Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 33 Records) |
Query Trace: CPT1A[original query] |
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Lack of association of CPT1A polymorphisms or haplotypes on hepatic lipid content or insulin resistance in Japanese individuals with type 2 diabetes mellitus. Metabolism: clinical and experimental 2007 May 56 (5): 656-61. Hirota Yushi, Ohara Takeshi, Zenibayashi Masako, Kuno Shin-ichi, Fukuyama Keiko, Teranishi Tetsuya, Kouyama Kunichi, Miyake Kazuaki, Maeda Eiichi, Kasuga Masa |
Carnitine palmitoyltransferase IA polymorphism P479L is common in Greenland Inuit and is associated with elevated plasma apolipoprotein A-I. Journal of lipid research 2009 Jun 50 (6): 1223-8. Rajakumar Chandheeb, Ban Matthew R, Cao Henian, Young T Kue, Bjerregaard Peter, Hegele Robert |
Prevalence and distribution of the c.1436C?T sequence variant of carnitine palmitoyltransferase 1A among Alaska Native infants. The Journal of pediatrics 2011 Jan 158 (1): 124-9. Gessner Bradford D, Gillingham Melanie B, Johnson Monique A, Richards C Sue, Lambert William E, Sesser David, Rien Leanne C, Hermerath Cheryl A, Skeels Michael R, Birch Stephanie, Harding Cary O, Wood Thalia, Koeller David |
Carnitine palmitoyltransferase 1A (CPT1A) P479L prevalence in live newborns in Yukon, Northwest Territories, and Nunavut. Molecular genetics and metabolism 0 101 (2-3): 200-4. Collins Sorcha A, Sinclair Graham, McIntosh Sarah, Bamforth Fiona, Thompson Robert, Sobol Isaac, Osborne Geraldine, Corriveau Andre, Santos Maria, Hanley Brendan, Greenberg Cheryl R, Vallance Hilary, Arbour Lau |
Evidence for an association between infant mortality and a carnitine palmitoyltransferase 1A genetic variant. Pediatrics 2010 Nov 126 (5): 945-51. Gessner Bradford D, Gillingham Melanie B, Birch Stephanie, Wood Thalia, Koeller David |
Genetic polymorphisms in carnitine palmitoyltransferase 1A gene are associated with variation in body composition and fasting lipid traits in Yup'ik Eskimos. Journal of lipid research 2012 Jan 53 (1): 175-84. Lemas Dominick J, Wiener Howard W, O'Brien Diane M, Hopkins Scarlett, Stanhope Kimber L, Havel Peter J, Allison David B, Fernandez Jose R, Tiwari Hemant K, Boyer Bert |
Variants in CPT1A, FADS1, and FADS2 are Associated with Higher Levels of Estimated Plasma and Erythrocyte Delta-5 Desaturases in Alaskan Eskimos. Frontiers in genetics 2012 3 86. Voruganti V Saroja, Higgins Paul B, Ebbesson Sven O E, Kennish John, Göring Harald H H, Haack Karin, Laston Sandra, Drigalenko Eugene, Wenger Charlotte R, Harris William S, Fabsitz Richard R, Devereux Richard B, Maccluer Jean W, Curran Joanne E, Carless Melanie A, Johnson Matthew P, Moses Eric K, Blangero John, Umans Jason G, Howard Barbara V, Cole Shelley A, Comuzzie Anthony Ge |
Carnitine palmitoyltransferase I and sudden unexpected infant death in British Columbia First Nations. Pediatrics 2012 Oct . Sinclair GB, Collins S, Popescu O, McFadden D, Arbour L, Vallance HD |
Association of a genetic variant of carnitine palmitoyltransferase 1A with infections in Alaska Native children. The Journal of pediatrics 2013 Aug . Gessner BD, Gillingham MB, Wood T, Koeller DM |
Genome-wide analysis of cold adaptation in indigenous Siberian populations. PloS one 2014 9 (5): e98076. Cardona Alexia, Pagani Luca, Antao Tiago, Lawson Daniel J, Eichstaedt Christina A, Yngvadottir Bryndis, Shwe Ma Than Than, Wee Joseph, Romero Irene Gallego, Raj Srilakshmi, Metspalu Mait, Villems Richard, Willerslev Eske, Tyler-Smith Chris, Malyarchuk Boris A, Derenko Miroslava V, Kivisild Toom |
