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 *

72 related articles for article (PubMed ID: 7806231)

  • 1. The fibulin-1 gene (FBLN1) is located on human chromosome 22 and on mouse chromosome 15.
    Mattei MG; Pan TC; Zhang RZ; Timpl R; Chu ML
    Genomics; 1994 Jul; 22(2):437-8. PubMed ID: 7806231
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fibulin-2 (FBLN2): human cDNA sequence, mRNA expression, and mapping of the gene on human and mouse chromosomes.
    Zhang RZ; Pan TC; Zhang ZY; Mattei MG; Timpl R; Chu ML
    Genomics; 1994 Jul; 22(2):425-30. PubMed ID: 7806230
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Localization of the human gene for fibulin-1 (FBLN1) to chromosome band 22q13.3.
    Korenberg JR; Chen XN; Tran H; Argraves WS
    Cytogenet Cell Genet; 1995; 68(3-4):192-3. PubMed ID: 7842734
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Assignment of the CD45-AP gene to the centromeric end of mouse chromosome 19 and human chromosome 11q13.1-q13.3.
    Takai S; Kozak CA; Kitamura K; Takeda A
    Genomics; 1996 Dec; 38(3):429-31. PubMed ID: 8975722
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cloning of the cDNA encoding human tissue inhibitor of metalloproteinases-3 (TIMP-3) and mapping of the TIMP3 gene to chromosome 22.
    Apte SS; Mattei MG; Olsen BR
    Genomics; 1994 Jan; 19(1):86-90. PubMed ID: 8188246
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Mapping of the ceruloplasmin gene on human and laboratory mouse chromosomes by direct in situ hybridization].
    Baranov VS; Shvartsman AL; Gorbunova VN; Gaĭtskhoki VS; Neĭfakh SA
    Genetika; 1985 Mar; 21(3):409-19. PubMed ID: 3886485
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Mapping of the transferrin gene in laboratory rats, mice and man by direct in situ hybridization].
    Baranov VS; Shvartsman AL; Gorbunova VN; Ryskov AP; Timchenko NA
    Genetika; 1984 Oct; 20(10):1584-93. PubMed ID: 6548721
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Sequence homologies and linkage group conservation of the human and mouse Cenpc genes.
    McKay S; Thomson E; Cooke H
    Genomics; 1994 Jul; 22(1):36-40. PubMed ID: 7959789
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mapping of two genes encoding members of a distinct subfamily of MAX interacting proteins: MAD to human chromosome 2 and mouse chromosome 6, and MXI1 to human chromosome 10 and mouse chromosome 19.
    Edelhoff S; Ayer DE; Zervos AS; Steingrímsson E; Jenkins NA; Copeland NG; Eisenman RN; Brent R; Disteche CM
    Oncogene; 1994 Feb; 9(2):665-8. PubMed ID: 8290278
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Transcript mapping of the human chromosome 11q12-q13.1 gene-rich region identifies several newly described conserved genes.
    Cooper PR; Nowak NJ; Higgins MJ; Church DM; Shows TB
    Genomics; 1998 May; 49(3):419-29. PubMed ID: 9615227
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular cloning of a human RP105 homologue and chromosomal localization of the mouse and human RP105 genes (Ly64 and LY64).
    Miura Y; Miyake K; Yamashita Y; Shimazu R; Copeland NG; Gilbert DJ; Jenkins NA; Inazawa J; Abe T; Kimoto M
    Genomics; 1996 Dec; 38(3):299-304. PubMed ID: 8975706
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Comparative mapping of mouse and rat chromosomes by fluorescence in situ hybridization.
    Grützner F; Himmelbauer H; Paulsen M; Ropers HH; Haaf T
    Genomics; 1999 Feb; 55(3):306-13. PubMed ID: 10049585
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactyly.
    Debeer P; Schoenmakers EF; Twal WO; Argraves WS; De Smet L; Fryns JP; Van De Ven WJ
    J Med Genet; 2002 Feb; 39(2):98-104. PubMed ID: 11836357
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Assignment of the human pancreatic regenerating (REG) gene to chromosome 2p12.
    Perfetti R; Hawkins AL; Griffin CA; Egan JM; Zenilman ME; Shuldiner AR
    Genomics; 1994 Mar; 20(2):305-7. PubMed ID: 8020983
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Evolutionary breakpoints on human chromosome 21.
    Davisson MT; Bechtel LJ; Akeson EC; Fortna A; Slavov D; Gardiner K
    Genomics; 2001 Nov; 78(1-2):99-106. PubMed ID: 11707078
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genomewide homozygosity mapping and molecular analysis of a candidate gene located on 22q13 (fibulin-1) in a previously undescribed vitreoretinal dystrophy.
    Weigell-Weber M; Sarra GM; Kotzot D; Sandkuijl L; Messmer E; Hergersberg M
    Arch Ophthalmol; 2003 Aug; 121(8):1184-8. PubMed ID: 12912698
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The common fragile site FRA16D and its associated gene WWOX are highly conserved in the mouse at Fra8E1.
    Krummel KA; Denison SR; Calhoun E; Phillips LA; Smith DI
    Genes Chromosomes Cancer; 2002 Jun; 34(2):154-67. PubMed ID: 11979549
    [TBL] [Abstract][Full Text] [Related]  

  • 18. YAC contigs of the Rab1 and wobbler (wr) spinal muscular atrophy gene region on proximal mouse chromosome 11 and of the homologous region on human chromosome 2p.
    Wedemeyer N; Lengeling A; Ronsiek M; Korthaus D; Baer K; Wuttke M; Jockusch H
    Genomics; 1996 Mar; 32(3):447-54. PubMed ID: 8838809
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Expression and functional analysis of fibulin-1 (Fbln1) during normal and abnormal placental development of the mouse.
    Singh U; Sun T; Larsson T; Elliott RW; Kostka G; Fundele RH
    Placenta; 2006; 27(9-10):1014-21. PubMed ID: 16338003
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Structure and chromosomal localization of the human PD-1 gene (PDCD1).
    Shinohara T; Taniwaki M; Ishida Y; Kawaichi M; Honjo T
    Genomics; 1994 Oct; 23(3):704-6. PubMed ID: 7851902
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.