Zobrazeno 1 - 10
of 193
pro vyhledávání: '"Irina Sokolova"'
Publikováno v:
PhytoKeys, Vol 247, Iss , Pp 219-248 (2024)
The study provides nomenclatural history, morphological characteristics and taxonomy of Cocconeis baicalensis and C. skvortzowii described by B.V. Skvortzov from Lake Baikal. The lecto- and epitypification of the names are made, based on the K.I. Mey
Externí odkaz:
https://doaj.org/article/275c1ea5e78b4053a231f646528650a3
Autor:
Irina Sokolova, Ilya Makarov
Publikováno v:
IEEE Access, Vol 12, Pp 127637-127654 (2024)
This paper explores the linguistic complexity of constructed auxiliary languages (conlangs) with two primary goals: evaluating their complexity using established linguistic criteria and developing a novel, interpretable method for quantifying languag
Externí odkaz:
https://doaj.org/article/74ed7bcd67c04ea793bb35a9f95ca26a
Autor:
Julya Sorokina, Irina Sokolova, Mariya Majorina, Anastasia Ungur, Vasiliy Troitskiy, Amir Tukhvatulin, Bogdan Melnik, Yury Belyi
Publikováno v:
Biomolecules, Vol 13, Iss 6, p 1012 (2023)
In a previous study, we demonstrated that the Clostridioides difficile VirB4-like ATPase forms oligomers in vitro. In the current investigation, to study the observed phenomenon in more detail, we prepared a library of VirB4-derived peptides (delVirB
Externí odkaz:
https://doaj.org/article/ced56fb895af43379b4b9d91375dca71
Autor:
Irina Sokolova
Publikováno v:
States and Regions. Series: Public Administration. :56-61
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d22dafd9ab99bb497bc3798ba02600c
https://doi.org/10.32840/1813-3401.2023.1.9
https://doi.org/10.32840/1813-3401.2023.1.9
Autor:
Belyi, Julya Sorokina, Irina Sokolova, Mariya Majorina, Anastasia Ungur, Vasiliy Troitskiy, Amir Tukhvatulin, Bogdan Melnik, Yury
Publikováno v:
Biomolecules; Volume 13; Issue 6; Pages: 1012
In a previous study, we demonstrated that the Clostridioides difficile VirB4-like ATPase forms oligomers in vitro. In the current investigation, to study the observed phenomenon in more detail, we prepared a library of VirB4-derived peptides (delVirB
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::b37504ee089a6c7d41fb12f9430ac2ab
Autor:
Martin J. van den Bent, Peter J. Ansell, Kyle D. Holen, Maria Guseva, Andrew M. Scott, Hui K. Gan, Priya Kumthekar, David Maag, Anahita Bhathena, Erica Gomez, Xin Lu, Zheng Zha, Carolyn Mullen, Rupinder Kular, Ekaterina Pestova, Minghao Song, Irina Sokolova, Lisa Roberts-Rapp, Andrew B. Lassman
Purpose:Patients with glioblastoma (GBM) have a poor prognosis and are in desperate need of better therapies. As therapeutic decisions are increasingly guided by biomarkers, and EGFR abnormalities are common in GBM, thus representing a potential ther
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15671a97fee370559bbe15233ea8d7b6
https://doi.org/10.1158/1078-0432.c.6527364.v1
https://doi.org/10.1158/1078-0432.c.6527364.v1
Autor:
Martin J. van den Bent, Peter J. Ansell, Kyle D. Holen, Maria Guseva, Andrew M. Scott, Hui K. Gan, Priya Kumthekar, David Maag, Anahita Bhathena, Erica Gomez, Xin Lu, Zheng Zha, Carolyn Mullen, Rupinder Kular, Ekaterina Pestova, Minghao Song, Irina Sokolova, Lisa Roberts-Rapp, Andrew B. Lassman
Supplementary Table S2. Concordance of FISH and WES results. Supplementary Table S3. Point mutations identified in EGFR. Supplementary Table S4. Concordance of FISH and RT-PCR results. Supplementary Table S5. Concordance of FISH and RNAseq results. S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e1792b7fc7dba0544047eaf0284e3fa
https://doi.org/10.1158/1078-0432.22469823
https://doi.org/10.1158/1078-0432.22469823
Autor:
Ai Zhang, Irina Sokolova, Alain Domissy, Joshua Davis, Lee Rao, Kagistia Hana Utami, Yanling Wang, Randi J Hagerman, Mahmoud A Pouladi, Pietro Sanna, Michael J Boland, Jeanne F Loring
Publikováno v:
Stem cells translational medicine, vol 11, iss 6
Fragile X Syndrome (FXS), the leading monogenic cause of intellectual disability and autism spectrum disorder, is caused by expansion of a CGG trinucleotide repeat in the 5ʹ-UTR of the Fragile X Mental Retardation-1 (FMR1) gene. Epigenetic silencing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95a946f7476ded33b16512281e779589
https://doi.org/10.1093/stcltm/szac022
https://doi.org/10.1093/stcltm/szac022
Autor:
Zahra Arabi, Farrokh Ghahremaninejad, Richard K. Rabeler, Irina Sokolova, Maximilian Weigend, Shahin Zarre
Publikováno v:
TAXON. 71:608-629
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05b8bd0838b6b1c860678d6e71a7244c
https://doi.org/10.1002/tax.12688
https://doi.org/10.1002/tax.12688
Autor:
Alexander Sennikov, Irina Sokolova
Publikováno v:
Nordic Journal of Botany. 2023
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec40f006b9097b6794352edb80ccc96b
https://doi.org/10.1111/njb.03873
https://doi.org/10.1111/njb.03873