Кошки, гены и эволюция - Павел Михайлович Бородин

79 Kehler J. S. et al. Four independent mutations in the feline fibroblast growth factor 5 gene determine the long-haired phenotype in domestic cats. Heredity 6 (2007): 555–66.

80 Берг Р. Л. Суховей. Воспоминания генетика. М.: Памятники исторической мысли, 2003.

81 Batchelor T. The revival of the German Rex. 2006. https://www.pawpeds.com/cms/index.php/en/education/articles/history/revival-of-german-rex-en.

82 Корнуэльский рекс. https://cfa.org/cornish-rex/cornish-rex-article/.

83 Gandolfi B. et al. To the root of the curl: A signature of a recent selective sweep identifies a mutation that defines the Cornish Rex cat breed. PLoS One 6 (2013): e67105.

84 Manakhov A. D. et al. The curly coat phenotype of the Ural Rex feline breed is associated with a mutation in the lipase H gene. Animal Genetics 4 (2020): 584–89.

85 Девон-рекс. https://cfa.org/devon-rex/.

86 Gandolfi B. et al. The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71. Mammalian genome 21 (2010): 509–15.

87 Селкирк-рекс. https://cfa.org/breed/selkirk-rex/.

88 Gandolfi B. et al. A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats. Scientific reports 3 (2013): 2000.

89 Lasisi T. et al. Human scalp hair as a thermoregulatory adaptation. Proceedings of the National Academy of Sciences of the USA 24 (2023): e2301760120.

90 Fogh J. The nude mouse in experimental and clinical research. Elsevier, 2014.

91 Hartwell S. The uncensored origins of the Lykoi. 2018. http://messybeast.com/lykoi-story.htm.

92 Buckley R. M. et al. Werewolf, there wolf: variants in Hairless associated with hypotrichia and roaning in the lykoi cat breed. Genes 6 (2020): 682.

93 Gandolfi B. et al. A dominant TRPV4 variant underlies osteochondrodysplasia in Scottish fold cats. Osteoarthritis and cartilage 8 (2016): 1441–50.

94 Jackson O. F. Congenital bone lesions in cats with folded-ears. Bulletin of the Feline Advisory Bureau 14 (1975): 2–4.

95 Шотландская вислоухая. https://cfa.org/scottish-fold.

96 Malik R. et al. Osteochondrodysplasia in Scottish Fold Cats. Australian veterinary journal 2 (1999): 85–92.

97 Chang J. et al. Osteochondrodysplasia in three scottish fold cats. Journal of veterinary science 3 (2007): 307–9.

98 Slingerland L. I. et al. Cross-sectional study of the prevalence and clinical features of osteoarthritis in 100 cats. Veterinary journal 3 (2011): 304–9.

99 Takanosu M., Hattori Y. Osteochondrodysplasia in scottish fold cross-breed cats. The Journal of veterinary medical science 12 (2020): 1769–72.

100 Rorden C. et al. Radiographical Survey of Osteochondrodysplasia in Scottish Fold Cats caused by the TRPV4 gene variant. Human genetics 140 (2021): 1525–34.

101 Robinson R. The American curl cat. Journal of Heredity 6 (1989): 474–75.

102 Американский керл: балансирование на грани. https://cfa.org/american-curl-article/.

103 Little C. C. Four-ears, a recessive mutation in the cat. Journal of Heredity 2 (1957): 57.

104 Garcia F. Four-eared cat called Batman adopted from a Pittsburgh shelter. Independent, August 11, 2016.

105 Toureille C. Fur real! Kitten who was born with FOUR ears, loves to cuddle and is friends with two Golden Retrievers goes viral on Instagram. Daily Mail, November 14, 2021.

106 Cavanagh J. A. et al. Bulldog dwarfism in Dexter cattle is caused by mutations in ACAN. Mammalian genome 11 (2007): 808–14.

107 Struck A. K. et al. A structural UGDH variant associated with standard Munchkin cats. BMC genetics 1 (2020), 67.

108 Mestrinho L. A. et al. Open surgical correction combined with an external splint for correction of a non-compliant pectus excavatum in a cat. Journal of Feline Medicine and Surgery 2 (2012): 151–54.

