Human Genome Epidemiology Literature Finder
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Records 1 - 18 (of 18 Records) |
| Query Trace: Disease and MERTK[original query] |
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| Polymorphisms in the receptor tyrosine kinase MERTK gene are associated with multiple sclerosis susceptibility. PloS one 2011 6 (2): e16964. Ma Gerry Z M, Stankovich Jim, , Kilpatrick Trevor J, Binder Michele D, Field Judi |
| Effect of the Gas6 c.834+7G>A polymorphism and the interaction of known risk factors on AMD pathogenesis in Hungarian patients. PloS one 2012 7 (11): 11. Losonczy G, Vajas A, Takács L, Dzsudzsák E, Fekete A, Márhoffer E, Kardos L, Ajzner E, Hurtado B, de Frutos PG, Berta A, Balogh I |
| Vitamin K-dependent proteins GAS6 and Protein S and TAM receptors in patients of systemic lupus erythematosus: correlation with common genetic variants and disease activity. Arthritis research & therapy 2013 Mar 15 (2): 2. Recarte-Pelz P, Tassies D, Espinosa G, Hurtado B, Sala N, Cervera R, Reverter JC, Garcia de Frutos P |
| New candidates for CD4 T cell pathogenicity in experimental neuroinflammation and multiple sclerosis. Brain : a journal of neurology 2015 Apr 138 (Pt 4): 902-17. Hoppmann Nicola, Graetz Christiane, Paterka Magdalena, Poisa-Beiro Laura, Larochelle Catherine, Hasan Maruf, Lill Christina M, Zipp Frauke, Siffrin Volk |
| MERTK rs4374383 polymorphism affects the severity of fibrosis in non-alcoholic fatty liver disease. Journal of hepatology 2015 Oct . Petta Salvatore, Valenti Luca, Marra Fabio, Grimaudo Stefania, Tripodo Claudio, Bugianesi Elisabetta, Cammà Calogero, Cappon Andrea, Marco Vito Di, Maira Giovanni Di, Dongiovanni Paola, Rametta Raffaela, Gulino Alessandro, Mozzi Enrico, Orlando Emanuele, Maggioni Marco, Pipitone Rosaria Maria, Fargion Silvia, Craxì Anton |
| Common and Low Frequency Variants in MERTK Are Independently Associated with Multiple Sclerosis Susceptibility with Discordant Association Dependent upon HLA-DRB1*15:01 Status. PLoS genetics 2016 Mar 12 (3): e1005853. Binder Michele D, Fox Andrew D, Merlo Daniel, Johnson Laura J, Giuffrida Lauren, Calvert Sarah E, Akkermann Rainer, Ma Gerry Z M, , Perera Ashwyn A, Gresle Melissa M, Laverick Louise, Foo Grace, Fabis-Pedrini Marzena J, Spelman Timothy, Jordan Margaret A, Baxter Alan G, Foote Simon, Butzkueven Helmut, Kilpatrick Trevor J, Field Judi |
| CLINICAL PROGRESS IN INHERITED RETINAL DEGENERATIONS: GENE THERAPY CLINICAL TRIALS AND ADVANCES IN GENETIC SEQUENCING. Retina (Philadelphia, Pa.) 2016 Oct . Hafler Brian |
| An intronic LINE-1 insertion in MERTK is strongly associated with retinopathy in Swedish Vallhund dogs. PloS one 2017 8 12 (8): e0183021. Everson Richard, Pettitt Louise, Forman Oliver P, Dower-Tylee Olivia, McLaughlin Bryan, Ahonen Saija, Kaukonen Maria, Komáromy András M, Lohi Hannes, Mellersh Cathryn S, Sansom Jane, Ricketts Sally |
| MERTK rs4374383 variant predicts incident nonalcoholic fatty liver disease and diabetes: role of mononuclear cell activation and adipokine response to dietary fat. Human molecular genetics 2017 Mar . Musso Giovanni, Cassader Maurizio, De Michieli Franco, Paschetta Elena, Pinach Silvia, Saba Francesca, Bongiovanni Daria, Framarin Luciana, Berrutti Mara, Leone Nicola, Corvisieri Stefania, Parente Renato, Molinaro Federica, Sircana Antonio, Simona Bo, Gambino Rober |
