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Items: 1 to 20 of 6420

1.

Characterization of a Rare Nonpathogenic Methylenetetrahydrofolatereductase (MTHFR) Gene Mutation p.Lys215del in a Southern Italian family.

Palmirotta R, Lovero D, Silvestris E, Simone V, Lanotte L, Quaresmini D, Silvestris F.

Hum Mutat. 2016 Oct 21. doi: 10.1002/humu.23132. No abstract available.

PMID:
27768236
2.

Associations of recurrent miscarriages with chromosomal abnormalities, thrombophilia allelic polymorphisms and/or consanguinity in Saudi Arabia.

Turki RF, Assidi M, Banni HA, Zahed HA, Karim S, Schulten HJ, Abu-Elmagd M, Rouzi AA, Bajouh O, Jamal HS, Al-Qahtani MH, Abuzenadah AM.

BMC Med Genet. 2016 Oct 10;17(Suppl 1):69.

PMID:
27766963
3.

Toward optimal set of single nucleotide polymorphism investigation before IVF.

Ivanov AV, Dedul AG, Fedotov YN, Komlichenko EV.

Gynecol Endocrinol. 2016 Oct;32(sup2):11-18.

PMID:
27759448
4.

Interactions between lifestyle and MTHFR polymorphisms on homocysteine concentrations in young adults belonging to the 1982 Pelotas Birth Cohort.

Oliveira IO, Silva LP, Borges MC, Cruz OM, Tessmann JW, Motta JV, Seixas FK, Horta BL, Gigante DP.

Eur J Clin Nutr. 2016 Oct 19. doi: 10.1038/ejcn.2016.193.

PMID:
27759072
5.

Genetic variation and bone mineral density in long-term adult survivors of childhood cancer.

den Hoed MA, Pluijm SM, Stolk L, Uitterlinden AG, Pieters R, van den Heuvel-Eibrink MM.

Pediatr Blood Cancer. 2016 Dec;63(12):2212-2220. doi: 10.1002/pbc.26198.

PMID:
27578188
6.

The antihypertensive MTHFR gene polymorphism rs17367504-G is a possible novel protective locus for preeclampsia.

Thomsen LC, Mccarthy NS, Melton PE, Cadby G, Austgulen R, Nygård OK, Johnson MP, Brennecke S, Moses EK, Bjørge L, Iversen AC.

J Hypertens. 2016 Oct 17.

PMID:
27755385
7.

Clinical utility of folate pathway genetic polymorphisms in the diagnosis of autism spectrum disorders.

Shaik Mohammad N, Sai Shruti P, Bharathi V, Krishna Prasad C, Hussain T, Alrokayan SA, Naik U, Radha Rama Devi A.

Psychiatr Genet. 2016 Oct 17.

PMID:
27755291
8.

Impact of genetic variants of ATP binding cassette B1, AICAR transformylase/IMP cyclohydrolase, folyl-polyglutamatesynthetase, and methylenetetrahydrofolatereductase on methotrexate toxicity.

Sala-Icardo L, Lamana A, Ortiz AM, García Lorenzo E, Moreno Fresneda P, García-Vicuña R, González-Álvaro I.

Reumatol Clin. 2016 Oct 14. pii: S1699-258X(16)30101-2. doi: 10.1016/j.reuma.2016.08.006. English, Spanish.

PMID:
27751863
Free Article
9.

Mexican Childhood Acute Lymphoblastic Leukemia: A Pilot Study of the MDR1 and MTHFR Gene Polymorphisms and Their Associations with Clinical Outcomes.

Ramírez-Pacheco A, Moreno-Guerrero S, Alamillo I, Medina-Sanson A, Lopez B, Moreno-Galván M.

Genet Test Mol Biomarkers. 2016 Oct;20(10):597-602.

PMID:
27533339
10.

Functional characterization of missense mutations in severe methylenetetrahydrofolate reductase deficiency using a human expression system.

Burda P, Suormala T, Heuberger D, Schäfer A, Fowler B, Froese DS, Baumgartner MR.

J Inherit Metab Dis. 2016 Oct 14.

PMID:
27743313
11.

