Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Alfonso G Fernandez"'
Autor:
Brandon R Lowe, Rajesh K Yadav, Ryan A Henry, Patrick Schreiner, Atsushi Matsuda, Alfonso G Fernandez, David Finkelstein, Margaret Campbell, Satish Kallappagoudar, Carolyn M Jablonowski, Andrew J Andrews, Yasushi Hiraoka, Janet F Partridge
Publikováno v:
eLife, Vol 10 (2021)
Sequencing of cancer genomes has identified recurrent somatic mutations in histones, termed oncohistones, which are frequently poorly understood. Previously we showed that fission yeast expressing only the H3.3G34R mutant identified in aggressive ped
Externí odkaz:
https://doaj.org/article/1deea5202d2c4144a85ce645ef7c9d33
Autor:
Rajesh K Yadav, Carolyn M Jablonowski, Alfonso G Fernandez, Brandon R Lowe, Ryan A Henry, David Finkelstein, Kevin J Barnum, Alison L Pidoux, Yin-Ming Kuo, Jie Huang, Matthew J O’Connell, Andrew J Andrews, Arzu Onar-Thomas, Robin C Allshire, Janet F Partridge
Publikováno v:
eLife, Vol 6 (2017)
Recurrent somatic mutations of H3F3A in aggressive pediatric high-grade gliomas generate K27M or G34R/V mutant histone H3.3. H3.3-G34R/V mutants are common in tumors with mutations in p53 and ATRX, an H3.3-specific chromatin remodeler. To gain insigh
Externí odkaz:
https://doaj.org/article/6f07b04184fd448199fb62c77f4d0ff3
Publikováno v:
PLoS ONE, Vol 5, Iss 6, p e10933 (2010)
To gain a better understanding of the sequence patterns that characterize positioned nucleosomes, we first performed an analysis of the periodicities of the 256 tetranucleotides in a yeast genome-wide library of nucleosomal DNA sequences that was pre
Externí odkaz:
https://doaj.org/article/6336e6c4ee3941a1be223c2fa5f9d714
Autor:
Georgios E. Christakopoulos, Thiyagaraj Mayuranathan, Alfonso G. Fernandez, Kalin Mayberry, Yu Yao, Rahul Telange, Michael Dudley, Rachel Levine, Erin Dempsey, David R. Liu, Jonathan S Yen, Mitchell J. Weiss
Publikováno v:
Blood. 140:10660-10661
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5cfcb7175bd8587b8bcd734242c36094
https://doi.org/10.1182/blood-2022-169391
https://doi.org/10.1182/blood-2022-169391
Autor:
Laurent Kiger, Julia Keith, Abdullah Freiwan, Alfonso G. Fernandez, Heather Tillman, Brant E. Isakson, Mitchell J. Weiss, Christophe Lechauve
Publikováno v:
Antioxidants; Volume 11; Issue 1; Pages: 159
Antioxidants, Vol 11, Iss 159, p 159 (2022)
Antioxidants
Antioxidants, Vol 11, Iss 159, p 159 (2022)
Antioxidants
Interest in the structure, function, and evolutionary relations of circulating and intracellular globins dates back more than 60 years to the first determination of the three-dimensional structure of these proteins. Non-erythrocytic globins have been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81306558b4249120823f5d9c8727aa41
Autor:
Masayoshi Honda, Melchior Lauten, Marcus B. Valentine, Patrick Revy, Stéphane Coulon, Richa Sharma, Charnise Goodings, Caroline Kannengiesser, Fabian Beier, Melanie Boerries, Shondra M. Pruett-Miller, Sophie L Granger, Miriam Erlacher, Maria Spies, Axel Künstner, Megan A. Cooper, Jill A. Rosenfeld, Vincent Géli, Carole Saintomé, Victor B Pastor, Charlotte M. Niemeyer, Dmitri Churikov, Marcin W. Wlodarski, Sophia Polychronopoulou, Hauke Busch, Ti-Cheng Chang, Sandrine Hirschi, Louis Sanchez, Charikleia Kelaidi, Sushree S. Sahoo, Marc S. Wold, Alfonso G Fernandez, Sarah K. Nicholas
