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Journal Abstract Search

303 related items for PubMed ID: 9585428

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  • 3. 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
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  • 4. 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
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  • 6. Foal with Overo lethal white syndrome born to a registered quarter horse mare.
    Lightbody T.
    Can Vet J; 2002 Sep; 43(9):715-7. PubMed ID: 12240532
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  • 7. 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
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  • 8. 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 15; 41():52-56. PubMed ID: 30096357
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  • 9. 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 15; 30(3):182-4. PubMed ID: 27039359
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  • 12. [The "lethal white foal" syndrome].
    Blendinger C, Müller G, Bostedt H.
    Tierarztl Prax; 1994 Jun 15; 22(3):252-5. PubMed ID: 8048034
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  • 13. A mutation in endothelin-B receptor gene causes myenteric aganglionosis and coat color spotting in rats.
    Kunieda T, Kumagai T, Tsuji T, Ozaki T, Karaki H, Ikadai H.
    DNA Res; 1996 Apr 30; 3(2):101-5. PubMed ID: 8804863
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  • 15. Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease.
    Amiel J, Attié T, Jan D, Pelet A, Edery P, Bidaud C, Lacombe D, Tam P, Simeoni J, Flori E, Nihoul-Fékété C, Munnich A, Lyonnet S.
    Hum Mol Genet; 1996 Mar 30; 5(3):355-7. PubMed ID: 8852660
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  • 16. An equine chromosome 3 inversion is associated with the tobiano spotting pattern in German horse breeds.
    Haase B, Jude R, Brooks SA, Leeb T.
    Anim Genet; 2008 Jun 30; 39(3):306-9. PubMed ID: 18410476
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  • 17. 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
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  • 18. 3-D technology used to accurately understand equine ileocolonic aganglionosis.
    Muniz E, Lobo Ladd AA, Lobo Ladd FV, da Silva AA, Kmit FV, Borges AS, Teixeira R, da Mota LS, Belli CB, de Zoppa AL, da Silva LC, de Melo MP, Coppi AA.
    Cells Tissues Organs; 2013 Jul 29; 198(2):160-8. PubMed ID: 23886660
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