Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Satyakrishna Pentakota"'
Autor:
Iyer Aditya Mahadevan, Satyakrishna Pentakota, Raktim Roy, Utsa Bhaduri, Manchanahalli R. Satyanarayana Rao
Publikováno v:
Epigenetics & Chromatin, Vol 12, Iss 1, Pp 1-23 (2019)
Abstract Background TH2B is a major histone variant that replaces about 80–85% of somatic H2B in mammalian spermatocytes and spermatids. The post-translational modifications (PTMs) on TH2B have been well characterised in spermatocytes and spermatid
Externí odkaz:
https://doaj.org/article/0d88d5d3cacc465eb06dd01575ca849e
Autor:
Satyakrishna Pentakota, Keda Zhou, Charlotte Smith, Stefano Maffini, Arsen Petrovic, Garry P Morgan, John R Weir, Ingrid R Vetter, Andrea Musacchio, Karolin Luger
Publikováno v:
eLife, Vol 6 (2017)
Centromere protein (CENP) A, a histone H3 variant, is a key epigenetic determinant of chromosome domains known as centromeres. Centromeres nucleate kinetochores, multi-subunit complexes that capture spindle microtubules to promote chromosome segregat
Externí odkaz:
https://doaj.org/article/c10118af6b92425bb5254d424be03270
Autor:
Lisa Schubert, Ivo A Hendriks, Emil P T Hertz, Wei Wu, Selene Sellés‐Baiget, Saskia Hoffmann, Keerthana Stine Viswalingam, Irene Gallina, Satyakrishna Pentakota, Bente Benedict, Joachim Johansen, Katja Apelt, Martijn S Luijsterburg, Simon Rasmussen, Michael Lisby, Ying Liu, Michael L Nielsen, Niels Mailand, Julien P Duxin
Publikováno v:
EMBO Reports, 23(4). WILEY
Schubert, L, Hendriks, I A, Hertz, E P T, Wu, W, Sellés-Baiget, S, Hoffmann, S, Viswalingam, K S, Gallina, I, Pentakota, S, Benedict, B, Johansen, J, Apelt, K, Luijsterburg, M S, Rasmussen, S, Lisby, M, Liu, Y, Nielsen, M L, Mailand, N & Duxin, J P 2022, ' SCAI promotes error-free repair of DNA interstrand crosslinks via the Fanconi anemia pathway ', EMBO Reports, vol. 23, no. 4, e53639 . https://doi.org/10.15252/embr.202153639
Schubert, L, Hendriks, I A, Hertz, E P T, Wu, W, Sellés-Baiget, S, Hoffmann, S, Viswalingam, K S, Gallina, I, Pentakota, S, Benedict, B, Johansen, J, Apelt, K, Luijsterburg, M S, Rasmussen, S, Lisby, M, Liu, Y, Nielsen, M L, Mailand, N & Duxin, J P 2022, ' SCAI promotes error-free repair of DNA interstrand crosslinks via the Fanconi anemia pathway ', EMBO Reports, vol. 23, no. 4, e53639 . https://doi.org/10.15252/embr.202153639
DNA interstrand crosslinks (ICLs) are cytotoxic lesions that threaten genome integrity. The Fanconi anemia (FA) pathway orchestrates ICL repair during DNA replication, with ubiquitylated FANCI-FANCD2 (ID2) marking the activation step that triggers in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b635fe1b7eb375726bd27f3881f73f4
https://doi.org/10.15252/embr.202153639
https://doi.org/10.15252/embr.202153639
Autor:
Niels Mailand, Marta Gallo, Fabian Coscia, Nicholas M.I. Taylor, Matthias Mann, Peter Haahr, Satyakrishna Pentakota, Andreas Mund, Saskia Hoffmann
Publikováno v:
Hoffmann, S, Pentakota, S, Mund, A, Haahr, P, Coscia, F, Gallo, M, Mann, M, Taylor, N M I & Mailand, N 2020, ' FAM111 protease activity undermines cellular fitness and is amplified by gain-of-function mutations in human disease ', EMBO Reports, vol. 21, no. 10, e50662 . https://doi.org/10.15252/embr.202050662
EMBO Reports
EMBO Reports
Dominant missense mutations in the human serine protease FAM111A underlie perinatally lethal gracile bone dysplasia and Kenny–Caffey syndrome, yet how FAM111A mutations lead to disease is not known. We show that FAM111A proteolytic activity suppres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39b03638cd40615b1ed54997820a49ec
https://curis.ku.dk/ws/files/250485170/embr.202050662.pdf
https://curis.ku.dk/ws/files/250485170/embr.202050662.pdf
Autor:
