Functional SNPs in the SCGB3A2 promoter are associated with susceptibility to Graves' disease. (Q54500126)

30 May 2018

title

Functional SNPs in the SCGB3A2 promoter are associated with susceptibility to Graves' disease. (English)

1 reference

30 May 2018

author name string

Huai-Dong Song

1

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30 May 2018

Jun Liang

2

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30 May 2018

Jing-Yi Shi

3

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30 May 2018

Shuang-Xia Zhao

4

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30 May 2018

Zhi Liu

5

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30 May 2018

Jia-Jun Zhao

6

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30 May 2018

Yong-De Peng

7

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30 May 2018

Guan-Qi Gao

8

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30 May 2018

Jiong Tao

9

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30 May 2018

Chun-Ming Pan

10

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30 May 2018

Li Shao

11

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30 May 2018

Feng Cheng

12

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30 May 2018

Yi Wang

13

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30 May 2018

Guo-Yue Yuan

14

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30 May 2018

Chao Xu

15

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30 May 2018

Bing Han

16

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30 May 2018

Wei Huang

17

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30 May 2018

Xun Chu

18

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30 May 2018

Yi Chen

19

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30 May 2018

Yan Sheng

20

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30 May 2018

Rong-Ying Li

21

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30 May 2018

Qing Su

22

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30 May 2018

Ling Gao

23

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30 May 2018

Wei-Ping Jia

24

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30 May 2018

Li Jin

25

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30 May 2018

Ming-Dao Chen

26

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30 May 2018

Sai-Juan Chen

27

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30 May 2018

Zhu Chen

28

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30 May 2018

Jia-Lun Chen

29

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30 May 2018

publication date

6 January 2009

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30 May 2018

published in

Human Molecular Genetics

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30 May 2018

volume

18

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30 May 2018

issue

6

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30 May 2018

page(s)

1156-1170

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30 May 2018

Serum TSH, T(4), and thyroid antibodies in the United States population (1988 to 1994): National Health and Nutrition Examination Survey (NHANES III).

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

Searching for the autoimmune thyroid disease susceptibility genes: from gene mapping to gene function

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

SNPs in the promoter of a B cell-specific antisense transcript, SAS-ZFAT, determine susceptibility to autoimmune thyroid disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

A Genome-Wide Scan for Autoimmune Thyroiditis in the Old Order Amish: Replication of Genetic Linkage on Chromosome 5q11.2-q14.3

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

Replication of linkage studies of complex traits: an examination of variation in location estimates

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

Haploview: analysis and visualization of LD and haplotype maps

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

UGRP1, a uteroglobin/Clara cell secretory protein-related protein, is a novel lung-enriched downstream target gene for the T/EBP/NKX2.1 homeodomain transcription factor

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

Identification of uteroglobin-related protein 1 and macrophage scavenger receptor with collagenous structure as a lung-specific ligand-receptor pair

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

On the allelic spectrum of human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

The cytotoxic T lymphocyte antigen-4 is a major Graves' disease locus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

Betting odds and genetic associations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

Assessing the probability that a positive report is false: an approach for molecular epidemiology studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

Problems of reporting genetic associations with complex outcomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

Cell-type-specific expression of the rat thyroperoxidase promoter indicates common mechanisms for thyroid-specific gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

Characterization of a thyroid-specific enhancer located 5.5 kilobase pairs upstream of the human thyroid peroxidase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

The lung-specific surfactant protein B gene promoter is a target for thyroid transcription factor 1 and hepatocyte nuclear factor 3, indicating common factors for organ-specific gene expression along the foregut axis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

Transcriptional regulation of a mouse Clara cell-specific protein (mCC10) gene by the NKx transcription factor family members thyroid transciption factor 1 and cardiac muscle-specific homeobox protein (CSX).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

Interleukin-5 reduces the expression of uteroglobin-related protein (UGRP) 1 gene in allergic airway inflammation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

Decreased expression of uteroglobin-related protein 1 in inflamed mouse airways is mediated by IL-9.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

Interleukin-10 induces uteroglobin-related protein (UGRP) 1 gene expression in lung epithelial cells through homeodomain transcription factor T/EBP/NKX2.1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

A polymorphism in the human UGRP1 gene promoter that regulates transcription is associated with an increased risk of asthma

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

Association of uteroglobulin-related protein 1 with bronchial asthma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

Plasma UGRP1 levels associate with promoter G-112A polymorphism and the severity of asthma

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

Cloning of a novel bacteria-binding receptor structurally related to scavenger receptors and expressed in a subset of macrophages

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

Hematopoietic gene expression profile in zebrafish kidney marrow.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN442

21 January 2018

Identifiers

DOI

10.1093/HMG/DDN442

1 reference

30 May 2018

release_qynayvrq7bg47n2co62o26x5ha

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/qynayvrq7bg47n2co62o26x5ha

mapped directly with Wikidata item

24 November 2022

based on heuristic

PubMed ID

19126779

1 reference

30 May 2018