Zobrazeno 1 - 10
of 50
pro vyhledávání: '"M. g. Divashuk"'
Autor:
M. A. Samarina, D. S. Uliyanov, T. D. Mokhov, Ya. S. Meglitskaya, P. Yu. Krupin, G. I. Karlov, P. N. Kharchenko, S. I. Voronov, N. V. Davydova, M. G. Divashuk
Publikováno v:
Зерновое хозяйство России, Vol 0, Iss 4, Pp 33-40 (2024)
According to the Law “On Seed Production”, all varieties or hybrids included in the state register shall be provided for genetic passports, as well as making a list of plants’ species, the production of which is aimed at ensuring food security.
Externí odkaz:
https://doaj.org/article/846db98277f3479f8e86662d2d869bf0
Autor:
P. Yu. Kroupin, A. I. Yurkina, A. A. Kocheshkova, D. S. Ulyanov, G. I. Karlov, M. G. Divashuk
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 27, Iss 8, Pp 947-957 (2023)
Satellite repeats are a significant component of the genome of Triticeae and play a crucial role in the speciation. They are a valuable tool for studying these processes. Pseudoroegneria species play a special role among grasses, as they are consider
Externí odkaz:
https://doaj.org/article/830b7d47bbb44a82ac352bc3668732c3
Autor:
R. P. Myasnikov, N. N. Kuzina, D. A. Nefedova, A. V. Kiseleva, O. V. Kulikova, A. N. Meshkov, M. M. Kudryavtseva, E. A. Mershina, M. g. Divashuk, E. V. Ryzhkova, M. S. Kharlap, O. M. Drapkina
Publikováno v:
Российский кардиологический журнал, Vol 28, Iss 11 (2023)
Inherited cardiomyopathies (CMP) are a group of heterogeneous diseases characterized by myocardial disorders that is not caused by coronary artery disease, hypertension, valvular and congenital defects. With the development of imaging methods and mol
Externí odkaz:
https://doaj.org/article/edf30b19433b45eba60ff5615a6f1553
Autor:
M. M. Kudryavtseva, A. V. Kiseleva, R. P. Myasnikov, O. V. Kulikova, A. N. Meshkov, E. A. Mershina, R. K. Angarsky, Е. A. Sotnikova, M. G. Divashuk, A. A. Zharikova, S. N. Koretsky, D. A. Filatova, V. E. Sinitsyn, N. A. Sdvigova, V. I. Barsky, E. N. Basargina, O. M. Drapkina
Publikováno v:
Кардиоваскулярная терапия и профилактика, Vol 21, Iss 12 (2023)
Left ventricular non-compaction (LVNC) is a rare, genetically and phenotypically heterogeneous disease, which is often accompanied by diagnostic difficulties.Aim. To demonstrate several generations of a family with LVNC with various clinical and phen
Externí odkaz:
https://doaj.org/article/67bab5e29c354e2bbd78fca1a22a2182
Autor:
O. V. Kulikova, R. P. Myasnikov, A. N. Meshkov, E. A. Mershina, A. V. Kiseleva, E. A. Sotnikova, M. M. Kudryavtseva, M. S. Kharlap, M. G. Divashuk, A. A. Zharikova, R. K. Angarsky, S. N. Koretsky, D. А. Filatova, V. E. Sinitsyn, O. M. Drapkina
Publikováno v:
Кардиоваскулярная терапия и профилактика, Vol 21, Iss 12 (2023)
Aim. To demonstrate two generations of a family with a progressive course of left ventricular non-compaction (LVNC) and the presence of a RBM20 gene variant.Material and methods. Based on the multicenter registry of patients with LVNC, a family with
Externí odkaz:
https://doaj.org/article/d48cc8bc572a42b48a3d6746494439f6
Autor:
