MTRR (ген) (Kazakh Wikipedia)

Analysis of information sources in references of the Wikipedia article "MTRR (ген)" in Kazakh language version.

refsWebsite

Global rank Kazakh rank

17nih.gov

4^th place

16^th place

10doi.org

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7^th place

1worldcat.org

5^th place

37^th place

1uniprot.org

5,673^rd place

low place

doi.org

"The methionine synthase reductase 66A>G polymorphism is a maternal risk factor for spina bifida". Journal of Molecular Medicine 84 (12): 1047–54. December 2006. doi:10.1007/s00109-006-0093-x. ISSN 0946-2716. PMID 17024475. Дереккөз қатесі: Invalid <ref> tag; name "van der Lindenden Heijer2006" defined multiple times with different content
"Genetic variants in the folate pathway and the risk of neural tube defects: a meta-analysis of the published literature". PLOS ONE 8 (4): e59570. doi:10.1371/journal.pone.0059570. PMID 23593147. Дереккөз қатесі: Invalid <ref> tag; name "El-MaarriZhang2013" defined multiple times with different content
"Methionine synthase reductase 66A->G polymorphism is associated with increased plasma homocysteine concentration when combined with the homozygous methylenetetrahydrofolate reductase 677C->T variant". The Journal of Nutrition 134 (11): 2985–90. November 2004. doi:10.1093/jn/134.11.2985. PMID 15514263.
"Association of MTRR A66G polymorphism with cancer susceptibility: Evidence from 85 studies". Journal of Cancer 8 (2): 266–277. doi:10.7150/jca.17379. PMID 28243331.
"Polymorphisms of methionine synthase and methionine synthase reductase and risk of lung cancer: a case-control analysis". Pharmacogenetics and Genomics 15 (8): 547–55. August 2005. doi:10.1097/01.fpc.0000170916.96650.70. PMID 16006998. Дереккөз қатесі: Invalid <ref> tag; name "pmid16006998" defined multiple times with different content
"Additive Interaction of MTHFR C677T and MTRR A66G Polymorphisms with Being Overweight/Obesity on the Risk of Type 2 Diabetes". International Journal of Environmental Research and Public Health 13 (12): 1243. December 2016. doi:10.3390/ijerph13121243. PMID 27983710.
"Genetic heterogeneity among patients with methylcobalamin deficiency. Definition of two complementation groups, cblE and cblG". The Journal of Clinical Investigation 81 (6): 1690–4. June 1988. doi:10.1172/JCI113507. PMID 3384945.
"CblE type of homocystinuria due to methionine synthase reductase deficiency: clinical and molecular studies and prenatal diagnosis in two families". Journal of Inherited Metabolic Disease 25 (6): 461–76. October 2002. doi:10.1023/A:1021299117308. PMID 12555939.
"Genetic polymorphisms in folate and homocysteine metabolism as risk factors for DNA damage". European Journal of Human Genetics 11 (9): 671–8. September 2003. doi:10.1038/sj.ejhg.5201024. PMID 12939653. Дереккөз қатесі: Invalid <ref> tag; name "pmid12939653" defined multiple times with different content
"A common polymorphism in methionine synthase reductase increases risk of premature coronary artery disease". Journal of Cardiovascular Risk 7 (3): 197–200. June 2000. doi:10.1177/204748730000700306. PMID 11006889.

