Zobrazeno 1 - 10
of 23
pro vyhledávání: '"D. V. Osipova"'
Autor:
T. V. Markova, V. M. Kenis, S. S. Nikitin, E. V. Melchenko, T. S. Nagornova, D. V. Osipova, A. E. Alieva, Ya. S. Yugeno, E. Yu. Zakharova, E. L. Dadali
Publikováno v:
Нервно-мышечные болезни, Vol 12, Iss 2, Pp 37-46 (2022)
Background. Multiple epiphysal dysplasia (MED) type 1 (OMIM: 132400) is one of 7 genetic variants of this group of skeletal dysplasias described to date. The disease is caused by mutations in the COMP gene located on chromosome 19p13.1. The presence
Externí odkaz:
https://doaj.org/article/3e21228b2bc24db9bb3aecb71518e8be
Publikováno v:
Нервно-мышечные болезни, Vol 8, Iss 4, Pp 35-42 (2019)
Background. Patients with the chronic migraine frequently present with memory and attention complaints. However, the prevalence and phenotype of such impairment in chronic migraine have not been studied.Objective – to evaluate the prevalence of the
Externí odkaz:
https://doaj.org/article/2ab2a0f0dc384b34b4878e4f6e53d1e4
Publikováno v:
Нервно-мышечные болезни, Vol 8, Iss 3, Pp 34-42 (2018)
Over a half of chronic pain (CP) patients present with cognitive complaints, which increase their disability and impact quality of life. The paper reviews objective impairments in memory, attention, processing speed and executive function demonstrate
Externí odkaz:
https://doaj.org/article/b158ee169bf6467795194a9b2daa3599
Publikováno v:
Нервно-мышечные болезни, Vol 8, Iss 2, Pp 10-16 (2018)
Externí odkaz:
https://doaj.org/article/b63457ab1471488b9297eeb01993e334
Publikováno v:
Medical alphabet. 1:15-18
Cognitive impairment (CN) is widespread in migraines, but very little has been studied. There is evidence that these violations are present in patients with episodic migraine (EM) during an attack and in the interictal period. The purpose of this wor
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 119(2)
To evaluate the prevalence of objective cognitive impairment (CI) in patients with episodic migraine (EM) during the interictal period and in the chronic migraine (CM) population.Sixty-four patients with CM and 42 patients with low-frequency EM (less
Publikováno v:
Molecular Biology. 44:795-800
The selective 5-HT1A receptor silencer Freud-1 is known as one of the main factors participating in the transcriptional regulation of the serotonin brain 5-HT1A receptor. However, the role of Freud-1 in the mechanisms of genetically determined or exp
Autor:
Nina K. Popova, Darya Bazovkina, Alexander V. Kulikov, Vladimir S. Naumenko, D. V. Osipova, V. Yu. Dee
Publikováno v:
Bulletin of Experimental Biology and Medicine. 147:621-624
Congenic mice obtained by genome fragments transfer from one strain to another are a potent tool for studies of the molecular mechanisms of behavioral mutations. The 59-70 cM fragment of chromosome 13 containing the locus determining predisposition t
Publikováno v:
Journal of Neuroscience Methods. 170:197-203
In this study, we applied for real-time PCR the two-standard system that we had worked out previously for PCR with gel-detection of products. Genomic DNA of a known concentration was used as external standard and mRNA of the DNA-dependent RNA-polymer
Publikováno v:
Russian Journal of Genetics. 43:1408-1412
Brain neurotransmitter serotonin is involved in the regulation of many physiological functions and types of behavior. The key enzyme of serotonin synthesis in the brain is tryptophan hydroxylase-2 (TPH-2). Linkage between the C1473G polymorphism in g