|
REFERENCES
-
1. Margeta, V., Škorput, D., Djurkin Kušec, I., Kralik, Z., Kušec, G., &
Gvozdanović, K. (2025). A Comprehensive Review: Molecular and Genealogical Methods for
Preserving the Genetic Diversity of Pigs. Applied Sci, 15(6), 3394.
https://doi.org/10.3390/app15063394
-
2. Panigrahi, M., Rajawat, D., Nayak, S. S., Bose, A., Bharia, N., Singh, S.,
Sharma, A., & Dutt, T. (2025). Advancements in Animal Breeding: From Mendelian Genetics to
Machine Learning. Intern J of molecular Sci, 26(23), 11352.
https://doi.org/10.3390/ijms262311352
-
3. Krupa, E., Moravčíková, N., Krupová, Z., & Žáková, E. (2021). Assessment of
the Genetic Diversity of a Local Pig Breed Using Pedigree and SNP Data. Genes, 12(12), 1972.
https://doi.org/10.3390/genes12121972
-
4. Samorè, A. B., Buttazzoni, L., Gallo, M., Russo, V., & Fontanesi, L. (2015).
Genomic selection in a pig population including information from slaughtered full sibs of boars
within a sib-testing program. Animal : an Intern J of Animal Biosci, 9(5), 750–759.
https://doi.org/10.1017/S1751731114002924
-
5. Samorè, A. B., & Fontanesi, L. (2016). Genomic selection in pigs: state of the
art and perspectives. Italian J of Animal Sci, 15(2), 211–232.
https://doi.org/10.1080/1828051X.2016.1172034
-
6. Su, R., Lv, J., Xue, Y., Jiang, S., Zhou, L., Jiang, L., Tan, J., Shen, Z., Zhong,
P., & Liu, J. (2025). Genomic selection in pig breeding: comparative analysis of machine
learning algorithms. Genetics, Selection, Evolution : GSE, 57(1), 13.
https://doi.org/10.1186/s12711-025-00957-3
-
7. Biscarini, F., Nicolazzi, E. L., Stella, A., Boettcher, P. J., & Gandini, G. (2015).
Challenges and opportunities in genetic improvement of local livestock breeds. Frontiers in
Genetics, 6, 33. https://doi.org/10.3389/fgene.2015.00033
-
8. Misztal, I., Aguilar, I., Lourenco, D., Ma, L., Steibel, J. P., & Toro, M. (2021).
Emerging issues in genomic selection. J of Animal Sci, 99(6), skab092.
https://doi.org/10.1093/jas/skab092
-
9. Voitenko, S. L. (2024). Pigs of meat breeds in Ukraine and the need for the
revival of pig breeding. Animal Breeding and Genetics, 67, 29-45.
https://doi.org/10.31073/abg.67.04
-
10. Balatsky, V. N., Saienko, A. M., Pena, R. N., Buslyk, T. V., & Gibolenko, O. S.
(2015). Genetic diversity of pig breeds on ten production quantitative traits loci. Cytology and
Genetics, 49(5), 299–307. https://doi.org/10.3103/S0095452715050023
-
11. Balatsky, V., Bankovska, I., Pena, R. N., Saienko, A., Buslyk, T., Korinnyi, S., &
Doran, O. (2016). Polymorphisms of the porcine cathepsins, growth hormone-releasing
hormone and leptin receptor genes and their association with meat quality traits in Ukrainian
Large White breed. Molecular Biology Reports, 43(6), 517–526.
https://doi.org/10.1007/s11033-
016-3977-z
-
12. Balatsky, V. N., Oliinychenko, Y. K., Buslyk, T. V., Bankovska, I. B., Korinnyi, S.
N., Saienko, A. M., & Pochernyaev, K. F. (2021). Associations of QTL Region Genes of
Chromosome 2 with Meat Quality Traits and Productivity of the Ukrainian Large White Pig
Breed. Cytology and Genetics, 55(1), 53–62. https://doi.org/10.3103/S0095452721010023
-
13. Calderon Martinez, E., Ghattas Hasbun, P. E., Salolin Vargas, V. P., García-
González, O. Y., Fermin Madera, M. D., Rueda Capistrán, D. E., Campos Carmona, T.,
Sanchez Cruz, C., & Teran Hooper, C. (2025). A comprehensive guide to conduct a systematic
review and meta-analysis in medical research. Medicine, 104(33), e41868.
