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 *

145 related articles for article (PubMed ID: 7511123)

  • 1. Insertional mutation on mouse chromosome 18 with vestibular and craniofacial abnormalities.
    Ting CN; Kohrman D; Burgess DL; Boyle A; Altschuler RA; Gholizadeh G; Samuelson LC; Jang W; Meisler MH
    Genetics; 1994 Jan; 136(1):247-54. PubMed ID: 7511123
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Optic, olfactory, and vestibular dysmorphogenesis in the homozygous mouse insertional mutant Tg9257.
    Griffith AJ; Ji W; Prince ME; Altschuler RA; Meisler MH
    J Craniofac Genet Dev Biol; 1999; 19(3):157-63. PubMed ID: 10589397
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A transgenic insertional inner ear mutation on mouse chromosome 1.
    Friedman RA; Adir Y; Crenshaw EB; Ryan AF; Rosenfeld MG
    Laryngoscope; 2000 Apr; 110(4):489-96. PubMed ID: 10763993
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus.
    Keller SA; Jones JM; Boyle A; Barrow LL; Killen PD; Green DG; Kapousta NV; Hitchcock PF; Swank RT; Meisler MH
    Genomics; 1994 Sep; 23(2):309-20. PubMed ID: 7835879
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Heterozygosity mapping of partially congenic lines: mapping of a semidominant neurological mutation, Wheels (Whl), on mouse chromosome 4.
    Nolan PM; Sollars PJ; Bohne BA; Ewens WJ; Pickard GE; Bućan M
    Genetics; 1995 May; 140(1):245-54. PubMed ID: 7635289
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Transgene-induced mutation of the murine steel locus.
    Keller SA; Liptay S; Hajra A; Meisler MH
    Proc Natl Acad Sci U S A; 1990 Dec; 87(24):10019-22. PubMed ID: 1979872
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Perinatal lethality (ple): a mutation caused by integration of a transgene into distal mouse chromosome 15.
    Beier DR; Morton CC; Leder A; Wallace R; Leder P
    Genomics; 1989 May; 4(4):498-504. PubMed ID: 2744761
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The genomic structure of an insertional mutation in the dystonia musculorum locus.
    Brown A; Copeland NG; Gilbert DJ; Jenkins NA; Rossant J; Kothary R
    Genomics; 1994 Apr; 20(3):371-6. PubMed ID: 8034309
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Phenotypic characterization of the transgenic mouse insertional mutation, legless.
    McNeish JD; Thayer J; Walling K; Sulik KK; Potter SS; Scott WJ
    J Exp Zool; 1990 Feb; 253(2):151-62. PubMed ID: 2313245
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Close linkage of a transgene insertion site to the steel (Sl) locus on mouse chromosome 10.
    Beier DR; Chaillet JR; Schmidt EV; Leder P
    Genomics; 1991 Aug; 10(4):1003-8. PubMed ID: 1655629
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Insertional mutation of the hairless locus on mouse chromosome 14.
    Jones JM; Elder JT; Simin K; Keller SA; Meisler MH
    Mamm Genome; 1993 Nov; 4(11):639-43. PubMed ID: 8281013
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Phenotypic and molecular analysis of a transgenic insertional allele of the mouse Fused locus.
    Perry WL; Vasicek TJ; Lee JJ; Rossi JM; Zeng L; Zhang T; Tilghman SM; Costantini F
    Genetics; 1995 Sep; 141(1):321-32. PubMed ID: 8536979
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A new mouse insertional mutation that causes sensorineural deafness and vestibular defects.
    Alagramam KN; Kwon HY; Cacheiro NL; Stubbs L; Wright CG; Erway LC; Woychik RP
    Genetics; 1999 Aug; 152(4):1691-9. PubMed ID: 10430593
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Tight-skin (Tsk) maps on mouse chromosome 2 within the region of linkage homology with human chromosome 15.
    Douté RC; Clark SH
    Genomics; 1994 Jul; 22(1):223-5. PubMed ID: 7959775
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Evidence for allelism of the recessive insertional mutation add and the dominant mouse mutation extra-toes (Xt).
    Pohl TM; Mattei MG; Rüther U
    Development; 1990 Dec; 110(4):1153-7. PubMed ID: 1983115
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of the hotfoot (ho) locus by creation of an insertional mutation in a transgenic mouse.
    Gordon JW; Uehlinger J; Dayani N; Talansky BE; Gordon M; Rudomen GS; Neumann PE
    Dev Biol; 1990 Feb; 137(2):349-58. PubMed ID: 1689261
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic mapping of an insertional hydrocephalus-inducing mutation allelic to hy3.
    Robinson ML; Allen CE; Davy BE; Durfee WJ; Elder FF; Elliott CS; Harrison WR
    Mamm Genome; 2002 Nov; 13(11):625-32. PubMed ID: 12461648
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPO.
    Griffith AJ; Burgess DL; Kohrman DC; Yu J; Blaschak J; Blanton SH; Boehnke M; Hecht JT; Overhauser J; Meisler MH
    Genomics; 1996 Jun; 34(3):299-303. PubMed ID: 8786128
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Linkage mapping around the ragged (Ra) and wasted (wst) loci on distal mouse chromosome 2.
    Abbott C; Malas S; Pilz A; Pate L; Ali R; Peters J
    Genomics; 1994 Mar; 20(1):94-8. PubMed ID: 8020960
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mapping the mouse craniofacial mutation first arch (Far) to chromosome 2.
    Juriloff DM; Harris MJ
    J Hered; 1991; 82(5):402-5. PubMed ID: 1940283
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.