(Q44778051)

6 December 2017

title

A promoter variant of the ATP-binding cassette transporter A1 gene alters the HDL cholesterol level in the general Japanese population (English)

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6 December 2017

4

Yoshihiro Kokubo

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6 December 2017

Keisuke Shioji

1

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6 December 2017

Junko Nishioka

2

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6 December 2017

Hiroaki Naraba

3

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6 December 2017

Toshifumi Mannami

5

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6 December 2017

Nozomu Inamoto

6

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6 December 2017

Kei Kamide

7

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6 December 2017

Shin Takiuchi

8

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6 December 2017

Masayoshi Yoshii

9

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6 December 2017

Yoshikazu Miwa

10

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6 December 2017

Yuhei Kawano

11

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6 December 2017

Toshiyuki Miyata

12

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6 December 2017

Shunichi Miyazaki

13

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6 December 2017

Yoichi Goto

14

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6 December 2017

Hiroshi Nonogi

15

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6 December 2017

Naomi Tago

16

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6 December 2017

Naoharu Iwai

17

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6 December 2017

language of work or name

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21 February 2004

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Journal of Human Genetics

6 December 2017

published in

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6 December 2017

volume

49

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6 December 2017

issue

3

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6 December 2017

page(s)

141-147

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The zinc finger protein 202 (ZNF202) is a transcriptional repressor of ATP binding cassette transporter A1 (ABCA1) and ABCG1 gene expression and a modulator of cellular lipid efflux

6 December 2017

cites work

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12 December 2020

JSNP: a database of common gene variations in the Japanese population

1 reference

12 December 2020

Association between hypertension and the alpha-adducin, beta1-adrenoreceptor, and G-protein beta3 subunit genes in the Japanese population; the Suita study

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12 December 2020

High-density lipoprotein cholesterol and ischemic stroke in the elderly: the Northern Manhattan Stroke Study

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12 December 2020

Common and rare ABCA1 variants affecting plasma HDL cholesterol

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12 December 2020

The apoAI-CIII-AIV gene cluster

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12 December 2020

Aldehyde dehydrogenase 2 gene is a risk factor for myocardial infarction in Japanese men.

1 reference

12 December 2020

Efflux and atherosclerosis: the clinical and biochemical impact of variations in the ABCA1 gene

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12 December 2020

Mutations in the ABC 1 gene in familial HDL deficiency with defective cholesterol efflux

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12 December 2020

ApoE genotype does not predict lipid response to changes in dietary saturated fatty acids in a heterogeneous normolipidemic population. The DELTA Research Group. Dietary Effects on Lipoproteins and Thrombogenic Activity

1 reference

12 December 2020

Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease

1 reference

12 December 2020

Epsilon 4 allele of apolipoprotein E gene associates with lower blood pressure in young Japanese subjects: the Suita Study

1 reference

12 December 2020

New genetic variants in the apoA-I and apoC-III genes and familial combined hyperlipidemia

1 reference

12 December 2020

High-density single-nucleotide polymorphism (SNP) map of the 150-kb region corresponding to the human ATP-binding cassette transporter A1 (ABCA1) gene

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12 December 2020

Novel polymorphisms in promoter region of atp binding cassette transporter gene and plasma lipids, severity, progression, and regression of coronary atherosclerosis and response to therapy

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12 December 2020

A common Ile 823 Met variant of ATP-binding cassette transporter A1 gene (ABCA1) alters high density lipoprotein cholesterol level in Japanese population

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12 December 2020

Tangier disease. Report of a case and studies of lipid metabolism

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12 December 2020

The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease

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12 December 2020

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

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12 December 2020

Incidence of coronary heart disease and lipoprotein cholesterol levels. The Framingham Study.

1 reference

12 December 2020

Prevalence of asymptomatic carotid atherosclerotic lesions detected by high-resolution ultrasonography and its relation to cardiovascular risk factors in the general population of a Japanese city: the Suita study

1 reference

12 December 2020

Regulation and Mechanisms of ATP-Binding Cassette Transporter A1-Mediated Cellular Cholesterol Efflux

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12 December 2020

Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1

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12 December 2020

10.1007/S10038-004-0124-9

Identifiers

DOI

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6 December 2017

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