BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

108 related articles for article (PubMed ID: 9341881)

  • 21. Expression regulation and genomic organization of human polynucleotide phosphorylase, hPNPase(old-35), a Type I interferon inducible early response gene.
    Leszczyniecka M; Su ZZ; Kang DC; Sarkar D; Fisher PB
    Gene; 2003 Oct; 316():143-56. PubMed ID: 14563561
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mammalian G2 regulatory genes and their possible involvement in genetic instability in cancer cells.
    Okayama H; Nagata A; Igarashi M; Suto K; Jinno S
    Princess Takamatsu Symp; 1991; 22():231-8. PubMed ID: 1844245
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Definition of the minimal MEN1 candidate area based on a 5-Mb integrated map of proximal 11q13. The European Consortium on Men1, (GENEM 1; Groupe d'Etude des Néoplasies Endocriniennes Multiples de type 1).
    Courseaux A; Grosgeorge J; Gaudray P; Pannett AA; Forbes SA; Williamson C; Bassett D; Thakker RV; Teh BT; Farnebo F; Shepherd J; Skogseid B; Larsson C; Giraud S; Zhang CX; Salandre J; Calender A
    Genomics; 1996 Nov; 37(3):354-65. PubMed ID: 8938448
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Eighteen new polymorphic markers in the multiple endocrine neoplasia type 1 (MEN1) region.
    Manickam P; Guru SC; Debelenko LV; Agarwal SK; Olufemi SE; Weisemann JM; Boguski MS; Crabtree JS; Wang Y; Roe BA; Lubensky IA; Zhuang Z; Kester MB; Burns AL; Spiegel AM; Marx SJ; Liotta LA; Emmert-Buck MR; Collins FS; Chandrasekharappa SC
    Hum Genet; 1997 Nov; 101(1):102-8. PubMed ID: 9385379
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Cloning of mouse uncoupling protein 3 cDNA and 5'-flanking region, and its genetic map.
    Yoshitomi H; Yamazaki K; Tanaka I
    Gene; 1998 Jul; 215(1):77-84. PubMed ID: 9666083
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A putative human zinc-finger gene (ZFPL1) on 11q13, highly conserved in the mouse and expressed in exocrine pancreas. The European Consortium on MEN 1.
    Höppener JW; De Wit MJ; Simarro-Doorten AY; Roijers JF; van Herrewaarden HM; Lips CJ; Parente F; Quincey D; Gaudray P; Khodaei S; Weber G; Teh B; Farnebo F; Larsson C; Zhang CX; Calender A; Pannett AA; Forbes SA; Bassett JH; Thakker RV; Lemmens I; Van de Ven WJ; Kas K
    Genomics; 1998 Jun; 50(2):251-9. PubMed ID: 9653652
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Diverse modes of alternative splicing of human splicing factor SF1 deduced from the exon-intron structure of the gene.
    Krämer A; Quentin M; Mulhauser F
    Gene; 1998 Apr; 211(1):29-37. PubMed ID: 9573336
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Cloning and chromosomal location of a novel member of the myotonic dystrophy family of protein kinases.
    Zhao Y; Loyer P; Li H; Valentine V; Kidd V; Kraft AS
    J Biol Chem; 1997 Apr; 272(15):10013-20. PubMed ID: 9092543
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The genomic structure of two protein kinase CK2alpha genes of Xenopus laevis and features of the putative promoter region.
    Wilhelm V; Neckelman G; Allende JE; Allende CC
    Mol Cell Biochem; 2001 Nov; 227(1-2):175-83. PubMed ID: 11827169
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Isolation, cDNA, and genomic structure of a conserved gene (NOF) at chromosome 11q13 next to FAU and oriented in the opposite transcriptional orientation.
    Kas K; Lemahieu V; Meyen E; Van de Ven WJ; Merregaert J
    Genomics; 1996 Jun; 34(3):433-6. PubMed ID: 8786148
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genomic organization and transcriptional units at the myotonic dystrophy locus.
    Shaw DJ; McCurrach M; Rundle SA; Harley HG; Crow SR; Sohn R; Thirion JP; Hamshere MG; Buckler AJ; Harper PS
    Genomics; 1993 Dec; 18(3):673-9. PubMed ID: 7905855
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Evaluation and molecular characterization of EHD1, a candidate gene for Bardet-Biedl syndrome 1 (BBS1).
    Haider NB; Searby C; Galperin E; Mintz L; Horowitz M; Stone EM; Sheffield VC
    Gene; 1999 Nov; 240(1):227-32. PubMed ID: 10564830
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Ataxia-telangiectasia locus: sequence analysis of 184 kb of human genomic DNA containing the entire ATM gene.
    Platzer M; Rotman G; Bauer D; Uziel T; Savitsky K; Bar-Shira A; Gilad S; Shiloh Y; Rosenthal A
    Genome Res; 1997 Jun; 7(6):592-605. PubMed ID: 9199932
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Loss of heterozygosity in 11q13-14 regions in gastric neuroendocrine tumors not associated with multiple endocrine neoplasia type 1 syndrome.
    D'Adda T; Keller G; Bordi C; Höfler H
    Lab Invest; 1999 Jun; 79(6):671-7. PubMed ID: 10378509
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Assignment of the human FAU gene to a subregion of chromosome 11q13.
    Kas K; Schoenmakers E; van de Ven W; Weber G; Nordenskjöld M; Michiels L; Merregaert J; Larsson C
    Genomics; 1993 Aug; 17(2):387-92. PubMed ID: 8406491
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Sequence analysis and transcript expression of the MEN1 gene in sporadic pituitary tumours.
    Farrell WE; Simpson DJ; Bicknell J; Magnay JL; Kyrodimou E; Thakker RV; Clayton RN
    Br J Cancer; 1999 Apr; 80(1-2):44-50. PubMed ID: 10389976
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The zebrafish fth1, slc3a2, men1, pc, fgf3 and cycd1 genes define two regions of conserved synteny between linkage group 7 and human chromosome 11q13.
    Yoder JA; Litman GW
    Gene; 2000 Dec; 261(2):235-42. PubMed ID: 11167010
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genomic organization of human myotonic dystrophy kinase-related Cdc42-binding kinase alpha reveals multiple alternative splicing and functional diversity.
    Tan I; Cheong A; Lim L; Leung T
    Gene; 2003 Jan; 304():107-15. PubMed ID: 12568720
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Is myotonic dystrophy a single-gene disorder?
    Johnson KJ; Boucher Ca; King SK; Winchester CL; Bailey ME; Hamilton GM; Carey N
    Biochem Soc Trans; 1996 May; 24(2):510-3. PubMed ID: 8736794
    [No Abstract]   [Full Text] [Related]  

  • 40. The search for the MEN1 gene. The European Consortium on MEN-1.
    J Intern Med; 1998 Jun; 243(6):441-6. PubMed ID: 9681841
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.