551631

29 September 2017

Global prevalence of diabetes: estimates for the year 2000 and projections for 2030

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2551631

29 September 2017

Decreased tolbutamide-stimulated insulin secretion in healthy subjects with sequence variants in the high-affinity sulfonylurea receptor gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2551631

29 September 2017

Identification and functional analysis of sulfonylurea receptor 1 variants in Japanese patients with NIDDM.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2551631

29 September 2017

Sequence variants in the sulfonylurea receptor (SUR) gene are associated with NIDDM in Caucasians

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2551631

29 September 2017

Human organic cation transporter (OCT1 and OCT2) gene polymorphisms and therapeutic effects of metformin.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2551631

27 June 2018

Central rather than overall obesity is related to diabetes in the Chinese population: the InterASIA study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2551631

4 September 2018

The E23K variant of KCNJ11 encoding the pancreatic beta-cell adenosine 5'-triphosphate-sensitive potassium channel subunit Kir6.2 is associated with an increased risk of secondary failure to sulfonylurea in patients with type 2 diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2551631

4 September 2018

Genetic studies of the sulfonylurea receptor gene locus in NIDDM and in morbid obesity among French Caucasians

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2551631

4 September 2018

Sulfonylurea receptor 1 gene variants are associated with gestational diabetes and type 2 diabetes but not with altered secretion of insulin

1 reference

https://pubmed.ncbi.nlm.nih.gov/18599530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sensitivity to sulphonylureas in patients with hepatocyte nuclear factor-1alpha gene mutations: evidence for pharmacogenetics in diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/18599530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis and classification of diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/18599530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SNPs in the KCNJ11-ABCC8 gene locus are associated with type 2 diabetes and blood pressure levels in the Japanese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/18599530

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.2337/DC07-2248

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

ResearchGate publication ID

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