Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Rem I. Sukernik"'
Autor:
Stanislav V. Dryomov, Elena B. Starikovskaya, Azhar M. Nazhmidenova, Igor V. Morozov, Rem I. Sukernik
Publikováno v:
BMC Evolutionary Biology, Vol 20, Iss 1, Pp 1-8 (2020)
Abstract Background We have described the diversity of complete mtDNA sequences from ‘relic’ groups of the Russian Far East, primarily the Nivkhi (who speak a language isolate with no clear relatedness to any others) and Oroki of Sakhalin, as wel
Externí odkaz:
https://doaj.org/article/74067ce749164277bc96d9337a0afab3
Autor:
Igor Morozov, Stanislav Dryomov, Elena B. Starikovskaya, Rem I. Sukernik, Azhar M Nazhmidenova
Publikováno v:
BMC Evolutionary Biology, Vol 20, Iss 1, Pp 1-8 (2020)
BMC Evolutionary Biology
BMC Evolutionary Biology
Background We have described the diversity of complete mtDNA sequences from ‘relic’ groups of the Russian Far East, primarily the Nivkhi (who speak a language isolate with no clear relatedness to any others) and Oroki of Sakhalin, as well as the
Autor:
Anatoly P. Derevianko, Rem I. Sukernik, Azhar M Nazhmidenova, David Reich, Nadin Rohland, Elena B. Starikovskaya, Stanislav Dryomov, Swapan Mallick, Sofia A Shalaurova, Rebecca Bernardos
Publikováno v:
PLoS ONE
PLoS ONE, Vol 16, Iss 1, p e0244228 (2021)
PLoS ONE, Vol 16, Iss 1, p e0244228 (2021)
The Central Siberian Plateau was the last geographic area in Eurasia to become habitable by modern humans after the Last Glacial Maximum (LGM). Through a comprehensive dataset of mitochondrial DNA (mtDNA) genomes retained in the remnats of earlier (
Autor:
Rem I. Sukernik, Elena B. Starikovskaya, Azhar M Nazhmidenova, I. O. Mazunin, Stanislav Dryomov, N. V. Volodko, Igor Y Bychkov, Sofia A Shalaurova
Publikováno v:
Cells
Volume 8
Issue 12
Volume 8
Issue 12
Our data first represent the variety of Leber&rsquo
s hereditary optic neuropathy (LHON) mutations in Western Siberia. LHON is a disorder caused by pathogenic mutations in mitochondrial DNA (mtDNA), inherited maternally and presents mainly in yo
s hereditary optic neuropathy (LHON) mutations in Western Siberia. LHON is a disorder caused by pathogenic mutations in mitochondrial DNA (mtDNA), inherited maternally and presents mainly in yo
Autor:
Rem I. Sukernik, Elena B. Starikovskaya, David Reich, Azhar M Nazhmidenova, Swapan Mallick, Stanislav Dryomov, Anatoly P. Derevianko, Rebecca Bernardos, Nadin Rohland, Sofia A Shalaurova
The Central Siberian Plateau was last geographic area in Eurasia to become habitable by modern humans after the Last Glacial Maximum (LGM). Through comprehensive mitochondrial DNA genomes retained in indigenous Siberian populations, the Ket, Tofalar,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5bd030726b2cb4dc55a5d5add11aac5
https://doi.org/10.1101/656181
https://doi.org/10.1101/656181
Autor:
Igor Morozov, Azhar M Nazhmidenova, Elena B. Starikovskaya, Andrei V Tabarev, Rem I. Sukernik, Stanislav Dryomov, Sophia A Shalaurova
Publikováno v:
European Journal of Human Genetics. 23:1399-1404
The patterns of prehistoric migrations across the Bering Land Bridge are far from being completely understood: there still exists a significant gap in our knowledge of the population history of former Beringia. Here, through comprehensive survey of m
Autor:
