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 *

47 related articles for article (PubMed ID: 24766504)

  • 1. Protein truncating variants of SLC30A8 reduce type 2 diabetes mellitus risk in humans.
    Yakala GK
    Clin Genet; 2014 Aug; 86(2):121-2. PubMed ID: 24766504
    [No Abstract]   [Full Text] [Related]  

  • 2. Zinc transport and diabetes risk.
    Pearson E
    Nat Genet; 2014 Apr; 46(4):323-4. PubMed ID: 24675520
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Loss-of-function mutations in SLC30A8 protect against type 2 diabetes.
    Flannick J; Thorleifsson G; Beer NL; Jacobs SB; Grarup N; Burtt NP; Mahajan A; Fuchsberger C; Atzmon G; Benediktsson R; Blangero J; Bowden DW; Brandslund I; Brosnan J; Burslem F; Chambers J; Cho YS; Christensen C; Douglas DA; Duggirala R; Dymek Z; Farjoun Y; Fennell T; Fontanillas P; Forsén T; Gabriel S; Glaser B; Gudbjartsson DF; Hanis C; Hansen T; Hreidarsson AB; Hveem K; Ingelsson E; Isomaa B; Johansson S; Jørgensen T; Jørgensen ME; Kathiresan S; Kong A; Kooner J; Kravic J; Laakso M; Lee JY; Lind L; Lindgren CM; Linneberg A; Masson G; Meitinger T; Mohlke KL; Molven A; Morris AP; Potluri S; Rauramaa R; Ribel-Madsen R; Richard AM; Rolph T; Salomaa V; Segrè AV; Skärstrand H; Steinthorsdottir V; Stringham HM; Sulem P; Tai ES; Teo YY; Teslovich T; Thorsteinsdottir U; Trimmer JK; Tuomi T; Tuomilehto J; Vaziri-Sani F; Voight BF; Wilson JG; Boehnke M; McCarthy MI; Njølstad PR; Pedersen O; ; ; Groop L; Cox DR; Stefansson K; Altshuler D
    Nat Genet; 2014 Apr; 46(4):357-63. PubMed ID: 24584071
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Study on protective gene mutations for T2DM appears to have strong implications for drug development.
    Caffrey MK
    Am J Manag Care; 2014 Mar; 20(4 Spec No.):E7. PubMed ID: 25618503
    [No Abstract]   [Full Text] [Related]  

  • 5. The hemochromatosis N144H mutation of SLC11A3 gene in patients with type 2 diabetes.
    Njajou OT; Vaessen N; Oostra B; Heutink P; Van Duijn CM
    Mol Genet Metab; 2002 Mar; 75(3):290-1. PubMed ID: 11914044
    [No Abstract]   [Full Text] [Related]  

  • 6. Mutations in the SLC30A8 gene are not a major cause of MODY or other forms of early-onset, autosomal dominant type 2 diabetes.
    Borowiec M; Thompson R; Powers C; Xu R; Dickey T; Doria A
    Diabetologia; 2007 Oct; 50(10):2224-6. PubMed ID: 17657472
    [No Abstract]   [Full Text] [Related]  

