Cargando…

Lack of association between methylenetetrahydrofolate reductase gene variants & essential tremor in Han Chinese

Detalles Bibliográficos
Autores principales:	He, Dan, Yuan, Lamei, Song, Zhi, Deng, Xiong, Chen, Yizhi, Lu, Hongwei, Deng, Hao
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2019
Materias:	Correspondence
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507536/ https://www.ncbi.nlm.nih.gov/pubmed/31115378 http://dx.doi.org/10.4103/ijmr.IJMR_432_17

Ejemplares similares

Systematic analysis of genetic variants in patients with essential tremor
por: Yuan, Lamei, et al.
Publicado: (2018)

Investigation of methylenetetrahydrofolate reductase tagging polymorphisms with colorectal cancer in Chinese Han population
por: Zhang, Sheng, et al.
Publicado: (2017)

Systematic analysis of genetic variants in Han Chinese patients with sporadic Parkinson’s disease
por: Yuan, Lamei, et al.
Publicado: (2016)

Methylenetetrahydrofolate reductase tagging polymorphisms are associated with risk of non-small cell lung cancer in eastern Chinese Han population
por: Ding, Hao, et al.
Publicado: (2017)

Identification of compound heterozygous DNAH11 variants in a Han‐Chinese family with primary ciliary dyskinesia
por: Xiong, Ying, et al.
Publicado: (2021)

Identification of DNAH17 Variants in Han-Chinese Patients With Left–Right Asymmetry Disorders
por: Yu, Xuehui, et al.
Publicado: (2022)

Methylenetetrahydrofolate Reductase 677T Allele Is a Risk Factor for Arterial Thrombosis in Chinese Han Patients with Antiphospholipid Syndrome
por: Tang, Zihan, et al.
Publicado: (2022)

Identification of a novel EVC variant in a Han‐Chinese family with Ellis‐van Creveld syndrome
por: Huang, Xiangjun, et al.
Publicado: (2019)

Association of methylenetetrahydrofolate reductase (MTHFR) variant C677T and risk of carotid atherosclerosis: a cross-sectional analysis of 730 Chinese Han adults in Chongqing
por: Peng, Xulei, et al.
Publicado: (2020)

Methylenetetrahydrofolate reductase and psychiatric diseases
por: Wan, Lin, et al.
Publicado: (2018)

Lack of Association of C677T Methylenetetrahydrofolate Reductase Polymorphism with Breast Cancer Risk in Mali
por: Diakite, Brehima, et al.
Publicado: (2023)

Methylenetetrahydrofolate Reductase Polymorphisms and Pregnancy Outcome
por: Turgal, Mert, et al.
Publicado: (2018)

Methylenetetrahydrofolate reductase tagging polymorphisms are associated with risk of esophagogastric junction adenocarcinoma: a case-control study involving 2,740 Chinese Han subjects
por: Ding, Guowen, et al.
Publicado: (2017)

Decreased Methylenetetrahydrofolate Reductase Activity Leads to Increased Sensitivity to para-Aminosalicylic Acid in Mycobacterium tuberculosis
por: Yu, Ji-fang, et al.
Publicado: (2022)

Digenic Variants in the TTN and TRAPPC11 Genes Co-segregating With a Limb-Girdle Muscular Dystrophy in a Han Chinese Family
por: Chen, Qian, et al.
Publicado: (2021)

Identification of novel pathogenic ABCA4 variants in a Han Chinese family with Stargardt disease
por: Xiang, Qin, et al.
Publicado: (2019)

Identification of a frame shift mutation in the CCDC151 gene in a Han-Chinese family with Kartagener syndrome
por: Deng, Sheng, et al.
Publicado: (2020)

Corrigendum: Digenic Variants in the TTN and TRAPPC11 Genes Co-segregating With a Limb-Girdle Muscular Dystrophy in a Han Chinese Family
por: Chen, Qian, et al.
Publicado: (2021)

The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura
por: Lea, Rod A, et al.
Publicado: (2004)