nih.gov

ncbi.nlm.nih.gov

Entrez Gene: MTRR 5-methyltetrahydrofolate-homocysteine methyltransferase reductase.
"The methionine synthase reductase 66A>G polymorphism is a maternal risk factor for spina bifida". Journal of Molecular Medicine 84 (12): 1047–54. December 2006. doi:10.1007/s00109-006-0093-x. ISSN 0946-2716. PMID 17024475. Дереккөз қатесі: Invalid <ref> tag; name "van der Lindenden Heijer2006" defined multiple times with different content
"Genetic variants in the folate pathway and the risk of neural tube defects: a meta-analysis of the published literature". PLOS ONE 8 (4): e59570. doi:10.1371/journal.pone.0059570. PMID 23593147. Дереккөз қатесі: Invalid <ref> tag; name "El-MaarriZhang2013" defined multiple times with different content
"Methionine synthase reductase 66A->G polymorphism is associated with increased plasma homocysteine concentration when combined with the homozygous methylenetetrahydrofolate reductase 677C->T variant". The Journal of Nutrition 134 (11): 2985–90. November 2004. doi:10.1093/jn/134.11.2985. PMID 15514263.
G">NM_002454.2(MTRR):c.1049A>G (p.Lys350Arg) AND not specified - ClinVar - NCBI. Тексерілді, 16 қыркүйек 2017.
G">NM_002454.2(MTRR):c.1349C>G (p.Pro450Arg) AND Disorders of Intracellular Cobalamin Metabolism - ClinVar - NCBI. Тексерілді, 16 қыркүйек 2017.
T">NM_002454.2(MTRR):c.1361C>T (p.Ser454Leu) Simple - Variation Report - ClinVar - NCBI. Тексерілді, 16 қыркүйек 2017.
A">NM_002454.2(MTRR):c.1459G>A (p.Gly487Arg) AND Inborn genetic diseases - ClinVar - NCBI. Тексерілді, 16 қыркүйек 2017.
T">NM_002454.2(MTRR):c.1573C>T (p.Arg525Ter) AND not provided - ClinVar - NCBI. Тексерілді, 16 қыркүйек 2017.
A">NM_002454.2(MTRR):c.1911G>A (p.Ala637=) Simple - Variation Report - ClinVar - NCBI. Тексерілді, 16 қыркүйек 2017.
"Association of MTRR A66G polymorphism with cancer susceptibility: Evidence from 85 studies". Journal of Cancer 8 (2): 266–277. doi:10.7150/jca.17379. PMID 28243331.
"Polymorphisms of methionine synthase and methionine synthase reductase and risk of lung cancer: a case-control analysis". Pharmacogenetics and Genomics 15 (8): 547–55. August 2005. doi:10.1097/01.fpc.0000170916.96650.70. PMID 16006998. Дереккөз қатесі: Invalid <ref> tag; name "pmid16006998" defined multiple times with different content
"Additive Interaction of MTHFR C677T and MTRR A66G Polymorphisms with Being Overweight/Obesity on the Risk of Type 2 Diabetes". International Journal of Environmental Research and Public Health 13 (12): 1243. December 2016. doi:10.3390/ijerph13121243. PMID 27983710.
"Genetic heterogeneity among patients with methylcobalamin deficiency. Definition of two complementation groups, cblE and cblG". The Journal of Clinical Investigation 81 (6): 1690–4. June 1988. doi:10.1172/JCI113507. PMID 3384945.
"CblE type of homocystinuria due to methionine synthase reductase deficiency: clinical and molecular studies and prenatal diagnosis in two families". Journal of Inherited Metabolic Disease 25 (6): 461–76. October 2002. doi:10.1023/A:1021299117308. PMID 12555939.
"Genetic polymorphisms in folate and homocysteine metabolism as risk factors for DNA damage". European Journal of Human Genetics 11 (9): 671–8. September 2003. doi:10.1038/sj.ejhg.5201024. PMID 12939653. Дереккөз қатесі: Invalid <ref> tag; name "pmid12939653" defined multiple times with different content
"A common polymorphism in methionine synthase reductase increases risk of premature coronary artery disease". Journal of Cardiovascular Risk 7 (3): 197–200. June 2000. doi:10.1177/204748730000700306. PMID 11006889.

uniprot.org

MTRR - Methionine synthase reductase - Homo sapiens (Human) - MTRR gene & protein. Тексерілді, 16 қыркүйек 2017. Дереккөз қатесі: Invalid <ref> tag; name "UniProt" defined multiple times with different content

worldcat.org

"The methionine synthase reductase 66A>G polymorphism is a maternal risk factor for spina bifida". Journal of Molecular Medicine 84 (12): 1047–54. December 2006. doi:10.1007/s00109-006-0093-x. ISSN 0946-2716. PMID 17024475. Дереккөз қатесі: Invalid <ref> tag; name "van der Lindenden Heijer2006" defined multiple times with different content