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Journal Abstract Search

183 related items for PubMed ID: 21358852

  • 1. Abnormally low serum acylcarnitine levels in narcolepsy patients.
    Miyagawa T, Miyadera H, Tanaka S, Kawashima M, Shimada M, Honda Y, Tokunaga K, Honda M.
    Sleep; 2011 Mar 01; 34(3):349-53A. PubMed ID: 21358852
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  • 2. Low carnitine palmitoyltransferase 1 activity is a risk factor for narcolepsy type 1 and other hypersomnia.
    Honda M, Shigematsu Y, Shimada M, Honda Y, Tokunaga K, Miyagawa T.
    Sleep; 2022 Oct 10; 45(10):. PubMed ID: 35810398
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  • 3. Effects of oral L-carnitine administration in narcolepsy patients: a randomized, double-blind, cross-over and placebo-controlled trial.
    Miyagawa T, Kawamura H, Obuchi M, Ikesaki A, Ozaki A, Tokunaga K, Inoue Y, Honda M.
    PLoS One; 2013 Oct 10; 8(1):e53707. PubMed ID: 23349733
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  • 4. Variant between CPT1B and CHKB associated with susceptibility to narcolepsy.
    Miyagawa T, Kawashima M, Nishida N, Ohashi J, Kimura R, Fujimoto A, Shimada M, Morishita S, Shigeta T, Lin L, Hong SC, Faraco J, Shin YK, Jeong JH, Okazaki Y, Tsuji S, Honda M, Honda Y, Mignot E, Tokunaga K.
    Nat Genet; 2008 Nov 10; 40(11):1324-8. PubMed ID: 18820697
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  • 5. Identification of the variations in the CPT1B and CHKB genes along with the HLA-DQB1*06:02 allele in Turkish narcolepsy patients and healthy persons.
    Cingoz S, Agilkaya S, Oztura I, Eroglu S, Karadeniz D, Evlice A, Altungoz O, Yilmaz H, Baklan B.
    Genet Test Mol Biomarkers; 2014 Apr 10; 18(4):261-8. PubMed ID: 24571861
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  • 8. Impact of L-carnitine in narcolepsy treatment: a systematic review on the effectiveness and safety.
    Salles C, Freitas MC, Cruz MME.
    Sleep Sci; 2022 Apr 10; 15(Spec 1):278-284. PubMed ID: 35273778
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  • 9. Evaluation of polygenic risks for narcolepsy and essential hypersomnia.
    Yamasaki M, Miyagawa T, Toyoda H, Khor SS, Liu X, Kuwabara H, Kano Y, Shimada T, Sugiyama T, Nishida H, Sugaya N, Tochigi M, Otowa T, Okazaki Y, Kaiya H, Kawamura Y, Miyashita A, Kuwano R, Kasai K, Tanii H, Sasaki T, Honda Y, Honda M, Tokunaga K.
    J Hum Genet; 2016 Oct 10; 61(10):873-878. PubMed ID: 27305985
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  • 11. A common haplotype of carnitine palmitoyltransferase 1b is associated with the metabolic syndrome.
    Auinger A, Rubin D, Sabandal M, Helwig U, Rüther A, Schreiber S, Foelsch UR, Döring F, Schrezenmeir J.
    Br J Nutr; 2013 Mar 14; 109(5):810-5. PubMed ID: 22809552
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  • 12. Polymorphisms in CPT1B and CPT2 have no significant effect on plasma carnitine levels in Japanese cancer patients.
    Hishida A, Watanabe R, Hattori Y, Okugawa Y, Shirai Y, Miki C.
    Nagoya J Med Sci; 2019 Aug 14; 81(3):477-487. PubMed ID: 31579338
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  • 14. Examination of carnitine palmitoyltransferase 1 abundance in white adipose tissue: implications in obesity research.
    Warfel JD, Vandanmagsar B, Dubuisson OS, Hodgeson SM, Elks CM, Ravussin E, Mynatt RL.
    Am J Physiol Regul Integr Comp Physiol; 2017 May 01; 312(5):R816-R820. PubMed ID: 28330968
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  • 17. Study of Carnitine/Acylcarnitine and Amino Acid Profile in Children and Adults With Acute Liver Failure.
    Sood V, Rawat D, Khanna R, Sharma S, Gupta PK, Alam S, Sarin SK.
    J Pediatr Gastroenterol Nutr; 2017 Jun 01; 64(6):869-875. PubMed ID: 28045774
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  • 19. Differential epigenetic and transcriptional response of the skeletal muscle carnitine palmitoyltransferase 1B (CPT1B) gene to lipid exposure with obesity.
    Maples JM, Brault JJ, Witczak CA, Park S, Hubal MJ, Weber TM, Houmard JA, Shewchuk BM.
    Am J Physiol Endocrinol Metab; 2015 Aug 15; 309(4):E345-56. PubMed ID: 26058865
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  • 20. Peroxisomes contribute to the acylcarnitine production when the carnitine shuttle is deficient.
    Violante S, Ijlst L, Te Brinke H, Koster J, Tavares de Almeida I, Wanders RJ, Ventura FV, Houten SM.
    Biochim Biophys Acta; 2013 Sep 15; 1831(9):1467-74. PubMed ID: 23850792
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