RET and PHOX2B genetic polymorphisms and Hirschsprung's disease susceptibility: a meta-analysis.

RET and PHOX2B genetic polymorphisms and Hirschsprung's disease susceptibility: a meta-analysis.

BACKGROUND: Many publications have evaluated the correlation between RET, PHOX2B polymorphisms and Hirschsprung's disease with conflicting results. We performed this meta-analysis to clarify the association of RET, PHOX2B polymorphisms with HSCR. METHODS: We searched Pubmed, Elsevier Science Di...

Full description

Bibliographic Details
Main Authors:	Chun-mei Liang, Dong-mei Ji, Xu Yuan, Ling-ling Ren, Juan Shen, Hai-yan Zhang
Format:	Article
Language:	English
Published:	Public Library of Science (PLoS) 2014-01-01
Series:	PLoS ONE
Online Access:	http://europepmc.org/articles/PMC3961244?pdf=render

Similar Items

A study on genetic polymorphism of RET proto-oncogene in Hirschsprung's disease in children
by: Madhu Kumari, et al.
Published: (2020-01-01)

RET single nucleotide polymorphism in Indonesians with sporadic Hirschsprung’s disease
by: Saryono Saryono, et al.
Published: (2016-02-01)

RET single nucleotide polymorphism in Indonesians with sporadic Hirschsprung’s disease
by: Saryono, et al.
Published: (2010-08-01)

Contributions of PHOX2B in the pathogenesis of Hirschsprung disease.
by: Raquel María Fernández, et al.
Published: (2013-01-01)

miRNA Profiling Reveals Dysregulation of RET and RET-Regulating Pathways in Hirschsprung's Disease.
by: Shuangshuang Li, et al.
Published: (2016-01-01)

Polymorphisms of the RET Gene in Hirschsprung Disease, Anorectal Malformation and Intestinal Pseudo-obstruction in Taiwan
by: Trang-Tiau Wu, et al.
Published: (2010-01-01)

Functional Studies on Novel RET Mutations and Their Implications for Genetic Counseling for Hirschsprung Disease
by: Hui Wang, et al.
Published: (2019-10-01)

RET transcriptional regulation by HOXB5 in Hirschsprung's disease
by: 朱江, et al.
Published: (2013)

Genetic variants in RET and risk of Hirschsprung's disease in Southeastern Chinese: a haplotype-based analysis
by: Gu Qinglong, et al.
Published: (2011-02-01)

RET mutational spectrum in Hirschsprung disease: evaluation of 601 Chinese patients.
by: Man-Ting So, et al.
Published: (2011-01-01)

Higher G allele frequency of RET C2307t>G polymorphism in female patients with Hirschsprung disease in Yogyakarta, Indonesia
by: Ahmad Hamim Sadewa, et al.
Published: (2008-05-01)

RET variants and haplotype analysis in a cohort of Czech patients with Hirschsprung disease.
by: Eliska Vaclavikova, et al.
Published: (2014-01-01)

Association between MTHFR genetic polymorphism and Parkinson’s disease susceptibility: a meta-analysis
by: Diao Hong-Mei, et al.
Published: (2019-08-01)

Whole Exome Sequencing Identifies a Novel Pathogenic RET Variant in Hirschsprung Disease
by: Wei Wu, et al.
Published: (2019-01-01)

Preliminary study shows novel variant detected in the screening of RET gene in Malaysian patients with Hirschsprung's disease
by: Nor Azian Abdul Murad, et al.
Published: (2017)

THE EFFECTS OF P22PHOX GENETIC POLYMORPHISMS AND NATURAL COMPOUNDS ON REACTIVE OXYGEN SPECIES FORMATION
by: Whitehouse, Scott David
Published: (2013)

Correlation analysis of IL-11 polymorphisms and Hirschsprung disease subtype susceptibility in Southern Chinese Children
by: Hong Zhang, et al.
Published: (2021-01-01)

Genetic polymorphisms of the SOX10 gene in Thai patients with sporadic Hirschsprung disease
by: Karun Eadyow, et al.
Published: (2020-06-01)

