Гены-кандидаты, ассоциированные с весом тела, у животных молочных пород крупного рогатого скота

Συγγραφείς: Юдин Н.С, Игошин А.В, Ларкин Д.М.

Πηγή: Письма в Вавиловский журнал генетики и селекции, Vol 11, Iss 1, Pp 5-11 (2025)

Θεματικοί όροι: крупный рогатый скот, молочная порода, вес тела, полногеномный анализ ассоциаций, ген-кандидат, Genetics, QH426-470

Περιγραφή αρχείου: electronic resource

Relation: https://pismavavilov.ru/wp-content/uploads/2025/03/003-Pisma-VJ_Yudin.pdf; https://doaj.org/toc/2686-8482

Σύνδεσμος πρόσβασης: https://doaj.org/article/d3753772f0e74d949c3d265289e7854f

Identification of genes associated with technological properties of cow milk using GWA analysis and gene ontology ; Выявление генов, ассоциированных с технологическими свойствами молока коров, с помощью GWA-анализа и генной онтологии

Συγγραφείς: M. V. Levchenko, G. G. Karlikova, G. K. Petryakova, I. A. Lashneva, A. A. Sermyagin, М. В. Левченко, Г. Г. Карликова, Г. К. Петрякова, И. А. Лашнева, А. А. Сермягин

Συνεισφορές: The research was carried out under the support of the Ministry of Science and Higher Education of the Russian Federation within the state assignment of the Federal Research Center for Animal Husbandry named after Academy Member L. K. Ernst No. FGGN-2024-0013, theme No. 124020200029-4)., Работа выполнена при поддержке Минобрнауки России в рамках Государственного задания ФГБНУ «Федеральный исследовательский центр животноводства – ВИЖ имени академика Л. К. Эрнста» (№ FGGN-2024-0013, рег. № 124020200029-4).

Πηγή: Agricultural Science Euro-North-East; Том 26, № 5 (2025); 1112-1124 ; Аграрная наука Евро-Северо-Востока; Том 26, № 5 (2025); 1112-1124 ; 2500-1396 ; 2072-9081

Θεματικοί όροι: сычужная свертываемость молока, Holstein breed, genome-wide association study, functional gene annotation, SNP markers, thermostability of milk, rennet coagulation of milk, голштинская порода, полногеномный анализ ассоциаций, функциональная аннотация генов, SNP-маркеры, термостабильность молока

Περιγραφή αρχείου: application/pdf

Relation: https://www.agronauka-sv.ru/jour/article/view/2232/950; Суровцев В. Н. Тенденции и перспективы развития молочного животноводства России: риски и возможности. Молочная промышленность. 2023;(2):12–16. DOI: https://doi.org/10.31515/1019-8946-2023-02-12-16 EDN: UQGWLO DOI: https://doi.org/10.31515/1019-8946-2023-02-12-16; Ларкина Т. А., Ширяев Г. В. GWAS как инструмент обнаружения SNPs у крупного рогатого скота для изучения их связи с воспроизводством, продуктивностью, ростом, поведением, болезнями. Аграрная наука. 2024;1(8):124–131. DOI: https://doi.org/10.32634/0869-8155-2024-385-8-124-131 EDN: FIMLEZ DOI: https://doi.org/10.32634/0869-8155-2024-385-8-124-131; Сермягин А. А., Быкова О. А., Лоретц О. Г., Костюнина А. В., Зиновьева Н. А. Оценка геномной вариабельности продуктивных признаков у животных голштинизированной черно-пестрой породы на основе GWAS-анализа и ROH паттернов. Сельскохозяйственная биология. 2020;55(2):257–274. 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Διαθεσιμότητα: https://www.agronauka-sv.ru/jour/article/view/2232
https://doi.org/10.30766/2072-9081.2025.26.5.1112-1124

Молекулярные маркеры адаптации к холодному климату у крупного рогатого скота

Πηγή: Письма в Вавиловский журнал генетики и селекции, Vol 9, Iss 1, Pp 5-14 (2023)

Θεματικοί όροι: полногеномный анализ ассоциаций, геном, крупный рогатый скот, молекулярный маркер, местная порода, Genetics, сравнительная геномика, холодный климат, адаптация, QH426-470, признаки отбора

