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 *

129 related articles for article (PubMed ID: 1889803)

  • 1. Localization of the panhypopituitary dwarf mutation (df) on mouse chromosome 11 in an intersubspecific backcross.
    Buckwalter MS; Katz RW; Camper SA
    Genomics; 1991 Jul; 10(3):515-26. PubMed ID: 1889803
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Pit-1 transcription factor gene is a candidate for the murine Snell dwarf mutation.
    Camper SA; Saunders TL; Katz RW; Reeves RH
    Genomics; 1990 Nov; 8(3):586-90. PubMed ID: 1981057
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Dwarf locus mutants lacking three pituitary cell types result from mutations in the POU-domain gene pit-1.
    Li S; Crenshaw EB; Rawson EJ; Simmons DM; Swanson LW; Rosenfeld MG
    Nature; 1990 Oct; 347(6293):528-33. PubMed ID: 1977085
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Transcript abundance in mouse pituitaries with altered growth hormone expression quantified by reverse transcriptase polymerase chain reaction implicates transcription factor Zn-16 in gene regulation in vivo.
    Wojtkiewicz PW; Phelps CJ; Hurley DL
    Endocrine; 2002 Jun; 18(1):67-74. PubMed ID: 12166626
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Reduced hypothalamic neuropeptide Y expression in growth hormone- and prolactin-deficient Ames and Snell dwarf mice.
    Hurley DL; Birch DV; Almond MC; Estrada IJ; Phelps CJ
    Endocrinology; 2003 Nov; 144(11):4783-9. PubMed ID: 12960004
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Postnatal reduction in number of hypothalamic tuberoinfundibular dopaminergic neurons in prolactin-deficient dwarf mice.
    Phelps CJ; Vaccarella MY; Romero MI; Hurley DL
    Neuroendocrinology; 1994 Mar; 59(3):189-96. PubMed ID: 7909141
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The little (lit) mutation cosegregates with the growth hormone releasing factor receptor on mouse chromosome 6.
    Chua SC; Hennessey K; Zeitler P; Leibel RL
    Mamm Genome; 1993; 4(10):555-9. PubMed ID: 8268652
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Postnatal regression of hypothalamic dopaminergic neurons in prolactin-deficient Snell dwarf mice.
    Phelps CJ
    Endocrinology; 2004 Dec; 145(12):5656-64. PubMed ID: 15345680
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic mapping and evaluation of candidate genes for spasmodic, a neurological mouse mutation with abnormal startle response.
    Buckwalter MS; Testa CM; Noebels JL; Camper SA
    Genomics; 1993 Aug; 17(2):279-86. PubMed ID: 8406478
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ames dwarf mice exhibit somatotrope commitment but lack growth hormone-releasing factor response.
    Gage PJ; Lossie AC; Scarlett LM; Lloyd RV; Camper SA
    Endocrinology; 1995 Mar; 136(3):1161-7. PubMed ID: 7867569
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Assessment of the primary adrenal cortical and pancreatic hormone basal levels in relation to plasma glucose and age in the unstressed Ames dwarf mouse.
    Borg KE; Brown-Borg HM; Bartke A
    Proc Soc Exp Biol Med; 1995 Nov; 210(2):126-33. PubMed ID: 7568282
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular basis of the little mouse phenotype and implications for cell type-specific growth.
    Lin SC; Lin CR; Gukovsky I; Lusis AJ; Sawchenko PE; Rosenfeld MG
    Nature; 1993 Jul; 364(6434):208-13. PubMed ID: 8391647
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Functional characterization of a human POU1F1 mutation associated with isolated growth hormone deficiency: a novel etiology for IGHD.
    Sobrier ML; Tsai YC; Pérez C; Leheup B; Bouceba T; Duquesnoy P; Copin B; Sizova D; Penzo A; Stanger BZ; Cooke NE; Liebhaber SA; Amselem S
    Hum Mol Genet; 2016 Feb; 25(3):472-83. PubMed ID: 26612202
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ames dwarf (Prop1(df)/Prop1(df)) mice display increased sensitivity of the major GH-signaling pathways in liver and skeletal muscle.
    Miquet JG; Muñoz MC; Giani JF; González L; Dominici FP; Bartke A; Turyn D; Sotelo AI
    Growth Horm IGF Res; 2010 Apr; 20(2):118-26. PubMed ID: 20022531
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Anterior pituitary cells defective in the cell-autonomous factor, df, undergo cell lineage specification but not expansion.
    Gage PJ; Roller ML; Saunders TL; Scarlett LM; Camper SA
    Development; 1996 Jan; 122(1):151-60. PubMed ID: 8565826
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pituitary lineage determination by the Prophet of Pit-1 homeodomain factor defective in Ames dwarfism.
    Sornson MW; Wu W; Dasen JS; Flynn SE; Norman DJ; O'Connell SM; Gukovsky I; Carrière C; Ryan AK; Miller AP; Zuo L; Gleiberman AS; Andersen B; Beamer WG; Rosenfeld MG
    Nature; 1996 Nov; 384(6607):327-33. PubMed ID: 8934515
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The Ames dwarf gene is required for Pit-1 gene activation.
    Andersen B; Pearse RV; Jenne K; Sornson M; Lin SC; Bartke A; Rosenfeld MG
    Dev Biol; 1995 Dec; 172(2):495-503. PubMed ID: 8612966
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Array-based expression analysis of mouse liver genes: effect of age and of the longevity mutant Prop1df.
    Dozmorov I; Bartke A; Miller RA
    J Gerontol A Biol Sci Med Sci; 2001 Feb; 56(2):B72-80. PubMed ID: 11213270
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Inherited ateliotic dwarfism in mice. Characteristics of the mutation, little, on chromosome 6.
    Eicher EM; Beamer WG
    J Hered; 1976; 67(2):87-91. PubMed ID: 1270792
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.