يعرض 1 - 20 نتائج من 2,864 نتيجة بحث عن '"DIHYDROPYRIMIDINE dehydrogenase"', وقت الاستعلام: 0.59s تنقيح النتائج
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    Academic Journal

    المؤلفون: Nguyen, D. Grace1 (AUTHOR), Morris, Sarah A.1 (AUTHOR), Hamilton, Alicia2 (AUTHOR), Kwange, Simeon O.1 (AUTHOR), Steuerwald, Nury2,3 (AUTHOR), Symanowski, James4 (AUTHOR), Moore, Donald C.5 (AUTHOR), Hanson, Sarah5 (AUTHOR), Mroz, Kaitlyn1 (AUTHOR), Lopes, Karine E.1 (AUTHOR), Larck, Chris5 (AUTHOR), Musselwhite, Laura3,6 (AUTHOR), Kadakia, Kunal C.3,6 (AUTHOR), Koya, Brinda6 (AUTHOR), Chai, Seungjean3,6 (AUTHOR), Osei-Boateng, Kwabena3,6 (AUTHOR), Kalapurakal, Sini6 (AUTHOR), Swift, Kristen6 (NURSE), Hwang, Jimmy3,6 (AUTHOR), Patel, Jai N.1,3 (AUTHOR) jai.patel@atriumhealth.org

    المصدر: JCO Precision Oncology. 12/1/2024, Vol. 8, p1-13. 13p.

  2. 2
    Academic Journal

    المؤلفون: Miteva-Marcheva, Nelly1 (AUTHOR) miteva_md@abv.bg, Ivanov, Hristo1 (AUTHOR), Bangieva-Ivanova, Elena1 (AUTHOR), Boyanov, Nikola2,3 (AUTHOR), Stoyanova, Vili1 (AUTHOR)

    المصدر: Biotechnology & Biotechnological Equipment. Dec2024, Vol. 38 Issue 1, p1-13. 13p.

  3. 3
    Academic Journal
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    Academic Journal

    المؤلفون: Launay, Manon1,2 (AUTHOR), Raymond, Laure3,4 (AUTHOR), Guitton, Jérôme2,5,6 (AUTHOR), Loriot, Marie-Anne4,7,8 (AUTHOR), Chatelut, Etienne2,9 (AUTHOR), Haufroid, Vincent4,10 (AUTHOR), Thomas, Fabienne2,4,9 (AUTHOR) thomas.fabienne@iuct-oncopole.fr, Etienne-Grimaldi, Marie-Christine2,4,11 (AUTHOR)

    المصدر: Clinical Chemistry & Laboratory Medicine. Nov2024, Vol. 62 Issue 12, p2415-2424. 10p.

  5. 5
    Academic Journal

    المؤلفون: Thompson, Jack T.1 (AUTHOR), Wood, David M.1,2 (AUTHOR), Dargan, Paul I.1,2 (AUTHOR) paul.dargan@gstt.nhs.uk

    المصدر: British Journal of Clinical Pharmacology. Oct2024, p1. 13p. 1 Illustration.

  6. 6
    Report

    المؤلفون: Servier

    المصدر: TRIFLUOX-DP: Safety of Trifluridine/Tipiracil as Replacement of Fluoropyrimidines (5-fluorouracil and Capecitabine) Based Chemotherapy as First Line Metastatic Colorectal or Gastroesophageal Cancer Regimens in Patients With Dihydropyrimidine Dehydrogenase Deficiency: a Phase II Trial

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  8. 8
    Academic Journal

    المؤلفون: Kato, Hiroyuki1 (AUTHOR) h.kato@med.nagoya‐cu.ac.jp, Sato, Motonori1 (AUTHOR), Naiki‐Ito, Aya1 (AUTHOR), Inaguma, Shingo1 (AUTHOR), Sano, Makoto2 (AUTHOR), Komura, Masayuki1 (AUTHOR), Nagayasu, Yuko1 (AUTHOR), Xiaochen, Kuang1 (AUTHOR), Kato, Akihisa3 (AUTHOR), Matsuo, Yoichi4 (AUTHOR), Ijichi, Hideaki5 (AUTHOR), Takahashi, Satoru1 (AUTHOR)

    المصدر: Cancer Medicine. Aug2024, Vol. 13 Issue 16, p1-11. 11p.

  9. 9
    Academic Journal

    المؤلفون: Medwid, Samantha1,2,3 (AUTHOR), Kim, Richard B.1,2,3 (AUTHOR) richard.kim@lhsc.on.ca

    المصدر: British Journal of Clinical Pharmacology. Aug2024, Vol. 90 Issue 8, p1763-1781. 19p.

  10. 10
    Academic Journal

    المؤلفون: Ikonnikova, Anna1 (AUTHOR) anyuik@gmail.com, Fedorinov, Denis2,3 (AUTHOR) fedorinov.denis@gmail.com, Gryadunov, Dmitry1 (AUTHOR) emel.marina85@gmail.com, Heydarov, Rustam4 (AUTHOR) rustam.heydarov@gmail.com, Lyadova, Marina2,5 (AUTHOR) dr.lyadova@gmail.com, Moskalenko, Alexey2 (AUTHOR) mansurgkokod@gmail.com, Mikhailovich, Vladimir4 (AUTHOR) v.mikhailovich@gmail.com, Emelyanova, Marina1,4 (AUTHOR), Lyadov, Vladimir2,3,5 (AUTHOR) vlyadov@gmail.com

    المصدر: International Journal of Molecular Sciences. Aug2024, Vol. 25 Issue 15, p8503. 13p.

