HuGE Literature Finder
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Records 1-19
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Mutations in folate transporter genes and risk for human myelomeningocele.
American journal of medical genetics. Part A 2017 Sep . Findley Tina O, Tenpenny Joy C, O'Byrne Michelle R, Morrison Alanna C, Hixson James E, Northrup Hope, Au Kit Si |
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MiR-pharmacogenetics of methotrexate in childhood B-cell acute lymphoblastic leukemia.
Pharmacogenetics and genomics 2016 Sep . Iparraguirre Leire, Gutierrez-Camino Angela, Umerez Maitane, Martin-Guerrero Idoia, Astigarraga Itziar, Navajas Aurora, Sastre Ana, Garcia de Andoin Nagore, Garcia-Orad Afri |
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Evaluation of proton-coupled folate transporter (SLC46A1) polymorphisms as risk factors for neural tube defects and oral clefts.
American journal of medical genetics. Part A 2016 Jan . VanderMeer Julia E, Carter Tonia C, Pangilinan Faith, Mitchell Adam, Kurnat-Thoma Emma, Kirke Peadar N, Troendle James F, Molloy Anne M, Munger Ronald G, Feldkamp Marcia L, Mansilla Maria A, Mills James L, Murray Jeff C, Brody Lawrence |
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SLC19A1, SLC46A1 and SLCO1B1 polymorphisms as predictors of methotrexate-related toxicity in Portuguese rheumatoid arthritis patients.
Toxicological sciences : an official journal of the Society of Toxicology 2014 Nov 142 (1): 196-209. Lima Aurea, Bernardes Miguel, Azevedo Rita, Monteiro Joaquim, Sousa Hugo, Medeiros Rui, Seabra Vít |
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Single nucleotide polymorphisms in CETP, SLC46A1, SLC19A1, CD36, BCMO1, APOA5, and ABCA1 are significant predictors of plasma HDL in healthy adults.
Lipids in health and disease 2013 12 66. Clifford Andrew J, Rincon Gonzalo, Owens Janel E, Medrano Juan F, Moshfegh Alanna J, Baer David J, Novotny Janet |
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Prediction of clinical non-response to methotrexate treatment in juvenile idiopathic arthritis.
Annals of the rheumatic diseases 2012 Sep 71 (9): 1484-9. Bulatovic Maja, Heijstek Marloes W, Van Dijkhuizen E H Pieter, Wulffraat Nico M, Pluijm Saskia M F, de Jonge Robe |
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Rare allelic variants determine folate status in an unsupplemented European population.
The Journal of nutrition 2012 Aug 142 (8): 1403-9. Pavlíková Markéta, Sokolová Jitka, Janosíková Bohumila, Melenovská Petra, Krupková Lucie, Zvárová Jana, Kozich Vikt |
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Regular Multivitamin Supplement Use, Single Nucleotide Polymorphisms in ATIC, SHMT2, and SLC46A1, and Risk of Ovarian Carcinoma.
Frontiers in genetics 2012 3 . Kelemen LE, Wang Q, Dinu I, Vierkant RA, Tsai YY, Cunningham JM, Phelan CM, Fridley BL, Amankwah EK, Iversen ES, Berchuck A, Schildkraut JM, Goode EL, Sellers TA |
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Associations between single nucleotide polymorphisms in iron-related genes and iron status in multiethnic populations.
PloS one 2012 7 (6): e38339. McLaren Christine E, McLachlan Stela, Garner Chad P, Vulpe Chris D, Gordeuk Victor R, Eckfeldt John H, Adams Paul C, Acton Ronald T, Murray Joseph A, Leiendecker-Foster Catherine, Snively Beverly M, Barcellos Lisa F, Cook James D, McLaren Gordon |
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Genetic polymorphisms in metabolic and cellular transport pathway of methotrexate impact clinical outcome of methotrexate monotherapy in Japanese patients with rheumatoid arthritis.
Drug metabolism and pharmacokinetics 2012 27 (2): 192-9. Kato Tomomi, Hamada Akinobu, Mori Shunsuke, Saito Hideyu |
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Interactions between genetic variants of folate metabolism genes and lifestyle affect plasma homocysteine concentrations in the Boston Puerto Rican population.