Σύνδεσμος πρόσβασης: https://doaj.org/article/3b0c505cdf5745289f0f0757cee4ea0f

Genotype imputation in human genomic studies ; Импутация генотипов в геномных исследованиях человека

Συγγραφείς: A. A. Berdnikova, I. V. Zorkoltseva, Y. A. Tsepilov, E. E. Elgaeva, А. А. Бердникова, И. В. Зоркольцева, Я. А. Цепилов, Е. Е. Елгаева

Πηγή: Vavilov Journal of Genetics and Breeding; Том 28, № 6 (2024); 628-639 ; Вавиловский журнал генетики и селекции; Том 28, № 6 (2024); 628-639 ; 2500-3259 ; 10.18699/vjgb-24-64

Θεματικοί όροι: ДНК-микрочип, genotyping, sequencing, genome-wide association study, human, DNA-microarray, генотипирование, секвенирование, полногеномный анализ ассоциаций, человек

Περιγραφή αρχείου: application/pdf

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Διαθεσιμότητα: https://vavilov.elpub.ru/jour/article/view/4292
https://doi.org/10.18699/vjgb-24-70

Problems with studying directional natural selection in humans ; Проблемы изучения направленного естественного отбора у человека

Συγγραφείς: S. V. Mikhailova, С. В. Михайлова

Συνεισφορές: This research was funded by Russian Science Foundation grant No. 22-28-00866. The English language was corrected by shevchuk-editing.com

Πηγή: Vavilov Journal of Genetics and Breeding; Том 27, № 6 (2023); 684-693 ; Вавиловский журнал генетики и селекции; Том 27, № 6 (2023); 684-693 ; 2500-3259 ; 10.18699/VJGB-23-65

Θεματικοί όροι: полногеномный анализ ассоциаций, Homo sapiens, fertility, adaptation, polygenic index, genome-wide association study, фертильность, адаптация, полигенный индекс

Περιγραφή αρχείου: application/pdf

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Διαθεσιμότητα: https://vavilov.elpub.ru/jour/article/view/3940
https://doi.org/10.18699/VJGB-23-79

Compilation and functional classification of telomere length-associated genes in humans and other animal species ; Компиляция и функциональная классификация генов, ассоциированных с длиной теломер, у человека и других видов животных

Συγγραφείς: E. V. Ignatieva, N. S. Yudin, D. M. Larkin, Е. В. Игнатьева, Н. С. Юдин, Д. М. Ларкин

Πηγή: Vavilov Journal of Genetics and Breeding; Том 27, № 3 (2023); 283-292 ; Вавиловский журнал генетики и селекции; Том 27, № 3 (2023); 283-292 ; 2500-3259 ; 10.18699/VJGB-23-24

Θεματικοί όροι: функциональный анализ, candidate genes, genome-wide association study, functional classification, гены-кандидаты, полногеномный анализ ассоциаций

Περιγραφή αρχείου: application/pdf

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Διαθεσιμότητα: https://vavilov.elpub.ru/jour/article/view/3739
https://doi.org/10.18699/VJGB-23-34

Полногеномные исследования миомы матки

Συγγραφείς: Алали, О. М., Чурносов, М. И.

Θεματικοί όροι: медицина, медицинская генетика, миома матки, полиморфизмы, полногеномный анализ ассоциаций, ассоциация, секвенирование экзонов, гены-кандидаты, репликативные исследования

Relation: http://dspace.bsu.edu.ru/handle/123456789/61838

Διαθεσιμότητα: http://dspace.bsu.edu.ru/handle/123456789/61838

Candidate genes for productivity identified by genome-wide association study with indicators of class in the Russian meat merino sheep breed ; Гены-кандидаты продуктивности, выявленные при полногеномном поиске ассоциаций с показателями классности у овец породы российский мясной меринос

Συγγραφείς: A. Y. Krivoruchko, O. A. Yatsyk, E. Y. Safaryan, А. Ю. Криворучко, О. А. Яцык, Е. Ю. Сафарян