Jüri Parik, Ene Metspalu, Susanne Nordenfelt, Gabriel Renaud, Andres Ruiz-Linares, Qiaomei Fu, Joseph Wee, Oleg Balanovsky, Hovhannes Sahakyan, Olga L. Posukh, Niru Chennagiri, George Ayodo, Doron M. Behar, Cheryl A. Winkler, Stanislav Dryomov, Iain Mathieson, Aashish R. Jha, Cynthia M. Beall, Iosif Lazaridis, Sarah A. Tishkoff, Draga Toncheva, Richard Villems, Damian Labuda, M. Syafiq Abdullah, Giovanni Poletti, Toomas Kivisild, Rem I. Sukernik, Yaniv Erlich, William Klitz, Anna Di Rienzo, Tor Hervig, Elena B. Starikovskaya, Levon Yepiskoposyan, Nick Patterson, David Comas, Jeffrey P. Spence, George Stamatoyannopoulos, Francois Balloux, Yun S. Song, David Reich, Cristian Capelli, Mark Lipson, Kumarasamy Thangaraj, Sergey Litvinov, Janet Kelso, Brenna M. Henn, Pontus Skoglund, Ugur Hodoglugil, Arti Tandon, Andrés Moreno-Estrada, Sriram Sankararaman, Carla Gallo, Elza Khusnutdinova, Lynn B. Jorde, Chris Tyler-Smith, Robert W. Mahley, Nadin Rohland, Elena Balanovska, Swapan Mallick, Choongwon Jeong, Antti Sajantila, Peter de Knijff, Mengyao Zhao, Michael J. Bamshad, Rita Khusainova, Thomas Willems, Sena Karachanak-Yankova, Heng Li, Irene Gallego Romero, Lalji Singh, Michael F. Hammer, W. Scott Watkins, Fernando Racimo, Svante Pääbo, George van Driem, Melissa Gymrek, Yali Xue, Mait Metspalu, Claudio M. Bravi
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
Nature
Nature, vol 538, iss 7624
SEDICI (UNLP)
Universidad Nacional de La Plata
instacron:UNLP
Nature, 538(7624), 201
Mallick, Swapan; Li, Heng; Lipson, Mark; Mathieson, Iain; Gymrek, Melissa; Racimo, Fernando; et al.(2016). The Simons Genome Diversity Project: 300 genomes from 142 diverse populations.. Nature, 538(7624), 201-206. doi: 10.1038/nature18964. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/71x1v1d2
instname
Nature
Nature, vol 538, iss 7624
SEDICI (UNLP)
Universidad Nacional de La Plata
instacron:UNLP
Nature, 538(7624), 201
Mallick, Swapan; Li, Heng; Lipson, Mark; Mathieson, Iain; Gymrek, Melissa; Racimo, Fernando; et al.(2016). The Simons Genome Diversity Project: 300 genomes from 142 diverse populations.. Nature, 538(7624), 201-206. doi: 10.1038/nature18964. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/71x1v1d2
Here we report the Simons Genome Diversity Project data set: high quality genomes from 300 individuals from 142 diverse populations. These genomes include at least 5.8 million base pairs that are not present in the human reference genome. Our analysi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d411cd6f6f44c0c1bb40fba811703cc
https://hdl.handle.net/1887/113776
https://hdl.handle.net/1887/113776
Autor:
Ilya O. Mazunin, N. P. Eltsov, Stanislav Dryomov, Elena B. Starikovskaya, Rem I. Sukernik, N. V. Volodko
Publikováno v:
American Journal of Physical Anthropology. 148:123-138
To fill remaining gaps in mitochondrial DNA diversity in the least surveyed eastern and western flanks of Siberia, 391 mtDNA samples (144 Tubalar from Altai, 87 Even from northeastern Siberia, and 160 Ulchi from the Russian Far East) were characteriz
Publikováno v:
Russian Journal of Genetics. 46:1386-1394
The mtDNA variation has been studied in representatives of the Russkoe Ust’e (n = 30), Kolyma (n = 31), and Markovo (n = 26) ethnic subgroups originating from Russian military men, hunters, and fishers who married local Yukaghir women and settled a
Publikováno v:
Molecular Biology. 44:665-681
Today there are described more than 400 point mutations and more than hundred of structural rearrangements of mitochondrial DNA associated with characteristic neuromuscular and other mitochondrial syndromes, from lethal in the neonatal period of life