Human Genome Epidemiology Literature Finder
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Records 1 - 24 (of 24 Records) |
| Query Trace: Disease and CYP27A1[original query] |
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| Systems biology-based analysis implicates a novel role for vitamin D metabolism in the pathogenesis of age-related macular degeneration. Human genomics 2011 Oct 5 (6): 538-68. Morrison Margaux A, Silveira Alexandra C, Huynh Nancy, Jun Gyungah, Smith Silvia E, Zacharaki Fani, Sato Hajime, Loomis Stephanie, Andreoli Michael T, Adams Scott M, Radeke Monte J, Jelcick Austin S, Yuan Yang, Tsiloulis Aristoteles N, Chatzoulis Dimitrios Z, Silvestri Giuliana, Kotoula Maria G, Tsironi Evangelia E, Hollis Bruce W, Chen Rui, Haider Neena B, Miller Joan W, Farrer Lindsay A, Hageman Gregory S, Kim Ivana K, Schaumberg Debra A, DeAngelis Margaret |
| Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS. PloS one 2012 7 (4): e35333. Diekstra Frank P, Saris Christiaan G J, van Rheenen Wouter, Franke Lude, Jansen Ritsert C, van Es Michael A, van Vught Paul W J, Blauw Hylke M, Groen Ewout J N, Horvath Steve, Estrada Karol, Rivadeneira Fernando, Hofman Albert, Uitterlinden Andre G, Robberecht Wim, Andersen Peter M, Melki Judith, Meininger Vincent, Hardiman Orla, Landers John E, Brown Robert H, Shatunov Aleksey, Shaw Christopher E, Leigh P Nigel, Al-Chalabi Ammar, Ophoff Roel A, van den Berg Leonard H, Veldink Jan |
| Vitamin D-related genetic variation, plasma vitamin D, and risk of lethal prostate cancer: a prospective nested case-control study. Journal of the National Cancer Institute 2012 May 104 (9): 690-9. Shui Irene M, Mucci Lorelei A, Kraft Peter, Tamimi Rulla M, Lindstrom Sara, Penney Kathryn L, Nimptsch Katharina, Hollis Bruce W, Dupre Natalie, Platz Elizabeth A, Stampfer Meir J, Giovannucci Edwa |
| Genetic sequence variants in vitamin D metabolism pathway genes, serum vitamin D level and outcome in head and neck cancer patients. International journal of cancer. Journal international du cancer 2012 Nov . Azad AK, Bairati I, Qiu X, Huang H, Cheng D, Liu G, Meyer F, Adjei A, Xu W |
| The Associations of Novel Vitamin D3 Metabolic Gene CYP27A1 Polymorphism, Adiponectin/Leptin Ratio, and Metabolic Syndrome in Middle-Aged Taiwanese Males. International journal of endocrinology 2015 2015 658151. Cheng Kai-Hung, Hsi Edward, Liu Chia-Chu, Huang Chun-Nung, Lee Yung-Chin, Chu Chih-Sheng, Bao Bo-Ying, Chang Chu-Fen, Huang Shu-Pin, Kuo Po-Lin, Lai Wen-T |
| Cerebrotendinous xanthomatosis: Possibility of founder mutation in CYP27A1 gene (c.526delG) in Eastern Indian and Surinamese population. Molecular genetics and metabolism reports 2015 Jun 3 33-5. Dutta Atanu Kumar, Danda Sumita, Muthusamy Karthik, Alexander Mathew, Sudhakar Sniya Valsa, Hansdak Samuel, Bandyopadhyay Rini, Bakhya Shree G B, Rekha |
| The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjects. Genetics in medicine : official journal of the American College of Medical Genetics 2017 Jul . Blauwendraat Cornelis, Wilke Carlo, Simón-Sánchez Javier, Jansen Iris E, Reifschneider Anika, Capell Anja, Haass Christian, Castillo-Lizardo Melissa, Biskup Saskia, Maetzler Walter, Rizzu Patrizia, Heutink Peter, Synofzik Matth |
| Prevalence, determinants and clinical correlates of vitamin D deficiency in patients with Chronic Obstructive Pulmonary Disease in London, UK. The Journal of steroid biochemistry and molecular biology 2018 01 175 138-145. Jolliffe David A, James Wai Yee, Hooper Richard L, Barnes Neil C, Greiller Claire L, Islam Kamrul, Bhowmik Angshu, Timms Peter M, Rajakulasingam Raj K, Choudhury Aklak B, Simcock David E, Hyppönen Elina, Walton Robert T, Corrigan Christopher J, Griffiths Christopher J, Martineau Adrian |
| CYP27A1, CYP24A1, and RXR-? Polymorphisms, Vitamin D, and Multiple Sclerosis: a Pilot Study. Journal of molecular neuroscience : MN 2018 Sep 66 (1): 77-84. Agnello Luisa, Scazzone Concetta, Lo Sasso Bruna, Ragonese Paolo, Milano Salvatore, Salemi Giuseppe, Ciaccio Marcel |
| Sterol 27-Hydroxylase Polymorphism Significantly Associates With Shorter Telomere, Higher Cardiovascular and Type-2 Diabetes Risk in Obese Subjects. Frontiers in endocrinology 2018 6 9 309. Pavanello Sofia, Angelici Laura, Hoxha Mirjam, Cantone Laura, Campisi Manuela, Tirelli Amedea Silvia, Vigna Luisella, Pesatori Angela Cecilia, Bollati Valenti |
