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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

96 related items for PubMed ID: 27039359

  • 21. Endothelin axis polymorphisms in patients with scleroderma.
    Fonseca C, Renzoni E, Sestini P, Pantelidis P, Lagan A, Bunn C, McHugh N, Welsh KI, Du Bois RM, Denton CP, Black C, Abraham D.
    Arthritis Rheum; 2006 Sep; 54(9):3034-42. PubMed ID: 16947775
    [Abstract] [Full Text] [Related]

  • 22. [Coding-sequence mutation and polymorphism analysis of EDNRB gene in patients with Hirschsprung's disease from Zhejiang region].
    Zhou MN, Li JC, Ding SP.
    Fen Zi Xi Bao Sheng Wu Xue Bao; 2006 Feb; 39(1):61-5. PubMed ID: 16944573
    [Abstract] [Full Text] [Related]

  • 23. Whole-genome sequencing reveals a large deletion in the MITF gene in horses with white spotted coat colour and increased risk of deafness.
    Henkel J, Lafayette C, Brooks SA, Martin K, Patterson-Rosa L, Cook D, Jagannathan V, Leeb T.
    Anim Genet; 2019 Apr; 50(2):172-174. PubMed ID: 30644113
    [Abstract] [Full Text] [Related]

  • 24. Endothelin receptor B2 (EDNRB2) is associated with the panda plumage colour mutation in Japanese quail.
    Miwa M, Inoue-Murayama M, Aoki H, Kunisada T, Hiragaki T, Mizutani M, Ito S.
    Anim Genet; 2007 Apr; 38(2):103-8. PubMed ID: 17313575
    [Abstract] [Full Text] [Related]

  • 25. 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 Apr; 14(6):e0217132. PubMed ID: 31170185
    [Abstract] [Full Text] [Related]

  • 26. Evaluation of a test for identification of Arabian horses heterozygous for the severe combined immunodeficiency trait.
    Shin EK, Perryman LE, Meek K.
    J Am Vet Med Assoc; 1997 Nov 15; 211(10):1268-70. PubMed ID: 9373363
    [Abstract] [Full Text] [Related]

  • 27. Genetic interactions between neurofibromin and endothelin receptor B in mice.
    Deo M, Huang JL, Van Raamsdonk CD.
    PLoS One; 2013 Nov 15; 8(3):e59931. PubMed ID: 23555837
    [Abstract] [Full Text] [Related]

  • 28. Evaluation of allele frequencies of inherited disease genes in subgroups of American Quarter Horses.
    Tryon RC, Penedo MC, McCue ME, Valberg SJ, Mickelson JR, Famula TR, Wagner ML, Jackson M, Hamilton MJ, Nooteboom S, Bannasch DL.
    J Am Vet Med Assoc; 2009 Jan 01; 234(1):120-5. PubMed ID: 19119976
    [Abstract] [Full Text] [Related]

  • 29. 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 01; 78(4):688-96. PubMed ID: 18077801
    [Abstract] [Full Text] [Related]

  • 30. SOX10, in combination with Sp1, regulates the endothelin receptor type B gene in human melanocyte lineage cells.
    Yokoyama S, Takeda K, Shibahara S.
    FEBS J; 2006 Apr 01; 273(8):1805-20. PubMed ID: 16623715
    [Abstract] [Full Text] [Related]

  • 31. Association of endothelin-beta receptor (EDNRB) gene variants in anorectal malformations.
    Moore SW, Zaahl MG.
    J Pediatr Surg; 2007 Jul 01; 42(7):1266-70. PubMed ID: 17618893
    [Abstract] [Full Text] [Related]

  • 32. [Effects of Kit gene on coat depigmentation in white horses].
    Bai DY, Yang LH, Unerhu U, Zhao YP, Zhao QN, Hasigaowa H, Dugarjaviin M.
    Yi Chuan; 2011 Nov 01; 33(11):1171-8. PubMed ID: 22120071
    [Abstract] [Full Text] [Related]

  • 33. 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]

  • 34. Transgenic expression of the endothelin-B receptor prevents congenital intestinal aganglionosis in a rat model of Hirschsprung disease.
    Gariepy CE, Williams SC, Richardson JA, Hammer RE, Yanagisawa M.
    J Clin Invest; 1998 Sep 15; 102(6):1092-101. PubMed ID: 9739043
    [Abstract] [Full Text] [Related]

  • 35. 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 Sep 15; 140(1):46-54. PubMed ID: 23635529
    [Abstract] [Full Text] [Related]

  • 36. Skin malformations in a neonatal foal tested homozygous positive for Warmblood Fragile Foal Syndrome.
    Monthoux C, de Brot S, Jackson M, Bleul U, Walter J.
    BMC Vet Res; 2015 Jan 31; 11():12. PubMed ID: 25637337
    [Abstract] [Full Text] [Related]

  • 37. [Clinical evaluation of the new coat colour macchiato in a male Franches-Montagnes horse].
    Blatter M, Haase B, Gerber V, Poncet PA, Leeb T, Rieder S, Henke D, Janett F, Burger D.
    Schweiz Arch Tierheilkd; 2013 Apr 31; 155(4):229-32. PubMed ID: 23531944
    [Abstract] [Full Text] [Related]

  • 38. Identification of aberrant promoter methylation of EDNRB gene in esophageal squamous cell carcinoma.
    Zhao BJ, Sun DG, Zhang M, Tan SN, Ma X.
    Dis Esophagus; 2009 Apr 31; 22(1):55-61. PubMed ID: 18564167
    [Abstract] [Full Text] [Related]

  • 39. [Molecular basis and applicability in equine color genetics].
    Li B, He XL, Zhao YP, Wang XJ, Manglai D, Zhang YR.
    Yi Chuan; 2010 Nov 31; 32(11):1133-40. PubMed ID: 21513164
    [Abstract] [Full Text] [Related]

  • 40. Cell-autonomous and cell non-autonomous signaling through endothelin receptor B during melanocyte development.
    Hou L, Pavan WJ, Shin MK, Arnheiter H.
    Development; 2004 Jul 31; 131(14):3239-47. PubMed ID: 15201217
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 5.