BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 24098150)

  • 1. A mutation in the SUV39H2 gene in Labrador Retrievers with hereditary nasal parakeratosis (HNPK) provides insights into the epigenetics of keratinocyte differentiation.
    Jagannathan V; Bannoehr J; Plattet P; Hauswirth R; Drögemüller C; Drögemüller M; Wiener DJ; Doherr M; Owczarek-Lipska M; Galichet A; Welle MM; Tengvall K; Bergvall K; Lohi H; Rüfenacht S; Linek M; Paradis M; Müller EJ; Roosje P; Leeb T
    PLoS Genet; 2013; 9(10):e1003848. PubMed ID: 24098150
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Abnormal keratinocyte differentiation in the nasal planum of Labrador Retrievers with hereditary nasal parakeratosis (HNPK).
    Bannoehr J; Balmer P; Stoffel MH; Jagannathan V; Gaschen V; Kühni K; Sayar B; Drögemüller M; Howald D; Wiener DJ; Leeb T; Welle MM; Müller EJ; Roosje PJ
    PLoS One; 2020; 15(3):e0225901. PubMed ID: 32119674
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A splice site variant in the SUV39H2 gene in Greyhounds with nasal parakeratosis.
    Bauer A; Nimmo J; Newman R; Brunner M; Welle MM; Jagannathan V; Leeb T
    Anim Genet; 2018 Apr; 49(2):137-140. PubMed ID: 29423952
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A mutation in the FAM83G gene in dogs with hereditary footpad hyperkeratosis (HFH).
    Drögemüller M; Jagannathan V; Becker D; Drögemüller C; Schelling C; Plassais J; Kaerle C; Dufaure de Citres C; Thomas A; Müller EJ; Welle MM; Roosje P; Leeb T
    PLoS Genet; 2014; 10(5):e1004370. PubMed ID: 24832243
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hereditary nasal parakeratosis in Labrador retrievers: 11 new cases and a retrospective study on the presence of accumulations of serum ('serum lakes') in the epidermis of parakeratotic dermatoses and inflamed nasal plana of dogs.
    Peters J; Scott DW; Erb HN; Miller WH
    Vet Dermatol; 2003 Aug; 14(4):197-203. PubMed ID: 12895224
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hereditary nasal parakeratosis in Labrador Retrievers.
    Pagé N; Paradis M; Lapointe JM; Dunstan RW
    Vet Dermatol; 2003 Apr; 14(2):103-10. PubMed ID: 12662268
    [TBL] [Abstract][Full Text] [Related]  

  • 7. SUV39H2 epigenetic silencing controls fate conversion of epidermal stem and progenitor cells.
    Balmer P; Hariton WVJ; Sayar BS; Jagannathan V; Galichet A; Leeb T; Roosje P; Müller EJ
    J Cell Biol; 2021 Apr; 220(4):. PubMed ID: 33604655
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A COL11A2 mutation in Labrador retrievers with mild disproportionate dwarfism.
    Frischknecht M; Niehof-Oellers H; Jagannathan V; Owczarek-Lipska M; Drögemüller C; Dietschi E; Dolf G; Tellhelm B; Lang J; Tiira K; Lohi H; Leeb T
    PLoS One; 2013; 8(3):e60149. PubMed ID: 23527306
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Activity and specificity of the human SUV39H2 protein lysine methyltransferase.
    Schuhmacher MK; Kudithipudi S; Kusevic D; Weirich S; Jeltsch A
    Biochim Biophys Acta; 2015 Jan; 1849(1):55-63. PubMed ID: 25459750
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genome-wide association study for hereditary ataxia in the Parson Russell Terrier and DNA-testing for ataxia-associated mutations in the Parson and Jack Russell Terrier.
    Gast AC; Metzger J; Tipold A; Distl O
    BMC Vet Res; 2016 Oct; 12(1):225. PubMed ID: 27724896
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A synonymous germline variant in a gene encoding a cell adhesion molecule is associated with cutaneous mast cell tumour development in Labrador and Golden Retrievers.
