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 *

144 related articles for article (PubMed ID: 36505279)

  • 1. Associations between
    Ma Q; Yang Y; Liu Y
    Am J Transl Res; 2022; 14(11):8407-8415. PubMed ID: 36505279
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Single nucleotide polymorphism of NKX2-5 gene with sporadic congenital heart disease in Chinese Bai population.
    Cao Y; Lan W; Li Y; Wei C; Zou H; Jiang L
    Int J Clin Exp Pathol; 2015; 8(11):14917-24. PubMed ID: 26823822
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic variations of NKX2-5 in sporadic atrial septal defect and ventricular septal defect in Chinese Yunnan population.
    Cao Y; Wang J; Wei C; Hou Z; Li Y; Zou H; Meng M; Wang W; Jiang L
    Gene; 2016 Jan; 575(1):29-33. PubMed ID: 26297999
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Frequency distribution of single nucleotide polymorphisms in P-selectin gene in Chinese Tibetan and Han populations.
    Zeng TT; Ye YX; Niu Q; Lu XJ; An YF; Li XP; Jiang H
    Gene; 2012 May; 499(2):352-6. PubMed ID: 22425972
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [NKX2.5 and TBX5 gene mutations in in vitro fertilization children with congenital heart disease].
    Yang JH; Xu XY; Mi HY; Jiang Y; Ma XM; Li L
    Zhongguo Dang Dai Er Ke Za Zhi; 2017 Jun; 19(6):652-657. PubMed ID: 28606231
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel Point Mutations in the
    Khatami M; Mazidi M; Taher S; Heidari MM; Hadadzadeh M
    Medicina (Kaunas); 2018 Jun; 54(3):. PubMed ID: 30344277
    [No Abstract]   [Full Text] [Related]  

  • 7. Investigation of Somatic NKX2-5 Mutations in Chinese Children with Congenital Heart Disease.
    Zheng J; Li F; Liu J; Xu Z; Zhang H; Fu Q; Wang J; Sun K
    Int J Med Sci; 2015; 12(7):538-43. PubMed ID: 26180509
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Single-nucleotide polymorphisms of NKX2.5 found in congenital heart disease patients of Mysore, South India.
    Dinesh SM; Kusuma L; Smitha R; Savitha MR; Krishnamurthy B; Narayanappa D; Ramachandra NB
    Genet Test Mol Biomarkers; 2010 Dec; 14(6):873-9. PubMed ID: 21091212
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Association of Maternal Diabetes Mellitus and Polymorphisms of the
    Zhao M; Diao J; Huang P; Li J; Li Y; Yang Y; Luo L; Zhang S; Chen L; Wang T; Zhu P; Qin J
    J Diabetes Res; 2020; 2020():3854630. PubMed ID: 33062711
    [TBL] [Abstract][Full Text] [Related]  

  • 10. AKT3, ANGPTL4, eNOS3, and VEGFA associations with high altitude sickness in Han and Tibetan Chinese at the Qinghai-Tibetan Plateau.
    Buroker NE; Ning XH; Zhou ZN; Li K; Cen WJ; Wu XF; Zhu WZ; Scott CR; Chen SH
    Int J Hematol; 2012 Aug; 96(2):200-13. PubMed ID: 22729570
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Preliminary exploration of transcription factor Nkx2.5 mutations and congenital heart diseases].
    Ding JD; Li KR; Zhang XL; Yao YY; Reng LQ; Tao SY; Fang X; Ma GS
    Zhonghua Yi Xue Za Zhi; 2009 Apr; 89(16):1114-6. PubMed ID: 19595143
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutations in EPAS1 in congenital heart disease in Tibetans.
    Pan H; Chen Q; Qi S; Li T; Liu B; Liu S; Ma X; Wang B
    Biosci Rep; 2018 Dec; 38(6):. PubMed ID: 30487161
    [No Abstract]   [Full Text] [Related]  

  • 13. Associations of NKX2-5 Genetic Polymorphisms with the Risk of Congenital Heart Disease: A Meta-analysis.
    Xie X; Shi X; Xun X; Rao L
    Pediatr Cardiol; 2016 Jun; 37(5):953-61. PubMed ID: 27033241
    [TBL] [Abstract][Full Text] [Related]  

  • 14. An EPAS1 haplotype is associated with high altitude polycythemia in male Han Chinese at the Qinghai-Tibetan plateau.
    Chen Y; Jiang C; Luo Y; Liu F; Gao Y
    Wilderness Environ Med; 2014 Dec; 25(4):392-400. PubMed ID: 25239027
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Association of Gene Polymorphisms in Wnt Signal Pathway with Tuberculosis in Chinese Tibetan Population.].
    Zhou WJ; Hu XJ; Zhang JY; Zhou Y; Wu LJ; Wang MJ; Wang N; Lu XJ; Ying BW
    Sichuan Da Xue Xue Bao Yi Xue Ban; 2016 Nov; 47(6):920-925. PubMed ID: 28598125
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic and functional analysis of the NKX2-5 gene promoter in patients with ventricular septal defects.
    Pang S; Shan J; Qiao Y; Ma L; Qin X; Wanyan H; Xing Q; Wu G; Yan B
    Pediatr Cardiol; 2012 Dec; 33(8):1355-61. PubMed ID: 22576768
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Screening NKX2.5 mutation in a sample of 230 Han Chinese children with congenital heart diseases.
    Zhang W; Li X; Shen A; Jiao W; Guan X; Li Z
    Genet Test Mol Biomarkers; 2009 Apr; 13(2):159-62. PubMed ID: 19371212
    [TBL] [Abstract][Full Text] [Related]  

  • 18. EPAS1 Gene Polymorphisms Are Associated With High Altitude Polycythemia in Tibetans at the Qinghai-Tibetan Plateau.
    Xu J; Yang YZ; Tang F; Ga Q; Tana W; Ge RL
    Wilderness Environ Med; 2015 Sep; 26(3):288-94. PubMed ID: 25792003
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association of NKX2-5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children.
    Behiry EG; Al-Azzouny MA; Sabry D; Behairy OG; Salem NE
    Mol Genet Genomic Med; 2019 May; 7(5):e612. PubMed ID: 30834692
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Differentiation analysis for estimating individual ancestry from the Tibetan Plateau by an archaic altitude adaptation EPAS1 haplotype among East Asian populations.
    Jiang L; Peng J; Huang M; Liu J; Wang L; Ma Q; Zhao H; Yang X; Ji A; Li C
    Int J Legal Med; 2018 Nov; 132(6):1527-1535. PubMed ID: 29428968
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.