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 *

191 related articles for article (PubMed ID: 31358688)

  • 1. Associations of
    Xie X; He Q; Huang L; Li L; Yao Y; Xia H; Zhao J; Zhong W; Zhang Y
    Biosci Rep; 2019 Aug; 39(8):. PubMed ID: 31358688
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Association Analysis of SLC6A20 Polymorphisms With Hirschsprung Disease.
    Lee JS; Oh JT; Kim JH; Seo JM; Kim DY; Park KW; Kim HY; Jung K; Park BL; Koh I; Shin HD
    J Pediatr Gastroenterol Nutr; 2016 Jan; 62(1):64-70. PubMed ID: 26049783
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Correlation analysis of IL-11 polymorphisms and Hirschsprung disease subtype susceptibility in Southern Chinese Children.
    Zhang H; Zhao JL; Zheng Y; Xie XL; Huang LH; Li L; Zhu Y; Lu LF; Hu TQ; Zhong W; He QM
    BMC Med Genomics; 2021 Jan; 14(1):21. PubMed ID: 33468134
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Common variation of the NSD1 gene is associated with susceptibility to Hirschsprung's disease in Chinese Han population.
    Yu XX; Chu X; Wu WJ; Wei ZL; Song HL; Bai MR; Lu YJ; Gu BL; Gong YM; Cai W
    Pediatr Res; 2021 Feb; 89(3):694-700. PubMed ID: 32380506
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Associations of CYP2B6 genetic polymorphisms with Hirschsprung's disease in a southern Chinese population.
    Liu Y; Lan C; Li B; Wang N; Zuo X; Huang L; Wu Y; Zhu Y
    J Clin Lab Anal; 2021 Dec; 35(12):e24074. PubMed ID: 34752660
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The single nucleotide polymorphisms in Smad-interacting protein 1 gene contribute to its ectopic expression and susceptibility in Hirschsprung's disease.
    Zhang S; Jiang K; Yuan Z; Wang W
    Exp Mol Pathol; 2014 Apr; 96(2):219-24. PubMed ID: 24576558
    [TBL] [Abstract][Full Text] [Related]  

  • 7. RET polymorphisms and the risk of Hirschsprung's disease in a Chinese population.
    Liu C; Jin L; Li H; Lou J; Luo C; Zhou X; Li JC
    J Hum Genet; 2008; 53(9):825-833. PubMed ID: 18612588
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Associations between common genetic variants in microRNAs and Hirschsprung disease susceptibility in Southern Chinese children.
    Wu Q; Zhao J; Zheng Y; Xie X; He Q; Zhu Y; Wang N; Huang L; Lu L; Hu T; Zeng J; Xia H; Zhang Y; Zhong W
    J Gene Med; 2021 Feb; 23(2):e3301. PubMed ID: 33294994
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease.
    Garcia-Barcelo MM; Tang CS; Ngan ES; Lui VC; Chen Y; So MT; Leon TY; Miao XP; Shum CK; Liu FQ; Yeung MY; Yuan ZW; Guo WH; Liu L; Sun XB; Huang LM; Tou JF; Song YQ; Chan D; Cheung KM; Wong KK; Cherny SS; Sham PC; Tam PK
    Proc Natl Acad Sci U S A; 2009 Feb; 106(8):2694-9. PubMed ID: 19196962
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic basis of Hirschsprung's disease.
    Tam PK; Garcia-Barceló M
    Pediatr Surg Int; 2009 Jul; 25(7):543-58. PubMed ID: 19521704
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The ITGB2 immunomodulatory gene (CD18), enterocolitis, and Hirschsprung's disease.
    Moore SW; Sidler D; Zaahl MG
    J Pediatr Surg; 2008 Aug; 43(8):1439-44. PubMed ID: 18675632
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Altered goblet cell function in Hirschsprung's disease.
    Nakamura H; Tomuschat C; Coyle D; O'Donnel AM; Lim T; Puri P
    Pediatr Surg Int; 2018 Feb; 34(2):121-128. PubMed ID: 29383490
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic variants of IL-11 associated with risk of Hirschsprung disease.
    Kim LH; Cheong HS; Shin JG; Seo JM; Kim DY; Oh JT; Kim HY; Jung K; Koh I; Kim JH; Shin HD
    Neurogastroenterol Motil; 2015 Oct; 27(10):1371-7. PubMed ID: 26172388
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Altered expression of IL36γ and IL36 receptor (IL1RL2) in the colon of patients with Hirschsprung's disease.
    Tomuschat C; O'Donnell AM; Coyle D; Puri P
    Pediatr Surg Int; 2017 Feb; 33(2):181-186. PubMed ID: 27853811
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Susceptibility of
    Wang B; Fang W; Qin D; He Q; Lan C
    Clin Exp Gastroenterol; 2023; 16():59-64. PubMed ID: 37215434
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Study of polymorphisms associated to Hirschsprung's disease].
    Vega Hernández L; Castaño González L; Belar Beitia O; Ruíz Aja E; Martínez Ezquerra N; López Alvarez-Buhilla P
    Cir Pediatr; 2011 Aug; 24(3):131-6. PubMed ID: 22295652
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Potential Association of INMT Nonsynonymous Variant (His46Pro) with Hirschsprung's Disease.
    Kim JY; Seo JM; Kim DY; Oh JT; Park KW; Kim HY; Jung K; Park BL; Kim JH; Shin HD
    Neonatology; 2015; 108(3):164-71. PubMed ID: 26183064
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Fine mapping of the NRG1 Hirschsprung's disease locus.
    Tang CS; Tang WK; So MT; Miao XP; Leung BM; Yip BH; Leon TY; Ngan ES; Lui VC; Chen Y; Chan IH; Chung PH; Liu XL; Wu XZ; Wong KK; Sham PC; Cherny SS; Tam PK; Garcia-Barceló MM
    PLoS One; 2011 Jan; 6(1):e16181. PubMed ID: 21283760
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Exome sequencing identified NRG3 as a novel susceptible gene of Hirschsprung's disease in a Chinese population.
    Yang J; Duan S; Zhong R; Yin J; Pu J; Ke J; Lu X; Zou L; Zhang H; Zhu Z; Wang D; Xiao H; Guo A; Xia J; Miao X; Tang S; Wang G
    Mol Neurobiol; 2013 Jun; 47(3):957-66. PubMed ID: 23315268
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic association of
    Ma Z; Zhong W; Song K; Chen J; Tian B; Chen Y; Li L; Lan C; Zhong W; He Q; Wu Y
    Transl Pediatr; 2024 Aug; 13(8):1395-1405. PubMed ID: 39263294
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.