Zobrazeno 1 - 10
of 12
pro vyhledávání: '"I. Y. Iourov"'
Publikováno v:
Обозрение психиатрии и медицинской психологии имени В.М. Бехтерева, Vol 0, Iss 4-1, Pp 80-81 (2019)
Genetic factors of mental illness are generally recognized. Here, it is shown that molecular karyotyping in combination with original bioinformatics methods offers the opportunity for effective uncovering genomic pathology, which may provide correct
Externí odkaz:
https://doaj.org/article/0e679808da4d49e6b18b3449adb5679d
Publikováno v:
Обозрение психиатрии и медицинской психологии имени В.М. Бехтерева, Vol 0, Iss 4-1, Pp 101-102 (2019)
Despite the large number of candidate genes for mental disorders, molecular mechanisms of the majority remain unknown. To fill this gap, we have studied genomic networks-candidates (instead of genes) in a group of children with brain disorders. The i
Externí odkaz:
https://doaj.org/article/69d3719347494d70b4db18ae170cba1d
Publikováno v:
Molecular Biology. 55:37-46
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69cb920a84397e19248c5dc2f118671e
https://doi.org/10.1134/s0026893321010155
https://doi.org/10.1134/s0026893321010155
Publikováno v:
Molekuliarnaia biologiia. 55(1)
Each neuron has 100-10000 connections (synapses) with other neural cells, therefore genome pathologies affecting a small proportion of brain cells are capable of causing dysfunction of the entire central nervous system (CNS). Recently, genome and chr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2c17f4792780122b2c401c3ec024bfea
https://pubmed.ncbi.nlm.nih.gov/33566024
https://pubmed.ncbi.nlm.nih.gov/33566024
Publikováno v:
V.M. BEKHTEREV REVIEW OF PSYCHIATRY AND MEDICAL PSYCHOLOGY. :101-102
Despite the large number of candidate genes for mental disorders, molecular mechanisms of the majority remain unknown. To fill this gap, we have studied genomic networks-candidates (instead of genes) in a group of children with brain disorders. The i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b52a848d54e7b232622cc2527cc7265
https://doi.org/10.31363/2313-7053-2019-4-1-101-102
https://doi.org/10.31363/2313-7053-2019-4-1-101-102
Autor:
Maria A Zelenova, Kurinnaia Os, Kirill S. Vasin, A.A. Kharlamova, S.I. Kutsev, I.A. Demidova, I. Y. Iourov, Yu. B. Yurov, Svetlana G. Vorsanova
Publikováno v:
Современные проблемы науки и образования (Modern Problems of Science and Education). :74-74
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f615ad92c822a34a37cff1c907224dd0
https://doi.org/10.17513/spno.30817
https://doi.org/10.17513/spno.30817
Autor:
I Y, Iourov, S G, Vorsanova, O S, Kurinnaaya, A D, Kolotii, I A, Demidova, V S, Kravets, Yu B, Yurov
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 114(1)
We examined 30 patients with a presumptive diagnosis of Prader-Willi and Angelman syndromes. In four patients, 15q11.2-q13 deletions were identified by cytogenetic techniques. The FISH method was used to study eight patients, in five of them microdel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5a6ea5f8f44f7beceaded0def26ca45c
https://pubmed.ncbi.nlm.nih.gov/24637817
https://pubmed.ncbi.nlm.nih.gov/24637817
Publikováno v:
TSitologiia i genetika. 42(5)
An approach towards construction of two-dimensional (2D) and three-dimensional (3D) profiles of interphase chromatin architecture by quantification of fluorescence in situ hybridization (FISH) signal intensity is proposed. The technique was applied f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6f8694070281aeb05cd858518be62f83
https://pubmed.ncbi.nlm.nih.gov/19140435
https://pubmed.ncbi.nlm.nih.gov/19140435
Publikováno v:
TSitologiia i genetika. 40(5)
We report on a case of chimerism and multiple abnormalities of chromosomes 21, Xand Yin spontaneous abortion specimen. To the best our knowledge the present case is the first documented chimera in a spontaneously aborted fetus. The application of int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::17fdfdbf23047227a17a258f23474643
https://pubmed.ncbi.nlm.nih.gov/17385415
https://pubmed.ncbi.nlm.nih.gov/17385415
Publikováno v:
TSitologiia i genetika. 40(3)
We report on two unrelated cases of pericentric inversion 46,XY,inv(7)(p11q21.1) associated with distinct pattern of malformation including mental retardation, development delay, ectrodactyly, facial dismorphism, high arched palate. Additionally, one
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::60ad3ecdc6cb72132448da7496d47fb2
https://pubmed.ncbi.nlm.nih.gov/16933852
https://pubmed.ncbi.nlm.nih.gov/16933852