Πηγή: Vavilov Journal of Genetics and Breeding; Том 24, № 8 (2020); 836-843 ; Вавиловский журнал генетики и селекции; Том 24, № 8 (2020); 836-843 ; 2500-3259 ; 10.18699/VJ20.67

Θεματικοί όροι: российский мясной меринос, SNP, genome-wide association study, GWAS, candidate gene, Russian meat merino, однонуклеотидный полиморфизм, полногеномный поиск ассоциаций, полногеномный анализ ассоциаций, ген-кандидат

Περιγραφή αρχείου: application/pdf

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Διαθεσιμότητα: https://vavilov.elpub.ru/jour/article/view/2843
https://doi.org/10.18699/VJ20.681

In silico mapping of coronary artery disease genes ; In silico поиск генов, контролирующих ишемическую болезнь сердца

Συγγραφείς: I. V. Zorkoltseva, N. M. Belonogova, G. R. Svishcheva, A. V. Kirichenko, T. I. Axenovich, И. В. Зоркольцева, Н. М. Белоногова, Г. Р. Свищёва, А. В. Кириченко, Т. И. Аксенович

Συνεισφορές: This work was supported by the Russian Ministry of Education and Science (project 0324-2019-0040) and the Russian Foundation for Basic Research (project 18-04-00076).

Πηγή: Vavilov Journal of Genetics and Breeding; Том 23, № 8 (2019); 1037-1046 ; Вавиловский журнал генетики и селекции; Том 23, № 8 (2019); 1037-1046 ; 2500-3259

Θεματικοί όροι: in silico картирование, gene-based association analysis, genome-wide association analysis, summary statistics, in silico mapping, полногеномный анализ ассоциаций, региональный анализ ассоциаций, суммарные статистики

Περιγραφή αρχείου: application/pdf

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Διαθεσιμότητα: https://vavilov.elpub.ru/jour/article/view/2396
https://doi.org/10.18699/VJ19.585

Genes related to the white face colour pattern in eight Russian cattle breeds ; Выявление генов, вовлеченных в контроль белой окраски головы, у восьми российских пород крупного рогатого скота

Συγγραφείς: N. S. Yudin, N. M. Belonogova, D. M. Larkin, Н. С. Юдин, Н. М. Белоногова, Д. М. Ларкин

Πηγή: Vavilov Journal of Genetics and Breeding; Том 22, № 2 (2018); 217-223 ; Вавиловский журнал генетики и селекции; Том 22, № 2 (2018); 217-223 ; 2500-3259

Θεματικοί όροι: доместикация, native populations, breed, colouring, white face, genome-wide association studies, SLC41A2, domestication, аборигенный скот, порода, окраска, белая голова, полногеномный анализ ассоциаций, ген SLC41A2

Περιγραφή αρχείου: application/pdf

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Διαθεσιμότητα: https://vavilov.elpub.ru/jour/article/view/1444
https://doi.org/10.18699/VJ18.350

Replication analysis of genome wide studies of atopic dermatitis in the Republic of Bashkortostan ; Репликация данных полногеномных анализов ассоциации атопического дерматита в Республике Башкортостан

Συγγραφείς: G. F. Gimalova, A. S. Karunas, Y. Y. Fedorova, E. R. Gumennaya, S. V. Levashova, E. I. Etkina, E. K. Khusnutdinova, Г. Ф. Гималова, А. С. Карунас, Ю. Ю. Федорова, Э. Р. Гуменная, С. В. Левашева, Э. И. Эткина, Э. К. Хуснутдинова

Πηγή: Medical Genetics; Том 15, № 4 (2016); 25-28 ; Медицинская генетика; Том 15, № 4 (2016); 25-28 ; 2073-7998

Θεματικοί όροι: polymorphic variants, полногеномный анализ ассоциации, гены, полиморфные варианты, atopic dermatitis, genome-wide association study, genes