Review article: the aetiology of primary Budd-Chiari syndrome - differences between the West and China.

Qi X, Han G, Guo X, De Stefano V, Xu K, Lu Z, Xu H, Mancuso A, Zhang W, Han X, Valla DC, Fan D.

Aliment Pharmacol Ther. 2016 Oct 13. doi: 10.1111/apt.13815. Review.

PMID:
27734511
12.

Thrombophilic Gene Mutations in Relation to Different Manifestations of Venous Thromboembolism: A Single Tertiary Center Study.

Bezgin T, Kaymaz C, Akbal Ö, Yılmaz F, Tokgöz HC, Özdemir N.

Clin Appl Thromb Hemost. 2016 Oct 11. pii: 1076029616672585.

PMID:
27729560
13.

Nicotinamide-N-Methyltransferase gene rs694539 variant and migraine risk.

Sazci A, Sazci G, Sazci B, Ergul E, Idrisoglu HA.

J Headache Pain. 2016 Dec;17(1):93.

PMID:
27726107
14.

Folate Deficiency Was Associated with Increased Alanine Aminotransferase and Glutamyl Transpeptidase Concentrations in a Chinese Hypertensive Population: A Cross-Sectional Study.

Li WX, Li W, Cao JQ, Yan H, Sun Y, Zhang H, Zhang Q, Tang L, Wang M, Huang JF, Liu D.

J Nutr Sci Vitaminol (Tokyo). 2016;62(4):265-271.

15.

Association of <i>MTHFR</i> (C677T) Gene Polymorphism With Breast Cancer in North India.

Waseem M, Hussain SR, Kumar S, Serajuddin M, Mahdi F, Sonkar SK, Bansal C, Ahmad MK.

Biomark Cancer. 2016 Sep 27;8:111-117.

16.

Riboflavin, MTHFR genotype and blood pressure: A personalized approach to prevention and treatment of hypertension.

McNulty H, Strain JJ, Hughes CF, Ward M.

Mol Aspects Med. 2016 Oct 6. pii: S0098-2997(16)30058-9. doi: 10.1016/j.mam.2016.10.002. Review.

PMID:
27720779
17.

Genetic variation associated with the occurrence and progression of neurological disorders.

Little J, Barakat-Haddad C, Martino R, Pringsheim T, Tremlett H, McKay KA, van Lieshout P, Walsh SJ, Gomes J, Krewski D.

Neurotoxicology. 2016 Oct 3. pii: S0161-813X(16)30198-X. doi: 10.1016/j.neuro.2016.09.018.

PMID:
27713094
18.

The impact of <i>MTHFR</i> 677C → T risk knowledge on changes in folate intake: findings from the Food4Me study.

O'Donovan CB, Walsh MC, Forster H, Woolhead C, Celis-Morales C, Fallaize R, Macready AL, Marsaux CF, Navas-Carretero S, San-Cristobal R, Kolossa S, Mavrogianni C, Lambrinou CP, Moschonis G, Godlewska M, Surwillo A, Bouwman J, Grimaldi K, Traczyk I, Drevon CA, Daniel H, Manios Y, Martinez JA, Saris WH, Lovegrove JA, Mathers JC, Gibney MJ, Brennan L, Gibney ER.

Genes Nutr. 2016 Sep 29;11:25.

19.

Moderate folic acid supplementation and MTHFD1-synthetase deficiency in mice, a model for the R653Q variant, result in embryonic defects and abnormal placental development.

Christensen KE, Hou W, Bahous RH, Deng L, Malysheva OV, Arning E, Bottiglieri T, Caudill MA, Jerome-Majewska LA, Rozen R.

Am J Clin Nutr. 2016 Oct 5. pii: ajcn139519.

PMID:
27707701
20.

Relationship between genetic polymorphisms of methylenetetrahydrofolate reductase and breast cancer chemotherapy response.

Yang L, Wang XW, Zhu LP, Wang HL, Wang B, Wu T, Zhao Q, JinSiHan DL, Wang XY.

Genet Mol Res. 2016 Sep 23;15(3). doi: 10.4238/gmr.15038679.

PMID:
27706773
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