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 *

173 related articles for article (PubMed ID: 22433413)

  • 1. [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]  

  • 2. Cloning and sequence analysis of SLC25A13 transcripts in human amniocytes.
    Zhang ZH; Zhao XJ; Song YZ; Tang XM; Zha QB
    Transl Pediatr; 2012 Oct; 1(2):85-90. PubMed ID: 26835269
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. 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]  

  • 5. [SLC25A13 gene mutation analysis in a pedigree of neonatal intrahepatic cholestasis caused by citrin deficiency].
    Song YZ; Ushikai M; Sheng JS; Iijima M; Kobayashi K
    Zhonghua Er Ke Za Zhi; 2007 Jun; 45(6):408-12. PubMed ID: 17880783
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Identification and diagnosis of three novel mutations in SLC25A13 gene of neonatal intrahepatic cholestasis caused by citrin deficiency].
    Song YZ; Sheng JS; Ushikai M; Hwu WL; Zhang CH; Kobayashi K
    Zhonghua Er Ke Za Zhi; 2008 Jun; 46(6):411-5. PubMed ID: 19099775
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Neonatal intrahepatic cholestasis caused by citrin deficiency: clinical and laboratory investigation of 13 subjects in mainland of China.
    Song YZ; Li BX; Chen FP; Liu SR; Sheng JS; Ushikai M; Zhang CH; Zhang T; Wang ZN; Kobayashi K; Saheki T; Zheng XY
    Dig Liver Dis; 2009 Sep; 41(9):683-9. PubMed ID: 19185551
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Neonatal intrahepatic cholestasis caused by citrin deficiency in two Malaysian siblings: outcome at one year of life.
    Thong MK; Boey CC; Sheng JS; Ushikai M; Kobayashi K
    Singapore Med J; 2010 Jan; 51(1):e12-4. PubMed ID: 20200759
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [Progresses and perspectives in the study on citrin deficiency].
    Lu YB; Peng F; Li MX; Kobayashi K; Saheki T
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Dec; 23(6):655-8. PubMed ID: 17160946
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [A difficult and complicated case study: neonatal intrahepatic cholestasis caused by citrin deficiency].
    Song YZ; Hao H; Ushikai M; Liu GS; Xiao X; Saheki T; Kobayashi K; Wang ZN
    Zhongguo Dang Dai Er Ke Za Zhi; 2006 Apr; 8(2):125-8. PubMed ID: 16613706
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Utilization of high-resolution melting analysis to screen patients with neonatal intrahepatic cholestasis caused by citrin deficiency].
    Wen PQ; Wang GB; Chen ZL; Cui D; Liu XH; Ying LF; Song P; Yuan Q; Chen SL; Liao JX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Apr; 29(2):167-71. PubMed ID: 22487826
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [SLC25A13 gene analysis in neonates with intrahepatic cholestasis caused by citrin deficiency].
    Wen PQ; Wang GB; Chen ZL; Cui D; Yuan Q; Song P; Chen SL; Liao JX; Li CR
    Zhongguo Dang Dai Er Ke Za Zhi; 2011 Apr; 13(4):303-8. PubMed ID: 21507300
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of a Large SLC25A13 Deletion via Sophisticated Molecular Analyses Using Peripheral Blood Lymphocytes in an Infant with Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency (NICCD): A Clinical and Molecular Study.
    Zheng QQ; Zhang ZH; Zeng HS; Lin WX; Yang HW; Yin ZN; Song YZ
    Biomed Res Int; 2016; 2016():4124263. PubMed ID: 27127784
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Neonatal intrahepatic cholestasis caused by citrin deficiency in Korean infants.
    Ko JS; Song JH; Park SS; Seo JK
    J Korean Med Sci; 2007 Dec; 22(6):952-6. PubMed ID: 18162705
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel mutation of the SLC25A13 gene in a Chinese patient with citrin deficiency detected by target next-generation sequencing.
    Liu G; Wei X; Chen R; Zhou H; Li X; Sun Y; Xie S; Zhu Q; Qu N; Yang G; Chu Y; Wu H; Lan Z; Wang J; Yang Y; Yi X
    Gene; 2014 Jan; 533(2):547-53. PubMed ID: 24161253
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The mutation spectrum of the SLC25A13 gene in Chinese infants with intrahepatic cholestasis and aminoacidemia.
    Fu HY; Zhang SR; Wang XH; Saheki T; Kobayashi K; Wang JS
    J Gastroenterol; 2011 Apr; 46(4):510-8. PubMed ID: 20927635
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Neonatal intrahepatic cholestasis caused by citrin deficiency: severe hepatic dysfunction in an infant requiring liver transplantation.
    Tamamori A; Okano Y; Ozaki H; Fujimoto A; Kajiwara M; Fukuda K; Kobayashi K; Saheki T; Tagami Y; Yamano T
    Eur J Pediatr; 2002 Nov; 161(11):609-13. PubMed ID: 12424587
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Multiple ovarian antral follicles in a preterm infant with neonatal intrahepatic cholestasis caused by citrin deficiency: a clinical, genetic and transcriptional analysis.
    Lin WX; Zhang ZH; Deng M; Cai XR; Song YZ
    Gene; 2012 Sep; 505(2):269-75. PubMed ID: 22710133
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.