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Andersson L.S., Axelsson J., Dubielzig R.R., Lindgren G., Ekesten B. Multiple congenital ocular anomalies in Icelandic horses BMC Veterinary Research, 2011 May 26; 7:21.
Andersson L.S., Juras L., Ramsey D.T., Eason-Butler J., Ewart S., Cothran G., Lindgren G. Equine Multiple Congenital Anomalies maps to f 4.9 megabase interval on horse chromosome 6 / BMC Genetics 2008. 9:88.
Andersson L.S., Lyberg K., Cothran G., Ramsey D.T., Juras L., Mikko S., Ekesten B., Ewart S., Lindgren G. Targeted analysis of four breeds narrows equine Multiple Congenital Ocular Anomalies locus to 208 kilobases / Mammalian Genome, 2011 June, 22(5-6):353-60.
Bellone R.R. Pleiotropic effects of pigmentation genes in horses / Animal Genetics, 2010, Volume 41 (Suppl. 2), 100-110.
Bellone R.R., Archer S., Wade C.M., Cuka-Lawson C., Haase B., Leeb T., Forsyth G., Sandmeyer L., Grahn B. Association analysis of candidate SNPs in TRPM1 with leopard complex spotting (LP) and congenital stationary night blindness (CSNB) in horses / Animal Genetics, Volume 41, Issue Supplement s2, December 2010. – P. 207.
Bellone R.R., Brooks S.A., Sandmeyer L., Murphy B.A., Forsyth G., Archer S., Bailey E., Grahn B. Different Gene Expression of TRPM1, the Potential Cause of Congenital Stationary Night Blindness and Coat Spotting Patterns (LP) in the Appaloosa Horse (Equus caballus) / Genetics, 2008 August, 179(4): 1861-1870.
Haase B., Obexer-Ruff G., Dolf G., Rieder S., Burger D., Poncet P.A., Gerber V., Howard J., Leeb T. Haematological parameters are normal in dominant white Franches-Montagnes horses carrying a KIT mutation / Veterinary Journal, 2010 June; 184(3): 315-7.
Harland M.M., Stewart A.J., Marshall A.E., Belknap E.B. Diagnosis of deafness in a horse by brainstem auditory evoked potential / Canadian Veterinary Journal, 2006, February; 47(2): 151-4.
Hauswirth R., Haase B., Blatter M., Brooks S.A., Burger D., Drögemüller C., Gerber V., Henke D., Janda J., Jude R., Magdesian K.G., Matthews J.M., Poncet P.-A., Svansson V., Tozaki T., Wilkinson-White L., Penedo M.C.T., Rieder S., Leeb T. Mutations in MITF and PAX3 Cause “Splashed White” and Other White Spotting Phenotypes in Horses / PLoS Genetics, April 2012.
Ishikawa Y., Mukoyama H., Matsuura T., Mukai T., Watanabe S. Establishments and biological characteristics of melanoma culture cell lines derived from aged grey horses / Journal of Equine Science, 33, 2000. – P. 75-82.Komáromy A.M., Rowlan J.S., La Croix N.C., Mangan B.G. Equine Multiple Congenital Ocular Anomalies (MCOA) syndrome in PMEL17 (Silver) mutant ponies: five cases / Veterinary Ophtalmology, 2011 September; 14(5):313-20.
Lightbody T. Foal with Overo lethal white syndrome born to a registered Quarter horse mare / The Canadian Veterinary Journal. La Revue vétérinaire canadienne, September 2002, Vol. 43, № 9. – P. 715-717.
Pielberg G., Golovko A., Sundström E., Curik I., Lennartsson J., Seltenhammer M.H., Druml T., Binns M., Fitzsimmons C., Lindgren G., Sandberg K., Baumung G., Vetterlein M., Strömberg S., Grabherr M., Wade C., Lindblad-Toh K., Pontén F., Heldin C.H., Sölkner J., Andersson L. A cis-acting regulatory mutation causes premature hair graying and susceptibility to melanoma in the horse / Nature Genetics, 2008, August, 40(8).
Rieder S., Stricker C., Joerg H., Dummer R., Stranzinger G. A comparative genetic approach for the investigation of ageing grey horse melanoma / Journal of Animal Breeding and Genetics, vol. 117(2), 2000. – P.73-82.
Sandmeyer L.S. Equine Recurrent Uveitis, July 2008, режим доступа: http://www.appaloosaproject.info/in...er_op=view_page&PAGE_id=40&MMN_position=68:68
Sandmeyer L.S., Breaux C.B., Archer S., Grahn B.H. Clinical and electroretinographic characteristics of congenital stationary night blindness in the Appaloosa and the association with the leopard complex / Veterinary Ophtalmology, 2007 November-December; 10(6): 368-75.
Santschi E.M., Vrotsos Paul D., Purdy A.K., Mickelson J.R. Incidence of the endothelin receptor B mutation that causes lethal white foal syndrome in white-patterned horses / American Journal of Veterinary Research, № 1, 2001. – P. 97-103.
Курская В. А. Распространение доминантного аллеля гена Silver в отечественных породах лошадей [Текст] // Инновационные технологии в сельском хозяйстве: материалы Междунар. науч. конф. (г. Москва, июнь 2015 г.). — М.: Буки-Веди, 2015. — С. 34-40.
Курская В. А. Масть в тяжеловозных породах: перспективы использования в качестве селекционируемого признака //
Иппология и ветеринария 2017, №2.