| Targeted Next-Generation Sequencing Reveals a Novel Frameshift Mutation in the MERTK Gene in a Chinese Family with Retinitis Pigmentosa. Genetic testing and molecular biomarkers 2018 2 22 (3): 165-169. Yang Mu, Li Shujin, Liu Wenjing, Yang Yeming, Zhang Lin, Zhang Shanshan, Jiang Zhilin, Yang Zhenglin, Zhu Xianj |
| The Myeloid-Epithelial-Reproductive Tyrosine Kinase (MERTK) rs4374383 Polymorphism Predicts Progression of Liver Fibrosis in Hepatitis C Virus-Infected Patients: A Longitudinal Study. Journal of clinical medicine 2018 Nov 7 (12): . Jiménez-Sousa María Ángeles, Gómez-Moreno Ana Zaida, Pineda-Tenor Daniel, Brochado-Kith Oscar, Sánchez-Ruano Juan José, Artaza-Varasa Tomas, Gómez-Sanz Alicia, Fernández-Rodríguez Amanda, Resino Salvad |
| Non-homologous recombination between Alu and LINE-1 repeats results in a 91 kb deletion in MERTK causing severe retinitis pigmentosa. Molecular vision 2018 11 24 667-678. Jonsson Frida, Burstedt Marie, Kellgren Therese G, Golovleva Iri |
| Mutations in MERTK are not associated with age-related macular degeneration. International ophthalmology 2018 Jan . Al-Khersan Hasenin, Kwong Alan, Grassi Michael |
| Association between Genetic Variations of MERTK and Chronic Obstructive Pulmonary Disease in Koreans. Journal of Korean medical science 2018 Feb 33 (7): e56. Kim Woo Jin, Park Hyo Jin, Choi Yang Ji, Kwon Eun Young, Kim Bo Min, Lee Jin Hwa, Chang Jung Hyun, Lee Kang Jihee, Choi Ji |
Genomewide Association Study of Acute Anterior Uveitis Identifies New Susceptibility Loci.
Investigative ophthalmology & visual science 2020 Jun 61 (6): 3. Huang Xiu-Feng, Li Zhixiu, De Guzman Erika, Robinson Philip, Gensler Lianne, Ward Michael M, Rahbar Mohammad Hossein, Lee MinJae, Weisman Michael H, Macfarlane Gary J, Jones Gareth T, Klingberg Eva, Forsblad-d'Elia Helena, McCluskey Peter, Wakefield Denis, Coombes Jeff S, Fiatarone Singh Maria A, Mavros Yorgi, Vlahovich Nicole, Hughes David C, Marzo-Ortega Helena, Van der Horste-Bruinsma Irene, O'Shea Finbar, Martin Tammy M, Rosenbaum James, Breban Maxime, Jin Zi-Bing, Leo Paul, Reveille John D, Wordsworth B Paul, Brown Matthew |
| Discovering Genotype Variants in an Infant with VACTERL through Clinical Exome Sequencing: A Support for Personalized Risk Assessment and Disease Prevention. Pediatric reports 2021 1 13 (1): 45-56. Pelizzo Gloria, Chiricosta Luigi, Mazzon Emanuela, Zuccotti Gian Vincenzo, Avanzini Maria Antonietta, Croce Stefania, Lima Mario, Bramanti Placido, Calcaterra Valer |
| Mer Tyrosine Kinase (MERTK) modulates liver fibrosis progression and hepatocellular carcinoma development. Frontiers in immunology 2022 8 13 926236. Pipitone Rosaria Maria, Calvaruso Vincenza, Di Marco Lorenza, Di Salvo Francesca, Gaggianesi Miriam, Lupo Giulia, Zito Rossella, La Mantia Claudia, Ramazzotti Matteo, Petta Salvatore, Di Marco Vito, Craxì Antonio, Grimaudo Stefan |
| [Neurofibromatosis type 1 associated with pheochromocytoma: a case report with a brief review of the literature]. Problemy endokrinologii 2024 5 70 (2): 53-64. A Y Lugovskaya, T A Britvin, L E Gurevich, I S Rog, L N Nefedova, I A Ilovayska |
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