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 *

63 related articles for article (PubMed ID: 9499429)

  • 1. Characterization of lpd (lipid defect): a novel mutation on mouse chromosome 16 associated with a defect in triglyceride metabolism.
    Wen XY; Bryce DM; Breitman ML
    Hum Mol Genet; 1998 Apr; 7(4):743-50. PubMed ID: 9499429
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Murine phosphatidylserine-specific phospholipase A1 (Ps-pla1) maps to chromosome 16 but is distinct from the lpd (lipid defect) locus.
    Wen XY; Stewart AK; Skaug J; Wei E; Tsui LC
    Mamm Genome; 2001 Feb; 12(2):129-32. PubMed ID: 11210182
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mouse microsomal triglyceride transfer protein large subunit: cDNA cloning, tissue-specific expression and chromosomal localization.
    Nakamuta M; Chang BH; Hoogeveen R; Li WH; Chan L
    Genomics; 1996 Apr; 33(2):313-6. PubMed ID: 8660984
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of a novel lipase gene mutated in lpd mice with hypertriglyceridemia and associated with dyslipidemia in humans.
    Wen XY; Hegele RA; Wang J; Wang DY; Cheung J; Wilson M; Yahyapour M; Bai Y; Zhuang L; Skaug J; Young TK; Connelly PW; Koop BF; Tsui LC; Stewart AK
    Hum Mol Genet; 2003 May; 12(10):1131-43. PubMed ID: 12719377
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A postimplantation lethal mutation induced by transgene insertion on mouse chromosome 8.
    Pravtcheva DD; Wise TL
    Genomics; 1995 Dec; 30(3):529-44. PubMed ID: 8825640
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. A novel transgenic mouse model of lysosomal storage disorder.
    Ortiz-Miranda S; Ji R; Jurczyk A; Aryee KE; Mo S; Fletcher T; Shaffer SA; Greiner DL; Bortell R; Gregg RG; Cheng A; Hennings LJ; Rittenhouse AR
    Am J Physiol Gastrointest Liver Physiol; 2016 Nov; 311(5):G903-G919. PubMed ID: 27659423
    [TBL] [Abstract][Full Text] [Related]  

  • 8. H beta 58, an insertional mutation affecting early postimplantation development of the mouse embryo.
    Radice G; Lee JJ; Costantini F
    Development; 1991 Mar; 111(3):801-11. PubMed ID: 1879343
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Genomic interval engineering of mice identifies a novel modulator of triglyceride production.
    Zhu Y; Jong MC; Frazer KA; Gong E; Krauss RM; Cheng JF; Boffelli D; Rubin EM
    Proc Natl Acad Sci U S A; 2000 Feb; 97(3):1137-42. PubMed ID: 10655497
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Localization of the tight junction protein gene TJP1 to human chromosome 15q13, distal to the Prader-Willi/Angelman region, and to mouse chromosome 7.
    Mohandas TK; Chen XN; Rowe LB; Birkenmeier EH; Fanning AS; Anderson JM; Korenberg JR
    Genomics; 1995 Dec; 30(3):594-7. PubMed ID: 8825647
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Cspg2 gene, disrupted in the hdf mutant, is required for right cardiac chamber and endocardial cushion formation.
    Mjaatvedt CH; Yamamura H; Capehart AA; Turner D; Markwald RR
    Dev Biol; 1998 Oct; 202(1):56-66. PubMed ID: 9758703
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cloning and characterization of the murine toll-like receptor 5 (Tlr5) gene: sequence and mRNA expression studies in Salmonella-susceptible MOLF/Ei mice.
    Sebastiani G; Leveque G; Larivière L; Laroche L; Skamene E; Gros P; Malo D
    Genomics; 2000 Mar; 64(3):230-40. PubMed ID: 10756091
    [TBL] [Abstract][Full Text] [Related]  

  • 16. His-1 and His-2: identification and chromosomal mapping of two commonly rearranged sites of viral integration in a myeloid leukemia.
    Askew DS; Bartholomew C; Buchberg AM; Valentine MB; Jenkins NA; Copeland NG; Ihle JN
    Oncogene; 1991 Nov; 6(11):2041-7. PubMed ID: 1682866
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Isolation and characterization of a pseudoautosomal region-specific genetic marker in C57BL/6 mice using genomic representational difference analysis.
    Kalcheva ID; Matsuda Y; Plass C; Chapman VM
    Proc Natl Acad Sci U S A; 1995 Dec; 92(26):12352-6. PubMed ID: 8618899
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular and phenotypic characterization of a new mouse insertional mutation that causes a defect in the distal vertebrae of the spine.
    Schrick JJ; Dickinson ME; Hogan BL; Selby PB; Woychik RP
    Genetics; 1995 Jul; 140(3):1061-7. PubMed ID: 7672577
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Transgenic mouse model of hemifacial microsomia: cloning and characterization of insertional mutation region on chromosome 10.
    Naora H; Kimura M; Otani H; Yokoyama M; Koizumi T; Katsuki M; Tanaka O
    Genomics; 1994 Oct; 23(3):515-9. PubMed ID: 7531669
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Positional cloning of the combined hyperlipidemia gene Hyplip1.
    Bodnar JS; Chatterjee A; Castellani LW; Ross DA; Ohmen J; Cavalcoli J; Wu C; Dains KM; Catanese J; Chu M; Sheth SS; Charugundla K; Demant P; West DB; de Jong P; Lusis AJ
    Nat Genet; 2002 Jan; 30(1):110-6. PubMed ID: 11753387
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.