https://doi.org/10.1097/MD.0000000000041868
-
14. Brignardello-Petersen, R., Santesso, N., & Guyatt, G. H. (2025). Systematic
reviews of the literature: an introduction to current methods. American J of Epidemiology,
194(2), 536–542. https://doi.org/10.1093/aje/kwae232
-
15. Randles, R., & Finnegan, A. (2023). Guidelines for writing a systematic review.
Nurse Education Today, 125, 105803. https://doi.org/10.1016/j.nedt.2023.105803
-
16. Ibatullin, M., Varchenko, O., Svynous I., Khakhula, B., & Dragan, O. (2019).
Organizational and economic bases of pig breeding in Ukraine. Intern J of Management and
Business Research, 9(1), 59–72.
-
17. Kramarenko, A. S., Karatieieva, O. I., Lіuta, I. M., & Kramarenko, S. S. (2024).
Genetic and non-genetic factors influencing piglet stillbirth risk. Regulatory Mechanisms in
Biosystems, 15(4), 875–881. https://doi.org/10.15421/0224126
-
18. Voloshynov, V., Povod, M., Mykhalko, O., Verbelchuk, T., Verbelchuk, S.,
Koberniuk, V., Lavryniuk, O., & Shcherbatiuk, N. (2024). The efficiency of pigs from different
genetic origins under industrial conditions in Ukraine. Online J of Animal and Feed Research,
14(4), 225–233. https://doi.org/10.51227/ojafr.2024.27
-
19. Ostapovets, L., & Starodub, L. (2016). Cytogenetical and biotechnological
methods for assessing boar reproductive potential. Bulgarian J of Agricultural Sci, 22, 123–126.
-
20. Balatskiĭ, V. N., & Lisovskiĭ, I. L. (1998). The genetic polymorphism of
somatotropin. TSitologiia i Genetika, 32(2), 92–104.
-
21. Burkina, V., Rasmussen, M. K., Oliinychenko, Y., & Zamaratskaia, G. (2019).
Porcine cytochrome 2A19 and 2E1. Basic and Clinical Pharmacology and Toxicology, 124(1),
32–39. https://doi.org/10.1111/bcpt.13121
-
22. Guo, L., Miao, Z., Ma, H., & Melnychuk, S. (2020). Effects of maternal vitamin D
3 during pregnancy on FASN and LIPE mRNA expression in offspring pigs. J of Agricultural Sci,
158(1–2), 128–135. https://doi.org/10.1017/S0021859620000210
-
23. Guo, L., Miao, Z., Ma, H., & Melnychuk, S. (2020). Effects of maternal vitamin
D3 concentration during pregnancy on adipogenic genes expression and serum biochemical
index in offspring piglets. J of Animal and Feed Sci, 29(2), 125–131.
https://doi.org/10.22358/jafs/124041/2020
-
24. Peka, M., & Balatsky, V. (2024). Bioinformatic approach to identifying causative
missense polymorphisms in animal genomes. BMC Genomics, 25(1).
https://doi.org/10.1186/s12864-024-11126-z
-
25. Peka, M., Balatsky, V., Saienko, A., & Tsereniuk, O. (2023). Bioinformatic
analysis of the effect of SNPs in the pig TERT gene on the structural and functional
characteristics of the enzyme to develop new genetic markers of productivity traits. BMC
Genomics, 24(1). https://doi.org/10.1186/s12864-023-09592-y
-
26. Pochernayev, K. K., Kiynitsa, K. I., Telegeev, G. D., Dybkov, M. V., & Malyuta,
S. S. (1996). M13 phage DNA probe informativity rising at studying pig genome. Biopolymers
and Cell, 12(3), 64–66. https://doi.org/10.7124/bc.00042F
-
27. Kubejko, J., Clop, A., Balatsky, V., Pochernyaev, K., Eghbalsaied, S., & Amills,
M. (2017). Mitochondrial DNA variation in Ukrainian wild boars. Animal Genetics, 48(6),
725–726. https://doi.org/10.1111/age.12592
-
28. Balatskiĭ V. N. (1992). Multiple forms of pig somatotropin. TSitologiia i Genetika,
26(5), 32–36.