Περιγραφή αρχείου: application/pdf

Relation: https://www.medgen-journal.ru/jour/article/view/112/100; Odhiambo JA, Williams HC, Clayton TO et al. Global variations in prevalence of eczema symptoms in children from ISAAC Phase Three. J Allergy Clin Immunol. 2009;124:1251-1258.; Schultz-Larsen F, Holm NV, Henningsen K. Atopic dermatitis: a genetic-epidemiologic study in a population-based twin study. J Am Acad Dermatol. 1993;28:719-23.; Williams HC. Clinical practice: atopic dermatitis. NEJM. 2005;352:2314-2324.; Esparza-Gordillo J, Weidinger S, Folster-Holst R et al. A common variant on chromosome 11q13 is associated with atopic dermatitis. Nat Genet. 2009;41:596-601.; Hughes-Davies L, Huntsman D, Ruas M et al. EMSY links the BRCA2 pathway to sporadic breast and ovarian cancer. Cell. 2003;115:523-535.; Ollendorff V, Szepetowski P, Mattei M-G et al. New gene in the homologous human 11q13-q14 and mouse 7F chromosomal regions. Mamm Genome. 1992;2:195-200.; Paternoster L, Standl M, Chen CM et al. Meta-analysis of genome-wide association studies identifies three new risk loci for atopic. Nat Genet. 2011;44(2):187-192.; Hirota T, Takahashi A, Kubo M et al. Genome-wide association study identifies eight new susceptibility loci for atopic dermatitis in the Japanese population. Nat Genet. 2012;44(11):1222-1226.; O’Regan GM, Campbell LE Irvine AD et al. Chromosome 11q13.5 variant associated with childhood eczema: an effect supplementary to filaggrin mutations. J Allergy Clin Immunol. 2010;125(1):170-4.; Ramasamy A, Curjuric I, Coin LJ, et al. A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order. J Allergy Clin Immunol. 2011;128(5):996-1005.; Li X, Ampleford EJ, Howard TD et al. The C11orf30-LRRC32 region is associated with total serum IgE levels in asthmatic patients. J Allergy Clin Immunol. 2012;129(2):575-578.; Ezell SA., Tsichlis PN. Akt1, EMSY, BRCA2 and type I IFN signaling: a novel arm of the IFN response. Transcription. 2012;3(6):305-309.

Διαθεσιμότητα: https://www.medgen-journal.ru/jour/article/view/112
https://doi.org/10.1234/XXXX-XXXX-2016-4-25-28

GENETIC ASPECTS OF SUICIDAL BEHAVIOR ; ГЕНЕТИЧЕСКИЕ АСПЕКТЫ СУИЦИДАЛЬНОГО ПОВЕДЕНИЯ

Συγγραφείς: A. G. Zainullina, Z. L. Khalilova, E. K. Khusnutdinova, А. Г. Зайнуллина, З. Л. Халилова, Э. К. Хуснутдинова

Συνεισφορές: Работа выполнена при финансовой поддержке гранта РГНФ (№11-06-00554а).

Πηγή: Medical Genetics; Том 12, № 3 (2013); 11-19 ; Медицинская генетика; Том 12, № 3 (2013); 11-19 ; 2073-7998

Θεματικοί όροι: эпигенетика, stress, molecular genetics, genome wide assotiation study, стресс, молекулярная генетика, полногеномный анализ ассоциаций

