These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

111 related articles for article (PubMed ID: 21470889)

  • 1. SLC25A13 gene mutations in Taiwanese patients with non-viral hepatocellular carcinoma.
    Chang KW; Chen HL; Chien YH; Chen TC; Yeh CT
    Mol Genet Metab; 2011 Jul; 103(3):293-6. PubMed ID: 21470889
    [TBL] [Abstract][Full Text] [Related]  

  • 2. High resolution melting analysis for the detection of SLC25A13 gene mutations in Taiwan.
    Lin JT; Hsiao KJ; Chen CY; Wu CC; Lin SJ; Chou YY; Shiesh SC
    Clin Chim Acta; 2011 Feb; 412(5-6):460-5. PubMed ID: 21134364
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Homozygous SLC25A13 mutation in a Taiwanese patient with adult-onset citrullinemia complicated with steatosis and hepatocellular carcinoma.
    Tsai CW; Yang CC; Chen HL; Hwu WL; Wu MZ; Liu KL; Wu MS
    J Formos Med Assoc; 2006 Oct; 105(10):852-6. PubMed ID: 17000460
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mitochondrial aspartate glutamate carrier (citrin) deficiency as the cause of adult-onset type II citrullinemia (CTLN2) and idiopathic neonatal hepatitis (NICCD).
    Saheki T; Kobayashi K
    J Hum Genet; 2002; 47(7):333-41. PubMed ID: 12111366
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Simple and rapid genetic testing for citrin deficiency by screening 11 prevalent mutations in SLC25A13.
    Kikuchi A; Arai-Ichinoi N; Sakamoto O; Matsubara Y; Saheki T; Kobayashi K; Ohura T; Kure S
    Mol Genet Metab; 2012 Apr; 105(4):553-8. PubMed ID: 22277121
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of two novel mutations in the SLC25A13 gene and detection of seven mutations in 102 patients with adult-onset type II citrullinemia.
    Yasuda T; Yamaguchi N; Kobayashi K; Nishi I; Horinouchi H; Jalil MA; Li MX; Ushikai M; Iijima M; Kondo I; Saheki T
    Hum Genet; 2000 Dec; 107(6):537-45. PubMed ID: 11153906
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [SLC25A13 gene mutations in Chinese infants with intrahepatic cholestasis and abnormal blood amino acids].
    Zhang SR; Wang JS; Wang XH; Zhu QR; Liu LY
    Zhonghua Gan Zang Bing Za Zhi; 2008 Jun; 16(6):445-8. PubMed ID: 18578996
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Cloning and sequence analysis of SLC25A13 transcripts in human amniocytes].
    Zhang ZH; Zhao XJ; Song YZ; Tang XM; Zha QB
    Zhongguo Dang Dai Er Ke Za Zhi; 2012 Mar; 14(3):221-5. PubMed ID: 22433413
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Analysis of SLC25A13 gene mutations and prenatal diagnosis for 20 families affected with citrin deficiency].
    Shi S; Tang X; Shi Z; Zha Q; Cheng Y; Zhang Z; Xiao X; Yang Y; Song Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Aug; 35(4):475-479. PubMed ID: 30098237
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Screening of SLC25A13 mutations in early and late onset patients with citrin deficiency and in the Japanese population: Identification of two novel mutations and establishment of multiple DNA diagnosis methods for nine mutations.
    Yamaguchi N; Kobayashi K; Yasuda T; Nishi I; Iijima M; Nakagawa M; Osame M; Kondo I; Saheki T
    Hum Mutat; 2002 Feb; 19(2):122-30. PubMed ID: 11793471
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Studies on the clinical manifestation and SLC25A13 gene mutation of Chinese patients with neonatal intrahepatic cholestasis caused by citrin deficiency].
    Xing YZ; Qiu WJ; Ye J; Han LS; Xu SS; Zhang HW; Gao XL; Wang Y; Gu XF
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr; 27(2):180-5. PubMed ID: 20376801
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Citrin deficiency as a cause of chronic liver disorder mimicking non-alcoholic fatty liver disease.
    Komatsu M; Yazaki M; Tanaka N; Sano K; Hashimoto E; Takei Y; Song YZ; Tanaka E; Kiyosawa K; Saheki T; Aoyama T; Kobayashi K
    J Hepatol; 2008 Nov; 49(5):810-20. PubMed ID: 18620775
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Analysis of SLC25A13 gene mutations in five infants with neonatal intrahepatic cholestasis caused by citrin deficiency].
    Xu J; Gao M; Lyu Y; Tang Y; Wei X; Yang L; Zhang K; Liu Y; Gai Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Feb; 35(1):34-38. PubMed ID: 29419856
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiency.
    Lu YB; Kobayashi K; Ushikai M; Tabata A; Iijima M; Li MX; Lei L; Kawabe K; Taura S; Yang Y; Liu TT; Chiang SH; Hsiao KJ; Lau YL; Tsui LC; Lee DH; Saheki T
    J Hum Genet; 2005; 50(7):338-346. PubMed ID: 16059747
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinicopathological characteristics of PIK3CA and HBx mutations in Korean patients with hepatocellular carcinomas.
    Kim DC; Chung WJ; Lee JH; Jang BK; Hwang JS; Kang KJ; Kwon SY
    APMIS; 2014 Oct; 122(10):1001-6. PubMed ID: 24673525
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Blood glucose and insulin and correlation of SLC25A13 mutations with biochemical changes in NICCD patients.
    Lu CT; Shi QP; Li ZJ; Li J; Feng L
    Exp Biol Med (Maywood); 2017 Jun; 242(12):1271-1278. PubMed ID: 28516797
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hepatic aflatoxin B1-DNA adducts and TP53 mutations in patients with hepatocellular carcinoma despite low exposure to aflatoxin B1 in southern Japan.
    Shirabe K; Toshima T; Taketomi A; Taguchi K; Yoshizumi T; Uchiyama H; Harimoto N; Kajiyama K; Egashira A; Maehara Y
    Liver Int; 2011 Oct; 31(9):1366-72. PubMed ID: 21745313
    [TBL] [Abstract][Full Text] [Related]  

  • 18. SLC25A13 gene analysis in citrin deficiency: sixteen novel mutations in East Asian patients, and the mutation distribution in a large pediatric cohort in China.
    Song YZ; Zhang ZH; Lin WX; Zhao XJ; Deng M; Ma YL; Guo L; Chen FP; Long XL; He XL; Sunada Y; Soneda S; Nakatomi A; Dateki S; Ngu LH; Kobayashi K; Saheki T
    PLoS One; 2013; 8(9):e74544. PubMed ID: 24069319
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular analysis of SLC25A13 gene in human peripheral blood lymphocytes: Marked transcript diversity, and the feasibility of cDNA cloning as a diagnostic tool for citrin deficiency.
    Zhang ZH; Lin WX; Deng M; Zhao XJ; Song YZ
    Gene; 2012 Dec; 511(2):227-34. PubMed ID: 23022256
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Six cases of citrin deficiency in Korea.
    Ko JM; Kim GH; Kim JH; Kim JY; Choi JH; Ushikai M; Saheki T; Kobayashi K; Yoo HW
    Int J Mol Med; 2007 Dec; 20(6):809-15. PubMed ID: 17982687
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.