-
29. Balatsky, V. N., Saenko, A. M., & Grishina, L. P. (2012). Polymorphism of the
estrogen receptor 1 locus in populations of pigs of different genotypes and its association with
reproductive traits of Large White sows. Cytology and Genetics, 46(4), 233–237.
https://doi.org/10.3103/S0095452712040020
-
30. Matiiuk, V. V., Saienko, A. M., Vashchenko, P. A., Slynko, V. H., Fesenko, O.
G., Peka, M. Y., & Tsereniuk, O. M. (2025). Association of polymorphisms in estrogen and
prolactin receptor genes with reproductive traits in sows of rare breeds. Regulatory Mechanisms
in Biosystems, 33(1), e25033. https://doi.org/10.15421/0225033
-
31. Syrovnev, G. I. (2014). Genetic polymorphism of FUT1 and MUC4 loci in a local
population of Ukrainian meat bread pigs. Cytology and Genetics, 48(5), 318–322.
https://doi.org/10.3103/S0095452714050119
-
32. Sukhno, V. V., Vashchenko, P. A., Saenko, A. M., Zhukorskyi, O. M.,
Tserenyuk, O. M., & Kryhina, N. V. (2022). Association of Fut1 and Slc11a1 gene
polymorphisms with productivity traits of Large White pigs. Regulatory Mechanisms in
Biosystems, 13(3), 225–230. https://doi.org/10.15421/022229
-
33. Balatskiĭ, V. N., & Pocherniaev, K. F. (1995). The polymorphic BsuRI restriction
site of the swine growth hormone gene. TSitologiia i Genetika, 29(1), 45–48.
34. Balatsky, V., Oliinychenko, Y., Sarantseva, N., Getya, A., Saienko, A., Vovk, V.,
& Doran, O. (2018). Association of single nucleotide polymorphisms in leptin (LEP) and leptin
receptor (LEPR) genes with backfat thickness and daily weight gain in Ukrainian Large White
pigs. Livestock Sci, 217, 157–161. https://doi.org/10.1016/j.livsci.2018.09.015
-
35. Balatsky, V. N., Oliinychenko, Y. K., Saienko, A. M., Buslyk, T. V., Bankovska,
I. B., Peka, M. Yu., & Doran, O. (2022). Associations of Polymorphisms in Leptin and Leptin
Receptor Genes with Meat Quality in Pigs of the Ukrainian Large White Breed. Cytology and
Genetics, 56(6), 513–525. https://doi.org/10.3103/S0095452722060020
-
36. Bordun, O., Khalak, V., Skliarenko, Y., Gutyj, B., Stadnytska, O., Ilchenko, M.,
Shevchenko, O., Kibenko, N., & Kravchenko, N. (2025). Evaluation of the Genotypes of Pigs of
Different Origins According to the RYR1 and LEP Genes. Acta Fytotechnica et Zootechnica,
28(1), 1–6. https://doi.org/10.15414/afz.2025.28.01.1-6
-
37. Lyadskiy, I. K., Getya, A. A., & Pochernyaev, K. F. (2011). Association of the
Asp298Asn polymorphism in the mc4r gene with back fat thickness in pigs of the Large White
breed. Cytology and Genetics, 45(2), 106–109.
-
38. Kozyr, V., Khalak, V., & Povod, M. (2019). DNA-type results swine for MS4R-
gene and its association with productivity. AgroLife Scientific J, 8(1), 128–133.