Publikováno v:
Blood
Blood, American Society of Hematology, 2021, ⟨10.1182/blood.2021011980⟩
Blood, 2021, ⟨10.1182/blood.2021011980⟩
Blood, 2022, 139 (7), pp.1039-1051. ⟨10.1182/blood.2021011980⟩
Blood, American Society of Hematology, 2021, ⟨10.1182/blood.2021011980⟩
Blood, 2021, ⟨10.1182/blood.2021011980⟩
Blood, 2022, 139 (7), pp.1039-1051. ⟨10.1182/blood.2021011980⟩
Human telomere biology disorders (TBD)/short telomere syndromes (STS) are heterogeneous disorders caused by inherited loss-of-function mutations in telomere-associated genes. Here, we identify 3 germline heterozygous missense variants in the RPA1 gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89d60362309a06fad91835f5abb3f0ae
https://hal.archives-ouvertes.fr/hal-03431979
https://hal.archives-ouvertes.fr/hal-03431979
Autor:
Janet F. Partridge, Brandon R Lowe, Yasushi Hiraoka, Carolyn M Jablonowski, Alfonso G Fernandez, Andrew J. Andrews, Rajesh K. Yadav, Margaret Campbell, Atsushi Matsuda, Patrick Schreiner, Ryan A. Henry, David Finkelstein, Satish Kallappagoudar
Publikováno v:
eLife, Vol 10 (2021)
eLife
eLife
Sequencing of cancer genomes has identified recurrent somatic mutations in histones, termed oncohistones, which are frequently poorly understood. Previously we showed that fission yeast expressing only the H3.3G34R mutant identified in aggressive ped
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5363386a4ffb88d405b41f53cc83ba81
https://doi.org/10.7554/elife.65369
https://doi.org/10.7554/elife.65369
Autor:
Margaret Campbell, Rajesh K. Yadav, Janet F. Partridge, Ryan A. Henry, Satish Kallappagoudar, Brandon R Lowe, Yasushi Hiraoka, Carolyn M Jablonowski, David Finkelstein, Andrew J. Andrews, Patrick Schreiner, Alfonso G Fernandez, Atsushi Matsuda
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25c9bd5f45118e83e61db9fbd78062dd
https://doi.org/10.7554/elife.65369.sa2
https://doi.org/10.7554/elife.65369.sa2
Autor:
Margaret Campbell, Carolyn M Jablonowski, Yasushi Hiraoka, David Finkelstein, Patrick Schreiner, Rajesh K. Yadav, Andrew J. Andrews, Atsushi Matsuda, Ryan A. Henry, Satish Kallappagoudar, Janet F. Partridge, Brandon R Lowe, Alfonso G Fernandez
Sequencing of cancer genomes has identified recurrent somatic mutations in histones, termed oncohistones, which are frequently poorly understood. Previously we showed that fission yeast expressing only the H3.3G34R mutant identified in aggressive ped
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4066323a96984fe10d5f49a9d5996b21
https://doi.org/10.1101/2020.12.10.419184
https://doi.org/10.1101/2020.12.10.419184
Autor:
Temesgen D. Fufa, Cynthia A. Pise-Masison, Clay Wakano, Alfonso G. Fernandez, Jung S. Byun, Kevin Gardner
Publikováno v:
Biochemical and Biophysical Research Communications. 465:5-11
The eleven-nineteen lysine-rich leukemia protein (ELL) is a key regulator of RNA polymerase II mediated transcription. ELL facilitates RNA polymerase II transcription pause site entry and release by dynamically interacting with p300 and the positive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da0f92c8c19cca17648f2e4c36521d09
https://doi.org/10.1016/j.bbrc.2015.07.072
https://doi.org/10.1016/j.bbrc.2015.07.072