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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

131 related items for PubMed ID: 28977675

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Genetic variants of the MRC1 gene and the IFNG gene are associated with leprosy in Han Chinese from Southwest China.
    Wang D, Feng JQ, Li YY, Zhang DF, Li XA, Li QW, Yao YG.
    Hum Genet; 2012 Jul; 131(7):1251-60. PubMed ID: 22392581
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Association analysis of the genetic polymorphisms with leprosy subtypes in Chinese Han population from Northern China.
    Wang C, Wang Z, Wang H, Pan Q, Fu X, Liu T, Yu G, Liu H, Zhang F.
    J Eur Acad Dermatol Venereol; 2018 Oct; 32(10):e377-e379. PubMed ID: 29575217
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Common variants of OPA1 conferring genetic susceptibility to leprosy in Han Chinese from Southwest China.
    Xiang YL, Zhang DF, Wang D, Li YY, Yao YG.
    J Dermatol Sci; 2015 Nov; 80(2):133-41. PubMed ID: 26360011
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. APOE rs405509 polymorphism and Parkinson's disease risk in the Chinese population.
    Huang M, Wang Y, Wang L, Chen B, Wang X, Hu Y.
    Neurosci Lett; 2020 Sep 25; 736():135256. PubMed ID: 32682842
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. The association of apolipoprotein E gene polymorphisms with cerebral palsy in Chinese infants.
    Xu Y, Wang H, Sun Y, Shang Q, Chen M, Li T, Zhu D, He L, Zhu C, Xing Q.
    Mol Genet Genomics; 2014 Jun 25; 289(3):411-6. PubMed ID: 24522486
    [Abstract] [Full Text] [Related]

  • 14. CUBN and NEBL common variants in the chromosome 10p13 linkage region are associated with multibacillary leprosy in Vietnam.
    Grant AV, Cobat A, Van Thuc N, Orlova M, Huong NT, Gaschignard J, Alter A, Ba NN, Thai VH, Abel L, Alcaïs A, Schurr E.
    Hum Genet; 2014 Jul 25; 133(7):883-93. PubMed ID: 24563210
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. The Association of MME microRNA Binding Site Polymorphism with the Risk of Late Onset Alzheimer's Disease in Northern Han Chinese.
    Liu CX, Tan L, Sun FR, Zhang W, Miao D, Tan MS, Wan Y, Tan CC, Yu JT, Tan L.
    Curr Neurovasc Res; 2017 Jul 25; 14(2):90-95. PubMed ID: 28294061
    [Abstract] [Full Text] [Related]

  • 17. Common variants in the PARL and PINK1 genes increase the risk to leprosy in Han Chinese from South China.
    Wang D, Zhang DF, Feng JQ, Li GD, Li XA, Yu XF, Long H, Li YY, Yao YG.
    Sci Rep; 2016 Nov 23; 6():37086. PubMed ID: 27876828
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Genetic variants in PVRL2-TOMM40-APOE region are associated with human longevity in a Han Chinese population.
    Lu F, Guan H, Gong B, Liu X, Zhu R, Wang Y, Qian J, Zhou T, Lan X, Wang P, Lin Y, Ma S, Lin H, Zhu X, Chen R, Zhu X, Shi Y, Yang Z.
    PLoS One; 2014 Nov 23; 9(6):e99580. PubMed ID: 24924924
    [Abstract] [Full Text] [Related]

  • 20. The polymorphism of the ATP-binding cassette transporter 1 gene modulates Alzheimer disease risk in Chinese Han ethnic population.
    Sun YM, Li HL, Guo QH, Wu P, Hong Z, Lu CZ, Wu ZY.
    Am J Geriatr Psychiatry; 2012 Jul 23; 20(7):603-11. PubMed ID: 22377775
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.