109 Lettice L. A. et al. Point mutations in a distant sonic hedgehog cis-regulator generate a variable regulatory output responsible for preaxial polydactyly. Human molecular genetics 7 (2008): 978–85.

110 Blanc I. et al. Unusual pattern of Sonic hedgehog expression in the polydactylous mouse mutant Hemimelic extra-toes. The International journal of developmental biology 46 (2002): 969–74.

111 Heus H. C. et al. A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36. Genomics 57 (1999): 342–51.

112 Dunn I. C. et al. The chicken polydactyly (Po) locus causes allelic imbalance and ectopic expression of Shh during limb development. Developmental dynamics 5 (2011): 1163–72.

113 Searle A. G. Hereditary split-hand in the domestic cat. Annals of eugenics 4 (1953): 279–82.

114 Wang H. et al. The pathogenic mechanism of syndactyly type V identified in a Hoxd13Q50R knock-in mice. Bone research 1 (2024): 21.

115 Buckingham K. J. et al. Multiple mutant T alleles cause haploinsufficiency of Brachyury and short tails in Manx cats. Mammalian genome 24 (2013): 400–08.

116 Haworth K. et al. Canine homolog of the T-box transcription factor T; failure of the protein to bind to its DNA target leads to a short-tail phenotype. Mammalian genome 12 (2001): 212–18.

117 Beddington R. S. et al. Brachyury – a gene affecting mouse gastrulation and early organogenesis. Development 1992: 157–65.

118 Kaempfer E. Kaempfer’s Japan: Tokugawa culture observed. University of Hawai’i Press, 1999.

119 Японский бобтейл. https://cfa.org/japanese-bobtail/.

120 Милн А. Винни-Пух и все-все-все. М.: Росмэн, 2021.

121 Xu X. et al. Whole genome sequencing identifies a missense mutation in HES7 associated with short tails in Asian domestic cats. Scientific reports 6 (2016): 31583.

122 Lyons L. A. et al. Whole genome sequencing in cats, identifies new models for blindness in AIPL1 and somite segmentation in HES7. BMC Genomics 17 (2016): 265.

123 Helgren J. A. Barron’s encyclopedia of cat breeds: a complete guide to the domestic cats of North America. NY: Barron’s Educational Series, Inc., 1997.

124 Willet C. E. et al. Canine disorder mirrors human disease: exonic deletion in HES7 causes autosomal recessive spondylocostal dysostosis in miniature Schnauzer dogs. Plos One. 2 (2015): e0117055.

125 Hytonen M. K. et al. Ancestral T-box mutation is present in many, but not all, short-tailed dog breeds. The Journal of heredity 2 (2008): 236–40.

126 Чехов А. П. Письмо к ученому соседу // Чехов А. П. Полное собрание сочинений и писем (в 30 т.). М.: Наука, 1974–1982.

127 Xia B. et al. On the genetic basis of tail-loss evolution in humans and apes. Nature 626 (2024): 1042–48.

128 Аульченко Ю. С. и др. Практическая и молекулярная генетика для начинающих. М.: Просвещение, 2024.

129 Бородин П. М. и др. Иммунофлуоресцентный анализ мейотической рекомбинации и интерференции у домашней кошки. Цитология 50 (2008): 60–64.

130 Segura J. et al. Evolution of recombination in eutherian mammals: insights into mechanisms that affect recombination rates and crossover interference. Proceedings. Biological sciences 280 (2013): 20131945.

131 Gobello C. Key aspects of domestic cat spermatogenesis. Reproduction in domestic animals 5 (2022): 459–64.

132 Wildt D. E. Fertilization in Cats // Dunbar B. S., O’Rand M. G. (eds). A Comparative Overview of Mammalian Fertilization. Boston: Springer US, 1991.

133 Knospe C. Periods and stages of the prenatal development of the domestic cat. Anatomia, histologia, embryologia 31 (2002): 37–51.

134 King V. et al. Evolution of the male-determining gene SRY-within the cat family Felidae. Genetics 175 (2007): 1855–67.

135 Vining B. et al. Diverse regulation but conserved function: SOX9 in vertebrate sex determination. Genes (Basel) 12 (2021): 486.

136 Foster J. W. et al. Evolution of sex determination