(Q50194515)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16941683%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

title

Investigation of the Lith1 candidate genes ABCB11 and LXRA in human gallstone disease (English)

1 reference

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29 December 2019

12

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29 December 2019

11

Stefan Schreiber

1 reference

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29 December 2019

3

Andre Franke

1 reference

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29 December 2019

author name string

Clemens Schafmayer

1

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29 December 2019

Jürgen Tepel

2

1 reference

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29 December 2019

Stephan Buch

4

1 reference

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29 December 2019

Sören Lieb

5

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29 December 2019

Marcus Seeger

6

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29 December 2019

Frank Lammert

7

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29 December 2019

Bernd Kremer

8

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29 December 2019

Ulrich R Fölsch

9

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29 December 2019

Fred Fändrich

10

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29 December 2019

language of work or name

English

0 references

publication date

1 September 2006

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29 December 2019

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29 December 2019

volume

44

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29 December 2019

issue

3

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29 December 2019

page(s)

650-657

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Polymorphisms at cholesterol 7alpha-hydroxylase, apolipoproteins B and E and low density lipoprotein receptor genes in patients with gallbladder stone disease

29 December 2019

cites work

1 reference

Independent risk factors for gallstone formation in a region with high cholelithiasis prevalence

21 January 2018

1 reference

7 January 2021

Familial incidence of gallstones

1 reference

7 January 2021

Genetic and environmental influences on symptomatic gallstone disease: a Swedish study of 43,141 twin pairs

1 reference

7 January 2021

Chromosomal organization of candidate genes involved in cholesterol gallstone formation: a murine gallstone map.

1 reference

7 January 2021

Lith1, a major gene affecting cholesterol gallstone formation among inbred strains of mice

1 reference

7 January 2021

Quantitative trait loci mapping for cholesterol gallstones in AKR/J and C57L/J strains of mice.

1 reference

7 January 2021

Lith genes control mucin accumulation, cholesterol crystallization, and gallstone formation in A/J and AKR/J inbred mice

1 reference

7 January 2021

FXR and ABCG5/ABCG8 as determinants of cholesterol gallstone formation from quantitative trait locus mapping in mice

1 reference

7 January 2021

Characterization of the mouse bile salt export pump overexpressed in the baculovirus system

1 reference

7 January 2021

Functional expression of the canalicular bile salt export pump of human liver

1 reference

7 January 2021

Enterohepatic bile salt transporters in normal physiology and liver disease

1 reference

7 January 2021

A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis

1 reference

7 January 2021

Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis

1 reference

7 January 2021

Bile Salt Export Pump Gene Mutations in Two Japanese Patients With Progressive Familial Intrahepatic Cholestasis

1 reference

7 January 2021

Impaired expression and function of the bile salt export pump due to three novel ABCB11 mutations in intrahepatic cholestasis

1 reference

7 January 2021

PPAR- and LXR-dependent pathways controlling lipid metabolism and the development of atherosclerosis

1 reference

7 January 2021

Nuclear receptors as targets for drug development: regulation of cholesterol and bile acid metabolism by nuclear receptors

1 reference

7 January 2021

The human ABCG1 gene: identification of LXR response elements that modulate expression in macrophages and liver

1 reference

7 January 2021

Liver X receptor alpha interferes with SREBP1c-mediated Abcd2 expression. Novel cross-talk in gene regulation.

1 reference

7 January 2021

UGT1A1 variation and gallstone formation in sickle cell disease

1 reference

7 January 2021

Coinheritance of Gilbert syndrome-associated UGT1A1 mutation increases gallstone risk in cystic fibrosis

1 reference

7 January 2021

Apolipoprotein B-100 Xba I gene polymorphism in gallbladder cancer

1 reference

7 January 2021

Apolipoprotein B-100 gene Xba I polymorphism and cholesterol gallstone disease

1 reference

7 January 2021

Apolipoprotein E polymorphism and lithogenic factors in gallbladder bile

1 reference

7 January 2021

Gallstone cholesterol content is related to apolipoprotein E polymorphism.

1 reference

7 January 2021

A genomewide search finds major susceptibility loci for gallbladder disease on chromosome 1 in Mexican Americans

1 reference

7 January 2021

An integrated system for high throughput TaqManTM based SNP genotyping

1 reference

7 January 2021

Pedigree disequilibrium tests for multilocus haplotypes.

1 reference

7 January 2021

A haplotype map of the human genome

1 reference

7 January 2021

Efficiency and power in genetic association studies

1 reference

7 January 2021

Haploview: analysis and visualization of LD and haplotype maps

1 reference

7 January 2021

Genetic analysis of cholesterol gallstone formation: searching for Lith (gallstone) genes

1 reference

7 January 2021

Age at onset as an indicator of familial risk of breast cancer

1 reference

7 January 2021

Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia.

1 reference

7 January 2021

Random-effects Cox proportional hazards model: general variance components methods for time-to-event data

1 reference

7 January 2021

Familial occurrence of gallstone disease. Incidence in parents of young patients

1 reference

7 January 2021

Gallstone prevalence in Germany: the Ulm Gallbladder Stone Study.

1 reference

7 January 2021

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

1 reference

7 January 2021

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

1 reference

7 January 2021

Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations

1 reference

7 January 2021

Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

1 reference

7 January 2021

Functional variants of OCTN cation transporter genes are associated with Crohn disease

1 reference

7 January 2021

Efficiency and consistency of haplotype tagging of dense SNP maps in multiple samples.

1 reference

7 January 2021

Genome-wide association studies for common diseases and complex traits

1 reference

7 January 2021

A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis

1 reference

7 January 2021

An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis

1 reference

7 January 2021

Identifiers

DOI

10.1002/HEP.21289

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16941683%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference