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Journals and Conferences
Huntington's disease (HD) is an autosomal-dominant neurological disorder caused by expanded CAG repeats in the Huntingtin (Htt) gene, but it is not known how this mutation causes neurodegeneration. Herein, we found that dysfunction of upstream binding factor-1 (UBF-1) is linked to reduced ribosomal DNA (rDNA) transcription in HD. We identified that UBF1… (More)
This study discusses two main questions: the direct medical costs and the clinical effectiveness of the hospital treatment with insulin of pregnant women with gestational diabetes (GD). A prospective study that includes 50 women with GD is performed. The pregnant women are divided into 2 groups: Group I (n=30) — pregnant women treated only with a diet; and… (More)
Copper accumulation and phosphatase activities of three Aspergillus species resistant to copper were compared to three copper-sensitive Rhizopus species. High level of acid phosphatases and decreased Cu2+-uptake were found with resistant in contrast to sensitive strains. The presence of copper(II) ions in the medium increased the production of acid… (More)
We report HLA-C*02:02:09 as a novel allele with a transition C->T at position 354.
The new allele HLA-B*52:23 differs from B*52:01:01 at position 208 in exon 2.
The new HLA-B*41:45N allele differs from B*41:02 by insertion of 21 nucleotides in exon 2.
We report a novel allele HLA-A*02:334 with the transition G→A at nucleotide position 282.
We report the new HLA-DRB1*14:99 allele differing from DRB1*14:01:01 by one nucleotide in exon 2.
We report the new HLA-A*11:192 allele differing from A*11:01 by one nucleotide in exon 2.