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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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Waits, L. P., Buckley-Beason, V. A., Johnson, W. E., Onorato, D., & McCarthy, T. (2006). A select panel of polymorphic microsatellite loci for individual identification of snow leopards (Panthera uncia)
(Vol. 7).
Abstract: Snow leopards (Panthera uncia) are elusive endangered carnivores found in remote mountain regions of Central Asia. New methods for identifying and counting snow leopards are needed for conservation and management efforts. To develop molecular genetic tools for individual identification of hair and faecal samples, we screened 50 microsatellite loci developed for the domestic cat (Felis catus) in 19 captive snow leopards. Forty-eight loci were polymorphic with numbers of alleles per locus ranging from two to 11. The probability of observing matching genotypes for unrelated individuals (2.1 x10-11) and siblings (7.5x10-5) using the 10 most polymorphic loci was low, suggesting that this panel would easily discriminate among individuals in the wild.
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Wajrak, A. (1994). Snow Leopard Skins in Poland (Polowanie Na Sniezna Pantere).
Abstract: Full Text: In 1991, Dr Andrzej Kruszewicz of the Institute of Ecology of the Polish Academy of Sciences saw a “quite fresh” snow leopard skin on sale by a Russian in a Warsaw market for three million Polish zlotys ($300). A few weeks later he saw another skin in a shop in the centre of Warsaw. In spring 1992, Marcin Waslawski from the Institute of Geography saw a snow leopard skin in the same market for the equivalent of $200. The seller was an Asian from a former Soviet Republic. In summer 1992, Wajrak himself saw a snow leopard skin in a hunters' shop in Warsaw and in winter saw one in the home of a Polish hunter, who said it was a gift from a Mongolian friend. In winter 1994, a student from Britain saw a Polish long coat of snow leopard skins in Bialowieza. Wajrak saw a skin in a Warsaw shop, which the owner said was 15-20 years old; he got it from a Polish diplomat who had been in Mongolia and had three snow leopard skins. The skin was priced at the equivalent of $1,000. Wajrak added that he had been told that it was possible to buy tiger skins from Russians in Poland and he was trying to find one; I have not heard from him since.
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Wang, X., & Schaller, G. B. (1996). Status of large mammals in Western Inner Mongolia, China. Journal of East China Normal University (Special Issue of Zoology), , 93–104.
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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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Wangchuk, T. R. (1992). Snow Leopard: Its Management with Emphasis on Bhutan.
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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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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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Wei, L., Wu, X., & Jiang, Z. (2008). The complete mitochondrial genome structure of snow leopard Panthera uncia.
Abstract: The complete mitochondrial genome (mtDNA) of snow leopard Panthera uncia was obtained by using the polymerase chain reaction (PCR) technique based on the PCR fragments of 30 primers we designed. The entire mtDNA sequence was 16 773 base pairs (bp) in length, and the base composition was: A-5,357ª“,Ž+bp (31.9%); C-4,444ª”,Ž+bp (26.5%); G-2,428ª“,Ž+bp (14.5%); T-4,544ª”,Ž+bp (27.1%). The structural characteristics [0] of the P. uncia mitochondrial genome were highly similar to these of Felis catus, Acinonyx jubatus, Neofelis nebulosa and other mammals. However, we found several distinctive features of the mitochondrial genome of Panthera unica. First, the termination codon of COIII was TAA, which differed from those of F. catus, A. jubatus and N. nebulosa. Second, tRNASer (AGY), which lacked the ''DHU'' arm, could not be folded into the typical cloverleaf-shaped structure. Third, in the control region, a long repetitive sequence in RS-2 (32ª“,Ž+bp) region was found with 2 repeats while one short repetitive segment (9ª”,Ž+bp) was found with 15 repeats in the RS-3 region. We performed phylogenetic analysis based on a 3 816ª",Ž+bp concatenated sequence of 12S rRNA, 16S rRNA, ND2, ND4, ND5, Cyt b and ATP8 for P. uncia and other related species, the result indicated that P. uncia and P. leo were the sister species, which was different from the previous findings. (c) 2008 Springer Science+Business Media B.V.
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Weilemann P. (1982). Experiences in births of snow leopards in Zurich Zoo. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 3 (Vol. 3, pp. 111–116). Helsinki: Helsinki Zoo.
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