Vashetko, E., Esipov A., Bykova, E., & Kreuzberg, E. (2005). Snow Leopard Bibliography. Central Asia (Abstracts).
Abstract: Bibliography of the Snow Leopard included publications on the studying various questions of ecology and conservation of the Snow Leopard in Central Asia (305) for the period 1873 to 2004. The most important works on this species in the region, as well as results of the analysis of timing of publications was described.
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Velte, F. (1982). Snow leopards at the Seneca Zoological Park, Rochester. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 3 (Vol. 3, pp. 55–58). Helsinki: Helsinki Zoo.
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Vogt, P. (1982). New enclosures for snow leopards (Uncia uncia) at Krefeld Zoo. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 3 (Vol. 3, pp. 67–70). Helsinki: Helsinki Zoo.
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Wahlberg, C., Tarkkanen, A., & Blomqvist, L. (1982). Further observations on the multiple ocular coloboma (MOC) in the snow leopard, Panthers uncia. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards (Vol. 3, pp. 139–144). Helsinki: Helsinki Zoo.
Abstract: The first observation of the occurrence of multiple ocular coloboma (MOC) in a snow leopard was reported in the International Pedigree Book of Snow Leopards Volume I in 1978 (1). The lesions in this syndrome consist of coloboma of the upper eye lid and uveal coloboma of the globe. Even colobomatous retinal cysts and retinal dysplasia have been noted. The ethiology of in all ten cases of MOC in the snow leopards kept at the Helsinki Zoo were described and discussed in detail in Volume II of the International Pedigree Book of Snow Leopards (2,3). Three cases of MOC in the snow leopards kept at Henry Doorly Zoo, Omaha, Ne., have been described by Phillips (4), one case is known of in Amsterdam (van Bree, personal communication), and two cases in Zoo Zurich (Isenbugel and Weilenmann, pers. comm.) The ethiology of the defect is still not known although various theories ranging from genetic to exogenous factors have been presented.
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Wahlberg, C. (1980). Autopsy findings and causes of death in captive snow leopards (Panthera uncia): a preliminary report. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards (Vol. 2, pp. 205–217). Helsinki: Helsinki Zoo.
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Wahlberg, C., & Tarkkanen, A. (1980). On the multiple ocular coloboma with retinal dysplasia (MOC) in snow leopards, Pantera uncia. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards (Vol. 2, pp. 183–194). Helsinki: Helsinki Zoo.
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Wangchuk, R., & Jackson, R. (2009). A Community-based Approach to Mitigating Livestock-Wildlife Conflict in Ladakh, India.
Abstract: Livestock depredation by snow leopard and wolf is widespread across the Himalayan region (Jackson et al. 1996, Jackson and Wangchuk 2001; Mishra 1997, Oli et al 1994). For example, in India's Kibber Wildlife Sanctuary, Mishra (1997) reported losses amounting to 18% of the livestock holdings and valued at about US $138 per household. The villagers claimed predation rates increased after establishment of the sanctuary, but
surveys indicated a dramatic increase in livestock numbers accompanying changes in animal husbandry systems (Mishra 2000).
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Ward, A. E. (1921). Game animals of Kashmir and adjacent hill provinces. J.of Bombay Natural Historical Society., 29, 23–35.
Abstract: comments that snow leopard may take blue sheep as prey
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Warren E.Johnson, E. E. (2006). The Late Miocene Radiation of Modern Felidae: A Genetic Assessment (Stephen J.O'Brien Emma Teeling Agostinho Antunes W. J. M. Jill Pecon-Slattery, Ed.) (Vol. 311). Washington D.C.
Abstract: Modern felid species descend from relatively recent (<11 million years ago) divergence and
speciation events that produced successful predatory carnivores worldwide but that have
confounded taxonomic classifications. A highly resolved molecular phylogeny with divergence dates
for all living cat species, derived from autosomal, X-linked, Y-linked, and mitochondrial gene
segments (22,789 base pairs) and 16 fossil calibrations define eight principal lineages produced
through at least 10 intercontinental migrations facilitated by sea-level fluctuations. A ghost lineage
analysis indicates that available felid fossils underestimate (i.e., unrepresented basal branch
length) first occurrence by an average of 76%, revealing a low representation of felid lineages
in paleontological remains. The phylogenetic performance of distinct gene classes showed that
Y-chromosome segments are appreciably more informative than mitochondrial DNA, X-linked,
or autosomal genes in resolving the rapid Felidae species radiation.
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Watanabe, M., Sugano, S., Togashi, T., Imai, J., Uchida, K., Yamaguchi, R., et al. (2000). Molecular cloning and phylogenetic analysis of canine beta-casein. DNA Seq, 11(3-4), 295–300.
Abstract: A canine beta-casein cDNA was isolated from mammary tissue by polymerase chain reaction (PCR) using degenerate primers. It encodes 250 amino acids protein containing the conserved sequence motif of beta- casein. It showed the highest homology with snow-leopard (Uncia uncia (55-62% identity). It also showed 44-53% identity with human, 33-42%, identity with mouse, 29-37%, identity with rat, 43-53% identity with rabbit, 41-48% identity with pig, 44-51% identity with cattle and 44- 50% identity with sheep. A 1.2-kb mRNA was detected in mammary tissue by Northern blot analysis. Phylogenetic analysis revealed that canine beta-casein formed a branch with lesser panda and snow leopard, which were grouped into carnivore.
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