R. P. Myasnikov, O. V. Kulikova, A. N. Meshkov, A. V. Kiseleva, A. O. Shumarina, S. N. Koretskiy, A. A. Zharikova, M. G. Divashuk, M. S. Kharlap, S. E. Serduk, E. A. Mershina, V. E. Sinitsyn, S. A. Boytsov, O. M. Drapkina
Publikováno v:
Рациональная фармакотерапия в кардиологии, Vol 16, Iss 3, Pp 383-391 (2020)
Left ventricular non-compaction (LVNC) is a genetically determined cardiomyopathy characterized by different variants of the clinical course. LVNC family cases allow to study in more details the role of genetic factors in cardiomyopathy pathogenesis
Externí odkaz:
https://doaj.org/article/71d202fcac474e7a99374b3c444066f8
Autor:
O. V. Kulikova, R. P. Myasnikov, A. N. Meshkov, M. M. Kudryavtseva, E. A. Mershina, A. V. Kiseleva, M. G. Divashuk, M. S. Kharlap, S. N. Koretsky, V. E. Sinitsyn, O. M. Drapkina
Publikováno v:
Российский кардиологический журнал, Vol 26, Iss 10 (2021)
Left ventricular non-compaction is a heterogeneous heart disease with various phenotypic and clinical manifestations. The article presents the results of clinical, instrumental and molecular genetic investigations of a family with diagnosed left vent
Externí odkaz:
https://doaj.org/article/1500037c6a8848898de5e870a5d3a46e
Autor:
A. G. Chernook, P. Yu. Kroupin, L. A. Bespalova, V. V. Panchenko, V. Ya. Kovtunenko, M. S. Bazhenov, L. A. Nazarova, G. I. Karlov, A. Yu. Kroupina, M. G. Divashuk
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 23, Iss 7, Pp 916-925 (2019)
Alleles of the genes, conferring a dwarfing phenotype, play a crucial role in wheat breeding, as they not only reduce plant height, ensuring their resistance to lodging, but also have a number of positive and negative pleiotropic effects on plant pro
Externí odkaz:
https://doaj.org/article/7efe024bad6340db89eebed77b57c3a9
Autor:
R. P. Myasnikov, A. A. Bukaeva, O. V. Kulikova, A. I. Ershova, A. V. Petukhova, E. D. Zotova, A. N. Meshkov, E. A. Mershina, A. V. Kiseleva, M. G. Divashuk, P. S. Pilyus, M. S. Kharlap, V. M. Mikova, S. N. Koretsky, L. A. Gandaeva, V. E. Sinitsyn, E.. N. Basargina, S. A. Boytsov, E. A. Snigir, A. I. Akinshina, D. A. Kashtanova, V. V. Makarov, V. S. Yudin, O. M. Drapkina
Publikováno v:
Российский кардиологический журнал, Vol 26, Iss 1S (2021)
The article presents the examination of three generations of a family with diagnosed left ventricular noncompaction (LVNC) and various phenotypic manifestations of the disease (isolated, hypertrophic and dilated type of LVNC). As a result of a molecu
Externí odkaz:
https://doaj.org/article/0ce62cb7901e4c04af8ca2327cf631cb
Autor:
R. P. Myasnikov, A. V. Kulikova, A. N. Meshkov, E. A. Mershina, A. V. Kiseleva, M. V. Klimushina, M. G. Divashuk, O. V. Kurilova, P. S. Pilyus, M. S. Kharlap, S. N. Koretsky, O. M. Larina, V. E. Sinitsyn, L. A. Gandaeva, V. I. Barsky, E. N. Basargina, S. A. Boytsov, O. M. Drapkina
Publikováno v:
Российский кардиологический журнал, Vol 25, Iss 10 (2020)
The article presents the results of clinical, instrumental and molecular genetic tests of three generations of a family with inherited cardiomyopathy caused by a new variant in the MYBPC3 gene. A specific feature of this case is the phenotypic hetero
Externí odkaz:
https://doaj.org/article/aa052b86ac63415ba12b5f05d4c973e4