Prevalence of lumbosacral transitional vertebra among 4816 consecutive patients with low back pain: A computed tomography, magnetic resonance imaging, and plain radiographic study with novel classification schema

Autor: Vadim A Byvaltsev, Andrei A Kalinin, Valery V Shepelev, Yurii Ya Pestryakov, Marat A Aliyev, Dmitriy V Hozeev, Mikhail Y Biryuchkov, Rustem A Kundubayev, K Daniel Riew

Publikováno v: Journal of Craniovertebral Junction and Spine, Vol 14, Iss 1, Pp 35-43 (2023)

Study Design: A retrospective single-center study. Background: The prevalence of the lumbosacral anomalies remains controversial. The existing classification to characterize these anomalies is more complex than necessary for clinical use. Purpose: To

Externí odkaz: https://doaj.org/article/f6ba885af3944294bbb0a205dcb1e0e4

The influence of heterotopic ossification on clinical and radiological out- comes after total lumbar disc replacement with M6-L prosthesis: a multicenter study

Autor: Vadim A. Byvaltsev, Yury Ya. Pestrjakov, Valery V. Shepelev, Ivan A. Stepanov

Publikováno v: Хирургия позвоночника, Vol 14, Iss 4, Pp 69-75 (2017)

Objective. To assess the degree of influence of heterotopic ossification on the motion amplitude of the operated segment and on clinical outcomes in patients after total intervertebral disc replacement. Material and Methods. Results of total replace

Externí odkaz: https://doaj.org/article/1846ee9b01c642d7a5714d0dc33e8081

The variation and evolution of complete human centromeres

Autor: Glennis A. Logsdon, Allison N. Rozanski, Fedor Ryabov, Tamara Potapova, Valery A. Shepelev, Yafei Mao, Mikko Rautiainen, Sergey Koren, Sergey Nurk, David Porubsky, Julian K. Lucas, Kendra Hoekzema, Katherine M. Munson, Jennifer L. Gerton, Adam M. Phillippy, Ivan A. Alexandrov, Evan E. Eichler

Publikováno v: bioRxiv

We completely sequenced and assembled all centromeres from a second human genome and used two reference sets to benchmark genetic, epigenetic, and evolutionary variation within centromeres from a diversity panel of humans and apes. We find that centr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3ae3628f75ed75dbf113c54b0b4a540
https://europepmc.org/articles/PMC10312506/

The complete sequence of a human Y chromosome

Autor: Arang Rhie, Sergey Nurk, Monika Cechova, Savannah J. Hoyt, Dylan J. Taylor, Nicolas Altemose, Paul W. Hook, Sergey Koren, Mikko Rautiainen, Ivan A. Alexandrov, Jamie Allen, Mobin Asri, Andrey V. Bzikadze, Nae-Chyun Chen, Chen-Shan Chin, Mark Diekhans, Paul Flicek, Giulio Formenti, Arkarachai Fungtammasan, Carlos Garcia Giron, Erik Garrison, Ariel Gershman, Jennifer Gerton, Patrick G.S. Grady, Andrea Guarracino, Leanne Haggerty, Reza Halabian, Nancy F. Hansen, Robert Harris, Gabrielle A. Hartley, William T. Harvey, Marina Haukness, Jakob Heinz, Thibaut Hourlier, Robert M. Hubley, Sarah E. Hunt, Stephen Hwang, Miten Jain, Rupesh K. Kesharwani, Alexandra P. Lewis, Heng Li, Glennis A. Logsdon, Julian K. Lucas, Wojciech Makalowski, Christopher Markovic, Fergal J. Martin, Ann M. Mc Cartney, Rajiv C. McCoy, Jennifer McDaniel, Brandy M. McNulty, Paul Medvedev, Alla Mikheenko, Katherine M. Munson, Terence D. Murphy, Hugh E. Olsen, Nathan D. Olson, Luis F. Paulin, David Porubsky, Tamara Potapova, Fedor Ryabov, Steven L. Salzberg, Michael E.G. Sauria, Fritz J. Sedlazeck, Kishwar Shafin, Valery A. Shepelev, Alaina Shumate, Jessica M. Storer, Likhitha Surapaneni, Angela M. Taravella Oill, Françoise Thibaud-Nissen, Winston Timp, Marta Tomaszkiewicz, Mitchell R. Vollger, Brian P. Walenz, Allison C. Watwood, Matthias H. Weissensteiner, Aaron M. Wenger, Melissa A. Wilson, Samantha Zarate, Yiming Zhu, Justin M. Zook, Evan E. Eichler, Rachel O’Neill, Michael C. Schatz, Karen H. Miga, Kateryna D. Makova, Adam M. Phillippy

The human Y chromosome has been notoriously difficult to sequence and assemble because of its complex repeat structure including long palindromes, tandem repeats, and segmental duplications. As a result, more than half of the Y chromosome is missing

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d38b477c2daccca72d1302cd2225927d
https://doi.org/10.1101/2022.12.01.518724

The evolutionary origin of man can be traced in the layers of defunct ancestral alpha satellites flanking the active centromeres of human chromosomes.

Autor: Valery A Shepelev, Alexander A Alexandrov, Yuri B Yurov, Ivan A Alexandrov

Publikováno v: PLoS Genetics, Vol 5, Iss 9, p e1000641 (2009)

Alpha satellite domains that currently function as centromeres of human chromosomes are flanked by layers of older alpha satellite, thought to contain dead centromeres of primate progenitors, which lost their function and the ability to homogenize sa

Externí odkaz: https://doaj.org/article/f5b9518b8f634d499547ce1de15b8625