Polymorphisms in genes involved in fatty acid ß-oxidation interact with dietary fat intakes to modulate the plasma TG response to a fish oil supplementation. Nutrients 2014 6 (3): 1145-63. Bouchard-Mercier Annie, Rudkowska Iwona, Lemieux Simone, Couture Patrick, Vohl Marie-Clau |
Evidence for an association between infant mortality and homozygosity for the arctic variant of carnitine palmitoyltransferase 1A. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Jan . Gessner Bradford D, Wood Thalia, Johnson Monique A, Richards Carolyn Sue, Koeller David |
Genome- and epigenome-wide association study of hypertriglyceridemic waist in Mexican American families. Clinical epigenetics 2016 8 6. Mamtani Manju, Kulkarni Hemant, Dyer Thomas D, Göring Harald H H, Neary Jennifer L, Cole Shelley A, Kent Jack W, Kumar Satish, Glahn David C, Mahaney Michael C, Comuzzie Anthony G, Almasy Laura, Curran Joanne E, Duggirala Ravindranath, Blangero John, Carless Melanie |
DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation. American journal of human genetics 2017 Dec 101 (6): 888-902. Richard Melissa A, Huan Tianxiao, Ligthart Symen, Gondalia Rahul, Jhun Min A, Brody Jennifer A, Irvin Marguerite R, Marioni Riccardo, Shen Jincheng, Tsai Pei-Chien, Montasser May E, Jia Yucheng, Syme Catriona, Salfati Elias L, Boerwinkle Eric, Guan Weihua, Mosley Thomas H, Bressler Jan, Morrison Alanna C, Liu Chunyu, Mendelson Michael M, Uitterlinden André G, van Meurs Joyce B, , Franco Oscar H, Zhang Guosheng, Li Yun, Stewart James D, Bis Joshua C, Psaty Bruce M, Chen Yii-Der Ida, Kardia Sharon L R, Zhao Wei, Turner Stephen T, Absher Devin, Aslibekyan Stella, Starr John M, McRae Allan F, Hou Lifang, Just Allan C, Schwartz Joel D, Vokonas Pantel S, Menni Cristina, Spector Tim D, Shuldiner Alan, Damcott Coleen M, Rotter Jerome I, Palmas Walter, Liu Yongmei, Paus Tomáš, Horvath Steve, O'Connell Jeffrey R, Guo Xiuqing, Pausova Zdenka, Assimes Themistocles L, Sotoodehnia Nona, Smith Jennifer A, Arnett Donna K, Deary Ian J, Baccarelli Andrea A, Bell Jordana T, Whitsel Eric, Dehghan Abbas, Levy Daniel, Fornage Myri |
The p.P479L variant in CPT1A is associated with infectious disease in a BC First Nation. Paediatrics & child health 2019 4 24 (2): e111-e115. Sinclair Graham, Collins Sorcha, Arbour Laura, Vallance Hila |
Genetic study of the Arctic CPT1A variant suggests that its effect on fatty acid levels is modulated by traditional Inuit diet. European journal of human genetics : EJHG 2020 6 28 (11): 1592-1601. Senftleber Ninna, Jørgensen Marit Eika, Jørsboe Emil, Imamura Fumiaki, Forouhi Nita Gandhi, Larsen Christina Lytken, Bjerregaard Peter, Hansen Torben, Albrechtsen Ande |
Association of the CPT1A p.P479L Metabolic Gene Variant With Childhood Respiratory and Other Infectious Illness in Nunavut. Frontiers in pediatrics 2021 7 9 678553. Collins Sorcha A, Edmunds Sharon, Akearok Gwen Healey, Thompson J Robert, Erickson Anders C, Hildes-Ripstein Elske, Miners Amber, Somerville Martin, Goldfarb David M, Rockman-Greenberg Cheryl, Arbour Lau |
The impact of CPT1B rs470117, LEPR rs1137101 and BDNF rs6265 polymorphisms on the risk of developing obesity in an Italian population. Obesity research & clinical practice 2021 Jun . Ricci Claudia, Marzocchi Carlotta, Riolo Giulia, Ciuoli Cristina, Benenati Nicoletta, Bufano Annalisa, Tirone Andrea, Voglino Costantino, Vuolo Giuseppe, Castagna Maria Grazia, Cantara Silv |
Neonatal hypoglycemia and the CPT1A P479L variant in term newborns: A retrospective cohort study of Inuit newborns from Kivalliq Nunavut. Paediatrics & child health 2021 6 26 (4): 218-227. Collins Sorcha A, Hildes-Ripstein Gertrude Elizabeth, Thompson James Robert, Edmunds Sharon, Miners Amber, Rockman-Greenberg Cheryl, Arbour Lau |
