Cargando…

Association between the methylene tetrahydrofolate reductase gene C677T mutation and colchicine unresponsiveness in Behcet’s disease

PURPOSE: Behcet’s disease (BD) is a multisystemic immunoinflammatory disorder characterized by mucocutaneous, ocular, vascular, and central nervous system manifestations. The common methylene tetrahydrofolate reductase (MTHFR) gene C677T mutation is a known risk factor for thrombosis. The aim of thi...

Descripción completa

Detalles Bibliográficos
Autores principales:	Karakus, Nevin, Yigit, Serbulent, Kalkan, Goknur, Rustemoglu, Aydin, Inanir, Ahmet, Gul, Ulker, Pancar, Gunseli Sefika, Akkanet, Songul, Ates, Omer
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Molecular Vision 2012
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388981/ https://www.ncbi.nlm.nih.gov/pubmed/22773907

Ejemplares similares

Association of IL-4 gene VNTR variant with deep venous thrombosis in Behçet’s disease and its effect on ocular involvement
por: Inanir, Ahmet, et al.
Publicado: (2013)

Clinical significance of NCOA5 gene rs2903908 polymorphism in Behçet's disease
por: Rustemoglu, Aydin, et al.
Publicado: (2017)

Association of MTHFR gene C677T mutation with diabetic peripheral neuropathy and diabetic retinopathy
por: Yigit, Serbulent, et al.
Publicado: (2013)

The effects of 755 nm alexandrite laser on skin dryness and pruritus
por: Pancar, Gunseli Sefika, et al.
Publicado: (2020)

Significant association between insertion/deletion polymorphism of the angiotensin-convertig enzyme gene and ankylosing spondylitis
por: Inanır, Ahmet, et al.
Publicado: (2012)

Common Mediterranean Fever (MEFV) Gene Mutations Associated with Ankylosing Spondylitis in Turkish Population
por: Yigit, Serbulent, et al.
Publicado: (2012)

MTHFR Gene C677T Mutation and ACE Gene I/D Polymorphism in Turkish Patients with Osteoarthritis
por: Inanir, Ahmet, et al.
Publicado: (2013)

Red Cell Distribution Width and Mean Platelet Volume in Patients With Pityriasis Rosea
por: Pancar, Gunseli Sefika, et al.
Publicado: (2016)

Laboratory informatics based evaluation of methylene tetrahydrofolate reductase C677T genetic test overutilization
por: Cohen, David A., et al.
Publicado: (2013)

Role of Hyperhomocysteinemia and Methylene Tetrahydrofolate Reductase C677T Polymorphism in Idiopathic Portal Vein Thrombosis
por: Ghaznavi, Habib, et al.
Publicado: (2016)

Study of C677T Methylene Tetrahydrofolate Reductase Gene Polymorphism as a Risk Factor for Neural Tube Defects
por: Goyal, Anjalika, et al.
Publicado: (2021)

Investigation of Associations between Obesity and LEP G2548A and LEPR 668A/G Polymorphisms in a Turkish Population
por: Şahın, Server, et al.
Publicado: (2013)

Histopathologic Study of Pathergy Test in Behçet's Disease
por: Ozluk, Ekin, et al.
Publicado: (2014)

Conjunctival Ulcers in Behcet's Disease and Response to Colchicine
por: Kaur, Ishmeet, et al.
Publicado: (2020)

Treatment of familial mediterranean fever with canakinumab in patients who are unresponsive to colchicine
por: Berdeli, Afig, et al.
Publicado: (2019)

The C677 Mutation in Methylene Tetrahydrofolate Reductase Gene: Correlation with Uric Acid and Cardiovascular Risk Factors in Elderly Korean men
por: Hong, Young Seoub, et al.
Publicado: (2004)

Association of homocysteine and methylene tetrahydrofolate reductase (MTHFR C677T) gene polymorphism with coronary artery disease (CAD) in the population of North India
por: Tripathi, Rajneesh, et al.
Publicado: (2010)

Association of the methylene-tetrahydrofolate reductase gene rs1801133 C677T variant with serum homocysteine levels, and the severity of coronary artery disease
por: Bouzidi, Nadia, et al.
Publicado: (2020)