Satyakrishna Pentakota, Manchanahalli R. Satyanarayana Rao, Raktim Roy, Iyer Aditya Mahadevan, Utsa Bhaduri
Publikováno v:
Epigenetics & Chromatin
Mahadevan, I A, Pentakota, S, Roy, R, Bhaduri, U & Satyanarayana Rao, M R 2019, ' TH2BS11ph histone mark is enriched in the unsynapsed axes of the XY body and predominantly associates with H3K4me3-containing genomic regions in mammalian spermatocytes ', Epigenetics & Chromatin, vol. 12, no. 1, 53 . https://doi.org/10.1186/s13072-019-0300-y
Epigenetics & Chromatin, Vol 12, Iss 1, Pp 1-23 (2019)
Mahadevan, I A, Pentakota, S, Roy, R, Bhaduri, U & Satyanarayana Rao, M R 2019, ' TH2BS11ph histone mark is enriched in the unsynapsed axes of the XY body and predominantly associates with H3K4me3-containing genomic regions in mammalian spermatocytes ', Epigenetics & Chromatin, vol. 12, no. 1, 53 . https://doi.org/10.1186/s13072-019-0300-y
Epigenetics & Chromatin, Vol 12, Iss 1, Pp 1-23 (2019)
BACKGROUND: TH2B is a major histone variant that replaces about 80-85% of somatic H2B in mammalian spermatocytes and spermatids. The post-translational modifications (PTMs) on TH2B have been well characterised in spermatocytes and spermatids. However
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2bf5bdb500c75bc2513b6d5d220d430
http://europepmc.org/articles/PMC6731575
http://europepmc.org/articles/PMC6731575
Autor:
Iyer Mahadevan, Satyakrishna Pentakota, Raktim Roy, Utsa Bhaduri, Manchanahalli Satyanarayana Rao
Additional file 1: Figure S1. Validation of H2B-specific antibody. H2B antibody was successfully generated in rabbits and the staining pattern was found to not coincide with the XY body in the pachytene spermatocyte. A Fragmentation table for the PTM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcd1a66d3c0b267b77ed34e43b634948
Autor:
Satyakrishna Pentakota, Manchanahalli R. Satyanarayana Rao, Iyer Aditya Mahadevan, Utsa Bhaduri, Raktim Roy
Various studies have focussed on understanding the repertoire and biological function of the post-translational modifications that occur on testis-specific histone variants like TH2B, Transition Proteins etc. In our attempt to decipher the unique fun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee20ed04bed298bf6b1573c2b6f2f930
Autor:
Satyakrishna Pentakota, Keda Zhou, Charlotte Smith, Stefano Maffini, Arsen Petrovic, Garry P Morgan, John R Weir, Ingrid R Vetter, Andrea Musacchio, Karolin Luger
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb1e92473f267e423de786eb81b041ce
https://doi.org/10.7554/elife.33442.031
https://doi.org/10.7554/elife.33442.031
Autor:
Andrea Musacchio, Ingrid R. Vetter, Garry Morgan, Karolin Luger, John R. Weir, Satyakrishna Pentakota, Stefano Maffini, Keda Zhou, Arsen Petrovic, Charlotte M. Smith
Publikováno v:
eLife
eLife, Vol 6 (2017)
eLife, Vol 6 (2017)
Centromere protein (CENP) A, a histone H3 variant, is a key epigenetic determinant of chromosome domains known as centromeres. Centromeres nucleate kinetochores, multi-subunit complexes that capture spindle microtubules to promote chromosome segregat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3869e515d62f83dcac7e4ff7f8ccb21e
Autor:
Josef Fischböck, Sabine Wohlgemuth, Doro Vogt, Arsen Petrovic, Alex C. Faesen, Andrea Musacchio, John R. Weir, Dongqing Pan, Jenny Keller, Marion E. Pesenti, Franz Herzog, Satyakrishna Pentakota, Kerstin Klare, Federica Basilico
Publikováno v:
Nature
Chromosomes are carriers of genetic material and their accurate transfer from a mother cell to its two daughters during cell division is of paramount importance for life. Kinetochores are crucial for this process, as they connect chromosomes with mic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a810dcb147882562d6c87b11349bfcc6