Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: FTL[original query] |
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Screening of ferritin light polypeptide 460-461InsA mutation in Parkinson's disease patients in North America. Neuroscience letters 2002 Dec 335 (2): 144-6. Chen Rong, Langston J William, Chan P |
Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype. Journal of human genetics 2006 51 (8): 645-51. Costa Maria do Carmo, Teixeira-Castro Andreia, Constante Marco, Magalhães Marina, Magalhães Paula, Cerqueira Joana, Vale José, Passão Vitorina, Barbosa Célia, Robalo Conceição, Coutinho Paula, Barros José, Santos Manuela M, Sequeiros Jorge, Maciel Patríc |
HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screening. Genetic testing 2007 11 (3): 269-75. Barton James C, Acton Ronald T, Leiendecker-Foster Catherine, Lovato Laura, Adams Paul C, McLaren Gordon D, Eckfeldt John H, McLaren Christine E, Reboussin David M, Gordeuk Victor R, Speechley Mark R, Reiss Jacob A, Press Richard D, Dawkins Fitzroy W, |
HD phenocopies--possible role of Saitohin gene. The International journal of neuroscience 2008 Mar 118 (3): 391-7. Jankovi? N, Kecmanovi? M, Dimitrijevi? R, Keckarevi? Markovi? M, Dobrici? V, Keckarevi? D, Savi? Pavicevi? D, Romac |
Association of glutathione S-transferase M1 and T1 gene polymorphisms and oxidative stress markers in preterm labor. Clinical biochemistry 2010 Sep 43 (13-14): 1124-8. Mustafa M D, Pathak Rahul, Ahmed Tanzeel, Ahmed Rafat S, Tripathi A K, Guleria Kiran, Banerjee B |
Noncoding variation of the gene for ferritin light chain in hereditary and age-related cataract. Molecular vision 2013 19 835-44. Bennett Thomas M, Maraini Giovanni, Jin Chongfei, Sun Wenmin, Hejtmancik J Fielding, Shiels Al |
Hereditary hemochromatosis type 1 phenotype modifiers in Italian patients. The controversial role of variants in HAMP, BMP2, FTL and SLC40A1 genes. Blood cells, molecules & diseases 2015 Jun 55 (1): 71-5. Radio Francesca Clementina, Majore Silvia, Aurizi Caterina, Sorge Fiammetta, Biolcati Gianfranco, Bernabini Sara, Giotti Irene, Torricelli Francesca, Giannarelli Diana, De Bernardo Carmelilia, Grammatico Pao |
Next-generation sequencing of hereditary hemochromatosis-related genes: Novel likely pathogenic variants found in the Portuguese population. Blood cells, molecules & diseases 2016 Oct 61 10-5. Faria Ricardo, Silva Bruno, Silva Catarina, Loureiro Pedro, Queiroz Ana, Fraga Sofia, Esteves Jorge, Mendes Diana, Fleming Rita, Vieira Luís, Gonçalves João, Faustino Pau |
MicroRNA Expression Analysis in Serum of Patients with Congenital Hemochromatosis and Age-Related Macular Degeneration (AMD). Medical science monitor : international medical journal of experimental and clinical research 2017 Aug 23 4050-4060. Szemraj Maciej, Oszajca Katarzyna, Szemraj Janusz, Jurowski Pio |
Detergent Insoluble Proteins and Inclusion Body-Like Structures Immunoreactive for PRKDC/DNA-PK/DNA-PKcs, FTL, NNT, and AIFM1 in the Amygdala of Cognitively Impaired Elderly Persons. Journal of neuropathology and experimental neurology 2018 Jan 77 (1): 21-39. Gal Jozsef, Chen Jing, Katsumata Yuriko, Fardo David W, Wang Wang-Xia, Artiushin Sergey, Price Douglas, Anderson Sonya, Patel Ela, Zhu Haining, Nelson Peter |
Hepcidin-regulating iron metabolism genes and pancreatic ductal adenocarcinoma: a pathway analysis of genome-wide association studies. The American journal of clinical nutrition 2021 7 114 (4): 1408-1417. Julián-Serrano Sachelly, Yuan Fangcheng, Wheeler William, Benyamin Beben, Machiela Mitchell J, Arslan Alan A, Beane-Freeman Laura E, Bracci Paige M, Duell Eric J, Du Mengmeng, Gallinger Steven, Giles Graham G, Goodman Phyllis J, Kooperberg Charles, Marchand Loic Le, Neale Rachel E, Shu Xiao-Ou, Van Den Eeden Stephen K, Visvanathan Kala, Zheng Wei, Albanes Demetrius, Andreotti Gabriella, Ardanaz Eva, Babic Ana, Berndt Sonja I, Brais Lauren K, Brennan Paul, Bueno-de-Mesquita Bas, Buring Julie E, Chanock Stephen J, Childs Erica J, Chung Charles C, Fabiánová Eleonora, Foretová Lenka, Fuchs Charles S, Gaziano J Michael, Gentiluomo Manuel, Giovannucci Edward L, Goggins Michael G, Hackert Thilo, Hartge Patricia, Hassan Manal M, Holcátová Ivana, Holly Elizabeth A, Hung Rayjean I, Janout Vladimir, Kurtz Robert C, Lee I-Min, Malats Núria, McKean David, Milne Roger L, Newton Christina C, Oberg Ann L, Perdomo Sandra, Peters Ulrike, Porta Miquel, Rothman Nathaniel, Schulze Matthias B, Sesso Howard D, Silverman Debra T, Thompson Ian M, Wactawski-Wende Jean, Weiderpass Elisabete, Wenstzensen Nicolas, White Emily, Wilkens Lynne R, Yu Herbert, Zeleniuch-Jacquotte Anne, Zhong Jun, Kraft Peter, Li Dounghui, Campbell Peter T, Petersen Gloria M, Wolpin Brian M, Risch Harvey A, Amundadottir Laufey T, Klein Alison P, Yu Kai, Stolzenberg-Solomon Rachael |
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- Page last updated:Apr 22, 2024
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