Περιγραφή αρχείου: application/pdf

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Genome-Wide Association Study of Antidepressant Treatment-Emergent Suicidal Ideation // Neuropsychopharmacology. — 2012. — Vol. 37. — P. 797-807.; Neves F., Malloy-Diniz L., Romano-Silva M. et al. The role of BDNF genetic polymorphisms in bipolar disorder with psychiatric comorbidi-ies // J. Af-ect. Di-ord. — 2011. — Vol. 131(1-3). — P. 307-311.; Papiol S., Arias B., Gasto C. et al. Genetic variability at HPA axis in major depression and clinical response to antidepressant treatment // Journal of Afec-ive Disorders. — 2007. — Vol. 104. — P. 83-90.; Perlis R. H., Huang J., Purcell S. et al. Genome-Wide Association Study of Suicide Attempts in Mood Disorder Patients // Am. J. Psychiatry. — 2010. — Vol. 167. — P.1499-1507.; Perroud N., Uher R., Ng M.Y. et al. Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP proj ect // The Pharmacogenomics Journal. — 2012. — Vol. 12. — P. 68-77.; Pivac N., Pregelj P., Niko-ac M. et al. The association between catechol-O-methyl-transferase Val108/158Met polymorphism and suicide // Genes Brain Behav. — 2011. — Vol. 10(5). — P. 565-569.; Pregelj P., Nedic G., Paska A. et al. The association between brain-derived neurotrophic factor polymorphism (BDNF Val66Met) and suicide // J. Affect. Disord. — 2011. — Vol. 128(3). — P. 287-290.; Roy A., Hodgkinson C., De Luca V. Two HPA axis genes, CRHBP and FKBP5, interact with childhood trauma to increase the risk for suicidal behavior // Journal of Psychiatric Research. — 2012. — Vol. 46. — P. 72-79.; Schosser A., Butler A.W., Ising M. et al. Genomewide Association Scan of Suicidal Thoughts and Behaviour in Major Depression // PLoS ONE. — 2011. — Vol. 6 (7). — e20690.; Sekiguchi H., Iritani S., Habuchi C. et al. Impairment of the tyrosine hydroxylase neuronal network in the orbitofrontal cortex of a genetically modified mouse model of schizophrenia // Brain Research. — 2011. — Vol. 1392. — P. 47-53.; Sequeira A., Mamdani F., Ernst C. et al. Global bram gene expression analysis links glutamatergic and GABAergic alterations to suicide and major depression // PLoS One. — 2009. — Vol. 4(8). — e6585.; Serretti A., Calati R., Giegling I. et al. Serotonin receptor HTR1A and HTR2C variants and personality traits in suicide attem-p-ers and con-rols // J. Psychiatr. Res. — 2009. — Vol. 43(5). — P. 519-525.; Sher L. Dopamine and the pathophysiology of suicidal behavior in alcoholism // Med. Hypotheses. — 2006. — Vol. 66(5). — P. 1043-1044.; Sokolowski M., Ben-Efraim Y., Wasserman J, Wasser-man D. Glutamatergic GRIN2B and polyaminergic ODC1 genes in suicide attempts: associations and gene-environment interactions with childhood/adolescent physical assault // Mol. Psychiatry. — 2012. doi:10.1038/mp.2012.112.; Suda A., Kawanishi C., Kishida I. et al. Dopamine D2 recep-or gene polymorphisms are associated with suicide attempt in the Japanese population//Neuropsychobiology. — 2009. — Vol. 59(2). — P. 130-134.; Tatro E.T., Nguyen T.B., Bousman C.A. Correlation of major depressive disorder symptoms with FKBP5 but not FKBP4 expression in human immunodeficiency virus-infected individuals // J. Neurovirol. — 2010. — Vol. 16(5). — P. 399-404.; Videtic A., Peternelj T., Zupanc T. et al. Promoter and functional polymorphisms of HTR2C and suicide victims // Genes Brain Behav. — 2009. — Vol. 8(5). — P. 541-555.; Videtic A., Zupanc T., Pregelj P. et al. Suicide, stress and serotonin receptor 1A promoter polymorphism -1019C>G in Slovenian suicide victims // Eur. Arch. Psychiatry Clin. Neurosci. — 2009. — Vol. 259(4). — P. 234-238.; Wasserman D. (Ed.) Suicide. An unnecessary death // Martin Dunitz, London. — 2001. — P. 287.; Wasserman D., Wasserman J., Rozanov V., Sokolowski M. depression in suicidal males: genetic risk variants in the CRHR1 gene // Genes, Brai n and Behavior. — 2009. — Vol. 8. — P. 72-77.; Willour V., Chen H., Toolan J. et al. Family-based association of FKBP5 in bipolar disorder // Molecular psychiatry. — 2009. — Vol. 14. — P. 261-268.; Yanagi M., Shirakawa O., Kitamura N. et al. Association of 14-3-3 gene haplotype with completed suicide in Japanese // J. Hum. Genet. — 2005. — Vol. 50. — P. 210-216.; Za-sman G., Patya M., Frisch A. et al. Association of polymorphisms of the serotonergic pathways with clinical traits of impul-sive-aggression and suicidality in adolescents: a multi-center study // World J. Biol. Psychiatry. — 2011. — Vol. 12(1). — P. 33-41.; Zubenko G., Maher B., Hughes H. et al. 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Διαθεσιμότητα: https://www.medgen-journal.ru/jour/article/view/28
https://doi.org/10.1234/XXXX-XXXX-2013-3-11-19

