(Q46678805)

English

The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population

scientific article published on 26 August 2005

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16132950

The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population (English)

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16132950

type 2 diabetes

0 references

metabolic syndrome

1 reference

based on heuristic

inferred from title

Juliana Chung-ngor Chan

9

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16132950

8

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G I Bell

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16132950

author name string

M C Y Ng

1

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16132950

K Miyake

2

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16132950

W Y So

3

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16132950

E W M Poon

4

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16132950

V K L Lam

5

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16132950

J K Y Li

6

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16132950

N J Cox

7

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16132950

publication date

26 August 2005

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16132950

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16132950

48

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16132950

10

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16132950

2018-2024

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16132950

https://scigraph.springernature.com/pub.10.1007/s00125-005-1914-0

0 references

Replication of Linkage of Familial Combined Hyperlipidemia to Chromosome 1q With Additional Heterogeneous Effect of Apolipoprotein A-I/C-III/A-IV Locus

1 reference

https://api.crossref.org/works/10.1007%2FS00125-005-1914-0

21 January 2018

Factors of insulin resistance syndrome--related phenotypes are linked to genetic locations on chromosomes 6 and 7 in nondiabetic mexican-americans

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: diagnosis and classification of diabetes mellitus provisional report of a WHO consultation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increasing the power and efficiency of disease-marker case-control association studies through use of allele-sharing information

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative-trait loci influencing body-mass index reside on chromosomes 7 and 13: the National Heart, Lung, and Blood Institute Family Heart Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The allelic architecture of human disease genes: common disease-common variant... or not?

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rational inferences about departures from Hardy-Weinberg equilibrium

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variation in USF1 shows haplotype effects, gene : gene and gene : environment associations with glucose and lipid parameters in the European Atherosclerosis Research Study II.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Growing evidence for diabetes susceptibility genes from genome scan data

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

GOLD--graphical overview of linkage disequilibrium

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide Scan for Type 2 Diabetes Loci in Hong Kong Chinese and Confirmation of a Susceptibility Locus on Chromosome 1q21-q25

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1).

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Executive Summary of The Third Report of The National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, And Treatment of High Blood Cholesterol In Adults (Adult Treatment Panel III)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of the metabolic syndrome to 1q23-q31 in Hispanic families: the Insulin Resistance Atherosclerosis Study Family Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

USF1 implicated in the aetiology of familial combined hyperlipidaemia and the metabolic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide scan for metabolic syndrome and related quantitative traits in Hong Kong Chinese and confirmation of a susceptibility locus on chromosome 1q21-q25.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A statistical method for identification of polymorphisms that explain a linkage result

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family-based tests of association in the presence of linkage

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage strategies for genetically complex traits. I. Multilocus models

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A New Statistical Method for Haplotype Reconstruction from Population Data

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A comprehensive linkage analysis for myocardial infarction and its related risk factors

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homeostasis model assessment: insulin resistance and ?-cell function from fasting plasma glucose and insulin concentrations in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Power and sample size calculations for case-control genetic association tests when errors are present: application to single nucleotide polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/16132950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00125-005-1914-0

1 reference

https://api.fatcat.wiki/v0/release/7vqezivponblbhha5fy72rvtxu

30 July 2022

based on heuristic

mapped directly with Wikidata item

release_7vqezivponblbhha5fy72rvtxu

1 reference

https://api.fatcat.wiki/v0/release/7vqezivponblbhha5fy72rvtxu

30 July 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

https://api.fatcat.wiki/v0/release/7vqezivponblbhha5fy72rvtxu

30 July 2022

based on heuristic

mapped directly with Wikidata item

ResearchGate publication ID

0 references

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