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96 related items for PubMed ID: 27039359

  • 1. 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; 30(3):182-4. PubMed ID: 27039359
    [Abstract] [Full Text] [Related]

  • 2. A dinucleotide mutation in the endothelin-B receptor gene is associated with lethal white foal syndrome (LWFS); a horse variant of Hirschsprung disease.
    Yang GC, Croaker D, Zhang AL, Manglick P, Cartmill T, Cass D.
    Hum Mol Genet; 1998 Jun; 7(6):1047-52. PubMed ID: 9580670
    [Abstract] [Full Text] [Related]

  • 3. 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; 9(6):426-31. PubMed ID: 9585428
    [Abstract] [Full Text] [Related]

  • 4. Validation of high-resolution melting analysis as a diagnostic tool for endothelin receptor B mutation in American Paint horses and allele frequency estimation.
    Badial PR, Teixeira RBC, Delfiol DJZ, da Mota LSLS, Borges AS.
    Mol Cell Probes; 2018 Oct; 41():52-56. PubMed ID: 30096357
    [Abstract] [Full Text] [Related]

  • 5. 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; 62(1):97-103. PubMed ID: 11197568
    [Abstract] [Full Text] [Related]

  • 6. 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; 9(4):306-9. PubMed ID: 9530628
    [Abstract] [Full Text] [Related]

  • 7. Overo lethal white foal syndrome: equine model of aganglionic megacolon (Hirschsprung disease).
    McCabe L, Griffin LD, Kinzer A, Chandler M, Beckwith JB, McCabe ER.
    Am J Med Genet; 1990 Jul; 36(3):336-40. PubMed ID: 2363434
    [Abstract] [Full Text] [Related]

  • 8. Genotyping of friesian horses to detect a hydrocephalus-associated c.1423C>T mutation in B3GALNT2 using PCR-RFLP and PCR-PIRA methods: Frequency in stallion horses in México.
    Ayala-Valdovinos MA, Galindo-García J, Sánchez-Chiprés D, Duifhuis-Rivera T.
    Mol Cell Probes; 2017 Apr; 32():69-71. PubMed ID: 28011345
    [Abstract] [Full Text] [Related]

  • 9. A novel simple genotyping assay for detection of the 'Gait keeper' mutation in DMRT3 and allele frequencies in Azteca and Costa Rican Saddle Horse breeds.
    Ayala-Valdovinos MA, Galindo-García J, Sánchez-Chiprés D, Duifhuis-Rivera T, Anguiano-Estrella R.
    Mol Cell Probes; 2020 Apr; 50():101506. PubMed ID: 31917254
    [Abstract] [Full Text] [Related]

  • 10. Extrinsic innervation of ileum and pelvic flexure of foals with ileocolonic aganglionosis.
    Giancola F, Gentilini F, Romagnoli N, Spadari A, Turba ME, Giunta M, Sadeghinezhad J, Sorteni C, Chiocchetti R.
    Cell Tissue Res; 2016 Oct; 366(1):13-22. PubMed ID: 27230228
    [Abstract] [Full Text] [Related]

  • 11. Pleiotropic effects of pigmentation genes in horses.
    Bellone RR.
    Anim Genet; 2010 Dec; 41 Suppl 2():100-10. PubMed ID: 21070283
    [Abstract] [Full Text] [Related]

  • 12. Mutation analysis of endothelin-B receptor gene in patients with Hirschsprung disease in Taiwan.
    Lin YC, Lai HS, Hsu WM, Lee PI, Chen HL, Chang MH.
    J Pediatr Gastroenterol Nutr; 2008 Jan; 46(1):36-40. PubMed ID: 18162831
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. 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]

  • 15. Whole-genome SNP association in the horse: identification of a deletion in myosin Va responsible for Lavender Foal Syndrome.
    Brooks SA, Gabreski N, Miller D, Brisbin A, Brown HE, Streeter C, Mezey J, Cook D, Antczak DF.
    PLoS Genet; 2010 Apr 15; 6(4):e1000909. PubMed ID: 20419149
    [Abstract] [Full Text] [Related]

  • 16. Association between population structure and allele frequencies of the glycogen synthase 1 mutation in the Austrian Noriker draft horse.
    Druml T, Grilz-Seger G, Neuditschko M, Brem G.
    Anim Genet; 2017 Feb 15; 48(1):108-112. PubMed ID: 27476720
    [Abstract] [Full Text] [Related]

  • 17. 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 Feb 15; 7(12):e53020. PubMed ID: 23300849
    [Abstract] [Full Text] [Related]

  • 18. Rolling Nagoya mouse strain (PROD-rol/rol) with classic piebald mutation.
    Yoshimoto T, Aoyama Y, Kim TY, Niimi K, Takahashi E, Itakura C.
    J Vet Med Sci; 2014 Aug 15; 76(8):1093-8. PubMed ID: 24758835
    [Abstract] [Full Text] [Related]

  • 19. Evaluation of deafness in American Paint Horses by phenotype, brainstem auditory-evoked responses, and endothelin receptor B genotype.
    Magdesian KG, Williams DC, Aleman M, Lecouteur RA, Madigan JE.
    J Am Vet Med Assoc; 2009 Nov 15; 235(10):1204-11. PubMed ID: 19912043
    [Abstract] [Full Text] [Related]

  • 20. Evidence for origin of lavender foal syndrome among Egyptian Arabian horses in Egypt.
    AbouEl Ela NH, El Araby IE, Saleh AA, Abd El-Fattah AH, Hagag NM, Brooks SA, Radwan MA, Kalbfleisch T.
    Equine Vet J; 2023 May 15; 55(3):487-493. PubMed ID: 35665534
    [Abstract] [Full Text] [Related]

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