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139 related items for PubMed ID: 23300849

  • 1. Familiar hypopigmentation syndrome in sheep associated with homozygous deletion of the entire endothelin type-B receptor gene.
    Lühken G, Fleck K, Pauciullo A, Huisinga M, Erhardt G.
    PLoS One; 2012; 7(12):e53020. PubMed ID: 23300849
    [Abstract] [Full Text] [Related]

  • 2. Dual-color high-resolution fiber-FISH analysis on lethal white syndrome carriers in sheep.
    Pauciullo A, Fleck K, Lühken G, Di Berardino D, Erhardt G.
    Cytogenet Genome Res; 2013; 140(1):46-54. PubMed ID: 23635529
    [Abstract] [Full Text] [Related]

  • 3. Spatially restricted hypopigmentation associated with an Ednrbs-modifying locus on mouse chromosome 10.
    Rhim H, Dunn KJ, Aronzon A, Mac S, Cheng M, Lamoreux ML, Tilghman SM, Pavan WJ.
    Genome Res; 2000 Jan; 10(1):17-29. PubMed ID: 10645946
    [Abstract] [Full Text] [Related]

  • 4. Clinical variability of Waardenburg-Shah syndrome in patients with proximal 13q deletion syndrome including the endothelin-B receptor locus.
    Tüysüz B, Collin A, Arapoğlu M, Suyugül N.
    Am J Med Genet A; 2009 Oct; 149A(10):2290-5. PubMed ID: 19764031
    [Abstract] [Full Text] [Related]

  • 5. QTL analysis of modifiers for pigmentary disorder in rats carrying Ednrb sl mutations.
    Huang J, Dang R, Torigoe D, Li A, Lei C, Sasaki N, Wang J, Agui T.
    Sci Rep; 2016 Jan 22; 6():19697. PubMed ID: 26796131
    [Abstract] [Full Text] [Related]

  • 6. B-lymphocyte-intrinsic and -extrinsic defects in secretory immunoglobulin A production in the neural crest-conditional deletion of endothelin receptor B model of Hirschsprung-associated enterocolitis.
    Medrano G, Cailleux F, Guan P, Kuruvilla K, Barlow-Anacker AJ, Gosain A.
    FASEB J; 2019 Jun 22; 33(6):7615-7624. PubMed ID: 30908942
    [Abstract] [Full Text] [Related]

  • 7. QTL analysis identifies a modifier locus of aganglionosis in the rat model of Hirschsprung disease carrying Ednrb(sl) mutations.
    Dang R, Torigoe D, Sasaki N, Agui T.
    PLoS One; 2011 Jun 22; 6(11):e27902. PubMed ID: 22132166
    [Abstract] [Full Text] [Related]

  • 8. A missense mutation in the endothelin-B receptor gene is associated with Lethal White Foal Syndrome: an equine version of Hirschsprung disease.
    Metallinos DL, Bowling AT, Rine J.
    Mamm Genome; 1998 Jun 22; 9(6):426-31. PubMed ID: 9585428
    [Abstract] [Full Text] [Related]

  • 9. Effects of endothelin receptor type-A and type-B antagonists on prostaglandin F2alpha-induced luteolysis of the sheep corpus luteum.
    Doerr MD, Goravanahally MP, Rhinehart JD, Inskeep EK, Flores JA.
    Biol Reprod; 2008 Apr 22; 78(4):688-96. PubMed ID: 18077801
    [Abstract] [Full Text] [Related]

  • 10. New test for endothelin receptor type B (EDNRB) mutation genotyping in horses.
    Ayala-Valdovinos MA, Galindo-García J, Sánchez-Chiprés D, Duifhuis-Rivera T.
    Mol Cell Probes; 2016 Jun 22; 30(3):182-4. PubMed ID: 27039359
    [Abstract] [Full Text] [Related]

  • 11. Endothelin receptor B polymorphism associated with lethal white foal syndrome in horses.
    Santschi EM, Purdy AK, Valberg SJ, Vrotsos PD, Kaese H, Mickelson JR.
    Mamm Genome; 1998 Apr 22; 9(4):306-9. PubMed ID: 9530628
    [Abstract] [Full Text] [Related]

  • 12. Cloning and association analysis of KIT and EDNRB polymorphisms with dominant white coat color in the Chinese raccoon dog (Nyctereutes procyonoides procyonoides).
    Yan SQ, Bai CY, Qi SM, Li ML, Si S, Li YM, Sun JH.
    Genet Mol Res; 2015 Jun 12; 14(2):6549-54. PubMed ID: 26125860
    [Abstract] [Full Text] [Related]

  • 13. Targeted and natural (piebald-lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice.
    Hosoda K, Hammer RE, Richardson JA, Baynash AG, Cheung JC, Giaid A, Yanagisawa M.
    Cell; 1994 Dec 30; 79(7):1267-76. PubMed ID: 8001159
    [Abstract] [Full Text] [Related]

  • 14. Null mutation of endothelin receptor type B gene in spotting lethal rats causes aganglionic megacolon and white coat color.
    Gariepy CE, Cass DT, Yanagisawa M.
    Proc Natl Acad Sci U S A; 1996 Jan 23; 93(2):867-72. PubMed ID: 8570650
    [Abstract] [Full Text] [Related]

  • 15. A deletion in the endothelin-B receptor gene is responsible for the Waardenburg syndrome-like phenotypes of WS4 mice.
    Ohtani S, Shinkai Y, Horibe A, Katayama K, Tsuji T, Matsushima Y, Tachibana M, Kunieda T.
    Exp Anim; 2006 Oct 23; 55(5):491-5. PubMed ID: 17090968
    [Abstract] [Full Text] [Related]

  • 16. Null mutation of the endothelin receptor type B gene causes embryonic death in the GK rat.
    Wang J, Dang R, Miyasaka Y, Hattori K, Torigoe D, Okamura T, Tag-Ei-Din-Hassan HT, Morimatsu M, Mashimo T, Agui T.
    PLoS One; 2019 Oct 23; 14(6):e0217132. PubMed ID: 31170185
    [Abstract] [Full Text] [Related]

  • 17. Incidence of the endothelin receptor B mutation that causes lethal white foal syndrome in white-patterned horses.
    Santschi EM, Vrotsos PD, Purdy AK, Mickelson JR.
    Am J Vet Res; 2001 Jan 23; 62(1):97-103. PubMed ID: 11197568
    [Abstract] [Full Text] [Related]

  • 18. Deletion in the OA1 gene in a family with congenital X linked nystagmus.
    Preising M, Op de Laak JP, Lorenz B.
    Br J Ophthalmol; 2001 Sep 23; 85(9):1098-103. PubMed ID: 11520764
    [Abstract] [Full Text] [Related]

  • 19. Hirschsprung disease is associated with an L286P mutation in the fifth transmembrane domain of the endothelin-B receptor in the N-ethyl-N-nitrosourea-induced mutant line.
    Chen B, Ouyang HL, Wang WH, Yin YH, Yan LN, Yang B, Xue ZF.
    Exp Anim; 2016 Jul 29; 65(3):245-51. PubMed ID: 26923755
    [Abstract] [Full Text] [Related]

  • 20. Interactions between Sox10 and EdnrB modulate penetrance and severity of aganglionosis in the Sox10Dom mouse model of Hirschsprung disease.
    Cantrell VA, Owens SE, Chandler RL, Airey DC, Bradley KM, Smith JR, Southard-Smith EM.
    Hum Mol Genet; 2004 Oct 01; 13(19):2289-301. PubMed ID: 15294878
    [Abstract] [Full Text] [Related]

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