Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Iris Kolder"'
Autor:
Raygene Martier, Jolanda M. Liefhebber, Jana Miniarikova, Tom van der Zon, Jolanda Snapper, Iris Kolder, Harald Petry, Sander J. van Deventer, Melvin M. Evers, Pavlina Konstantinova
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 14, Iss , Pp 593-608 (2019)
The most common pathogenic mutation in amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) is an intronic GGGGCC (G4C2) repeat in the chromosome 9 open reading frame 72 (C9orf72) gene. Cellular toxicity due to RNA foci and dipeptide
Externí odkaz:
https://doaj.org/article/84305642532d46c7a5bc8e546a17f209
Autor:
Siana Nkya Mtatiro, Tarjinder Singh, Helen Rooks, Josephine Mgaya, Harvest Mariki, Deogratius Soka, Bruno Mmbando, Evarist Msaki, Iris Kolder, Swee Lay Thein, Stephan Menzel, Sharon E Cox, Julie Makani, Jeffrey C Barrett
Publikováno v:
PLoS ONE, Vol 9, Iss 11, p e111464 (2014)
Fetal hemoglobin (HbF) is an important modulator of sickle cell disease (SCD). HbF has previously been shown to be affected by variants at three loci on chromosomes 2, 6 and 11, but it is likely that additional loci remain to be discovered.We conduct
Externí odkaz:
https://doaj.org/article/36304838133a4c1aa3a02d07da489ce3