Presidential Decree of the Russian Federation of February 28, 2024 no. 145 “About the Strategy of Scientific Technology Development of the Russian Federation”.

Gustavsson, I., Standard karyotype of the domestic pig, Hereditas, 1988, vol. 109, pp. 151—157. https://doi.org/10.1111/j.1601-5223.1988.tb00351.x

Article  CAS  PubMed  Google Scholar 

Adega, F., Chaves, R., and Guedes-Pinto, H., Chromosome restriction enzyme digestion in domestic pig (Sus scrofa) constitutive heterochromatin arrangement, Genes Genet. Syst., 2005, vol. 80, pp. 49—56. https://doi.org/10.1266/ggs.80.49

Article  CAS  PubMed  Google Scholar 

Hansen, K.M., Sequential Q- and C-band staining of pig chromosomes, and some comments on C-band polymorphism and C-band technique, Hereditas, 1982, vol. 96, pp. 183—189. https://doi.org/10.1111/j.1601-5223.1982.tb00848.x

Article  CAS  PubMed  Google Scholar 

Quilter, C.R., Blott, S.C., Mileham, A.J., et al., A mapping and evolutionary study of porcine sex chromosome gene, Mamm. Genome, 2002, vol. 13, pp. 588—594. https://doi.org/10.1007/s00335-002-3026-1

Article  CAS  PubMed  Google Scholar 

Cornefert-Jensen, F., Hare, W.C., and Abt, D.A., Identification of the sex chromosomes of the domestic pig, J. Hered., 1968, vol. 59, pp. 251—255. https://doi.org/10.1093/oxfordjournals.jhered.a107710

Article  CAS  PubMed  Google Scholar 

Grunwald, D., Geffrotin, C., Chardon, P., et al., Swine chromosomes: flow sorting and spot blot hybridization, Cytometry, 1986, vol. 7, pp. 582—588. https://doi.org/10.1002/cyto.990070613

Article  CAS  PubMed  Google Scholar 

Thomsen, P.D., Hindkjaer, J., and Christensen, K., Assignment of a porcine male-specific DNA repeat to Y-chromosomal heterochromatin, Cytogenet. Cell Genet., 1992, vol. 61, pp. 152—154. https://doi.org/10.1159/000133395

Article  CAS  PubMed  Google Scholar 

Alföldi, J., Skaletsky, H., Graves, T., et al., Sequence of the mouse Y chromosome, Conference presentation 18th International Mouse Genome Conference, Seattle, 2004.

Alföldi, J.E., Sequence of the mouse Y chromosome, PhD Thesis, Massachusetts: Massachusetts Inst. Technol., 2008.

Hamilton, C.K., Revay, T., Domander, R., et al., A large expansion of the HSFY gene family in cattle shows dispersion across Yq and testis-specific expression, PLoS One, 2011, vol. 6, no. 3, p. e17790. https://doi.org/10.1371/journal.pone.0017790

Article  CAS  PubMed  PubMed Central  Google Scholar 

Horng, Y.-M. and Huang, M.-C., Male-specific DNA sequences in pigs, Theriogenology, 2003, vol. 59, pp. 841—848. https://doi.org/10.1016/S0093-691X(02)01150-0

Article  CAS  PubMed  Google Scholar 

Pérez-Pérez, J. and Barragán, C., Isolation of four pig male-specific DNA fragments by RDA, Anim. Genet., 1998, vol. 29, pp. 157—158.

PubMed  Google Scholar 

Skinner, B.M., Lachani, K., Sargent, C.A., and Affara, N.A., Regions of XY homology in the pig X chromosome and the boundary of the pseudoautosomal region, BMC Genet., 2013, vol. 14, no. 3. https://doi.org/10.1186/1471-2156-14-3

Park, J., Cho, Y.G., Kim, J.K., and Kim, H.H., STS and PUDP deletion identified by targeted panel sequencing with CNV analysis in X-linked ichthyosis, Genes (Basel), 2023, vol. 14, no. 10, p. 1925. https://doi.org/10.3390/genes14101925

Article  CAS  PubMed  PubMed Central  Google Scholar 

Moghaddam, S., Houshangi, A.F., Eshratkhah, B., and Allahvirdizadeh, R., Clinical report of a Holstein’s calf with ichthyosis, Vet. Res. Forum, 2021, vol. 12, no. 1, pp. 133—135. https://doi.org/10.30466/vrf.2020.117113.2783

Article  PubMed  PubMed Central  Google Scholar 

Câmara, A.C.L., Borges, P.A.C., Paiva, S.A., and Pierezan, F., Ichthyosis fetalis in a cross-bred lamb, Vet. Dermatol., 2017, vol. 28, pp. 516—525. https://doi.org/10.1111/vde.12459

Article  PubMed  Google Scholar 

Belknap, E.B. and Dunstan, R.W., Congenital ichthyosis in a llama, J. Am. Vet. Med. Assoc., 1990, vol. 197, no. 6, pp. 764—767.