    Biasoli D; Compston-Garnett L; Ricketts SL; Birand Z; Courtay-Cahen C; Fineberg E; Arendt M; Boerkamp K; Melin M; Koltookian M; Murphy S; Rutteman G; Lindblad-Toh K; Starkey M
    PLoS Genet; 2019 Mar; 15(3):e1007967. PubMed ID: 30901340
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A deletion in the VLDLR gene in Eurasier dogs with cerebellar hypoplasia resembling a Dandy-Walker-like malformation (DWLM).
    Gerber M; Fischer A; Jagannathan V; Drögemüller M; Drögemüller C; Schmidt MJ; Bernardino F; Manz E; Matiasek K; Rentmeister K; Leeb T
    PLoS One; 2015; 10(2):e0108917. PubMed ID: 25668033
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evaluation of the dynactin 1 gene in Leonbergers and Labrador Retrievers with laryngeal paralysis.
    Holt DE; Brown DC; Henthorn PS
    Am J Vet Res; 2016 Oct; 77(10):1114-20. PubMed ID: 27668583
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Parakeratosis in skin is associated with loss of inhibitor of differentiation 4 via promoter methylation.
    Ruchusatsawat K; Wongpiyabovorn J; Protjaroen P; Chaipipat M; Shuangshoti S; Thorner PS; Mutirangura A
    Hum Pathol; 2011 Dec; 42(12):1878-87. PubMed ID: 21663940
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A loss-of-function variant in SUV39H2 identified in autism-spectrum disorder causes altered H3K9 trimethylation and dysregulation of protocadherin β-cluster genes in the developing brain.
    Balan S; Iwayama Y; Ohnishi T; Fukuda M; Shirai A; Yamada A; Weirich S; Schuhmacher MK; Dileep KV; Endo T; Hisano Y; Kotoshiba K; Toyota T; Otowa T; Kuwabara H; Tochigi M; Watanabe A; Ohba H; Maekawa M; Toyoshima M; Sasaki T; Nakamura K; Tsujii M; Matsuzaki H; Zhang KYJ; Jeltsch A; Shinkai Y; Yoshikawa T
    Mol Psychiatry; 2021 Dec; 26(12):7550-7559. PubMed ID: 34262135
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A Large Deletion in the
    Bauer A; De Lucia M; Jagannathan V; Mezzalira G; Casal ML; Welle MM; Leeb T
    G3 (Bethesda); 2017 Sep; 7(9):3115-3121. PubMed ID: 28739597
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Epigenetic regulation of surfactant protein A gene (SP-A) expression in fetal lung reveals a critical role for Suv39h methyltransferases during development and hypoxia.
    Benlhabib H; Mendelson CR
    Mol Cell Biol; 2011 May; 31(10):1949-58. PubMed ID: 21402781
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A frameshift mutation in the cubilin gene (CUBN) in Border Collies with Imerslund-Gräsbeck syndrome (selective cobalamin malabsorption).
    Owczarek-Lipska M; Jagannathan V; Drögemüller C; Lutz S; Glanemann B; Leeb T; Kook PH
    PLoS One; 2013; 8(4):e61144. PubMed ID: 23613799
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Caspase-14-deficient mice are more prone to the development of parakeratosis.
    Hoste E; Denecker G; Gilbert B; Van Nieuwerburgh F; van der Fits L; Asselbergh B; De Rycke R; Hachem JP; Deforce D; Prens EP; Vandenabeele P; Declercq W
    J Invest Dermatol; 2013 Mar; 133(3):742-750. PubMed ID: 23014340
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Isolation and characterization of Suv39h2, a second histone H3 methyltransferase gene that displays testis-specific expression.
    O'Carroll D; Scherthan H; Peters AH; Opravil S; Haynes AR; Laible G; Rea S; Schmid M; Lebersorger A; Jerratsch M; Sattler L; Mattei MG; Denny P; Brown SD; Schweizer D; Jenuwein T
    Mol Cell Biol; 2000 Dec; 20(24):9423-33. PubMed ID: 11094092
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.