Two novel mutations in exon 3 of PHOX2B gene: think about congenital central hypoventilation syndrome in patients with Hirschsprung disease
by: Maria Giovanna Paglietti, et al.
Published: (2019-04-01)

Induction of RET dependent and independent pro-inflammatory programs in human peripheral blood mononuclear cells from Hirschsprung patients.
by: Marta Rusmini, et al.
Published: (2013-01-01)

The A930G polymorphism ofP22phox (CYBA) gene but not C242T variation is associated with hypertension: a meta-analysis.
by: Yu-Wang Qin, et al.
Published: (2013-01-01)

Correction: Induction of RET Dependent and Independent Pro-Inflammatory Programs in Human Peripheral Blood Mononuclear Cells from Hirschsprung Patients
by: Marta Rusmini, et al.
Published: (2013-01-01)

Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population.
by: Belinda K Cornes, et al.
Published: (2010-01-01)

RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family
by: Elisangela P. S. Quedas, et al.
Published: (2012-01-01)

Correction: Induction of RET Dependent and Independent Pro-Inflammatory Programs in Human Peripheral Blood Mononuclear Cells from Hirschsprung Patients.
by: Marta Rusmini, et al.
Published: (2013-01-01)

The advances of genetics research on Hirschsprung's disease
by: Juntao Ke, et al.
Published: (2018-09-01)

Comprehensive analysis of <it>RET </it>common and rare variants in a series of Spanish Hirschsprung patients confirms a synergistic effect of both kinds of events
by: Castaño Luis, et al.
Published: (2011-10-01)

Sequence characterization of RET in 117 Chinese Hirschsprung disease families identifies a large burden of de novo and parental mosaic mutations
by: Qian Jiang, et al.
Published: (2019-10-01)

Relationship of the p22phox (CYBA) gene polymorphism C242T with risk of coronary artery disease: a meta-analysis.
by: Zhijun Wu, et al.
Published: (2013-01-01)

Correction: Relationship of the p22phox () Gene Polymorphism C242T with Risk of Coronary Artery Disease: A Meta-Analysis.
by: Zhijun Wu, et al.
Published: (2013-01-01)

Association between NADPH oxidase p22(phox) C242T polymorphism and ischemic cerebrovascular disease: a meta-analysis.
by: Bing-Hu Li, et al.
Published: (2013-01-01)

Significant Association of rs2147555 Genetic Polymorphism in the EDNRB Gene with Hirschsprung Disease in Southern Chinese Children
by: Yi Zheng, et al.
Published: (2020-01-01)

Correction: Relationship of the p22phox (CYBA) Gene Polymorphism C242T with Risk of Coronary Artery Disease: A Meta-Analysis
by: Zhijun Wu, et al.
Published: (2013-01-01)

P.049 THE P22PHOX -930A/G POLYMORPHISM OF NADPH OXIDASE: AN INDEPENDENT GENETIC DETERMINANT OF WAVE REFLECTIONS
by: P. Xaplanteris, et al.
Published: (2007-08-01)

The Association between PTPN22 Genetic Polymorphism and Juvenile Idiopathic Arthritis (JIA) Susceptibility: An Updated Meta-Analysis
by: Yazhen DI, et al.
Published: (2015-10-01)

Molecular Basis of Medullary Thyroid Carcinoma: The Role of RET Polymorphisms
by: Ana Luiza Maia, et al.
Published: (2011-12-01)

Exercise Training Attenuates Upregulation of p47phox and p67phox in Hearts of Diabetic Rats
by: Neeru M. Sharma, et al.
Published: (2016-01-01)

Polymorphisms of the NADPH Oxidase p22phox Gene in a Caucasian Population with Intracranial Aneurysms
by: Krex, Dietmar, et al.
Published: (2014)

Genetic mutation in Hirschsprungs/congenital central hypoventilation syndrome
by: Christina Schreiner, et al.
Published: (2021-06-01)

Molecular-genetic analysis of Hirschsprung's disease in South Africa
by: Julies, Monique G.
Published: (2012)