39. Khalak, V. (2020). Fattening and meat qualities of store pigs of large white
breed of different intra-breed differentiation by melanocortin-4 receptor gene (MC4R). Scientific
Horizons, 23(9), 30–37. https://doi.org/10.48077/scihor.23(9).2020.30-37
-
40. Khalak, V., Horchanok, A., Kuzmenko, O., Lytvyschenko, L., Prysiazhniuk, N.,
& Bordun, A. (2021). Interior profile of young pigs of different genotypes and the use of its
components for early prediction of quantitative characters. AgroLife Scientific J, 10(2), 92–98.
https://doi.org/10.17930/AGL2021211
-
41. Khalak, V., Voloshchuk, V., Gutyj, B., Zasucha, L., Onyshchenko, A., Ilchenko,
M., Ofilenko, N., Pokhyl, V., Pundyk, V., Bezaltychna, O., & Stadnytska, О. (2023). Young pig
fattening and meat quality due to varying formation intensities in early ontogenesis and two
genotypes of the melanocortin receptor 4 (Mc4r) gene. Veterinarska Stanica, 54(6), 613–624.
https://doi.org/10.46419/vs.54.6.10
-
42. Zhukorskyi, O. M., Tsereniuk, O. M., Sukhno, T. V., Saienko, A. M., Polishchuk,
A. A., Chereuta, Y. V., Shaferivskyi, B. S., & Vashchenko, P. A. (2023). The influence of
genotype and feeding level of gilts on their further reproductive performance. Regulatory
Mechanisms in Biosystems, 14(2), 312–318. https://doi.org/10.15421/022346
-
43. Tsereniuk, O. M., Vashchenko, P. A., Khokhlov, A. M., Tsybenko, V. H.,
Shostia, G. M., Saenko, A. M., Peka, M. Y., & Zhukorskyi, O. M. (2023). Comparative
characteristics of polymorphisms of melanocortin 4 and ryanodine 1 receptor genes of Myrhorod
pigs before and after the African swine fever outbreak. Regulatory Mechanisms in Biosystems,
14(4), 601–608. https://doi.org/10.15421/022387
-
44. Vashchenko, P. A., Zhukorskyi, O. M., Saenko, A. M., Khokhlov, A. M., Usenko,
S. O., Kryhina, N. V., Sukhno, T. V., & Tsereniuk, O. M. (2023). The influence of feeding level
on the growth of pigs depending on their genotype. Regulatory Mechanisms in Biosystems,
14(1), 112–117. https://doi.org/10.15421/022317
-
45. Khalak, V., Bordun, O., Skliarenko, Y., Gutyj, B., Zasukha, L., Horchanok, A.,
Kuzmenko, O., & Prisjazhnjuk, N. (2025). Study of Polymorphism of the MC4R Locus in Pigs of
the Large White Breed. Acta Fytotechnica et Zootechnica, 28(4), 282–287.
https://doi.org/10.15414/afz.2025.28.04.282-287
-
46. Balatskiĭ, V. N., & Metlitskaia, E. N. (2001). DNA diagnosis of porcine stress
syndrome and RYRI genotype association with viability of young pigs. TSitologiia i genetika,
35(3), 43–49.
-
47. Tsereniuk, O. M., Bobrytska, O. M., Miroshnikova, O. S., & Danchuk, O. V.
(2020). DNA-type results of Landrace sows for RYR1-gene and its association with productivity.
