Vladislav S Baranov
Saint Petersburg State University
143 Papers
575 Citations
Vladislav S Baranov is an academic researcher from Saint Petersburg State University. The author has contributed to research in topics: Population & SMA*. The author has an hindex of 19, co-authored 138 publications. Previous affiliations of Vladislav S Baranov include Russian Academy & Kirov Military Medical Academy.
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Papers
•Journal Article
Biochip development for polymorphism analysis in biotransformation system genes
Glotov aS,T. V. Nasedkina,Ivashchenko Te,R A Iurasov,Sergey Surzhikov,S. V. Pan'kov,Alexander V. Chudinov,Vladislav S Baranov,Alexander S. Zasedatelev +8 more
TL;DR: The efficiency of using the method of allele-specific hybridization with biochips for identification of individual genetic polymorphism is shown and it is believed that the bioch chips can be also a convenient tool in pharmacogenetics researches.
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DYNC1H1 gene methylation correlates with severity of spinal muscular atrophy
TL;DR: Significantly decreased methylation of CpG islands within exon 37 of the DYNC1H1 gene was observed in patients with a severe SMA manifestation compared to mildly affected SMA patients (types III–IV), which provides new information on peculiarities of methylation in clinically different types of SMA Patients and gives a clue for identification of new SMA modifiers.
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Allele frequencies and molecular diagnosis in haemophilia A and B patients from russia and from some Asian Republics of the former U.S.S.R.
M. V. Aseev,V. Surin,K. Baboev,N. Gornostaeva,T Kuznetzova,Tatyana K Kascheeva,T. Ivaschenko,G. Solovyev,A. Mikhailov,V. Lebedev,L. Papaian,T. Andreeva,Dm. Amoashyi,V. Vakharlovsky,Vladislav S Baranov +14 more
TL;DR: RFLP analysis of some intra‐ and extra‐genic polymorphic sites of Factor VIII (FVIII) and Factor IX (FIX) genes with relevant DNA probes or by polymerase chain reaction (PCR) was carried out in Slavic populations from the European part of Russia and also in the native ethnic groups of Uzbekistan and Kazahstan.
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Characterization of iRGD-Ligand Modified Arginine-Histidine-Rich Peptides for Nucleic Acid Therapeutics Delivery to αvβ3 Integrin-Expressing Cancer Cells
Anna Egorova,Alexander Selutin,Marianna Maretina,Sergei Alekseevich Selkov,Vladislav S Baranov,A. V. Kiselev +5 more
TL;DR: It is demonstrated that the peptide carrier RGD1 can be considered as promising candidate for development of NA therapeutics delivery systems useful in cancer gene therapy.
MED12 gene mutations in women with uterine myoma
N. S. Osinovskaya,T. E. Ivashchenko,A. K. Dolinskii,I. Yu. Sultanov,Svetlana Ghimbovschi,Eric P. Hoffman,V. F. Bezhenar,Vladislav S Baranov +7 more
TL;DR: It was shown that somatic mutations in the MED12 gene occur in 73% of cases with deletions of varying sizes and missense mutations being most common at codon 44.
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