Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: CPT2[original query] |
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Haplotype analysis of carnitine transporters and left ventricular mass in human essential hypertension. Journal of renal nutrition : the official journal of the Council on Renal Nutrition of the National Kidney Foundation 2005 Jan 15 (1): 2-7. Tripodi Grazia, Modica Rossana, Stella Alessandra, Bigatti Giada, Bianchi Giuseppe, Stella Pao |
High frequency of ETFDH c.250G>A mutation in Taiwanese patients with late-onset lipid storage myopathy. Clinical genetics 2010 Dec 78 (6): 565-9. Lan M-Y, Fu M-H, Liu Y-F, Huang C-C, Chang Y-Y, Liu J-S, Peng C-H, Chen S |
A common haplotype of carnitine palmitoyltransferase 1b is associated with the metabolic syndrome. The British journal of nutrition 2013 Mar 109 (5): 810-5. Auinger A, Rubin D, Sabandal M, Helwig U, Rüther A, Schreiber S, Foelsch U R, Döring F, Schrezenmeir |
Carnitine palmitoyltransferase 2 gene polymorphism is a genetic risk factor for sudden unexpected death in infancy. Brain & development 2014 Jun 36 (6): 479-83. Yamamoto Takuma, Tanaka Hidekazu, Emoto Yuko, Umehara Takahiro, Fukahori Yuki, Kuriu Yukiko, Matoba Ryoji, Ikematsu Kazu |
Single nucleotide polymorphism in CPT1B and CPT2 genes and its association with blood carnitine levels in acute myocardial infarction patients. Gene 2013 Jul 523 (1): 76-81. Khan Haseeb Ahmad, Alhomida Abdullah Sal |
Abbreviated half-lives and impaired fuel utilization in carnitine palmitoyltransferase II variant fibroblasts. PloS one 2015 10 (3): e0119936. Yao Min, Cai Min, Yao Dengfu, Xu Xi, Yang Rongrong, Li Yuting, Zhang Yuanyuan, Kido Hiroshi, Yao Dengbi |
Genetic evaluation of AMPD1, CPT2, and PGYM metabolic enzymes in patients with chronic fatigue syndrome. Genetics and molecular research : GMR 2016 15 (3): . Maltese P E, Venturini L, Poplavskaya E, Bertelli M, Cecchin S, Granato M, Nikulina S Y, Salmina A, Aksyutina N, Capelli E, Ricevuti G, Lorusso |
Carnitine palmitoyl transferase 2 polymorphism may be associated with enterovirus 71 severe infection in a Chinese population. Archives of virology 2016 Feb . Liu Peipei, Liu Xiangping, Hu Jingfei, Han Zhenliang, Li Fei, Wang Yuanyuan, Song Long, Chen Zong |
Thermolabile polymorphism of carnitine palmitoyltransferase 2: A genetic risk factor of overall acute encephalopathy. Brain & development 2019 7 41 (10): 862-869. Shibata Akiko, Kasai Mariko, Hoshino Ai, Miyagawa Taku, Matsumoto Hiroshi, Yamanaka Gaku, Kikuchi Kenjiro, Kuki Ichiro, Kumakura Akira, Hara Shinya, Shiihara Takashi, Yamazaki Sawako, Ohta Masayasu, Yamagata Takanori, Takanashi Jun-Ichi, Kubota Masaya, Oka Akira, Mizuguchi Masas |
Association of the Polymorphism of rs1799822 on Carnitine Palmitoyltransferase II Gene with Severe Enterovirus 71 Encephalitis in Chinese Children. Journal of molecular neuroscience : MN 2019 Jun . Guo Ya, Zhang Yu, Liu Peipei, Li Fei, Xin Dandan, He Hongfang, Liu Yedan, Yang Chengqing, Chen Zong |
Exome-Based Rare-Variant Analyses in CKD. Journal of the American Society of Nephrology : JASN 2019 May . Cameron-Christie Sophia, Wolock Charles J, Groopman Emily, Petrovski Slavé, Kamalakaran Sitharthan, Povysil Gundula, Vitsios Dimitrios, Zhang Mengqi, Fleckner Jan, March Ruth E, Gelfman Sahar, Marasa Maddalena, Li Yifu, Sanna-Cherchi Simone, Kiryluk Krzysztof, Allen Andrew S, Fellström Bengt C, Haefliger Carolina, Platt Adam, Goldstein David B, Gharavi Ali |
Polymorphisms in CPT1B and CPT2 have no significant effect on plasma carnitine levels in Japanese cancer patients. Nagoya journal of medical science 2019 Aug 81 (3): 477-487. Hishida Asahi, Watanabe Ryosuke, Hattori Yuta, Okugawa Yoshinaga, Shirai Yumiko, Miki Chik |
Endogenous genetic risk factor for serious heatstroke: the thermolabile phenotype of carnitine palmitoyltransferase II variant. Acute medicine & surgery 2019 Jan 6 (1): 25-29. Oda Jun, Yukioka Tetsuo, Azuma Kazunari, Arai Takao, Chida Junji, Kido Hiros |
Effects of fasting, feeding and exercise on plasma acylcarnitines among subjects with CPT2D, VLCADD and LCHADD/TFPD. Molecular genetics and metabolism 2020 9 131 (1-2): 90-97. Elizondo Gabriela, Matern Dietrich, Vockley Jerry, Harding Cary O, Gillingham Melanie |
Whole-exome sequencing in a family with a monozygotic twin pair concordant for schizophrenia and a follow-up case-control study of identified de-novo variants. Psychiatric genetics 2020 2 30 (2): 60-63. Hoya Satoshi, Watanabe Yuichiro, Nunokawa Ayako, Otsuka Ikuo, Shibuya Masako, Igeta Hirofumi, Hishimoto Akitoyo, Someya Toshiyu |
Mitochondrial molecular genetic results in a South African cohort: divergent mitochondrial and nuclear DNA findings. Journal of clinical pathology 2020 10 75 (1): 34-38. Meldau Surita, Owen Elizabeth Patricia, Khan Kashief, Riordan Gillian Tra |
Increased Cancer Prevalence in Peripartum Cardiomyopathy. JACC. CardioOncology 2021 8 1 (2): 196-205. Pfeffer Tobias J, Schlothauer Stella, Pietzsch Stefan, Schaufelberger Maria, Auber Bernd, Ricke-Hoch Melanie, List Manuel, Berliner Dominik, Abou Moulig Valeska, König Tobias, Arany Zolt, Sliwa Karen, Bauersachs Johann, Hilfiker-Kleiner Deni |
Recurrent acute necrotizing encephalopathy in a boy with RANBP2 mutation and thermolabile CPT2 variant: The first case of ANE1 in Japan. Brain & development 2021 6 43 (8): 873-878. Ohashi Eri, Hayakawa Itaru, Murofushi Yuka, Kawai Michiko, Suzuki-Muromoto Sato, Abe Yuichi, Yoshida Michiko, Kono Naoko, Kosaki Rika, Hoshino Ai, Mizuguchi Masashi, Kubota Masa |
Whole-Exome Sequencing Identifies a Novel CPT2 Mutation in a Pedigree With Gout. Frontiers in cell and developmental biology 2022 4 10 802635. Guo Yong, Jin Jing, Zhou Zhenni, Chen Yihui, Sun Li, Zhang Chunwu, Xia Xiao |
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 |
Genetic and environmental risk factors of acute infection-triggered encephalopathy. Frontiers in neuroscience 2023 2 17 1119708. Mizuguchi Masashi, Shibata Akiko, Kasai Mariko, Hoshino |
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- Page last updated:Mar 25, 2024
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