Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Lennart Österman"'
Autor:
Ida Maria Westin, Frida Jonsson, Lennart Österman, Monica Holmberg, Marie Burstedt, Irina Golovleva
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract Retinitis pigmentosa (RP) is a clinically and genetically heterogeneous group of inherited retinal degenerations. The ortholog of Drosophila eyes shut/spacemaker, EYS on chromosome 6q12 is a major genetic cause of recessive RP worldwide, wit
Externí odkaz:
https://doaj.org/article/7d1c0a553203498cb63fcaadea9dd10e
Autor:
Karthik Aripaka, Shyam Kumar Gudey, Guangxiang Zang, Alexej Schmidt, Samaneh Shabani Åhrling, Lennart Österman, Anders Bergh, Jonas von Hofsten, Marene Landström
Publikováno v:
EBioMedicine, Vol 45, Iss , Pp 192-207 (2019)
Background: Tumour necrosis factor receptor associated factor 6 (TRAF6) promotes inflammation in response to various cytokines. Aberrant Wnt3a signals promotes cancer progression through accumulation of β-Catenin. Here we investigated a potential ro
Externí odkaz:
https://doaj.org/article/be1819560a984ed19d17d131ce016b1a
Publikováno v:
PLoS ONE, Vol 11, Iss 10, p e0165453 (2016)
Hereditary myopathy with lactic acidosis (HML) is an autosomal recessive disease caused by an intronic one-base mutation in the iron-sulfur cluster assembly (ISCU) gene, resulting in aberrant splicing. The incorrectly spliced transcripts contain a 10
Externí odkaz:
https://doaj.org/article/bc3cd8cbee0c4c9c9463bf202260e426
Autor:
Monica Holmberg, Lennart Österman, Irina Golovleva, Frida Jonsson, Ida Maria Westin, Marie Burstedt
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Scientific Reports
Scientific Reports
Retinitis pigmentosa (RP) is a clinically and genetically heterogeneous group of inherited retinal degenerations. The ortholog of Drosophila eyes shut/spacemaker, EYS on chromosome 6q12 is a major genetic cause of recessive RP worldwide, with prevale
Autor:
Shyam Kumar Gudey, Samaneh Shabani Åhrling, Jonas von Hofsten, Anders Bergh, Karthik Aripaka, Guangxiang Zang, Maréne Landström, Lennart Österman, Alexej Schmidt
Publikováno v:
EBioMedicine
Background Tumour necrosis factor receptor associated factor 6 (TRAF6) promotes inflammation in response to various cytokines. Aberrant Wnt3a signals promotes cancer progression through accumulation of β-Catenin. Here we investigated a potential rol
Publikováno v:
Molecular Genetics & Genomic Medicine
Background Hereditary myopathy with lactic acidosis (HML) is an autosomal recessive disease caused by an intron mutation in the iron‐sulfur cluster assembly (ISCU) gene. The mutation results in aberrant splicing, where part of the intron is retaine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b80ccebc41232c68005799a2650dbc1c
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-153102
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-153102
Autor:
Monica Holmberg, Ida Maria Westin, Ola Sandgren, Lennart Österman, Irina Golovleva, Frida Jonsson, Marie Burstedt
Publikováno v:
Acta ophthalmologica. 96(7)
Inherited retinal dystrophies (IRDs) represent a group of progressive conditions affecting the retina. There is a great genetic heterogeneity causing IRDs, and to date, more than 260 genes are associated with IRDs. Stargardt disease, type 1 (STGD1) o
Autor:
Makoto Kobayashi, Vladyslav Krylov, Takeshi Matsuda, Leif J. Jönsson, R. Mehdiyev, J. Timmermans, Jochen Kaminski, M. S. Dixit, Yang Gao, Oliver Schäfer, Gilles De Lentdecker, Claus Kleinwort, Astrid Münnich, Katsumasa Ikematsu, Björn Lundberg, Fan Zhang, Junping Tian, Y. Kato, Amir Noori Shirazi, R. Yonamine, Sudeb Bhattacharya, Oleg Bezshyyko, Serguei Ganjour, Ulf Mjörnmark, Supratik Mukhopadhyay, Deb Sankar Bhattacharya, Vincent Hedberg, Keisuke Fujii, Anders Nils Erik Oskarsson, Philippe Gros, Ivor Fleck, Tohru Takahashi, Maksym Titov, Ralf Diener, Wenxin Wang, Tomohisa Ogawa, Yifan Yang, Ronald Settles, D. Tsionou, Ulrich Werthenbach, Takahiro Fusayasu, Martin Killenberg, Yulan Li, P. Colas, S. Caiazza, Alain Bellerive, Klaus Dehmelt, Ties Behnke, M. Riallot, Akira Sugiyama, Zhenwei Yang, Shin ichi Kawada, Nayana Majumdar, Annika Vauth, Takashi Watanabe, Klaus Kurt Desch, Klaus Zenker, D. Peterson, Peter Hayman, Bo Li, Purba Bhattacharya, Lennart Österman, Stefan Roth, Christoph Rosemann, M. Lupberger, Oxana Smirnova, Peter Schade, David Attié, F. Müller
Publikováno v:
Nucl.Instrum.Meth.A
Nucl.Instrum.Meth.A, 2017, 856, pp.109-118. 〈10.1016/j.nima.2016.11.002〉
Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment
Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment, Elsevier, 2017, 856, pp.109-118. ⟨10.1016/j.nima.2016.11.002⟩
Nucl.Instrum.Meth.A, 2017, 856, pp.109-118. ⟨10.1016/j.nima.2016.11.002⟩
Nucl.Instrum.Meth.A, 2017, 856, pp.109-118. 〈10.1016/j.nima.2016.11.002〉
Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment
Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment, Elsevier, 2017, 856, pp.109-118. ⟨10.1016/j.nima.2016.11.002⟩
Nucl.Instrum.Meth.A, 2017, 856, pp.109-118. ⟨10.1016/j.nima.2016.11.002⟩
For the International Large Detector concept at the planned International Linear Collider, the use of time projection chambers (TPC) with micro-pattern gas detector readout as the main tracking detector is investigated. In this paper, results from a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74094d014319b4a8bca9d321c7bf9554
https://hal.archives-ouvertes.fr/hal-01554956
https://hal.archives-ouvertes.fr/hal-01554956
Autor:
H. Appelshäuser, Ketil Røed, Filippo Costa, Dieter Røhrich, Tivadar Kiss, Rune Langøy, Stefan Kirsch, Jørgen André Lien, Arild Velure, Erno David, Kjetil Ullaland, Tako Gunji, Lennart Österman, Chengxin Zhao, Christian Lippmann, Johan Alme, Lars Karlot Stubberud Bratrud, Anders Nils Erik Oskarsson, Attiq Ur Rehman, Shiming Yang, Meghan Stuart, Torsten Alt, Andrew John Castro, Yoko Sekiguchi
This paper presents the first performance results of the ALICE TPC Readout Control Unit 2 (RCU2). With the upgraded hardware typology and the new readout scheme in FPGA design, the RCU2 is designed to achieve twice the readout speed of the present Re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::739ba1c472e6ace16595d4c4da169565
http://hdl.handle.net/10852/53076
http://hdl.handle.net/10852/53076
Publikováno v:
PLoS ONE, Vol 11, Iss 10, p e0165453 (2016)
PLoS ONE
PLoS ONE
Hereditary myopathy with lactic acidosis (HML) is an autosomal recessive disease caused by an intronic one-base mutation in the iron-sulfur cluster assembly (ISCU) gene, resulting in aberrant splicing. The incorrectly spliced transcripts contain a 10