Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 59 Records) |
Query Trace: CYP27A1[original query] |
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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 |
Vitamin D receptor genotype influences risk of upper respiratory infection. The British journal of nutrition 2018 Aug 1-10. Jolliffe David A, Greiller Claire L, Mein Charles A, Hoti Mimoza, Bakhsoliani Eteri, Telcian Aurica G, Simpson Angela, Barnes Neil C, Curtin John A, Custovic Adnan, Johnston Sebastian L, Griffiths Christopher J, Walton Robert T, Martineau Adrian |
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 |
Impact of CYP2R1, CYP27A1 and CYP27B1 genetic polymorphisms controlling vitamin D metabolism on susceptibility to hepatitis C virus infection in a high-risk Chinese population. Archives of virology 2019 Sep . Yang Jing-Jing, Fan Hao-Zhi, Tian Ting, Wu Meng-Ping, Xie Chao-Nan, Huang Peng, Yu Rong-Bin, Yi Hong-Gang, Zhang Yun, Wang J |
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 |
Vitamin D Receptor Polymorphism and DHCR7 Contribute to the Abnormal Interplay Between Vitamin D and Lipid Profile in Rheumatoid Arthritis. Scientific reports 2019 2 9 (1): 2546. Rodríguez-Carrio Javier, Alperi-López Mercedes, Naves-Díaz Manuel, Dusso Adriana, López Patricia, Ballina-García Francisco Javier, Cannata-Andía Jorge B, Suárez A |
Next-generation sequencing study reveals the broader variant spectrum of hereditary spastic paraplegia and related phenotypes. Neurogenetics 2019 2 20 (1): 27-38. Elert-Dobkowska Ewelina, Stepniak Iwona, Krysa Wioletta, Ziora-Jakutowicz Karolina, Rakowicz Maria, Sobanska Anna, Pilch Jacek, Antczak-Marach Dorota, Zaremba Jacek, Sulek An |
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 |
Association of vitamin D gene polymorphisms in children with asthma - A systematic review. Heliyon 2020 9 6 (9): e04795. Ashok Narmada, Kirubakaran Richard, Saraswathy Rad |
Exploratory Genome-Wide Interaction Analysis of Nonsteroidal Anti-inflammatory Drugs and Predicted Gene Expression on Colorectal Cancer Risk. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2020 7 29 (9): 1800-1808. Wang Xiaoliang, Su Yu-Ru, Petersen Paneen S, Bien Stephanie, Schmit Stephanie L, Drew David A, Albanes Demetrius, Berndt Sonja I, Brenner Hermann, Campbell Peter T, Casey Graham, Chang-Claude Jenny, Gallinger Steven J, Gruber Stephen B, Haile Robert W, Harrison Tabitha A, Hoffmeister Michael, Jacobs Eric J, Jenkins Mark A, Joshi Amit D, Li Li, Lin Yi, Lindor Noralane M, Marchand Loïc Le, Martin Vicente, Milne Roger, Maclnnis Robert, Moreno Victor, Nan Hongmei, Newcomb Polly A, Potter John D, Rennert Gad, Rennert Hedy, Slattery Martha L, Thibodeau Steve N, Weinstein Stephanie J, Woods Michael O, Chan Andrew T, White Emily, Hsu Li, Peters Ulri |
Association of common genetic variants with vitamin D status in Malaysian children with epilepsy. Seizure 2020 May 79 103-111. Kong Ann Nie, Fong Choong Yi, Ng Ching Ching, Mohamed Ahmad Rithauddin, Khoo Teik Beng, Ng Rui Lun, Jalaludin Muhammad Yazid, Nadarajaw Thiyag |
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 |
Dysregulation of vitamin D synthesis pathway genes in colorectal cancer: A case-control study. Journal of clinical laboratory analysis 2020 Oct e23617. Sadeghi Hossein, Kamaliyan Zeeba, Mohseni Roohollah, Sahebi Unes, Nazemalhosseini-Mojarad Ehsan, Aghaei Naser, Zali Mohammad Reza, Asadzadeh Aghdaei Hamid, Mirfakhraie Reza, Moshiri Ar |
Association of genetic variations in the vitamin D pathway with susceptibility to tuberculosis in Kazakhstan. Molecular biology reports 2020 Jan . Sadykov Mukhtar, Azizan Azliyati, Kozhamkulov Ulan, Akilzhanova Ainur, Yerezhepov Dauren, Salfinger Max, Chan Chee K |
Association of vitamin D pathway genes polymorphisms with pulmonary tuberculosis susceptibility in a Chinese population. Genes & nutrition 2021 Apr 16 (1): 6. Zhang Tian-Ping, Chen Shuang-Shuang, Zhang Gen-You, Shi Si-Jiu, Wei Li, Li Hong-Mi |
First case series of Polish patients with cerebrotendinous xanthomatosis and systematic review of cases from the 21st century. Clinical genetics 2021 10 101 (2): 190-207. Badura-Stronka Magdalena, Hirschfeld Adam Sebastian, Winczewska-Wiktor Anna, Budzy?ska Edyta, Jakubiuk-Tomaszuk Anna, Piontek Anita, Steinborn Barbara, Kozubski Wojcie |
Prevalence of cerebrotendinous xanthomatosis in cases with idiopathic bilateral juvenile cataract in ophthalmology clinics in Turkey. Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus 2021 10 25 (5): 269.e1-269.e6. Atilla Huban, Coskun Turgay, Elibol Bulent, Kadayifcilar Sibel, Altinel Serdar, |
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 |
Comprehensive Analysis of Copy Number Variation, Nucleotide Mutation, and Transcription Level of PPAR Pathway-Related Genes in Endometrial Cancer. PPAR research 2022 1 2022 5572258. Tang Minghui, Wang Jingyao, Fan Liangshe |
Genetic Characteristics of Latvian Patients with Familial Hypercholesterolemia: The First Analysis from Genome-Wide Sequencing. Journal of clinical medicine 2023 8 12 (15): . Gustavs Latkovskis, Raimonds Rescenko-Krums, Georgijs Nesterovics, Monta Briviba, Vita Saripo, Dainus Gilis, Elizabete Terauda, Ruta Meiere, Gunda Skudrina, Andrejs Erglis, Joana Rita Chora, Mafalda Bourbon, Janis Klovi |
Identification of genetic mechanisms underlying lipid metabolism-mediated tumor immunity in head and neck squamous cell carcinoma. BMC medical genomics 2023 5 16 (1): 110. Shaokun Liu, Shuning Wang, Zhenlin Wa |
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 |
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- Page last updated:Apr 16, 2024
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