Zobrazeno 1 - 10
of 93
pro vyhledávání: '"Pa, Slominskiĭ"'
Autor:
Ta, Kolomin, Agapova TIu, Agniullin IaV, Si, Shram, Maria Shadrina, Pa, Slominskiĭ, Sa, Limborskaia, If, Miasoedov
Publikováno v:
Europe PubMed Central
The effect of single and course administration of Selank (Thr-Lys-Pro-Arg-Pro-Gly-Pro) in the dose 200 microg/kg on the rat hippocampus transcriptional profile were studied using cDNA microarray technology. It was shown that mRNA levels of 36 genes c
Autor:
Fedotova EIu, Ao, Chechetkin, Maria Shadrina, Pa, Slominskiĭ, Ia, Ivanova-Smolenskaia, Sn, Illarioshkin
Publikováno v:
Europe PubMed Central
An abnormal hyperechogenecity of substantia nigra is thought to be the most characteristic sonographic feature in Parkinson's disease (PD). However specificity and sensitivity of the ultrasound method should be refined. Using transcranial sonography,
Autor:
Ev, Semenova, Maria Shadrina, Pa, Slominskiĭ, Sn, Illarioshkin, Bagyeva GKh, Av, Karabanov, Ia, Ivanova-Smolenskaia, Sa, Limborskaia
Publikováno v:
Europe PubMed Central
Fifty-two patients that had ParkinsonTs disease with autosomal dominant type of inheritance were analyzed for the presence of duplications and triplications in exons 4--6 of alpha-synuclein gene using real-time PCR with Taq-Man probes. No mutations i
Publikováno v:
Europe PubMed Central
Allele frequency distributions of the insertion/deletion (I/D) polymorphism of the angiotensin-converting enzyme (ACE) gene and the M235T polymorphism of the angiotensinogen gene was studied in a random sample of the indigenous population of the Sakh
Autor:
Ev, Filatova, Maria Shadrina, Av, Karabanov, Pa, Slominskiĭ, Sn, Illarioshkin, Ia, Ivanova-Smolenskaia, Sa, Limborskaia
Publikováno v:
Europe PubMed Central
Parkinson's disease (PD) is the second most common progressive neurodegenerative disorder characterized by the degeneration of dopaminergic neurons. Detecting changes in gene expression in untreated de novo patients with PD is important for understan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::db1aa06d9238e5d198566dd3243a2f8c
http://europepmc.org/abstract/med/21790007
http://europepmc.org/abstract/med/21790007
Publikováno v:
Europe PubMed Central
Polymorphism of the (CA)n repetitive sequence in the angiotensinogen gene was studied in a random sample of Russian males from the Moscow population and in a sample of patients with coronary heart disease. Thirteen allelic variants of this microsatel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::88827f559038b8a30e23715fbbcc1dcb
http://europepmc.org/abstract/med/9589857
http://europepmc.org/abstract/med/9589857
Autor:
Sn, Popova, Pa, Slominskiĭ, Sn, Galushkin, La, Tarskaia, Viktor Spitsyn, Ia, Guseva, Sa, Limborskaia
Publikováno v:
Europe PubMed Central
Polymorphism of highly polymorphic triplet repeats CTG of the 3'-untranslated region of the myotonin protein kinase gene and CAG of the genes associated with dentatorobral-pallidoluysian atrophy (DRPLA, or Hew River syndrome) and spinocerebellar atax
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::b011aca6c299769f075cec8c360b0cb0
http://europepmc.org/abstract/med/12500681
http://europepmc.org/abstract/med/12500681
Publikováno v:
Europe PubMed Central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::cca386e6c20ad44f5399e923343b9ae6
http://europepmc.org/abstract/med/9173245
http://europepmc.org/abstract/med/9173245
Publikováno v:
Europe PubMed Central
The IVS9-675CA polymorphism of the HIF-1alpha gene was analyzed in patients with acute ischemic stroke and in a control group. The genotype and allele frequencies proved to significantly differ between the two groups. Allele C and genotypes containin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0a235ed81d5a31d766def5afc037d2ef
http://europepmc.org/abstract/med/16871792
http://europepmc.org/abstract/med/16871792
Autor:
Sn, Popova, Pa, Slominskiĭ, Sn, Galushkin, Viktor Spitsyn, Ia, Guseva, Na, Bebiakova, Sa, Limborskaia
Publikováno v:
Europe PubMed Central
Frequencies of the wild-type and null genotypes of the GSTM1 and GSTT1 genes were established in healthy donors from several Russian populations (ethnic Russians from the towns of Oshevensk and Kholmogory, Arkhangel'sk oblast; ethnic Khants; ethnic K
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::f298c0b0ff6818e6aafe94e76fc98cfb
http://europepmc.org/abstract/med/11898621
http://europepmc.org/abstract/med/11898621