The protective effects of the methylenetetrahydrofolate reductase rs1801131 variant among Saudi smokers
por: Almutairi, Mikhlid H., et al.
Publicado: (2021)

Lack of association of methylenetetrahydrofolate reductase 677C>T mutation with coronary artery disease in a Pakistani population
por: Iqbal, M Perwaiz, et al.
Publicado: (2005)

Methylenetetrahydrofolate reductase polymorphism and susceptibility to breast cancer
por: Campbell, Ian G, et al.
Publicado: (2002)

Thiopurine S-Methyltransferase and Methylenetetrahydrofolate Reductase Polymorphisms in Leukemia
por: KÜPELİ, Serhan
Publicado: (2015)

Association of methylenetetrahydrofolate reductase C677T polymorphism and serum lipid levels in the Guangxi Bai Ku Yao and Han populations
por: Zhang, Lin, et al.
Publicado: (2010)

Increased Medical Comorbidities in Essential Tremor—A Wake-up Call?
por: Louis, Elan D.
Publicado: (2022)

Methylenetetrahydrofolate reductase C677T polymorphism and diabetic retinopathy risk: a meta-analysis of the Chinese population
por: Xu, Wei-hai, et al.
Publicado: (2019)

Novel SCN5A and GPD1L Variants Identified in Two Unrelated Han-Chinese Patients With Clinically Suspected Brugada Syndrome
por: Yuan, Meng, et al.
Publicado: (2021)

Prognostic Relevance of Methylenetetrahydrofolate Reductase Polymorphisms for Prostate Cancer
por: Lin, Victor C., et al.
Publicado: (2016)

Methylenetetrahydrofolate Reductase Polymorphism and Premature Coronary Artery Disease
por: Zaghloul, Ahmed, et al.
Publicado: (2019)

Clinical presentation of seven patients with Methylenetetrahydrofolate reductase deficiency
por: Aljassim, Nada, et al.
Publicado: (2020)

Lack of association between methylenetetrahydrofolate reductase C677T polymorphism, HPV infection and cervical intraepithelial neoplasia in Brazilian women
por: Silva, Nayara Nascimento Toledo, et al.
Publicado: (2019)

COL1A2 p.Gly1066Val variant identified in a Han Chinese family with osteogenesis imperfecta type I
por: Wang, Mingyuan, et al.
Publicado: (2019)

Genetic variants in 3′-UTRs of methylenetetrahydrofolate reductase (MTHFR) predict colorectal cancer susceptibility in Koreans
por: Joo Jeon, Young, et al.
Publicado: (2015)

Methylenetetrahydrofolate reductase A1298C genetic variant & risk of schizophrenia: A meta-analysis
por: Rai, Vandana, et al.
Publicado: (2017)

Associations of Genetic Variants of Methylenetetrahydrofolate Reductase and Serum Folate Levels with Metabolic Parameters in Patients with Schizophrenia
por: Chen, Chun-Hsin, et al.
Publicado: (2021)

Methylenetetrahydrofolate reductase gene polymorphisms in the risk of polycystic ovary syndrome and ovarian cancer
por: Xiong, Ying, et al.
Publicado: (2020)

The Polymorphisms in Methylenetetrahydrofolate Reductase, Methionine Synthase, Methionine Synthase Reductase, and the Risk of Colorectal Cancer
por: Zhou, Daijun, et al.
Publicado: (2012)

Novel CLCN7 mutation identified in a Han Chinese family with autosomal dominant osteopetrosis-2
por: Deng, Hao, et al.
Publicado: (2016)

Lack of association of TP73 rare variants with amyotrophic lateral sclerosis in a Chinese cohort
por: Li, Chunyu, et al.
Publicado: (2022)

The Association of Methylenetetrahydrofolate Reductase Genotypes with the Risk of Childhood Leukemia in Taiwan
por: Pei, Jen-Sheng, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_u4il6k5q4ofhk2a5n2th53n9oo