Study of Acute Liver Failure in Children Using Next Generation Sequencing Technology. The Journal of pediatrics 2021 5 236 124-130. Hegarty Robert, Gibson Philippa, Sambrotta Melissa, Strautnieks Sandra, Foskett Pierre, Ellard Sian, Baptista Julia, Lillis Suzanne, Bansal Sanjay, Vara Roshni, Dhawan Anil, Grammatikopoulos Tassos, Thompson Richard |
Association of CPT1A gene polymorphism with the risk of gestational diabetes mellitus: a case-control study. Journal of assisted reproduction and genetics 2021 Mar . Ren Qingwen, Guo Mengzhu, Yang Feifei, Han Tianbi, Du Wenqiong, Zhao Feng, Li Jinbo, Li Wangjun, Feng Yongliang, Wang Suping, Zhang Yawei, Wu Weiw |
Three Novel and One Potential Hotspot CPT1A Variants in Chinese Patients With Carnitine Palmitoyltransferase 1A Deficiency. Frontiers in pediatrics 2021 12 9 771922. Zhang Weifeng, Chen Yanru, Lin Chunmei, Peng Weilin, Fu Qingliu, Lin Yimi |
Newborn Screening for Mitochondrial Carnitine-Acylcarnitine Cycle Disorders in Zhejiang Province, China. Frontiers in genetics 2022 4 13 823687. Zhou Duo, Cheng Yi, Yin Xiaoshan, Miao Haixia, Hu Zhenzhen, Yang Jianbin, Zhang Yu, Wu Benqing, Huang Xinw |
Association of Inherited Genetic Factors With Drug-Induced Hepatic Damage Among Children With Acute Lymphoblastic Leukemia. JAMA network open 2022 12 5 (12): e2248803. Yang Wenjian, Karol Seth E, Hoshitsuki Keito, Lee Shawn, Larsen Eric C, Winick Naomi, Carroll William L, Loh Mignon L, Raetz Elizabeth A, Hunger Stephen P, Winter Stuart S, Dunsmore Kimberly P, Devidas Meenakshi, Relling Mary V, Yang Jun |
Neutrophil trafficking to the site of infection requires Cpt1a-dependent fatty acid ?-oxidation. Communications biology 2022 12 5 (1): 1366. Pham Ly, Komalavilas Padmini, Eddie Alex M, Thayer Timothy E, Greenwood Dalton L, Liu Ken H, Weinberg Jaclyn, Patterson Andrew, Fessel Joshua P, Boyd Kelli L, Schafer Jenny C, Kuck Jamie L, Shaver Aaron C, Flaherty David K, Matlock Brittany K, Wijers Christiaan D M, Serezani C Henrique, Jones Dean P, Brittain Evan L, Rathmell Jeffrey C, Noto Michael |
Whole Exome Sequencing in Multi-Incident Families Identifies Novel Candidate Genes for Multiple Sclerosis. International journal of molecular sciences 2022 10 23 (19): . Horjus Julia, van Mourik-Banda Tineke, Heerings Marco A P, Hakobjan Marina, De Witte Ward, Heersema Dorothea J, Jansen Anne J, Strijbis Eva M M, de Jong Brigit A, Slettenaar Astrid E J, Zeinstra Esther M P E, Hoogervorst Erwin L J, Franke Barbara, Kruijer Wiebe, Jongen Peter J, Visser Leo J, Poelmans Gee |
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 |
Impact of genetic variants involved in the lipid metabolism pathway on progression free survival in patients receiving bevacizumab-based chemotherapy in metastatic colorectal cancer: a retrospective analysis of FIRE-3 and MAVERICC trials. EClinicalMedicine 2023 2 57 101827. Wang Jingyuan, Millstein Joshua, Yang Yan, Stintzing Sebastian, Arai Hiroyuki, Battaglin Francesca, Kawanishi Natsuko, Soni Shivani, Zhang Wu, Mancao Christoph, Cremolini Chiara, Liu Tianshu, Heinemann Volker, Falcone Alfredo, Shen Lin, Lenz Heinz-Jos |
Weighted gene co-expression network analysis for hub genes in colorectal cancer. Pharmacological reports : PR 2023 12 . Zheng Xu, Jianing Wang, Guosheng Wa |
Metabolic heterogeneity in early-stage lung adenocarcinoma revealed by RNA-seq and scRNA-seq. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2023 1 . Zhang Yang, Shi Jiang, Luo Junfang, Liu Cong, Zhu Li |
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- Page last updated:Apr 16, 2024
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