Курская В. А. Наследственные заболевания лошадей тяжеловозных пород // Иппология и ветеринария, в печати.
Andersson L.S., Juras L., Ramsey D.T., Eason-Butler J., Ewart S., Cothran G., Lindgren G. Equine Multiple Congenital Anomalies maps to f 4.9 megabase interval on horse chromosome 6 / BMC Genetics 2008. 9:88.
Andersson L.S., Lyberg K., Cothran G., Ramsey D.T., Juras L., Mikko S., Ekesten B., Ewart S., Lindgren G. Targeted analysis of four breeds narrows equine Multiple Congenital Ocular Anomalies locus to 208 kilobases / Mammalian Genome, 2011 June, 22(5-6):353-60.
Bellone R.R. Pleiotropic effects of pigmentation genes in horses / Animal Genetics, 2010, Volume 41 (Suppl. 2), 100-110.
Bellone R.R., Archer S., Wade C.M., Cuka-Lawson C., Haase B., Leeb T., Forsyth G., Sandmeyer L., Grahn B. Association analysis of candidate SNPs in TRPM1 with leopard complex spotting (LP) and congenital stationary night blindness (CSNB) in horses / Animal Genetics, Volume 41, Issue Supplement s2, December 2010. – P. 207.
Bellone R.R., Brooks S.A., Sandmeyer L., Murphy B.A., Forsyth G., Archer S., Bailey E., Grahn B. Different Gene Expression of TRPM1, the Potential Cause of Congenital Stationary Night Blindness and Coat Spotting Patterns (LP) in the Appaloosa Horse (Equus caballus) / Genetics, 2008 August, 179(4): 1861-1870.
Haase B., Obexer-Ruff G., Dolf G., Rieder S., Burger D., Poncet P.A., Gerber V., Howard J., Leeb T. Haematological parameters are normal in dominant white Franches-Montagnes horses carrying a KIT mutation / Veterinary Journal, 2010 June; 184(3): 315-7.
Harland M.M., Stewart A.J., Marshall A.E., Belknap E.B. Diagnosis of deafness in a horse by brainstem auditory evoked potential / Canadian Veterinary Journal, 2006, February; 47(2): 151-4.
Hauswirth R., Haase B., Blatter M., Brooks S.A., Burger D., Drögemüller C., Gerber V., Henke D., Janda J., Jude R., Magdesian K.G., Matthews J.M., Poncet P.-A., Svansson V., Tozaki T., Wilkinson-White L., Penedo M.C.T., Rieder S., Leeb T. Mutations in MITF and PAX3 Cause “Splashed White” and Other White Spotting Phenotypes in Horses / PLoS Genetics, April 2012.
Ishikawa Y., Mukoyama H., Matsuura T., Mukai T., Watanabe S. Establishments and biological characteristics of melanoma culture cell lines derived from aged grey horses / Journal of Equine Science, 33, 2000. – P. 75-82.Komáromy A.M., Rowlan J.S., La Croix N.C., Mangan B.G. Equine Multiple Congenital Ocular Anomalies (MCOA) syndrome in PMEL17 (Silver) mutant ponies: five cases / Veterinary Ophtalmology, 2011 September; 14(5):313-20.
Lightbody T. Foal with Overo lethal white syndrome born to a registered Quarter horse mare / The Canadian Veterinary Journal. La Revue vétérinaire canadienne, September 2002, Vol. 43, № 9. – P. 715-717.
Pielberg G., Golovko A., Sundström E., Curik I., Lennartsson J., Seltenhammer M.H., Druml T., Binns M., Fitzsimmons C., Lindgren G., Sandberg K., Baumung G., Vetterlein M., Strömberg S., Grabherr M., Wade C., Lindblad-Toh K., Pontén F., Heldin C.H., Sölkner J., Andersson L. A cis-acting regulatory mutation causes premature hair graying and susceptibility to melanoma in the horse / Nature Genetics, 2008, August, 40(8).
Rieder S., Stricker C., Joerg H., Dummer R., Stranzinger G. A comparative genetic approach for the investigation of ageing grey horse melanoma / Journal of Animal Breeding and Genetics, vol. 117(2), 2000. – P.73-82.
Sandmeyer L.S. Equine Recurrent Uveitis, July 2008, режим доступа: http://www.appaloosaproject.info/in...er_op=view_page&PAGE_id=40&MMN_position=68:68
Sandmeyer L.S., Breaux C.B., Archer S., Grahn B.H. Clinical and electroretinographic characteristics of congenital stationary night blindness in the Appaloosa and the association with the leopard complex / Veterinary Ophtalmology, 2007 November-December; 10(6): 368-75.
Santschi E.M., Vrotsos Paul D., Purdy A.K., Mickelson J.R. Incidence of the endothelin receptor B mutation that causes lethal white foal syndrome in white-patterned horses / American Journal of Veterinary Research, № 1, 2001. – P. 97-103.
Курская В. А. Распространение доминантного аллеля гена Silver в отечественных породах лошадей [Текст] // Инновационные технологии в сельском хозяйстве: материалы Междунар. науч. конф. (г. Москва, июнь 2015 г.). — М.: Буки-Веди, 2015. — С. 34-40.
Курская В. А. Масть в тяжеловозных породах: перспективы использования в качестве селекционируемого признака //
Иппология и ветеринария 2017, №2.
Курская В. А. Наследственные заболевания лошадей тяжеловозных пород // Иппология и ветеринария, в печати.