  • 7. Association between FTO, MC4R, SLC30A8, and KCNQ1 gene variants and type 2 diabetes in Saudi population.
    Bazzi MD; Nasr FA; Alanazi MS; Alamri A; Turjoman AA; Moustafa AS; Alfadda AA; Pathan AA; Parine NR
    Genet Mol Res; 2014 Dec; 13(4):10194-203. PubMed ID: 25501231
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Association between rs13266634 C/T polymorphisms of solute carrier family 30 member 8 (SLC30A8) and type 2 diabetes, impaired glucose tolerance, type 1 diabetes--a meta-analysis.
    Xu K; Zha M; Wu X; Yu Z; Yu R; Xu X; Chen H; Yang T
    Diabetes Res Clin Pract; 2011 Feb; 91(2):195-202. PubMed ID: 21131091
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A non-synonymous variant in SLC30A8 is not associated with type 1 diabetes in the Danish population.
    Brorsson C; Bergholdt R; Sjögren M; Eising S; Sørensen KM; Hougaard DM; Orho-Melander M; Groop L; Pociot F
    Mol Genet Metab; 2008 Jul; 94(3):386-8. PubMed ID: 18400535
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association of genetic variations in TCF7L2, SLC30A8, HHEX, LOC387761, and EXT2 with Type 2 diabetes mellitus in Tunisia.
    Kifagi C; Makni K; Boudawara M; Mnif F; Hamza N; Abid M; Granier C; Ayadi H
    Genet Test Mol Biomarkers; 2011 Jun; 15(6):399-405. PubMed ID: 21510814
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Association analysis of genetic polymorphisms of TCF7L2, CDKAL1, SLC30A8, HHEX genes and microvascular complications of type 2 diabetes mellitus].
    Fu LL; Lin Y; Yang ZL; Yin YB
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Apr; 29(2):194-9. PubMed ID: 22487833
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Association of SLC30A8 gene polymorphism with type 2 diabetes, evidence from 46 studies: a meta-analysis.
    Fan M; Li W; Wang L; Gu S; Dong S; Chen M; Yin H; Zheng J; Wu X; Jin J; Jiang X; Cai J; Liu P; Zheng C
    Endocrine; 2016 Aug; 53(2):381-94. PubMed ID: 26832344
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Role of high-risk variants in the development of impaired glucose metabolism was modified by birth weight in Han Chinese.
    Zhang Y; Xiao X; Zhang Z; Ma X; Xu T; Li W; Feng K; Sun Q; Zhang Q
    Diabetes Metab Res Rev; 2015 Nov; 31(8):790-5. PubMed ID: 26109524
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Association between type 2 diabetes in Uygur and polymorphisms of SLC30A8 and its interaction with smoking].
    Su Y; Wang Z; Yao H; Wang T; Ma Q; Zhu J; Wang S; Ma Y
    Zhonghua Liu Xing Bing Xue Za Zhi; 2015 Oct; 36(10):1167-71. PubMed ID: 26837367
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic mutations you want.
    Williams SC
    Proc Natl Acad Sci U S A; 2016 Mar; 113(10):2554-7. PubMed ID: 26957571
    [No Abstract]   [Full Text] [Related]  

  • 16. Interactions between zinc transporter-8 gene (SLC30A8) and plasma zinc concentrations for impaired glucose regulation and type 2 diabetes.
    Shan Z; Bao W; Zhang Y; Rong Y; Wang X; Jin Y; Song Y; Yao P; Sun C; Hu FB; Liu L
    Diabetes; 2014 May; 63(5):1796-803. PubMed ID: 24306209
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Gender-dependent associations of CDKN2A/2B, KCNJ11, POLI, SLC30A8, and TCF7L2 variants with type 2 diabetes in (North African) Tunisian Arabs.
    Turki A; Al-Zaben GS; Khirallah M; Marmouch H; Mahjoub T; Almawi WY
    Diabetes Res Clin Pract; 2014 Mar; 103(3):e40-3. PubMed ID: 24485399
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hemochromatosis caused by mutations in the iron-regulatory proteins ferroportin and H ferritin.
    Press RD
    Mol Diagn; 2001 Dec; 6(4):347. PubMed ID: 11774199
    [No Abstract]   [Full Text] [Related]  

  • 19. [Polymorphic markers TCF7L2 rs12255372 and SLC30A8 rs13266634 confer susceptibility to type 2 diabetes in a Russian population].
    Potapov VA; Shamkhalova MN; Smetanina SA; Bel'chikova LN; Suplotova LA; Shestakova MV; Nosikov VV
    Genetika; 2010 Aug; 46(8):1123-31. PubMed ID: 20873210
    [TBL] [Abstract][Full Text] [Related]  

  • 20. New antigenic targets in type 1 diabetes.
    Wenzlau JM; Hutton JC; Davidson HW
    Curr Opin Endocrinol Diabetes Obes; 2008 Aug; 15(4):315-20. PubMed ID: 18594270
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.