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128 related items for PubMed ID: 24758835
1. 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; 76(8):1093-8. PubMed ID: 24758835 [Abstract] [Full Text] [Related]
2. Piebald mutation on a C57BL/6J background. Fukushima S, Niimi K, Takahashi E. J Vet Med Sci; 2015 Feb; 77(2):161-6. PubMed ID: 25328005 [Abstract] [Full Text] [Related]
3. 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. PubMed ID: 16500897 [Abstract] [Full Text] [Related]
4. Age-dependent kainate sensitivity in heterozygous rolling Nagoya Cav2.1 channel mutant mice. Kim TY, Yoshimoto T, Aoyama Y, Niimi K, Takahashi E, Itakura C. Pharmacol Biochem Behav; 2014 Sep 21; 124():250-9. PubMed ID: 24992728 [Abstract] [Full Text] [Related]
5. GABAA Receptor Expression in the Forebrain of Ataxic Rolling Nagoya Mice. Nielsen EO, Kaja S. Biol Med (Aligarh); 2014 Sep 21; 6(1):. PubMed ID: 25309056 [Abstract] [Full Text] [Related]
6. Reduced voltage sensitivity of activation of P/Q-type Ca2+ channels is associated with the ataxic mouse mutation rolling Nagoya (tg(rol)). Mori Y, Wakamori M, Oda S, Fletcher CF, Sekiguchi N, Mori E, Copeland NG, Jenkins NA, Matsushita K, Matsuyama Z, Imoto K. J Neurosci; 2000 Aug 01; 20(15):5654-62. PubMed ID: 10908603 [Abstract] [Full Text] [Related]
7. Analysis of the protective effects of a neuronal Cav2.1 calcium channel in brain injury. Kim TY, Yoshimoto T, Aoyama Y, Niimi K, Takahashi E. Neuroscience; 2016 Jan 28; 313():110-21. PubMed ID: 26616403 [Abstract] [Full Text] [Related]
8. Differential cerebellar GABAA receptor expression in mice with mutations in CaV2.1 (P/Q-type) calcium channels. Kaja S, Payne AJ, Nielsen EØ, Thompson CL, van den Maagdenberg AM, Koulen P, Snutch TP. Neuroscience; 2015 Sep 24; 304():198-208. PubMed ID: 26208839 [Abstract] [Full Text] [Related]
9. Nucleotide sequence of endothelin-B receptor gene reveals origin of piebald mutation in laboratory mouse. Kumagai T, Wada A, Tsudzuki M, Nishimura M, Kunieda T. Exp Anim; 1998 Oct 24; 47(4):265-9. PubMed ID: 10067171 [Abstract] [Full Text] [Related]
10. 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 24; 9(1):15-9. PubMed ID: 9434939 [Abstract] [Full Text] [Related]
11. Hypoalgesic behaviors of P/Q-type voltage-gated Ca2+ channel mutant mouse, rolling mouse Nagoya. Fukumoto N, Obama Y, Kitamura N, Niimi K, Takahashi E, Itakura C, Shibuya I. Neuroscience; 2009 Apr 21; 160(1):165-73. PubMed ID: 19248821 [Abstract] [Full Text] [Related]
12. 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]
13. Impaired growth and differentiation of diploid but not immortal melanoblasts from endothelin receptor B mutant (piebald) mice. Sviderskaya EV, Easty DJ, Bennett DC. Dev Dyn; 1998 Dec 30; 213(4):452-63. PubMed ID: 9853966 [Abstract] [Full Text] [Related]
14. Protein expression pattern in cerebellum of Cav2.1 mutant, tottering-6j mice. Kim TY, Niimi K, Takahashi E. Exp Anim; 2016 Jul 29; 65(3):207-14. PubMed ID: 26887908 [Abstract] [Full Text] [Related]
15. Zebrin II expressing Purkinje cell phenotype-related and -unrelated cerebellar abnormalities in Cav2.1 mutant, rolling mouse Nagoya. Sawada K, Fukui Y. ScientificWorldJournal; 2010 Oct 12; 10():2032-8. PubMed ID: 20953553 [Abstract] [Full Text] [Related]
16. Anatomic modifications in the enteric nervous system of JF1 mice with the classic piebald mutation. Dang R, Sasaki N, Torigoe D, Agui T. J Vet Med Sci; 2012 Mar 12; 74(3):391-4. PubMed ID: 22067082 [Abstract] [Full Text] [Related]
17. 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 12; 38(2):103-8. PubMed ID: 17313575 [Abstract] [Full Text] [Related]
18. 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 12; 55(5):491-5. PubMed ID: 17090968 [Abstract] [Full Text] [Related]
19. 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. PubMed ID: 9371807 [Abstract] [Full Text] [Related]
20. Age-related spatial and nonspatial short-term memory in Cav2.1alpha1 mutant mice, Rolling Nagoya. Takahashi E, Niimi K, Itakura C. Behav Brain Res; 2009 Dec 01; 204(1):241-5. PubMed ID: 19467269 [Abstract] [Full Text] [Related] Page: [Next] [New Search]