5,10-methylene tetrahydrofolate reductase C677T gene polymorphism, homocysteine concentration and the extent of premature coronary artery disease in southern Iran
por: Senemar, Sara, et al.
Publicado: (2013)

In Vivo Rate of Formaldehyde Condensation with Tetrahydrofolate
por: He, Hai, et al.
Publicado: (2020)

The Second Class of Tetrahydrofolate (THF-II) Riboswitches Recognizes the Tetrahydrofolic Acid Ligand via Local Conformation Changes
por: Zhang, Minmin, et al.
Publicado: (2022)

Associations Among Methylene Tetrahydrofolate Reductase rs1801133 C677T Gene Variant, Food Groups, and Non-alcoholic Fatty Liver Disease Risk in the Chinese Population
por: Hao, Xiaoyan, et al.
Publicado: (2021)

Bioengineering of crop plants for improved tetrahydrofolate production
por: Chaudhary, Bhupendra, et al.
Publicado: (2017)

Methionine synthase supports tumor tetrahydrofolate pools
por: Ghergurovich, Jonathan M., et al.
Publicado: (2021)

MTHFR SNPs (Methyl Tetrahydrofolate Reductase, Single Nucleotide Polymorphisms) C677T and A1298C Prevalence and Serum Homocysteine Levels in >2100 Hypofertile Caucasian Male Patients
por: Clément, Arthur, et al.
Publicado: (2022)

Two Cases of Acute Leukopenia Induced by Colchicine with Concurrent Immunosuppressants Use in Behçet's Disease
por: Lee, Kyu-Yeop, et al.
Publicado: (2008)

Methylene-tetrahydrofolate reductase contributes to allergic airway disease
por: Eyring, Kenneth R., et al.
Publicado: (2018)

Neutrophil‐mediated mechanisms of damage and in‐vitro protective effect of colchicine in non‐vascular Behçet’s syndrome
por: Bettiol, Alessandra, et al.
Publicado: (2021)

Biochemical validation of a second class of tetrahydrofolate riboswitches in bacteria
por: Chen, Xi, et al.
Publicado: (2019)

Effectiveness of the Full Outline of UnResponsiveness Score in Patients With Acute Ischemic Stroke
por: Atiş, Şeref Emre, et al.
Publicado: (2022)

Promiscuous and Adaptable Enzymes Fill “Holes” in the Tetrahydrofolate Pathway in Chlamydia Species
por: Adams, Nancy E., et al.
Publicado: (2014)

Structures in Tetrahydrofolate Methylation in Desulfitobacterial Glycine Betaine Metabolism at Atomic Resolution
por: Badmann, Thomas, et al.
Publicado: (2019)

Colchicine therapy for deep vein thrombosis in a patient with vascular-type Behçet disease: A case report
por: Nonaka, Daishi, et al.
Publicado: (2020)

Relationship between granulomatous lobular mastitis and methylene tetrahydrofolate reductase gene polymorphism
por: Lei, Qing-Ran, et al.
Publicado: (2020)

P03-009 - Experiences of in pediatric Behçet uveitis
por: Sozeri, B, et al.
Publicado: (2013)

Time-resolved x-ray crystallography capture of a slow reaction tetrahydrofolate intermediate
por: Cao, Hongnan, et al.
Publicado: (2019)

Contribution of genetic polymorphism of methylene tetrahydrofolate reductase on the effect of methotrexate in ectopic pregnancy patients
por: Deng, Jie, et al.
Publicado: (2019)

Methylene tetrahydrofolate reductase gene mutation in sickle cell anaemia patients in Lagos, Nigeria
por: Adelekan, Oluwaseun Olabisi, et al.
Publicado: (2019)

Tailored extraction and ion mobility-mass spectrometry enables isotopologue analysis of tetrahydrofolate vitamers
por: Mitic, Bernd M., et al.
Publicado: (2023)

Colchicine
por: Ben-Chetrit, Eldad
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_72t4vrlrf39v10017rh6d4oj3k