Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Daria A. Larina"'
Autor:
Tatiana A. Shnaider, Anna A. Khabarova, Ksenia N. Morozova, Anastasia M. Yunusova, Sophia A. Yakovleva, Anastasia S. Chvileva, Ekaterina R. Wolf, Elena V. Kiseleva, Elena V. Grigor’eva, Viktori Y. Voinova, Maria A. Lagarkova, Ekaterina A. Pomerantseva, Elizaveta V. Musatova, Alexander V. Smirnov, Anna V. Smirnova, Diana S. Stoklitskaya, Tatiana I. Arefieva, Daria A. Larina, Tatiana V. Nikitina, Inna E. Pristyazhnyuk
Publikováno v:
Cells, Vol 12, Iss 23, p 2702 (2023)
Cohen syndrome is an autosomal recessive disorder caused by VPS13B (COH1) gene mutations. This syndrome is significantly underdiagnosed and is characterized by intellectual disability, microcephaly, autistic symptoms, hypotension, myopia, retinal dys
Externí odkaz:
https://doaj.org/article/46fae80a53d840f5ae947d70a2822115
Autor:
Tatiana N Melnik, Maria A Majorina, Daria S Larina, Ivan A Kashparov, Ekaterina N Samatova, Anatoly S Glukhov, Bogdan S Melnik
Publikováno v:
PLoS ONE, Vol 9, Iss 6, p e98645 (2014)
At present it is unclear which interactions in proteins reveal the presence of intermediate states, their stability and formation rate. In this study, we have investigated the effect of substitutions of hydrophobic amino acid residues in the hydropho
Externí odkaz:
https://doaj.org/article/790183bf70a74d40ac87c4ce8fddddd4
Autor:
Anatoly S. Glukhov, Ivan A. Kashparov, Daria S. Larina, Bogdan S. Melnik, Maria A. Majorina, Ekaterina Samatova, Tatiana N. Melnik
Publikováno v:
PLoS ONE
PLoS ONE, Vol 9, Iss 6, p e98645 (2014)
PLoS ONE, Vol 9, Iss 6, p e98645 (2014)
At present it is unclear which interactions in proteins reveal the presence of intermediate states, their stability and formation rate. In this study, we have investigated the effect of substitutions of hydrophobic amino acid residues in the hydropho