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: 38997957)

  • 1. Different Founding Effects Underlie Dominant Blue Eyes (DBE) in the Domestic Cat.
    Abitbol M; Dufaure de Citres C; Rudd Garces G; Lühken G; Lyons LA; Gache V
    Animals (Basel); 2024 Jun; 14(13):. PubMed ID: 38997957
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A PAX3 insertion in the Celestial breed and certain feline breeding lines with dominant blue eyes.
    Abitbol M; Couronné A; Dufaure de Citres C; Gache V
    Anim Genet; 2024 Aug; 55(4):670-675. PubMed ID: 38644700
    [TBL] [Abstract][Full Text] [Related]  

  • 3. PAX3 haploinsufficiency in Maine Coon cats with dominant blue eyes and hearing loss resembling the human Waardenburg syndrome.
    Rudd Garces G; Farke D; Schmidt MJ; Letko A; Schirl K; Abitbol M; Leeb T; Lyons LA; Lühken G
    G3 (Bethesda); 2024 Sep; 14(9):. PubMed ID: 38869246
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic heterogeneity of polydactyly in Maine Coon cats.
    Hamelin A; Conchou F; Fusellier M; Duchenij B; Vieira I; Filhol E; Dufaure de Citres C; Tiret L; Gache V; Abitbol M
    J Feline Med Surg; 2020 Dec; 22(12):1103-1113. PubMed ID: 32067556
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Endogenous retrovirus insertion in the KIT oncogene determines white and white spotting in domestic cats.
    David VA; Menotti-Raymond M; Wallace AC; Roelke M; Kehler J; Leighty R; Eizirik E; Hannah SS; Nelson G; Schäffer AA; Connelly CJ; O'Brien SJ; Ryugo DK
    G3 (Bethesda); 2014 Aug; 4(10):1881-91. PubMed ID: 25085922
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Precision medicine validation: identifying the
    Ontiveros ES; Ueda Y; Harris SP; Stern JA;
    J Feline Med Surg; 2019 Dec; 21(12):1086-1093. PubMed ID: 30558461
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic epidemiology of blood type, disease and trait variants, and genome-wide genetic diversity in over 11,000 domestic cats.
    Anderson H; Davison S; Lytle KM; Honkanen L; Freyer J; Mathlin J; Kyöstilä K; Inman L; Louviere A; Chodroff Foran R; Forman OP; Lohi H; Donner J
    PLoS Genet; 2022 Jun; 18(6):e1009804. PubMed ID: 35709088
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Absence of known feline MYH7 and MYBPC3 variants in a diverse cohort of cats with hypertrophic cardiomyopathy.
    O'Donnell K; Adin D; Atkins CE; DeFrancesco T; Keene BW; Tou S; Meurs KM
    Anim Genet; 2021 Aug; 52(4):542-544. PubMed ID: 33970514
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prevalence of congenital sensorineural deafness in a population of client-owned purebred kittens in the United Kingdom.
    Mari L; Freeman J; Van Dijk J; De Risio L
    J Vet Intern Med; 2019 Jul; 33(4):1707-1713. PubMed ID: 31144374
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Golden cats: A never-ending story!
    Abitbol M; Dargar T; Gache V
    Anim Genet; 2022 Oct; 53(5):715-718. PubMed ID: 35703390
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations in MITF and PAX3 cause "splashed white" and other white spotting phenotypes in horses.
    Hauswirth R; Haase B; Blatter M; Brooks SA; Burger D; Drögemüller C; Gerber V; Henke D; Janda J; Jude R; Magdesian KG; Matthews JM; Poncet PA; Svansson V; Tozaki T; Wilkinson-White L; Penedo MC; Rieder S; Leeb T
    PLoS Genet; 2012; 8(4):e1002653. PubMed ID: 22511888
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Evaluation of the prevalence of congenital sensorineural deafness in a population of 72 client-owned purebred white cats examined from 2007 to 2021.
    Annemarie K; Liliana R; Małgorzata K; Andrzej P
    BMC Vet Res; 2022 Jul; 18(1):287. PubMed ID: 35869465
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Whole genome sequencing in cats, identifies new models for blindness in AIPL1 and somite segmentation in HES7.
    Lyons LA; Creighton EK; Alhaddad H; Beale HC; Grahn RA; Rah H; Maggs DJ; Helps CR; Gandolfi B
    BMC Genomics; 2016 Mar; 17():265. PubMed ID: 27030474
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association of A31P and A74T polymorphisms in the myosin binding protein C3 gene and hypertrophic cardiomyopathy in Maine Coon and other breed cats.
    Wess G; Schinner C; Weber K; Küchenhoff H; Hartmann K
    J Vet Intern Med; 2010; 24(3):527-32. PubMed ID: 20412438
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A new Finnish flavor of feline coat coloration, "salmiak," is associated with a 95-kb deletion downstream of the KIT gene.
    Anderson H; Salonen M; Toivola S; Blades M; Lyons LA; Forman OP; Hytönen MK; Lohi H
    Anim Genet; 2024 Aug; 55(4):676-680. PubMed ID: 38721753
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Werewolf, There Wolf: Variants in
    Buckley RM; Gandolfi B; Creighton EK; Pyne CA; Bouhan DM; LeRoy ML; Senter DA; Gobble JR; Abitbol M; Lyons LA;
    Genes (Basel); 2020 Jun; 11(6):. PubMed ID: 32580512
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new domestic cat genome assembly based on long sequence reads empowers feline genomic medicine and identifies a novel gene for dwarfism.
    Buckley RM; Davis BW; Brashear WA; Farias FHG; Kuroki K; Graves T; Hillier LW; Kremitzki M; Li G; Middleton RP; Minx P; Tomlinson C; Lyons LA; Murphy WJ; Warren WC
    PLoS Genet; 2020 Oct; 16(10):e1008926. PubMed ID: 33090996
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats.
    Gandolfi B; Alhaddad H; Joslin SE; Khan R; Filler S; Brem G; Lyons LA
    Sci Rep; 2013; 3():2000. PubMed ID: 23770706
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Not another type of potato: MC1R and the russet coloration of Burmese cats.
    Gustafson NA; Gandolfi B; Lyons LA
    Anim Genet; 2017 Feb; 48(1):116-120. PubMed ID: 27671997
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cystinuria Associated with Different SLC7A9 Gene Variants in the Cat.
    Mizukami K; Raj K; Osborne C; Giger U
    PLoS One; 2016; 11(7):e0159247. PubMed ID: 27404572
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.