Современные проблемы и достижения фундаментальной и клинической медицины

Συγγραφείς: ХУБЕРТ Е. БЛЮМ

Θεματικοί όροι: ОРГАНИЗАЦИЯ ПО ИЗУЧЕНИЮ ГЕНОМА ЧЕЛОВЕКА,ПОЛНОГЕНОМНЫЙ АНАЛИЗ АССОЦИАЦИЙ,ПРОЕКТ "МИКРОБИОМ ЧЕЛОВЕКА",ОДИНОЧНЫЙ НУКЛЕОТИДНЫЙ ПОЛИМОРФИЗМ,СИГНАТУРЫ ГЕНОВ,АНАЛИЗ МАССИВОВ ДАННЫХ,HUMAN GENOME ORGANIZATION,GENOME-WIDE ASSOCIATION STUDIES,HUMAN MICROBIOME PROJECT,SINGLE NUCLEOTIDE POLYMORPHISM,GENE SIGNATURES,ARRAY ANALYSES

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Глютеновая энтеропатия с позиций полногеномного анализа ассоциаций (GWAS)

Συγγραφείς: ВОХМЯНИНА НАТАЛЬЯ ВАСИЛЬЕВНА, ВАВИЛОВА ТАТЬЯНА ВЛАДИМИРОВНА

Θεματικοί όροι: ЦЕЛИАКИЯ,CELIAC DISEASE,ИММУННО-ОПОСРЕДОВАННЫЕ БОЛЕЗНИ,ПОЛНОГЕНОМНЫЙ АНАЛИЗ АССОЦИАЦИЙ,GENOME-WIDE ASSOCIATION STUDIES,HLA-ГЕНЫ,IMMUNE-RELATED DISEASE,GWAS,HLA-GENE

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SEARCH OF TUBERCULOSIS SUSCEPTIBILITY GENES USING THE RESULTS OF GENOME-WIDE ASSOCIATION STUDY OF CROHN’S DISEASE ; ПОИСК ГЕНОВ ПОДВЕРЖЕННОСТИ ТУБЕРКУЛЕЗУ С ИСПОЛЬЗОВАНИЕМ РЕЗУЛЬТАТОВ ПОЛНОГЕНОМНОГО ИССЛЕДОВАНИЯ БОЛЕЗНИ КРОНА

Συγγραφείς: A. Rudko A., M. Freidin B., Ye. Bragina Yu., A. An R., V. Puzyryov P., А. Рудко А., М. Фрейдин Б., Е. Брагина Ю., А. Ан Р., В. Пузырёв П.

Πηγή: Bulletin of Siberian Medicine; Том 12, № 3 (2013); 61-68 ; Бюллетень сибирской медицины; Том 12, № 3 (2013); 61-68 ; 1819-3684 ; 1682-0363 ; 10.20538/1682-0363-2013-12-3

Θεματικοί όροι: tuberculosis, Crohn’s disease, polymorphism, genome-wide association study, candidate genes, predisposition, association, туберкулез, болезнь Крона, полиморфизм, полногеномный анализ ассоциаций, гены-кандидаты, подверженность, ассоциация

