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 *

113 related articles for article (PubMed ID: 24466774)

  • 1. [Gene detection of GPD1-L and the association with sudden unexplained death syndrome in young adults].
    Xu XL; Wang W; Liu C; Hou YD; Huang L; Liu CH; Li Y; Cheng JD
    Fa Yi Xue Za Zhi; 2013 Oct; 29(5):348-52. PubMed ID: 24466774
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome.
    Van Norstrand DW; Valdivia CR; Tester DJ; Ueda K; London B; Makielski JC; Ackerman MJ
    Circulation; 2007 Nov; 116(20):2253-9. PubMed ID: 17967976
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Is sudden unexplained nocturnal death syndrome in Southern China a cardiac sodium channel dysfunction disorder?
    Liu C; Tester DJ; Hou Y; Wang W; Lv G; Ackerman MJ; Makielski JC; Cheng J
    Forensic Sci Int; 2014 Mar; 236():38-45. PubMed ID: 24529773
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Postmortem genetic screening of SNPs in RyR2 gene in sudden unexplained nocturnal death syndrome in the southern Chinese Han population.
    Huang L; Liu C; Tang S; Su T; Cheng J
    Forensic Sci Int; 2014 Feb; 235():14-8. PubMed ID: 24447446
    [TBL] [Abstract][Full Text] [Related]  

  • 5. GJA1 gene variations in sudden unexplained nocturnal death syndrome in the Chinese Han population.
    Wu Q; Wu Y; Zhang L; Zheng J; Tang S; Cheng J
    Forensic Sci Int; 2017 Jan; 270():178-182. PubMed ID: 27992820
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Correlation between Genetic Variants and Polymorphism of Caveolin and Sudden Unexplained Death].
    Wu FY; Tang XH; Gai LL; Kong XP; Hao B; Huang EW; Shi H; Sheng LH; Quan L; Liu SP; Luo B
    Fa Yi Xue Za Zhi; 2017 Apr; 33(2):114-119. PubMed ID: 29231014
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [KCNQ1, KCNH2, KCNE1 and KCNE2 potassium channels gene variants in sudden manhood death syndrome].
    Zhao QH; Liu C; Lu LW; Lü GL; Liu H; Tang SB; Quan L; Cheng JD
    Fa Yi Xue Za Zhi; 2012 Oct; 28(5):337-41, 346. PubMed ID: 23213782
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Association of common and rare variants of SCN10A gene with sudden unexplained nocturnal death syndrome in Chinese Han population.
    Zhang L; Zhou F; Huang L; Wu Q; Zheng J; Wu Y; Yin K; Cheng J
    Int J Legal Med; 2017 Jan; 131(1):53-60. PubMed ID: 27272739
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation analysis of the glycerol-3 phosphate dehydrogenase-1 like (GPD1L) gene in Japanese patients with Brugada syndrome.
    Makiyama T; Akao M; Haruna Y; Tsuji K; Doi T; Ohno S; Nishio Y; Kita T; Horie M
    Circ J; 2008 Oct; 72(10):1705-6. PubMed ID: 18762705
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic variants in KCNE1, KCNQ1, and NOS1AP in sudden unexplained death during daily activities in Chinese Han population.
    Huang J; Wang X; Hao B; Chen Y; Liu H; Quan L; Tang D; Sheng L; Li M; Huang E; Liu C; Luo B
    J Forensic Sci; 2015 Mar; 60(2):351-6. PubMed ID: 25639344
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Postmortem molecular analysis of KCNQ1, KCNH2, KCNE1 and KCNE2 genes in sudden unexplained nocturnal death syndrome in the Chinese Han population.
    Liu C; Zhao Q; Su T; Tang S; Lv G; Liu H; Quan L; Cheng J
    Forensic Sci Int; 2013 Sep; 231(1-3):82-7. PubMed ID: 23890619
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Correlation of NOS1AP gene polymorphisms with sudden unexpected death in Chinese Han population].
    Huang JL; Hao B; Wang XG; Liu H; Li M; Quan L; Sheng LH; Liu C; Luo B
    Fa Yi Xue Za Zhi; 2014 Feb; 30(1):27-30, 35. PubMed ID: 24804380
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Biallelic mutations in GPD1 gene in a Chinese boy mainly presented with obesity, insulin resistance, fatty liver, and short stature.
    Li N; Chang G; Xu Y; Ding Y; Li G; Yu T; Yao R; Li J; Shen Y; Wang X; Wang J
    Am J Med Genet A; 2017 Dec; 173(12):3189-3194. PubMed ID: 28944580
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of the G994T polymorphism in exon 9 of plasma platelet-activating factor acetylhydrolase gene as a risk factor for polycystic ovary syndrome.
    Fan P; Liu HW; Wang XS; Zhang F; Song Q; Li Q; Wu HM; Bai H
    Hum Reprod; 2010 May; 25(5):1288-94. PubMed ID: 20185515
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel homozygous mutation in the glycerol-3-phosphate dehydrogenase 1 gene in a Chinese patient with transient infantile hypertriglyceridemia: a case report.
    Li JQ; Xie XB; Feng JY; Chen L; Abuduxikuer K; Lu Y; Li YC; Wang JS
    BMC Gastroenterol; 2018 Jun; 18(1):96. PubMed ID: 29940878
    [TBL] [Abstract][Full Text] [Related]  

  • 16. HCN4 Gene Variations in Sudden Unexplained Nocturnal Death Syndrome in the Southern Han Chinese Population.
    Wu Q; Zhao Q; Yin K; Hu BJ; Cheng J
    J Forensic Sci; 2019 Jul; 64(4):1112-1118. PubMed ID: 30452770
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Germline mutation analysis of hPMS2 gene in Chinese families with hereditary nonpolyposis colorectal cancer.
    Sheng X; Zhou HH; Zhou XY; Du X; Zhang TM; Cai SJ; Sheng WQ; Shi DR
    World J Gastroenterol; 2010 Aug; 16(30):3847-52. PubMed ID: 20698049
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations in the SCN5A gene: evidence for a link between long QT syndrome and sudden death?
    Kiehne N; Kauferstein S
    Forensic Sci Int Genet; 2007 Jun; 1(2):170-4. PubMed ID: 19083750
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Association of the exon 8 and intron 8 polymorphisms of the human urate transporter 1 gene with primary hyperuricemia in Chinese Han population].
    Meng DM; Han L; Miao ZM; Li CG
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Dec; 27(6):659-63. PubMed ID: 21154327
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Proinflammatory cytokine gene polymorphisms among Hashimoto's thyroiditis patients.
    Chen RH; Chang CT; Chen WC; Tsai CH; Tsai FJ
    J Clin Lab Anal; 2006; 20(6):260-5. PubMed ID: 17115419
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.