  11. 11
    Academic Journal

    المؤلفون: Ambrodji, Alisa1,2 (AUTHOR) alisa.ambrodji@extern.insel.ch, Sadlon, Angélique1 (AUTHOR) angelique.sadlon@insel.ch, Amstutz, Ursula1 (AUTHOR) ursula.amstutz@insel.ch, Hoch, Dennis3 (AUTHOR) dennis.hoch@insel.ch, Berger, Martin D.3 (AUTHOR) martin.berger@insel.ch, Bastian, Sara4 (AUTHOR) sara.bastian@ksgr.ch, Offer, Steven M.5 (AUTHOR) steven-offer@uiowa.edu, Largiadèr, Carlo R.1 (AUTHOR) carlo.largiader@insel.ch

    المصدر: International Journal of Molecular Sciences. Jul2024, Vol. 25 Issue 14, p7599. 15p.

    مصطلحات جغرافية: EUROPE

  12. 12
    Report

    المصدر: Prospective Study of the Clinical, Genomic, Pharmacological, Laboratory, and Dietary Determinates of Pyrimidine and Purine Metabolism Disorders
    Shchelochkov OA, Manoli I, Juneau P, Sloan JL, Ferry S, Myles J, Schoenfeld M, Pass A, McCoy S, Van Ryzin C, Wenger O, Levin M, Zein W, Huryn L, Snow J, Chlebowski C, Thurm A, Kopp JB, Chen KY, Venditti CP. Severity modeling of propionic acidemia using clinical and laboratory biomarkers. Genet Med. 2021 Aug;23(8):1534-1542. doi: 10.1038/s41436-021-01173-2. Epub 2021 May 18.
    Sloan JL, Johnston JJ, Manoli I, Chandler RJ, Krause C, Carrillo-Carrasco N, Chandrasekaran SD, Sysol JR, O'Brien K, Hauser NS, Sapp JC, Dorward HM, Huizing M; NIH Intramural Sequencing Center Group; Barshop BA, Berry SA, James PM, Champaigne NL, de Lonlay P, Valayannopoulos V, Geschwind MD, Gavrilov DK, Nyhan WL, Biesecker LG, Venditti CP. Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria. Nat Genet. 2011 Aug 14;43(9):883-6. doi: 10.1038/ng.908.
    Balasubramaniam S, Duley JA, Christodoulou J. Inborn errors of purine metabolism: clinical update and therapies. J Inherit Metab Dis. 2014 Sep;37(5):669-86. doi: 10.1007/s10545-014-9731-6. Epub 2014 Jun 28.
    Shchelochkov OA, Manoli I, Sloan JL, Ferry S, Pass A, Van Ryzin C, Myles J, Schoenfeld M, McGuire P, Rosing DR, Levin MD, Kopp JB, Venditti CP. Chronic kidney disease in propionic acidemia. Genet Med. 2019 Dec;21(12):2830-2835. doi: 10.1038/s41436-019-0593-z. Epub 2019 Jun 28.
    Balasubramaniam S, Duley JA, Christodoulou J. Inborn errors of pyrimidine metabolism: clinical update and therapy. J Inherit Metab Dis. 2014 Sep;37(5):687-98. doi: 10.1007/s10545-014-9742-3. Epub 2014 Jul 17.
    Chu Y, Sun S, Huang Y, Gao Q, Xie X, Wang P, Li J, Liang L, He X, Jiang Y, Wang M, Yang J, Chen X, Zhou C, Zhao Y, Ding F, Zhang Y, Wu X, Bai X, Wu J, Wei X, Chen X, Yue Z, Fang X, Huang Q, Wang Z, Huang R. Metagenomic analysis revealed the potential role of gut microbiome in gout. NPJ Biofilms Microbiomes. 2021 Aug 9;7(1):66. doi: 10.1038/s41522-021-00235-2.
    Han ST, Kim AC, Garcia K, Schimmenti LA, Macnamara E, Network UD, Gahl WA, Malicdan MC, Tifft CJ. PUS7 deficiency in human patients causes profound neurodevelopmental phenotype by dysregulating protein translation. Mol Genet Metab. 2022 Mar;135(3):221-229. doi: 10.1016/j.ymgme.2022.01.103. Epub 2022 Feb 1.

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    Academic Journal
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    Academic Journal
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    Academic Journal
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    Academic Journal
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    Academic Journal
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    Academic Journal

    المؤلفون: Loison, Gaspard1 (AUTHOR), Bouges Le Royer, Hélène2 (AUTHOR), Marsili, Sabrina1,3 (AUTHOR), Brice, Aurélie1,3 (AUTHOR), Vintejoux, Julien1,3 (AUTHOR), Yakoubi, Malika1,3 (AUTHOR), Sirgue, Hélène1,3 (AUTHOR), Chatelut, Etienne1,3 (AUTHOR), Etienne-Grimaldi, Marie-Christine2 (AUTHOR), Thomas, Fabienne1,3,4,5 (AUTHOR) thomas.fabienne@iuct-oncopole.fr

    المصدر: Clinical Chemistry & Laboratory Medicine. May2024, Vol. 62 Issue 6, pe129-e131. 3p.

  20. 20
    Academic Journal