Article  CAS  PubMed  Google Scholar 

Holmes, R.S., Vertebrate patatin-like phospholipase domain-containing protein 4 (PNPLA4) genes and proteins: a gene with a role in retinol metabolism, 3 Biotech., 2012, vol. 2, pp. 277—286. https://doi.org/10.1007/s13205-012-0063-7

Gray, K.A., Yates, B., Seal, R.L., et al., Genenames.org: the HGNC resources in 2015, Nucleic Acids Res., 2015, vol. 43, no. D1, pp. D1079—D1085. https://doi.org/10.1093/nar/gku1071

Article  CAS  PubMed  Google Scholar 

Dodé, C. and Hardelin, J.P., Kallmann syndrome, Eur. J. Hum. Genet., 2009, vol. 17, no. 2, pp. 139—146. https://doi.org/10.1038/ejhg.2008.206

Article  CAS  PubMed  Google Scholar 

MacColl, G., Bouloux, P., and Quinton, R., Kallmann syndrome: adhesion, afferents, and anosmia, Neuron, 2002, vol. 34, no. 5, pp. 675—678. https://doi.org/10.1016/s0896-6273(02)00720-1

Article  CAS  PubMed  Google Scholar 

Prakash, S.K., Paylor, R., Jenna, S., et al., Functional analysis of ARHGAP6, a novel GTPase-activating protein for RhoA, Hum. Mol. Genet., 2000, vol. 9, no. 4, pp. 477—488. https://doi.org/10.1093/hmg/9.4.477

Article  CAS  PubMed  Google Scholar 

Brunet, T., McWalter, K., Mayerhanser, K., et al., Defining the genotypic and phenotypic spectrum of X-linked MSL3-related disorder, Genet. Med., 2021, vol. 23, no. 2, pp. 384—395. https://doi.org/10.1038/s41436-020-00993-y

Article  CAS  PubMed  Google Scholar 

Deciphering Developmental Disorders Study: Prevalence and architecture of de novo mutations in developmental disorders, Nature, 2017, vol. 542, pp. 433—438. https://doi.org/10.1038/nature21062

Lucas, C.G., Spate, A.M., Samuel, M.S., et al., A novel swine sex-linked marker and its application across different mammalian species, Transgenic Res., 2020, vol. 29, pp. 395—407. https://doi.org/10.1007/s11248-020-00204-z

Article  CAS  PubMed  PubMed Central  Google Scholar 

O’Connor, E., Eisenhaber, B., Dalley, J., et al., Species specific membrane anchoring of nyctalopin, a small leucine-rich repeat protein, Hum. Mol. Genet., 2005, vol. 14, no. 13, pp. 1877—1887. https://doi.org/10.1093/hmg/ddi194

Article  CAS  PubMed  Google Scholar 

Huang, T.N. and Hsueh, Y.P., CASK point mutation regulates protein–protein interactions and NR2b promoter activity, Biochem. Biophys. Res Commun., 2009, vol. 382, no. 1, pp. 219—222. https://doi.org/10.1016/j.bbrc.2009.03.015

Article  CAS  PubMed  Google Scholar 

Najm, J., Horn, D., Wimplinger, I., et al., Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum, Nat. Genet., 2008, vol. 40, pp. 1065—1067. https://doi.org/10.1038/ng.194

Article  CAS  PubMed  Google Scholar 

Atasoy, D., Schoch, S., Ho, A., et al., Deletion of CASK in mice is lethal and impairs synaptic function, Proc. Natl. Acad. Sci. U.S.A., 2007, vol. 104, no. 7, pp. 2525—2530. https://doi.org/10.1073/pnas.0611003104

Article  CAS  PubMed  PubMed Central  Google Scholar 

Engemaier, E., Römpler, H., Schöneberg, T., and Schulz, A., Genomic and supragenomic structure of the nucleotide-like G-protein-coupled receptor GPR34, Genomics, 2006, vol. 87, no. 2, pp. 254—264. https://doi.org/10.1016/j.ygeno.2005.10.001

Article  CAS  PubMed  Google Scholar 

Engel, K.M., Schröck, K., Teupser, D., et al., Reduced food intake and body weight in mice deficient for the G protein-coupled receptor GPR82, PLoS One, 2011, vol. 6, no. 12, p. e29400. https://doi.org/10.1371/journal.pone.0029400

Article  CAS  PubMed  PubMed Central  Google Scholar 

Sallmann, G.B., Bray, P.J., Rogers, S., et al., Scanning the ocular albinism 1 (OA1) gene for polymorphisms in congenital nystagmus by DHPLC, Ophthalmic Genet., 2006, vol. 27, pp. 43—49. https://doi.org/10.1080/13816810600677834

Article  CAS  PubMed