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 *

64 related articles for article (PubMed ID: 10851274)

  • 21. Mutation screening and identification of a sequence variation in the human ob gene coding region.
    Considine RV; Considine EL; Williams CJ; Nyce MR; Zhang P; Opentanova I; Ohannesian JP; Kolaczynski JW; Bauer TL; Moore JH; Caro JF
    Biochem Biophys Res Commun; 1996 Mar; 220(3):735-9. PubMed ID: 8607834
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mutations in the hepatocyte nuclear factor-4alpha gene in Japanese with non-insulin-dependent diabetes: a nucleotide substitution in the polypyrimidine tract of intron 1b.
    Sakurai K; Seki N; Fujii R; Yagui K; Tokuyama Y; Shimada F; Makino H; Suzuki Y; Hashimoto N; Saito Y; Egashira T; Matsui K; Kanatsuka A
    Horm Metab Res; 2000 Aug; 32(8):316-20. PubMed ID: 10983627
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Sulfonylurea receptor 1 gene variants are associated with gestational diabetes and type 2 diabetes but not with altered secretion of insulin.
    Rissanen J; Markkanen A; Kärkkäinen P; Pihlajamäki J; Kekäläinen P; Mykkänen L; Kuusisto J; Karhapää P; Niskanen L; Laakso M
    Diabetes Care; 2000 Jan; 23(1):70-3. PubMed ID: 10857971
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mutation analysis of NR0B2 among 1545 Danish men identifies a novel c.278G>A (p.G93D) variant with reduced functional activity.
    Echwald SM; Andersen KL; Sørensen TI; Larsen LH; Andersen T; Tonooka N; Tomura H; Takeda J; Pedersen O
    Hum Mutat; 2004 Nov; 24(5):381-7. PubMed ID: 15459958
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Cytochemical analysis of pancreatic islet hypercytolipidemia following diabetes (db/db) and obese (ob/ob) mutation expression: influence of genomic background.
    Garris DR; Garris BL
    Pathobiology; 2004; 71(5):231-40. PubMed ID: 15459481
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Association between Pro12Ala polymorphism of the PPAR-gamma2 gene and insulin sensitivity in Brazilian patients with type-2 diabetes mellitus.
    Tavares V; Hirata RD; Rodrigues AC; Monte O; Salles JE; Scalissi N; Speranza AC; Hirata MH
    Diabetes Obes Metab; 2005 Sep; 7(5):605-11. PubMed ID: 16050954
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [SSCP (single strand conformation polymorphism) analysis for detection of point mutations. A technique and its limits exemplified by dominantly inherited forms of diabetes (MODY)].
    Ziemssen F; Schnepf R; Pfeiffer A
    Med Klin (Munich); 2001 Sep; 96(9):515-20. PubMed ID: 11603114
    [TBL] [Abstract][Full Text] [Related]  

  • 28. No abnormalities of reg1 alpha and reg1 beta gene associated with diabetes mellitus.
    Banchuin N; Boonyasrisawat W; Pulsawat P; Vannasaeng S; Deerochanawong C; Sriussadaporn S; Ploybutr S; Pasurakul T; Yenchitsomanus PT
    Diabetes Res Clin Pract; 2002 Feb; 55(2):105-11. PubMed ID: 11796176
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The adipocyte specific transcription factor C/EBPalpha modulates human ob gene expression.
    Miller SG; De Vos P; Guerre-Millo M; Wong K; Hermann T; Staels B; Briggs MR; Auwerx J
    Proc Natl Acad Sci U S A; 1996 May; 93(11):5507-11. PubMed ID: 8643605
    [TBL] [Abstract][Full Text] [Related]  

  • 30. High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes.
    Lehto M; Wipemo C; Ivarsson SA; Lindgren C; Lipsanen-Nyman M; Weng J; Wibell L; Widén E; Tuomi T; Groop L
    Diabetologia; 1999 Sep; 42(9):1131-7. PubMed ID: 10447526
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Nucleotide sequences at intron 6 and exon 7 junction of fibroblast growth factor receptor 2 and rapid mutational analysis in Apert syndrome].
    Wada C; Ishigaki M; Toyo-oka Y; Yamabe H; Ohnuki Y; Takada F; Yamazaki Y; Ohtani H
    Rinsho Byori; 1996 May; 44(5):435-8. PubMed ID: 8676562
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Metabolic effects of the Gly1057Asp polymorphism in IRS-2 and interactions with obesity.
    Stefan N; Kovacs P; Stumvoll M; Hanson RL; Lehn-Stefan A; Permana PA; Baier LJ; Tataranni PA; Silver K; Bogardus C
    Diabetes; 2003 Jun; 52(6):1544-50. PubMed ID: 12765968
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Polymorphism in intron 2 of islet amyloid polypeptide gene is associated with lower low-density lipoprotein cholesterol in nondiabetic subjects and in type 2 diabetic patients.
    Rojas I; Gomis R; Casals E; Quintó LI; Franco C; Novials A
    Endocrine; 2002 Nov; 19(2):185-9. PubMed ID: 12588049
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genetic analysis of the insulin receptor gene in Chinese patients with extreme insulin resistance.
    Lee WJ; Sheu WH; Shu SG; Yao YE
    Zhonghua Yi Xue Za Zhi (Taipei); 1998 Nov; 61(11):636-42. PubMed ID: 9872020
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Detection of heterozygous mutations in the RB1 gene in retinoblastoma patients using single-strand conformation polymorphism analysis and polymerase chain reaction sequencing.
    Hogg A; Onadim Z; Baird PN; Cowell JK
    Oncogene; 1992 Jul; 7(7):1445-51. PubMed ID: 1352398
    [TBL] [Abstract][Full Text] [Related]  

  • 36. PAX6 gene variations associated with aniridia in south India.
    Neethirajan G; Krishnadas SR; Vijayalakshmi P; Shashikant S; Sundaresan P
    BMC Med Genet; 2004 Apr; 5():9. PubMed ID: 15086958
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Characterisation of CAH alleles with non-radioactive DNA single strand conformation polymorphism analysis of the CYP21 gene.
    Bobba A; Iolascon A; Giannattasio S; Albrizio M; Sinisi A; Prisco F; Schettini F; Marra E
    J Med Genet; 1997 Mar; 34(3):223-8. PubMed ID: 9132494
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genetic variants in promoters and coding regions of the muscle glycogen synthase and the insulin-responsive GLUT4 genes in NIDDM.
    Bjørbaek C; Echwald SM; Hubricht P; Vestergaard H; Hansen T; Zierath J; Pedersen O
    Diabetes; 1994 Aug; 43(8):976-83. PubMed ID: 8039605
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Detection of mutations in insulin-receptor gene in NIDDM patients by analysis of single-stranded conformation polymorphisms.
    O'Rahilly S; Choi WH; Patel P; Turner RC; Flier JS; Moller DE
    Diabetes; 1991 Jun; 40(6):777-82. PubMed ID: 2040394
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Linkage and molecular scanning analyses of MODY3/hepatocyte nuclear factor-1 alpha gene in typical familial type 2 diabetes: evidence for novel mutations in exons 8 and 10.
    Elbein SC; Teng K; Yount P; Scroggin E
    J Clin Endocrinol Metab; 1998 Jun; 83(6):2059-65. PubMed ID: 9626139
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.