36 research outputs found
Are developmental hemoglobin changes related to the origin of stem cells and site of erythropoiesis?
Semantic interference in the picture-word interference task: Is there a pre-lexical conceptual contribution to the effect?
Here we provide materials, experimental lists, data and analyses scripts (for R) used for analyses reported in:
Jescheniak, J. D., Wöhner, S., Bethcke, H. S., and Beaupain, M. C. (2019). Semantic interference in the picture-word interference task:
Is there a pre-lexical conceptual contribution to the effect?
We preregistered our study, see: https://aspredicted.org/s557m.pd
Molecular cloning and complete primary sequence of human erythrocyte porphobilinogen deaminase.
We have cloned and sequenced a cDNA clone coding for human erythrocyte porphobilinogen deaminase. It encompasses the translated region, part of the 5' and the 3' untranslated regions. The deduced 344 amino acid sequence is consistent with the molecular weight and the partial amino-acid sequence of the NH2 terminal of the purified erythrocyte enzyme. Southern analysis of human genomic DNA shows that its gene is present as a single copy in the human genome and Northern analysis demonstrates the presence of a single size species of mRNA in erythroid and non-erythroid tissues and in several cultured cell lines. Quantitative determinations indicate that the amount of PBG-D mRNA is modulated both by the erythroid nature of the tissue and by cell proliferation, probably at the transcriptional level
Structure of the gene for human uroporphyrinogen decarboxylase.
Uroporphyrinogen decarboxylase, the fifth enzyme of the heme biosynthetic pathway, is an housekeeping enzyme whose activity is enhanced during erythropoietic differentiation. We have previously shown that this increased activity was in part accounted for by an enhanced transcription of the gene in erythropoietic tissues. To elucidate further the tissue specific regulation of an housekeeping gene we have isolated the human URO-D gene and determined its organization. The cloned gene comprises 10 exons spread over 3 Kb. Two transcriptional start sites were determined and analysis of 900 bp of the 5' flanking region suggests a very simple structural organization for the URO-D gene promoter. We also show that this gene is functional when transfected into mouse fibroblasts, and that its promoter is sensitive to a viral enhancer
Workplace involvement in technological innovation in the European Community Volume II - Issues of participation
Vol. 2 of 2Available from British Library Document Supply Centre- DSC:OP-EC/3166 / BLDSC - British Library Document Supply CentreSIGLEGBUnited Kingdo