Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Gloria Sheynkman"'
Autor:
Guy Karlebach, Robin Steinhaus, Daniel Danis, Maeva Devoucoux, Olga Anczuków, Gloria Sheynkman, Dominik Seelow, Peter N. Robinson
Publikováno v:
npj Genomic Medicine, Vol 9, Iss 1, Pp 1-10 (2024)
Abstract Numerous factors regulate alternative splicing of human genes at a co-transcriptional level. However, how alternative splicing depends on the regulation of gene expression is poorly understood. We leveraged data from the Genotype-Tissue Expr
Externí odkaz:
https://doaj.org/article/39c63d49bd6b460c87475b63ca1475dd
Autor:
Vladimir B. C. de Souza, Ben T. Jordan, Elizabeth Tseng, Elizabeth A. Nelson, Karen K. Hirschi, Gloria Sheynkman, Mark D. Robinson
Publikováno v:
Genome Biology, Vol 24, Iss 1, Pp 1-14 (2023)
Abstract Long-read RNA sequencing (lrRNA-seq) produces detailed information about full-length transcripts, including novel and sample-specific isoforms. Furthermore, there is an opportunity to call variants directly from lrRNA-seq data. However, most
Externí odkaz:
https://doaj.org/article/29a834968197445ca6a1f65ac1700bd1
Autor:
Karyn Schmidt, Johanna S. Carroll, Elaine Yee, Dolly D. Thomas, Leon Wert-Lamas, Steven C. Neier, Gloria Sheynkman, Justin Ritz, Carl D. Novina
Publikováno v:
Cell Reports, Vol 27, Iss 8, Pp 2493-2507.e4 (2019)
Summary: Melanoma is the deadliest form of skin cancer, affecting men more frequently and severely than women. Although recent studies suggest that differences in activity of the androgen receptor (AR) underlie the observed sex bias, little is known
Externí odkaz:
https://doaj.org/article/596f218635ae4074aba56476daea8a07
Autor:
Anoushka Joglekar, Wen Hu, Bei Zhang, Oleksandr Narykov, Mark Diekhans, Jennifer Balacco, Lishomwa C Ndhlovu, Teresa A Milner, Olivier Fedrigo, Erich D Jarvis, Gloria Sheynkman, Dmitry Korkin, M. Elizabeth Ross, Hagen U. Tilgner
RNA isoforms influence cell identity and function. Until recently, technological limitations prevented a genome-wide appraisal of isoform influence on cell identity in various parts of the brain. Using enhanced long-read single-cell isoform sequencin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00cf03d4f20784df665358b6066d9981
https://doi.org/10.1101/2023.04.02.535281
https://doi.org/10.1101/2023.04.02.535281
Autor:
Valérie de Crécy-lagard, Rocio Amorin de Hegedus, Cecilia Arighi, Jill Babor, Alex Bateman, Ian Blaby, Crysten Blaby-Haas, Alan J Bridge, Stephen K Burley, Stacey Cleveland, Lucy J Colwell, Ana Conesa, Christian Dallago, Antoine Danchin, Anita de Waard, Adam Deutschbauer, Raquel Dias, Yousong Ding, Gang Fang, Iddo Friedberg, John Gerlt, Joshua Goldford, Mark Gorelik, Benjamin M Gyori, Christopher Henry, Geoffrey Hutinet, Marshall Jaroch, Peter D Karp, Liudmyla Kondratova, Zhiyong Lu, Aron Marchler-Bauer, Maria-Jesus Martin, Claire McWhite, Gaurav D Moghe, Paul Monaghan, Anne Morgat, Christopher J Mungall, Darren A Natale, William C Nelson, Seán O’Donoghue, Christine Orengo, Katherine H O’Toole, Predrag Radivojac, Colbie Reed, Richard J Roberts, Dmitri Rodionov, Irina A Rodionova, Jeffrey D Rudolf, Lana Saleh, Gloria Sheynkman, Francoise Thibaud-Nissen, Paul D Thomas, Peter Uetz, David Vallenet, Erica Watson Carter, Peter R Weigele, Valerie Wood, Elisha M Wood-Charlson, Jin Xu
Valérie de Crécy-Lagard: et al.
Over the last 25 years, biology has entered the genomic era and is becoming a science of 'big data'. Most interpretations of genomic analyses rely on accurate functional annotations of the proteins encoded by mo
Over the last 25 years, biology has entered the genomic era and is becoming a science of 'big data'. Most interpretations of genomic analyses rely on accurate functional annotations of the proteins encoded by mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92bc0c0dc223190e4e256e36b3167003
Autor:
Vladimir B. C. de Souza, Ben T. Jordan, Elizabeth Tseng, Elizabeth A. Nelson, Karen K. Hirschi, Gloria Sheynkman, Mark D. Robinson
Long-read RNA sequencing (lrRNA-seq) produces detailed information about full-length transcripts, including novel and sample-specific isoforms. Furthermore, there is an opportunity to call variants directly from lrRNA-seq data. However, most state-of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::483b28b608c81a48edb0a395ddd3a8fc
https://doi.org/10.1101/2022.02.08.479579
https://doi.org/10.1101/2022.02.08.479579
Autor:
Anthony Abrantes, NaEshia Ancalade, Shadia Sekle, Fatima Memic, Anke Dijkstra, Elizabeth Tseng, Gloria Sheynkman, Jens Hjerling-Leffler, August Smit, Patrick Sullivan, Paola Giusti-Rodriguez
Publikováno v:
European Neuropsychopharmacology. 63:e156
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa61d9184af53af1facaaee0c08f9207
https://doi.org/10.1016/j.euroneuro.2022.07.286
https://doi.org/10.1016/j.euroneuro.2022.07.286