Public health nutrition 2011 Oct 14 (10): 1805-12. Huang Tao, Tucker Katherine L, Lee Yu-Chi, Crott Jimmy W, Parnell Laurence D, Shen Jian, Smith Caren E, Ordovas Jose M, Li Duo, Lai Chao-Qia |
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Assessment of hepatocyte growth factor in ovarian cancer mortality.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2011 Aug 20 (8): 1638-48. Goode Ellen L, Chenevix-Trench Georgia, Hartmann Lynn C, Fridley Brooke L, Kalli Kimberly R, Vierkant Robert A, Larson Melissa C, White Kristin L, Keeney Gary L, Oberg Trynda N, Cunningham Julie M, Beesley Jonathan, Johnatty Sharon E, Chen Xiaoqing, Goodman Katelyn E, Armasu Sebastian M, Rider David N, Sicotte Hugues, Schmidt Michele M, Elliott Elaine A, Høgdall Estrid, Kjær Susanne Krüger, Fasching Peter A, Ekici Arif B, Lambrechts Diether, Despierre Evelyn, Høgdall Claus, Lundvall Lene, Karlan Beth Y, Gross Jenny, Brown Robert, Chien Jeremy, Duggan David J, Tsai Ya-Yu, Phelan Catherine M, Kelemen Linda E, Peethambaram Prema P, Schildkraut Joellen M, Shridhar Vijayalakshmi, Sutphen Rebecca, Couch Fergus J, Sellers Thomas A, |
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The folate hydrolase 1561C>T polymorphism is associated with depressive symptoms in Puerto Rican adults.
Psychosomatic medicine 2011 Jun 73 (5): 385-92. Ye Xingwang, Lai Chao-Qiang, Crott Jimmy W, Troen Aron M, Ordovas Jose M, Tucker Katherine |
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Large-scale candidate gene analysis of HDL particle features.
PloS one 2011 6 (1): e14529. Kaess Bernhard M, Tomaszewski Maciej, Braund Peter S, Stark Klaus, Rafelt Suzanne, Fischer Marcus, Hardwick Robert, Nelson Christopher P, Debiec Radoslaw, Huber Fritz, Kremer Werner, Kalbitzer Hans Robert, Rose Lynda M, Chasman Daniel I, Hopewell Jemma, Clarke Robert, Burton Paul R, Tobin Martin D, Hengstenberg Christian, Samani Nilesh |
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Genetic associations of variants in genes encoding HIV-dependency factors required for HIV-1 infection.
The Journal of infectious diseases 2010 Dec 202 (12): 1836-45. Chinn Leslie W, Tang Minzhong, Kessing Bailey D, Lautenberger James A, Troyer Jennifer L, Malasky Michael J, McIntosh Carl, Kirk Gregory D, Wolinsky Steven M, Buchbinder Susan P, Gomperts Edward D, Goedert James J, O'Brien Stephen |
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Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
Diabetes care 2010 Oct 33 (10): 2250-3. Bailey Swneke D, Xie Changchun, Do Ron, Montpetit Alexandre, Diaz Rafael, Mohan Viswanathan, Keavney Bernard, Yusuf Salim, Gerstein Hertzel C, Engert James C, Anand Sonia, |
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Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
American journal of human genetics 2009 Nov 85 (5): 628-42. Talmud Philippa J, Drenos Fotios, Shah Sonia, Shah Tina, Palmen Jutta, Verzilli Claudio, Gaunt Tom R, Pallas Jacky, Lovering Ruth, Li Kawah, Casas Juan Pablo, Sofat Reecha, Kumari Meena, Rodriguez Santiago, Johnson Toby, Newhouse Stephen J, Dominiczak Anna, Samani Nilesh J, Caulfield Mark, Sever Peter, Stanton Alice, Shields Denis C, Padmanabhan Sandosh, Melander Olle, Hastie Claire, Delles Christian, Ebrahim Shah, Marmot Michael G, Smith George Davey, Lawlor Debbie A, Munroe Patricia B, Day Ian N, Kivimaki Mika, Whittaker John, Humphries Steve E, Hingorani Aroon D, , , |
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Associations between single nucleotide polymorphisms in folate uptake and metabolizing genes with blood folate, homocysteine, and DNA uracil concentrations.
The American journal of clinical nutrition 2008 Oct 88 (4): 1149-58. DeVos Lauren, Chanson Aurelie, Liu Zhenhua, Ciappio Eric D, Parnell Laurence D, Mason Joel B, Tucker Katherine L, Crott Jimmy |
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Heme carrier protein 1 (HCP1) genetic variants in the Hemochromatosis and Iron Overload Screening (HEIRS) Study participants.
Blood cells, molecules & diseases 0 42 (2): 150-4. Wang XinJing, Leiendecker-Foster Catherine, Acton Ronald T, Barton James C, McLaren Christine E, McLaren Gordon D, Gordeuk Victor R, Eckfeldt John |
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- Page last updated:Dec 5, 2019
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