白毛 (Japanese Wikipedia)

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

refsWebsite

Global rank Japanese rank

8nih.gov

4^th place

24^th place

6doi.org

2^nd place

6^th place

1oxfordjournals.org

1,389^th place

1,710^th place

1springerlink.com

2,569^th place

2,101^st 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"
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.
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.
Haase B, Brooks SA, Tozaki T, et al. (October 2009). “Seven novel KIT mutations in horses with white coat colour phenotypes”. Animal Genetics 40 (5): 623–9. doi:10.1111/j.1365-2052.2009.01893.x. PMID 19456317.
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 2008年9月4日閲覧。.
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.

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.
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.
Pulos WL, Hutt FB (1969). “Lethal dominant white in horses”. The Journal of Heredity 60 (2): 59–63. PMID 5816567.
Haase B, Brooks SA, Tozaki T, et al. (October 2009). “Seven novel KIT mutations in horses with white coat colour phenotypes”. Animal Genetics 40 (5): 623–9. doi:10.1111/j.1365-2052.2009.01893.x. PMID 19456317.
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 2008年9月4日閲覧。.
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.

ncbi.nlm.nih.gov

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.

oxfordjournals.org

jhered.oxfordjournals.org

Pulos WL, Hutt FB (1969). “Lethal dominant white in horses”. The Journal of Heredity 60 (2): 59–63. PMID 5816567.

springerlink.com

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 2008年9月4日閲覧。.