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Relation: https://bulletin.tomsk.ru/jour/article/view/340/346; Пузырёв В.П. Генетика мультифакториальных заболеваний: между прошлым и будущим // Мед. генетика. 2003. Т. 2, № 12. С. 498–508.; Пузырёв В.П. Феномно-геномные отношения и патогенетика многофакторных заболеваний // Вестн. РАМН. 2011. № 9. С. 17–27.; Рудко А.А., Фрейдин М.Б., Пузырёв В.П. Наследственная подверженность туберкулезу // Молекулярная медицина. 2011. № 3. С. 3–10.; Фрейдин М.Б., Рудко А.А., Колоколова О.В. и др. Сравнительный анализ структуры наследственной компоненты подверженности к туберкулезу у тувинцев и русских // Молекулярная биология. 2006. Т. 40, № 2. С. 252–262.; Azad A.K., Sadee W., Schlesinger L.S. Innate immune gene polymorphisms in tuberculosis // Infect. Immun. 2012. V. 80, № 20. P. 3343–3359.; Bamias G., Martin C., Marin M. et al. Expression, localization, and functional activity of TL1A, a novel Th1-polarizing cytokine in inflammatory bowel disease // J. Immun. 2003. V. 171. P. 4868–4874.; Bellamy R. Identifying genetic susceptibility factors for tuberculosis in Africans: a combined approach using a candidate gene study and a genome-wide screen // Clin. Sci. 2000. V. 98. P. 245–250.; Cantero-Recasens G., Fandos C., Rubio-Moscardo F. et al. The asthma-associated ORMDL3 gene product regulates endoplasmic reticulum-mediated calcium signaling and cellular stress // Hum. Molec. Genet. 2010. V. 19. p. 111–121.; Cooke G.S., Campbell S.J., Bennett S. et al. Mapping of a novel susceptibility locus suggests a role for MC3R and CTSZ in human tuberculosis // Am. J. Crit. Care Ved. 2008. V. 178. P. 203–207.; El Baghdadi J., Orlova M., Alter A. et al. An autosomal dominant major gene conferts predisposition to pulmonary tuberculosis in adults // J. Exp. Med. 2006. V. 203, № 7. P. 1679–1684.; Galanter J.M., Torgerson D., Gignoux C.R. et al. Cosmopolitan and ethnic-specific replication of genetic risk factors for asthma in 2 Latino populations // J. Allergy Clin. Immunol. 2011. V. 128. P. 37–43.; Hampe J., Franke A., Rosenstiel P., et al. A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1 // Nature Genet. 2007. V. 39. P. 207–211.; Hill A.V.S. Evolution, revolution and heresy in the genetics of infectious disease susceptibility // Phil. Trans. R. Soc. 2012. V. 367. P. 840–849.; Mahasirimongkol S., Yanai H., Nishida N. et al. Genomewide SNP-based linkage analysis of tuberculosis in Thais // Genes Immun. 2009. № 10. P. 77–83.; Mahasirimongkol S., Yanai H., Mushiroda T. et al. Genomewide association studies of tuberculosis in Asians identify atrisk locus for young tuberculosis // Journal of Human Genetics. 2012. V. 57. P. 363–367.; Miller E.N., Jamieson S.E., Joberty C. et al. Genome-widescans for leprosy and tuberculosis susceptibility genes in Brazilians // Genes Immun. 2004. V. 5 (1). P. 63–67.; Moffatt M.F., Gut I.G., Demenais F. et al. A large-scale, consortium-based genomewide association study of asthma // N. Engl. J. Med. 2010. V. 363 (13). P. 1211–1221.; Möller M., de Wit E., Hoal E.G. Past, present and future directions in human genetic susceptibility to tuberculosis // FEMS Immunol. Med. Microbiol. 2009. V. 2. P. 1–24.; Pearce N. What does the odds ratio estimate in a case-control study? // Int. J. Epidemiol. 1993. V. 26. P. 1189–1192.; Png E., Alisjahbana B., Sahiratmadja E. et al. A genomewide association study of pulmonary tuberculosis susceptibility in Indonesians // BMC Medical Genetics. V. 13, № 5. P. 1–9.; Songane M., Kleinnijenhuis J., Alisjahbana B. et al. Polymorphisms in autophagy genes and susceptibility to tuberculosis // PLoS One. 2012. V. 7 (8). P. e41618.; Stein C.M., Zalwango S., Malone L.L. Genome scan of M. tuberculosis infection and disease in Ugandans // PLoSONE. 2008. V. 3, № 12. P. 1–10.; The Wellcome Trust Case Control Consortium. Genome-wide association study of 14000 cases of seven common diseases and 3000 share controls // Nature. 2007. V. 447. P. 661–683.; Thye T., Vannberg F., Wong S. et al. Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2 // Nature Genome. 2010. V. 42, № 9. P. 739–741.; Vergne I., Singh S., Roberts E. et al. Autophagy in immune defense against Mycobacterium tuberculosis // Autophagy. 2006. V. 2, Iss. 3. P. 175–178.; Wong S.H., Hill A.V., Vannberg F.O. et al. Genome-wide association study of leprosy // N. Engl. J. Med. 2010. V. 362 (15). P. 1446–1447.; Zhernakova A., Van Diemen C.C., Wijmenga C. Detecting shared pathogenesis from the shared genetics of i mmunerelated diseases // Nat. Rev. Genet. 2009. V. 10 (1). P. 43–55.; https://bulletin.tomsk.ru/jour/article/view/340

