Zobrazeno 1 - 10
of 1 236
pro vyhledávání: '"Murtazina A"'
Autor:
Alek G. Erickson, Alessia Motta, Maria Eleni Kastriti, Steven Edwards, Fanny Coulpier, Emy Théoulle, Aliia Murtazina, Irina Poverennaya, Daniel Wies, Jeremy Ganofsky, Giovanni Canu, Francois Lallemend, Piotr Topilko, Saida Hadjab, Kaj Fried, Christiana Ruhrberg, Quenten Schwarz, Valerie Castellani, Dario Bonanomi, Igor Adameyko
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-16 (2024)
Abstract The sympathetic nervous system controls bodily functions including vascular tone, cardiac rhythm, and the “fight-or-flight response”. Sympathetic chain ganglia develop in parallel with preganglionic motor nerves extending from the neural
Externí odkaz:
https://doaj.org/article/98641f2716d646a285c21ce889f6b686
Autor:
Artem Borovikov, Andrey Marakhonov, Aysylu Murtazina, Kseniya Davydenko, Alexandra Filatova, Nailya Galeeva, Varvara Kadnikova, Natalya Ogorodova, Daria Gorodilova, Ilya Kanivets, Denis Pyankov, Konstantin Zherdev, Aleksandr Petel’guzov, Pavel Zubkov, Alexander Polyakov, Olga Shchagina, Mikhail Skoblov
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Multiple osteochondromas (MO) is a rare autosomal dominant skeletal disorder characterized by the development of multiple benign tumors known as osteochondromas. The condition is predominantly caused by loss-of-function variants in the EXT1 or EXT2 g
Externí odkaz:
https://doaj.org/article/9b18c72810344e36991efc0b72f3c6ef
Autor:
Aysylu Murtazina, Dmitrii Subbotin, Anna Kuchina, Olga Gilvanova, Daniil Degterev, Olga Shchagina, Tatiana Cherevatova, Maria Bulakh, Darya Sherstyukova, Oksana Ryzhkova, Olga Kurushina, Mikhail Skoblov, Artem Borovikov, Sergey Kutsev
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Recent research has sparked a discussion on the spectrum of diseases linked to the MATR3 gene associated with amyotrophic lateral sclerosis and distal myopathy with vocal cord and pharyngeal weakness (VCPDM). To date, fewer than 50 cases of VCPDM hav
Externí odkaz:
https://doaj.org/article/0e97c5b455b14c928a3ae1cdf362ce68
Autor:
Ionova, Sofya A.1 (AUTHOR) sofya.aydarovna.g@med-gen.ru, Murtazina, Aysylu F.1 (AUTHOR) aysylumurtazina@gmail.com, Marakhonov, Andrey A.1 (AUTHOR) marakhonov@generesearch.ru, Shchagina, Olga A.1 (AUTHOR) schagina@med-gen.ru, Ryadninskaya, Nina V.1 (AUTHOR) outremal@yandex.ru, Tebieva, Inna S.2,3 (AUTHOR) tebinna@mail.ru, Kadyshev, Vitaly V.1 (AUTHOR) vvh.kad@gmail.com, Borovikov, Artem O.1 (AUTHOR) borovikov33@gmail.com, Ginter, Evgeny K.1 (AUTHOR) ekginter@mail.ru, Kutsev, Sergey I.1 (AUTHOR) kutsev@mail.ru, Zinchenko, Rena A.1 (AUTHOR) renazinchenko@mail.ru
Publikováno v:
International Journal of Molecular Sciences. Sep2024, Vol. 25 Issue 17, p9734. 11p.
Autor:
Strizhitskaya, Olga1 (AUTHOR) i.r.myrtazina@spbu.ru, Murtazina, Inna1 (AUTHOR)
Publikováno v:
Social Sciences (2076-0760). Aug2024, Vol. 13 Issue 8, p388. 11p.
Publikováno v:
Историческая этнология, Vol 9, Iss 1, Pp 10-16 (2024)
The article opens a special issue of the journal “Historical Ethnology”, dedicated to the Tatar woman. Its authors, who acted as compilers and scientific editors of the issue, substantiate the research focus, chronology and source base of the pub
Externí odkaz:
https://doaj.org/article/0d9950a3427f4ccbadaa5f3f3db323a1
Autor:
Lyalya R. Murtazina
Publikováno v:
Историческая этнология, Vol 9, Iss 1, Pp 30-37 (2024)
The article analyses the views of a prominent representative of the Tatar emigration, teacher, journalist, and public figure Rukiya Mukhammadish on the Tatar woman and her role in the fate of the people. The work is accompanied by a publication writt
Externí odkaz:
https://doaj.org/article/217648d7968c46fdbf9711d7864692c4
Autor:
Olga Shchagina, Aysylu Murtazina, Polina Chausova, Mariya Orlova, Elena Dadali, Sergei Kurbatov, Sergey Kutsev, Aleksander Polyakov
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Introduction:Charcot–Marie–Tooth disease type 4C (CMT4C) OMIM#601596 stands out as one of the most prevalent forms of recessive motor sensory neuropathy worldwide. This disorder results from biallelic pathogenic variants in the SH3TC2 gene.Method
Externí odkaz:
https://doaj.org/article/3d34053f980542aab2439eedeeee24e9
Autor:
Hollinshead, F.K., Hanlon, D.W., Hou, W., Tasma, Z., Damani, T., Bouma, G.J., Murtazina, D.A., Chamley, L.
Publikováno v:
In Journal of Equine Veterinary Science August 2024 139
Autor:
Sofya A. Ionova, Aysylu F. Murtazina, Andrey A. Marakhonov, Olga A. Shchagina, Nina V. Ryadninskaya, Inna S. Tebieva, Vitaly V. Kadyshev, Artem O. Borovikov, Evgeny K. Ginter, Sergey I. Kutsev, Rena A. Zinchenko
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 17, p 9734 (2024)
Myotonic dystrophy type 1 (DM1) is a multisystem disorder with progressive myopathy and myotonia. The clinical study was conducted in the Republic of North Ossetia-Alania (RNOA), and in it 39 individuals from 17 unrelated families were identified wit
Externí odkaz:
https://doaj.org/article/86166c8852db4680a725410044d44bda