Zobrazeno 1 - 10
of 162
pro vyhledávání: '"Ivan Y Iourov"'
Autor:
Anna L Kaysheva, Artur T Kopylov, Tatyana O Pleshakova, Ivan Y Iourov, Svetlana G Vorsanova, Yuri B Yurov, Andrey A Shchetkin, Alexander I Archakov, Yuri D Ivanov
Publikováno v:
Biotecnología Aplicada, Vol 34, Iss 2, Pp 2211-2214 (2017)
Externí odkaz:
https://doaj.org/article/d6decb69f3e545ac85add159385503aa
Autor:
Yuri B Yurov, Ivan Y Iourov, Svetlana G Vorsanova, Thomas Liehr, Alexei D Kolotii, Sergei I Kutsev, Franck Pellestor, Alfia K Beresheva, Irina A Demidova, Viktor S Kravets, Viktor V Monakhov, Ilia V Soloviev
Publikováno v:
PLoS ONE, Vol 2, Iss 6, p e558 (2007)
BACKGROUND: Understanding the mechanisms underlying generation of neuronal variability and complexity remains the central challenge for neuroscience. Structural variation in the neuronal genome is likely to be one important mechanism for neuronal div
Externí odkaz:
https://doaj.org/article/c11353b297164747977eae106295b5a1
Autor:
Ivan Y. Iourov, Alexandr P. Gerasimov, Maria A. Zelenova, Natalya E. Ivanova, Oksana S. Kurinnaia, Yulia M. Zabrodskaya, Irina A. Demidova, Evgeny R. Barantsevich, Kirill S. Vasin, Alexey D. Kolotii, Vseslav V. Ushanov, Darya A. Sitovskaya, Timur B.-A. Lobzhanidze, Maria E. Iuditskaia, Nikita S. Iakushev, Muslim M. Zhumatov, Svetlana G. Vorsanova, Konstantin A. Samochernyh
Publikováno v:
Molecular Cytogenetics, Vol 16, Iss 1, Pp 1-18 (2023)
Abstract Molecular cytogenetic and cytogenomic studies have made a contribution to genetics of epilepsy. However, current genomic research of this devastative condition is generally focused on the molecular genetic aspects (i.e. gene hunting, detecti
Externí odkaz:
https://doaj.org/article/95d9c24d4b984991baed1086afb6fe00
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-6 (2020)
Abstract Background Somatic chromosomal mosaicism is the presence of cell populations differing with respect to the chromosome complements (e.g. normal and abnormal) in an individual. Chromosomal mosaicism is associated with a wide spectrum of diseas
Externí odkaz:
https://doaj.org/article/a810f723ae8f44fcbc76ba447ddfcd49
Autor:
Ivan Y. Iourov, Maria A. Zelenova
Publikováno v:
Current Bioinformatics. 17:883-887
Background: Technical advances and cost reduction have allowed for the worldwide popularity of array platforms. Otherwise called “molecular karyotyping”, it yields a large amount of CNV data, which is useless without interpretation. Objective: Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6cbb186fe61f2b0c29b337142131d7f0
https://doi.org/10.2174/1574893617666220907121155
https://doi.org/10.2174/1574893617666220907121155
Publikováno v:
Methods in Molecular Biology ISBN: 9781071626542
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3de16961afaac23bc0b7e0bbd933369f
https://doi.org/10.1007/978-1-0716-2655-9_10
https://doi.org/10.1007/978-1-0716-2655-9_10
Publikováno v:
Cytogenetics and Molecular Cytogenetics ISBN: 9781003223658
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::488e041ac359ca0500bab5a562944fa6
https://doi.org/10.1201/9781003223658-16
https://doi.org/10.1201/9781003223658-16
Autor:
Ivan Y. Iourov
Publikováno v:
Cytogenetics and Molecular Cytogenetics ISBN: 9781003223658
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43a9b21dc691ada7345d84a3b88f7be3
https://doi.org/10.1201/9781003223658-5
https://doi.org/10.1201/9781003223658-5
Autor:
Kirill S. Vasin, Svetlana G. Vorsanova, Yuri B. Yurov, Alexey D. Kolotii, I.V. Soloviev, Victor S. Kravets, Ivan Y. Iourov, Demidova Ia
Publikováno v:
RESEARCH RESULTS IN BIOMEDICINE. 7:257-271
Chromosome 18p deletion syndrome (18p-) is associated with a loss of chromosomal material of the short arm (partial monosomy); however, the whole short arm is lost in the majority of cases. The frequency of 18p- syndrome is 1:60000. The syndrome is c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9a1dec7e12cd4944e273c1e9d393182
https://doi.org/10.18413/2658-6533-2021-7-3-0-5
https://doi.org/10.18413/2658-6533-2021-7-3-0-5
Publikováno v:
Molecular cytogenetics. 15(1)
It is hard to believe that all the cells of a human brain share identical genomes. Indeed, single cell genetic studies have demonstrated intercellular genomic variability in the normal and diseased brain. Moreover, there is a growing amount of eviden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d49f7f83e6a65fadb98e7b6022e6d71
https://pubmed.ncbi.nlm.nih.gov/36266706
https://pubmed.ncbi.nlm.nih.gov/36266706