Διαθεσιμότητα: https://bulletin.tomsk.ru/jour/article/view/340
https://doi.org/10.20538/1682-0363-2013-3-61-68

ПОИСК ГЕНОВ ПОДВЕРЖЕННОСТИ ТУБЕРКУЛЕЗУ С ИСПОЛЬЗОВАНИЕМ РЕЗУЛЬТАТОВ ПОЛНОГЕНОМНОГО ИССЛЕДОВАНИЯ БОЛЕЗНИ КРОНА

Συγγραφείς: Рудко, Алексей, Фрейдин, Максим, Брагина, Елена, Ан, Адиля, Пузырёв, Валерий

Θεματικοί όροι: ТУБЕРКУЛЕЗ, БОЛЕЗНЬ КРОНА, CROHN'S DISEASE, ПОЛИМОРФИЗМ, ПОЛНОГЕНОМНЫЙ АНАЛИЗ АССОЦИАЦИЙ, ГЕНЫ-КАНДИДАТЫ, ПОДВЕРЖЕННОСТЬ, АССОЦИАЦИЯ

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Современные проблемы и достижения фундаментальной и клинической медицины

Πηγή: Вестник Адыгейского государственного университета. Серия 4: Естественно-математические и технические науки.

Θεματικοί όροι: 03 medical and health sciences, 0302 clinical medicine, ОРГАНИЗАЦИЯ ПО ИЗУЧЕНИЮ ГЕНОМА ЧЕЛОВЕКА,ПОЛНОГЕНОМНЫЙ АНАЛИЗ АССОЦИАЦИЙ,ПРОЕКТ 'МИКРОБИОМ ЧЕЛОВЕКА',ОДИНОЧНЫЙ НУКЛЕОТИДНЫЙ ПОЛИМОРФИЗМ,СИГНАТУРЫ ГЕНОВ,АНАЛИЗ МАССИВОВ ДАННЫХ,HUMAN GENOME ORGANIZATION,GENOME-WIDE ASSOCIATION STUDIES,HUMAN MICROBIOME PROJECT,SINGLE NUCLEOTIDE POLYMORPHISM,GENE SIGNATURES,ARRAY ANALYSES, 3. Good health

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Σύνδεσμος πρόσβασης: http://cyberleninka.ru/article/n/sovremennye-problemy-i-dostizheniya-fundamentalnoy-i-klinicheskoy-meditsiny
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Глютеновая энтеропатия с позиций полногеномного анализа ассоциаций (GWAS)

Πηγή: Вестник Санкт-Петербургского университета. Серия 11. Медицина.

Θεματικοί όροι: ЦЕЛИАКИЯ,CELIAC DISEASE,ИММУННО-ОПОСРЕДОВАННЫЕ БОЛЕЗНИ,ПОЛНОГЕНОМНЫЙ АНАЛИЗ АССОЦИАЦИЙ,GENOME-WIDE ASSOCIATION STUDIES,HLA-ГЕНЫ,IMMUNE-RELATED DISEASE,GWAS,HLA-GENE, 3. Good health

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Поиск генов подверженности туберкулезу с использованием результатов полногеномного исследования болезни Крона

Πηγή: Бюллетень сибирской медицины.

Θεματικοί όροι: 0301 basic medicine, 03 medical and health sciences, ТУБЕРКУЛЕЗ, БОЛЕЗНЬ КРОНА, CROHN'S DISEASE, ПОЛИМОРФИЗМ, ПОЛНОГЕНОМНЫЙ АНАЛИЗ АССОЦИАЦИЙ, ГЕНЫ-КАНДИДАТЫ, ПОДВЕРЖЕННОСТЬ, АССОЦИАЦИЯ, 3. Good health

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