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Results: 1 to 20 of 81

Similar articles for PubMed (Select 20497153)

1.

Endothelin receptor B (EDNRB) is not the causative gene of the English spotting locus in the domestic rabbit (Oryctolagus cuniculus).

Fontanesi L, Vargiolu M, Scotti E, Mazzoni M, Clavenzani P, De Giorgio R, Romeo G, Russo V.

Anim Genet. 2010 Dec;41(6):669-70. doi: 10.1111/j.1365-2052.2010.02084.x. No abstract available.

PMID:
20497153
2.

The KIT gene is associated with the english spotting coat color locus and congenital megacolon in Checkered Giant rabbits (Oryctolagus cuniculus).

Fontanesi L, Vargiolu M, Scotti E, Latorre R, Faussone Pellegrini MS, Mazzoni M, Asti M, Chiocchetti R, Romeo G, Clavenzani P, De Giorgio R.

PLoS One. 2014 Apr 15;9(4):e93750. doi: 10.1371/journal.pone.0093750. eCollection 2014.

3.
4.

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.

PMID:
8001159
5.
6.

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.

7.

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.

8.

Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons.

Baynash AG, Hosoda K, Giaid A, Richardson JA, Emoto N, Hammer RE, Yanagisawa M.

Cell. 1994 Dec 30;79(7):1277-85.

PMID:
8001160
9.

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.

PMID:
16947775
10.

Exclusion of EDNRB and KIT as the basis for white spotting in Border Collies.

Metallinos D, Rine J.

Genome Biol. 2000;1(2):RESEARCH0004. Epub 2000 Jul 28.

11.

Reduced expression of the endothelin receptor type B gene in piebald mice caused by insertion of a retroposon-like element in intron 1.

Yamada T, Ohtani S, Sakurai T, Tsuji T, Kunieda T, Yanagisawa M.

J Biol Chem. 2006 Apr 21;281(16):10799-807. Epub 2006 Feb 24.

12.

Endothelins and the color of mice: unraveling the etiopathogenesis of Hirschsprung's disease.

Sylvester FA, Griffiths AM.

J Pediatr Gastroenterol Nutr. 1995 Nov;21(4):478-9. No abstract available.

PMID:
8583305
13.

A new inbred strain JF1 established from Japanese fancy mouse carrying the classic piebald allele.

Koide T, Moriwaki K, Uchida K, Mita A, Sagai T, Yonekawa H, Katoh H, Miyashita N, Tsuchiya K, Nielsen TJ, Shiroishi T.

Mamm Genome. 1998 Jan;9(1):15-9. Erratum in: Mamm Genome 1998 Apr;9(4):344.

PMID:
9434939
14.
15.

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.

PMID:
11197568
16.

Molecular characterization of four induced alleles at the Ednrb locus.

Shin MK, Russell LB, Tilghman SM.

Proc Natl Acad Sci U S A. 1997 Nov 25;94(24):13105-10.

17.

Association of single nucleotide polymorphisms in endothelin family genes with the progression of atherosclerosis in patients with essential hypertension.

Yasuda H, Kamide K, Takiuchi S, Matayoshi T, Hanada H, Kada A, Yang J, Miwa Y, Yoshii M, Horio T, Yoshihara F, Nakamura S, Nakahama H, Tei C, Miyata T, Kawano Y.

J Hum Hypertens. 2007 Nov;21(11):883-92. Epub 2007 May 24.

PMID:
17525706
18.

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. Epub 2007 Feb 22.

PMID:
17313575
19.

A mouse model of Waardenburg syndrome type 4 with a new spontaneous mutation of the endothelin-B receptor gene.

Matsushima Y, Shinkai Y, Kobayashi Y, Sakamoto M, Kunieda T, Tachibana M.

Mamm Genome. 2002 Jan;13(1):30-5.

PMID:
11773966
20.

Tyrosinase and tyrosinase related protein 1 alleles specify domestic cat coat color phenotypes of the albino and brown loci.

Schmidt-K√ľntzel A, Eizirik E, O'Brien SJ, Menotti-Raymond M.

J Hered. 2005 Jul-Aug;96(4):289-301. Epub 2005 Apr 27.

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