16 research outputs found
INSITU LOCALIZATION OF SPECIFIC RNAS IN WHOLE FRUITING COLONIES OF SCHIZOPHYLLUM-COMMUNE
INSITU LOCALIZATION OF SPECIFIC RNAS IN DEVELOPING FRUIT BODIES OF THE BASIDIOMYCETE SCHIZOPHYLLUM-COMMUNE
cDNA clones representing mRNAs abundantly expressed during fruiting ofSchizophyllum commune were used to detect the cellular localization of these mRNAs in freeze-microtome sections of developing fruit bodies. An 18 S rRNA clone was isolated and used as a probe for total RNA. Both RNA and DNA probes with different labels were found suitable but the procedure finally adopted involvedin situ hybridization with nick-translated biotinylated DNA probes. To permit the probes to permeate the cell walls it was necessary to treat the sections with RNasedepletedTrichoderma harzianum wall-lytic enzymes before hybridization. Hybridization at different developmental stages showed that the specific mRNAs were abundantly expressed in specific areas of the fruit bodie
PHOTOREGULATION OF DIKARYON-SPECIFIC MESSENGER-RNAS AND PROTEINS BY UV-A LIGHT IN SCHIZOPHYLLUM-COMMUNE
PHOTOREGULATION OF DIKARYON-SPECIFIC MESSENGER-RNAS AND PROTEINS BY UV-A LIGHT IN SCHIZOPHYLLUM-COMMUNE
PHOTOREGULATION OF DIKARYON-SPECIFIC MESSENGER-RNAS AND PROTEINS BY UV-A LIGHT IN SCHIZOPHYLLUM-COMMUNE
EFFECT OF INBREEDING AND LIGHT ON MONOKARYOTIC AND DIKARYOTIC FRUITING IN THE HOMOBASIDIOMYCETE SCHIZOPHYLLUM-COMMUNE
EFFECT OF INBREEDING AND LIGHT ON MONOKARYOTIC AND DIKARYOTIC FRUITING IN THE HOMOBASIDIOMYCETE SCHIZOPHYLLUM-COMMUNE
A frequently occurring mutation that blocks the expression of fruiting genes in Schizophyllum commune
The association between age and inflammatory disease activity on MRI in relapse-onset multiple sclerosis during long-term follow-up
BACKGROUND: Inflammatory disease activity in multiple sclerosis (MS) decreases with advancing age. Previous work found a decrease in contrast enhancing lesions (CELs) with age. Here we describe the relation of age and MRI measures of inflammatory disease activity during long-term follow-up in a large real-world cohort of people with relapse-onset MS. METHODS: We investigated MRI data from the long-term observational Amsterdam MS cohort. We used logistic regression models and negative binomial generalized estimating equations to investigate the associations between age and radiological disease activity after a first clinical event. RESULTS: We included 1,063 participants, and 10,651 cranial MRIs. Median follow-up time was 6.1 years (IQR 2.4-10.9 years). Older participants had a significantly lower risk of CELs on baseline MRI (40-50 years vs. 50 years vs. 50 years vs. 50 years, a less aggressive treatment strategy might be appropriate compared to younger patients