Regulatory Mechanisms in Biosystems, 11(3), 431–437. https://doi.org/10.15421/022066
-
48. Zhukorskyi, O. M., Tsereniuk, O. M., Vashchenko, P. A., Khokhlov, A. M.,
Chereuta, Y. V., Akimov, O. V., & Kryhina, N. V. (2022). The effect of the ryanodine receptor
gene on the reproductive traits of Welsh sows. Regulatory Mechanisms in Biosystems, 13(4),
367–372. https://doi.org/10.15421/022248
-
49. Solé, E., González-Prendes, R., Oliinychenko, Y., Tor, M., Ros-Freixedes, R.,
Estany, J., & Pena, R. N. (2022). Transcriptome shifts triggered by vitamin A and SCD genotype
interaction in Duroc pigs. BMC Genomics, 23(1). https://doi.org/10.1186/s12864-021-08244-3
-
50. Vashchenko, P., Saienko, A., Sukhno, V., Tsereniuk, O., Babicz, M., Shkavro,
N., Smołucha, G., & Łuszczewska-Sierakowska, I. (2022). Association of NRAMP1 gene
polymorphism with the productive traits of the Ukrainian Large White pig. Medycyna
Weterynaryjna, 78(9). https://doi.org/10.21521/mw.6698
-
51. Saienko, A., Peka, M., Tsereniuk, O., Babicz, M., Kropiwiec-Domańska, K.,
Onyshchenko, A., Vashchenko, P., & Balatsky, V. (2023). Analysis of polymorphism and
development of a molecular-genetic system for genotyping by the telomerase reverse
transcriptase (TERT) gene. Biosystems Diversity, 31(4), 436–443.
https://doi.org/10.15421/012352
-
52. Hashim, H. O. & Al-Shuhaib, M. B. (2019). Exploring the Potential and
Limitations of PCR-RFLP and PCR-SSCP for SNP Detection: A Review. Journal of Applied
Biotechnology Reports, 6, 137-144. https://doi.org/10.29252/JABR.06.04.02
-
53. Leite, I. G. C., Benard, G., Cavalcanti, S. C., Bollela, V. R., Del Negro, G. M. B.,
Martinez, R., Gimenes, V. M. F., & Cocio, T. A. (2024). Comparison between PCR-RFLP and
sequencing techniques in the analysis of Paracoccidioides spp. biodiversity: limitations and
insights into species and variant differentiation. Mycopathologia, 189(6), 97.
https://doi.org/10.1007/s11046-024-00902-w
-
54. Mekonnen, K. T., Lee, D. H., Beyenssa, B. C., Son, A. Y., Cho, Y. G., & Seo, K.
S. (2025). Genome-wide association study identifies genetic variants associated with single-
parity reproductive loss in three commercial pig breeds. BMC Genomics, 26(1), 1054.
https://doi.org/10.1186/s12864-025-12255-9
-
55. Panda, S., Kumar, A., Gaur, G. K., Ahmad, S. F., Chauhan, A., Mehrotra, A., &
Dutt, T. (2023). Genome wide copy number variations using Porcine 60K SNP Beadchip in
Landlly pigs. Animal Biotechnology, 34(6), 1891–1899.
https://doi.org/10.1080/10495398.2022.2056047
-
56. Hong, Y., He, X., Wu, D., Ye, J., Zhang, Y., Wu, Z., & Tan, C. (2025). Genome
Selection and Genome-Wide Association Analyses for Litter Size Traits in Large White Pigs.
Animals : an open access journal from MDPI, 15(12), 1724.
https://doi.org/10.3390/ani15121724
-
57. Wang, X., Wang, L., Shi, L., Zhang, P., Li, Y., Li, M., Tian, J., Wang, L., & Zhao,
F. (2022). GWAS of Reproductive Traits in Large White Pigs on Chip and Imputed Whole-
Genome Sequencing Data. Intern J of Molecular Sci, 23(21), 13338.
https://doi.org/10.3390/ijms232113338
-
58. Du, H., Zhou, L., Liu, Z., Zhuo, Y., Zhang, M., Huang, Q., Lu, S., Xing, K.,
Jiang, L., & Liu, J. F. (2024). The 1000 Chinese Indigenous Pig Genomes Project provides
insights into the genomic architecture of pigs. Nature Communications, 15(1), 10137.
https://doi.org/10.1038/s41467-024-54471-z
-
59. Boichard, D., Ducrocq, V., Croiseau, P., & Fritz, S. (2016). Genomic selection in
domestic animals: Principles, applications and perspectives. Comptes Rendus Biologies, 339(7-
8), 274–277. https://doi.org/10.1016/j.crvi.2016.04.007
|