Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Sebastian DiLorenzo"'
Autor:
Tommaso De Marchi, Paul Theodor Pyl, Martin Sjöström, Susanne Erika Reinsbach, Sebastian DiLorenzo, Björn Nystedt, Lena Tran, Gyula Pekar, Fredrik Wärnberg, Irma Fredriksson, Per Malmström, Mårten Fernö, Lars Malmström, Johan Malmstöm, Emma Niméus
Publikováno v:
Communications Biology, Vol 6, Iss 1, Pp 1-14 (2023)
A proteogenomic analysis of matching primary breast cancer and ipsilateral breast tumor recurrence (IBTR) samples provides insight into the development of IBTR and may be useful in identifying biomarkers for IBTR formation.
Externí odkaz:
https://doaj.org/article/7fcdfaaf09f349e4a6ae38eff9a3e17b
Autor:
Fahmi Mesmar, Bingbing Dai, Ahmed Ibrahim, Linnea Hases, Mohammed Hakim Jafferali, Jithesh Jose Augustine, Sebastian DiLorenzo, Ya'an Kang, Yang Zhao, Jing Wang, Michael Kim, Chin‐Yo Lin, Anders Berkenstam, Jason Fleming, Cecilia Williams
Publikováno v:
Cancer Medicine, Vol 8, Iss 18, Pp 7705-7719 (2019)
Abstract Despite advances in cancer therapeutics, pancreatic cancer remains difficult to treat and often develops resistance to chemotherapies. We have evaluated a bioavailable genistein analogue, AXP107‐11 which has completed phase Ib clinical tri
Externí odkaz:
https://doaj.org/article/900afa4941d14028b0d39be55bc5e75d
Autor:
Maxime Garcia, Szilveszter Juhos, Malin Larsson, Pall I. Olason, Marcel Martin, Jesper Eisfeldt, Sebastian DiLorenzo, Johanna Sandgren, Teresita Díaz De Ståhl, Philip Ewels, Valtteri Wirta, Monica Nistér, Max Käller, Björn Nystedt
Publikováno v:
F1000Research, Vol 9 (2020)
Whole-genome sequencing (WGS) is a fundamental technology for research to advance precision medicine, but the limited availability of portable and user-friendly workflows for WGS analyses poses a major challenge for many research groups and hampers s
Externí odkaz:
https://doaj.org/article/05a73ce337a649f6a7c3c6a9bd0170ec
Autor:
Maxime Garcia, Szilveszter Juhos, Malin Larsson, Pall I. Olason, Marcel Martin, Jesper Eisfeldt, Sebastian DiLorenzo, Johanna Sandgren, Teresita Díaz De Ståhl, Philip Ewels, Valtteri Wirta, Monica Nistér, Max Käller, Björn Nystedt
Publikováno v:
F1000Research, Vol 9 (2020)
Whole-genome sequencing (WGS) is a fundamental technology for research to advance precision medicine, but the limited availability of portable and user-friendly workflows for WGS analyses poses a major challenge for many research groups and hampers s
Externí odkaz:
https://doaj.org/article/73960a360a4448db9833dbe29df58531
Autor:
C. Christofer Juhlin, Nima Rafati, Sebastian DiLorenzo, Jan Zedenius, Felix Haglund, Yi Chen, Johan O. Paulsson
Publikováno v:
The Journal of Clinical Endocrinology and Metabolism
Background The genomic and transcriptomic landscape of widely invasive follicular thyroid carcinomas (wiFTCs) and Hürthle cell carcinoma (HCC) are poorly characterized, and subsets of these tumors lack information on genetic driver events. Objective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dff11fc248454fedd96e52814d895c7b
http://europepmc.org/articles/PMC8530729
http://europepmc.org/articles/PMC8530729
Autor:
Teresita Díaz de Ståhl, Maxime Garcia, Valtteri Wirta, Sebastian DiLorenzo, Björn Nystedt, Max Käller, Pall I Olason, Marcel Martin, Jesper Eisfeldt, Szilveszter Juhos, Johanna Sandgren, Philip Ewels, Malin Larsson, Monica Nistér
Publikováno v:
F1000Research
Whole-genome sequencing (WGS) is a fundamental technology for research to advance precision medicine, but the limited availability of portable and user-friendly workflows for WGS analyses poses a major challenge for many research groups and hampers s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::127b93c8f0fb7791dbddeb088d495ebe
http://europepmc.org/articles/PMC7111497
http://europepmc.org/articles/PMC7111497
Autor:
Sebastian DiLorenzo, Björn Nystedt, Szilveszter Juhos, Monica Nistér, Jesper Eisfeldt, Max Käller, Pall I Olason, Malin Larsson, Valtteri Wirta, Marcel Martin, Johanna Sandgren, Maxime Garcia, Teresita Díaz de Ståhl
SummaryWhole-genome sequencing (WGS) is a cornerstone of precision medicine, but portable and reproducible open-source workflows for WGS analyses of germline and somatic variants are lacking. We present Sarek, a modular, comprehensive, and easy-to-in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c42fe83836a310c12f1071018dc8bdc
https://doi.org/10.1101/316976
https://doi.org/10.1101/316976
Autor:
Linda Olsson, Mikael Behrendtz, Marianne Rissler, Anders Isaksson, Anders Castor, Henrik Lilljebjörn, Per Wahlberg, Anders Lundmark, Kajsa Paulsson, Kristina B. Lundin-Ström, Andrea Biloglav, Sebastian DiLorenzo, Rebeqa Gunnarsson, Thoas Fioretos, Bertil Johansson
Publikováno v:
Leukemia
High-throughput sequencing was applied to investigate the mutation/methylation patterns on 1q and gene expression profiles in pediatric B-cell precursor acute lymphoblastic leukemia (BCP ALL) with/without (w/wo) dup(1q). Sequencing of the breakpoint
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec3387a968c68bfe20bdf6a59a0900f6
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-367402
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-367402
Autor:
Torbjörn Ramqvist, Nikolaos Tertipis, Cinzia Bersani, Linnea Haeggblom, Anders Näsman, Michael Mints, Tina Dalianis, Lars Sivars, Andreas Ährlund-Richter, Eva Munck-Wikland, Sebastian DiLorenzo
Publikováno v:
Oncotarget
// Cinzia Bersani 1 , Lars Sivars 1 , Linnea Haeggblom 1 , Sebastian DiLorenzo 2,3 , Michael Mints 4,5 , Andreas Ahrlund-Richter 1 , Nikolaos Tertipis 1 , Eva Munck-Wikland 6,7 , Anders Nasman 1 , Torbjorn Ramqvist 1,* and Tina Dalianis 1,* 1 Departm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1985a7c73e4fbebd7c95ccd828b9278d
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-136333
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-136333
Publikováno v:
Genome Biology
Whole-genome sequencing of tumor tissue has the potential to provide comprehensive characterization of genomic alterations in tumor samples. We present Patchwork, a new bioinformatic tool for allele-specific copy number analysis using whole-genome se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::876e8063b89275af8b3c4cd86556e309
https://doi.org/10.1186/gb-2013-14-3-r24
https://doi.org/10.1186/gb-2013-14-3-r24