| Genetic polymorphisms of the hepatic pathways of fatty liver disease after living donor liver transplantation. Liver international : official journal of the International Association for the Study of the Liver 2018 Jun . Chiu King-Wah, Goto Shigeru, Nakano Toshiaki, Hu Tsung-Hui, Chen Ding-Wei, Huang Kuang-Tzu, Hsu Li-Wen, Chen Chao-Lo |
| Unusual genetic variants associated with hypercholesterolemia in Argentina. Atherosclerosis 2018 10 277 256-261. Corral Pablo, Geller Andrew S, Polisecki Eliana Y, Lopez Graciela I, Bañares Virginia G, Cacciagiu Leonardo, Berg Gabriela, Hegele Robert A, Schaefer Ernst J, Schreier Laura |
| Molecular findings in children with inherited intrahepatic cholestasis. Pediatric research 2019 Aug . Wang Neng-Li, Lu Yi, Gong Jing-Yu, Xie Xin-Bao, Lin Jing, Abuduxikuer Kuerbanjiang, Zhang Mei-Hong, Wang Jian-S |
| Subclinical atherosclerosis and its progression are modulated by PLIN2 through a feed-forward loop between LXR and autophagy. Journal of internal medicine 2019 Jun . Saliba-Gustafsson P, Pedrelli M, Gertow K, Werngren O, Janas V, Pourteymour S, Baldassarre D, Tremoli E, Veglia F, Rauramaa R, Smit A J, Giral P, Kurl S, Pirro M, de Faire U, Humphries S E, Hamsten A, , Gonçalves I, Orho-Melander M, Franco-Cereceda A, Borén J, Eriksson P, Magné J, Parini P, Ehrenborg |
| Exonic variants of genes related to the vitamin D signaling pathway in the families of familial multiple sclerosis using whole-exome next generation sequencing. Brain and behavior 2019 3 9 (4): e01272. Pytel Vanesa, Matías-Guiu Jordi A, Torre-Fuentes Laura, Montero-Escribano Paloma, Maietta Paolo, Botet Javier, Álvarez Sara, Gómez-Pinedo Ulises, Matías-Guiu Jor |
| Relationship between rs4674344 CYP27A1 gene polymorphism and coronary artery disease in a Polish population. Kardiologia polska 2019 Nov . Iwanicka Joanna, Iwanicki Tomasz, Balcerzyk Anna, Niemiec Pawe?, Nowak Tomasz, Krauze Jolanta, Trautsolt Wanda, Ochalska-Tyka Anna, Grzeszczak W?adys?aw, ?ak Iwo |
| Distribution of variants in multiple vitamin D-related loci (DHCR7/NADSYN1, GC, CYP2R1, CYP11A1, CYP24A1, VDR, RXR? and RXR?) vary between European, East-Asian and Sub-Saharan African-ancestry populations. Genes & nutrition 2020 3 15 (1): 5. Jones Patrice, Lucock Mark, Chaplin George, Jablonski Nina G, Veysey Martin, Scarlett Christopher, Beckett Em |
| Cholestasis as a dominating symptom of patients with CYP27A1 mutations: An analysis of 17 Chinese infants. Journal of clinical lipidology 2020 Dec . Zhang Ping, Zhao Jing, Peng Xiao-Min, Qian Yan-Yan, Zhao Xue-Mei, Zhou Wen-Hao, Wang Jian-She, Wu Bing-Bing, Wang Hui-J |
| Role of Multiple Vitamin D-Related Polymorphisms in Multiple Sclerosis Severity: Preliminary Findings. Genes 2022 Jul 13 (8): . Agnello Luisa, Scazzone Concetta, Sasso Bruna Lo, Vidali Matteo, Giglio Rosaria Vincenza, Ciaccio Anna Maria, Ragonese Paolo, Salemi Giuseppe, Ciaccio Marcel |
| Prospective cholestanol screening of cerebrotendinous xanthomatosis among patients with juvenile-onset unexplained bilateral cataracts. Orphanet journal of rare diseases 2022 12 17 (1): 434. Fernández-Eulate Gorka, Martin Gilles C, Dureau Pascal, Speeg-Spatz Claude, Brassier Anais, Gillard Perrine, Bremond-Gignac Dominique, Thouvenin Dominique, Pagan Cecile, Lamari Foudil, Nadjar Ya |
| High Throughput Genetic Characterisation of Caucasian Patients Affected by Multi-Drug Resistant Rheumatoid or Psoriatic Arthritis. Journal of personalized medicine 2022 10 12 (10): . Tesolin Paola, Bertinetto Francesca Eleonora, Sonaglia Arianna, Cappellani Stefania, Concas Maria Pina, Morgan Anna, Ferrero Norma Maria, Zabotti Alen, Gasparini Paolo, Amoroso Antonio, Quartuccio Luca, Girotto Giorg |
| The Interaction Effect of 27-hydroxycholesterol Metabolism Disorder and CYP27A1 Single Nucleotide Polymorphisms in Mild Cognitive Impairment: Evidence from a Case-Control Study. Molecular nutrition & food research 2023 2 e2200576. Wang Lijing, Yu Huiyan, Hao Ling, Ju Mengwei, Feng Wenjing, Xiao Ro |
| Allelic prevalence and geographic distribution of cerebrotendinous xanthomatosis. Orphanet journal of rare diseases 2023 1 18 (1): 13. Pramparo Tiziano, Steiner Robert D, Rodems Steve, Jenkinson Cel |
| Apolipoprotein B gene expression and regulation in relation to Alzheimer's disease pathophysiology. Journal of lipid research 2024 10 100667. Gabriel Aumont-Rodrigue, Cynthia Picard, Anne Labonté, , Judes Poiri |
- Page last reviewed:Feb 1, 2024
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