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駁毛 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "駁毛" in Japanese language version.

refsWebsite
Global rank Japanese rank
7nih.gov
4th place
24th place
6doi.org
2nd place
6th place
1studbook.jp
low place
3,432nd place
1jockeyclub.com
low place
low place
1springerlink.com
2,569th place
2,101st place

doi.org

  • Brooks, Samantha; Ernest Bailey (2005). “Exon skipping in the KIT gene causes a sabino spotting pattern in horses”. Mammalian Genome 16 (11): 893–902. doi:10.1007/s00335-005-2472-y. PMID 16284805. "Chapter 3" 
  • Haase, B., S. A. Brooks, A. Schlumbaum, P. Azor, E. Bailey et al. (2007). “Allelic Heterogeneity at the Equine KIT Locus in Dominant White (W) Horses”. PLoS Genet 3 (11): e195. doi:10.1371/journal.pgen.0030195. 
  • Marklund, S; M Moller, K Sandberg, L Andersson (1999). “Close association between sequence polymorphism in the KIT gene and the roan coat color in horses”. Mammalian Genome 10 (3): 283–288. doi:10.1007/s003359900987. PMID 10051325. 
  • Metallinos, DL; Bowling AT, Rine J (June 1998). “A missense mutation in the endothelin-B receptor gene is associated with Lethal White Foal Syndrome: an equine version of Hirschsprung Disease”. Mammalian Genome (New York: Springer New York) 9 (6): 426–31. doi:10.1007/s003359900790. PMID 9585428. http://www.springerlink.com/content/xehe4p28y8p7cw98/ 2008年9月4日閲覧。. 
  • Brooks SA, Lear TL, Adelson DL, Bailey E. (2007). “A chromosome inversion near the KIT gene and the Tobiano spotting pattern in horses”. Cytogenet Genome Res. 119: 225-30. doi:10.1159/000112065. PMID 18253033. 
  • Bellone, Rebecca R; Brooks SA, Sandmeyer L, Murphy BA, Forsyth G, Archer S, Bailey E, Grahn B (August 2008). “Differential Gene Expression of TRPM1, the Potential Cause of Congenital Stationary Night Blindness and Coat Spotting Patterns (LP) in the Appaloosa Horse (Equus caballus)”. Genetics (Genetics Society of America) 179 (4): 1861–1870. doi:10.1534/genetics.108.088807. PMC 2516064. PMID 18660533. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2516064/. 

jockeyclub.com

registry.jockeyclub.com

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Brooks, Samantha; Ernest Bailey (2005). “Exon skipping in the KIT gene causes a sabino spotting pattern in horses”. Mammalian Genome 16 (11): 893–902. doi:10.1007/s00335-005-2472-y. PMID 16284805. "Chapter 3" 
  • Marklund, S; M Moller, K Sandberg, L Andersson (1999). “Close association between sequence polymorphism in the KIT gene and the roan coat color in horses”. Mammalian Genome 10 (3): 283–288. doi:10.1007/s003359900987. PMID 10051325. 
  • Metallinos, DL; Bowling AT, Rine J (June 1998). “A missense mutation in the endothelin-B receptor gene is associated with Lethal White Foal Syndrome: an equine version of Hirschsprung Disease”. Mammalian Genome (New York: Springer New York) 9 (6): 426–31. doi:10.1007/s003359900790. PMID 9585428. http://www.springerlink.com/content/xehe4p28y8p7cw98/ 2008年9月4日閲覧。. 
  • Brooks SA, Lear TL, Adelson DL, Bailey E. (2007). “A chromosome inversion near the KIT gene and the Tobiano spotting pattern in horses”. Cytogenet Genome Res. 119: 225-30. doi:10.1159/000112065. PMID 18253033. 
  • Bellone, Rebecca R; Brooks SA, Sandmeyer L, Murphy BA, Forsyth G, Archer S, Bailey E, Grahn B (August 2008). “Differential Gene Expression of TRPM1, the Potential Cause of Congenital Stationary Night Blindness and Coat Spotting Patterns (LP) in the Appaloosa Horse (Equus caballus)”. Genetics (Genetics Society of America) 179 (4): 1861–1870. doi:10.1534/genetics.108.088807. PMC 2516064. PMID 18660533. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2516064/. 

ncbi.nlm.nih.gov

pmc.ncbi.nlm.nih.gov

springerlink.com

studbook.jp