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Umeå University
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Lennart Österman

Contact

E-mail
lennart.osterman@umu.se
Phone

Works at

Affiliation
Affiliated as research fellow at Department of Medical Biosciences Section: Pathology
Location
By 6M, Sjukhusområdet Umeå universitet, 901 85 Umeå
EYS mutations and implementation of minigene assay for variant classification in EYS-associated retinitis pigmentosa in northern Sweden
Scientific Reports, Nature Publishing Group 2021, Vol. 11, (1)
Westin, Ida Maria; Jonsson, Frida; Österman, Lennart; et al.
TRAF6 function as a novel co-regulator of Wnt3a target genes in prostate cancer
EBioMedicine, Elsevier 2019, Vol. 45 : 192-207
Aripaka, Karthik; Gudey, Shyam Kumar; Zang, Guangxiang; et al.
ATP-binding cassette subfamily A, member 4 intronic variants c.4773+3A > G and c.5461-10T > C cause Stargardt disease due to defective splicing
Acta Ophthalmologica, John Wiley & Sons 2018, Vol. 96, (7) : 737-743
Jonsson, Frida; Westin, Ida Maria; Österman, Lennart; et al.
PTBP1 acts as a dominant repressor of the aberrant tissue-specific splicing of ISCU in hereditary myopathy with lactic acidosis
Molecular Genetics & Genomic Medicine, John Wiley & Sons 2018, Vol. 6, (6) : 887-897
Rawcliffe, Denise F. R.; Österman, Lennart; Nordin, Angelica; et al.
The High Level of Aberrant Splicing of ISCU in Slow-Twitch Muscle May Involve the Splicing Factor SRSF3
PLOS ONE, Public library science 2016, Vol. 11, (10)
Rawcliffe, Denise F. R.; Österman, Lennart; Lindsten, Hans; et al.
MBNL1 and RBM39 can activate the incorrect splicing of ISCU and the aberrant transcript is a target for nonsense-mediated decay
Rawcliffe, Denise F. R.; Johansson, Malin; Österman, Lennart; et al.
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