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 *

113 related articles for article (PubMed ID: 7958830)

  • 1. Mini-mouse: phenotypic characterization of a transgenic insertional mutant allelic to pygmy.
    Benson KF; Chada K
    Genet Res; 1994 Aug; 64(1):27-33. PubMed ID: 7958830
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mini-mouse: disruption of the pygmy locus in a transgenic insertional mutant.
    Xiang X; Benson KF; Chada K
    Science; 1990 Feb; 247(4945):967-9. PubMed ID: 2305264
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Reduced body growth and excessive incisor length in insertional mutants mapping to mouse Chromosome 13.
    Petznek H; Kappler R; Scherthan H; Müller M; Brem G; Aigner B
    Mamm Genome; 2002 Sep; 13(9):504-9. PubMed ID: 12370780
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Disruption of the mouse phospholipase C-beta1 gene in a beta-lactoglobulin transgenic line affects viability, growth, and fertility in mice.
    Ballester M; Molist J; Lopez-Bejar M; Sánchez A; Santaló J; Folch JM; Ibáñez E
    Gene; 2004 Oct; 341():279-89. PubMed ID: 15474310
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Gtl2lacZ, an insertional mutation on mouse chromosome 12 with parental origin-dependent phenotype.
    Schuster-Gossler K; Simon-Chazottes D; Guenet JL; Zachgo J; Gossler A
    Mamm Genome; 1996 Jan; 7(1):20-4. PubMed ID: 8903723
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The Ames dwarf gene, df, is required early in pituitary ontogeny for the extinction of Rpx transcription and initiation of lineage-specific cell proliferation.
    Gage PJ; Brinkmeier ML; Scarlett LM; Knapp LT; Camper SA; Mahon KA
    Mol Endocrinol; 1996 Dec; 10(12):1570-81. PubMed ID: 8961267
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Polydactyly in the Strong's luxoid mouse is suppressed by limb deformity alleles.
    Vogt TF; Leder P
    Dev Genet; 1996; 19(1):33-42. PubMed ID: 8792607
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Stereocilia defects in waltzer (Cdh23), shaker1 (Myo7a) and double waltzer/shaker1 mutant mice.
    Holme RH; Steel KP
    Hear Res; 2002 Jul; 169(1-2):13-23. PubMed ID: 12121736
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Analysis of growth hormone genes in mice with genetic defects of growth hormone expression.
    Phillips JA; Beamer WG; Bartke A
    J Endocrinol; 1982 Mar; 92(3):405-7. PubMed ID: 7069343
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The petit rat (pet/pet), a new semilethal mutant dwarf rat with thymic and testicular anomalies.
    Chiba J; Suzuki K; Suzuki H
    Comp Med; 2008 Dec; 58(6):551-9. PubMed ID: 19149412
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Utility and limits of Hprt-Cre technology in generating mutant mouse embryos.
    Zaremba KM; Reeder AL; Kowalkowski A; Girma E; Nichol PF
    J Surg Res; 2014 Apr; 187(2):386-93. PubMed ID: 24360120
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The pygmy (pg) mutant of the mouse--a model of the human pygmy.
    Rimoin DL; Richmond L
    J Clin Endocrinol Metab; 1972 Sep; 35(3):467-8. PubMed ID: 5051369
    [No Abstract]   [Full Text] [Related]  

  • 14. Transketolase haploinsufficiency reduces adipose tissue and female fertility in mice.
    Xu ZP; Wawrousek EF; Piatigorsky J
    Mol Cell Biol; 2002 Sep; 22(17):6142-7. PubMed ID: 12167708
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Elongation of the epiphyseal trabecular bone in transgenic mice carrying a klotho gene locus mutation that leads to a syndrome resembling aging.
    Yamashita T; Nifuji A; Furuya K; Nabeshima Y; Noda M
    J Endocrinol; 1998 Oct; 159(1):1-8. PubMed ID: 9795335
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Phenotypic characterization of the Komeda miniature rat Ishikawa, an animal model of dwarfism caused by a mutation in Prkg2.
    Tsuchida A; Yokoi N; Namae M; Fuse M; Masuyama T; Sasaki M; Kawazu S; Komeda K
    Comp Med; 2008 Dec; 58(6):560-7. PubMed ID: 19149413
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hydrocephalus in the Otx2+/- mutant mouse.
    Makiyama Y; Shoji S; Mizusawa H
    Exp Neurol; 1997 Nov; 148(1):215-21. PubMed ID: 9398463
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Estrogenic restoration of functional pancreatic islet cytoarchitecture in diabetes (db/db) mutant C57BL/KsJ mice: relationship to estradiol localization, systemic glycemia, and persistent hyperinsulinemia.
    Garris DR; Garris BL
    Cell Tissue Res; 2005 Feb; 319(2):231-42. PubMed ID: 15654653
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Human stanniocalcin-2 exhibits potent growth-suppressive properties in transgenic mice independently of growth hormone and IGFs.
    Gagliardi AD; Kuo EY; Raulic S; Wagner GF; DiMattia GE
    Am J Physiol Endocrinol Metab; 2005 Jan; 288(1):E92-105. PubMed ID: 15367391
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.