Zobrazeno 51 - 59
of 59
pro vyhledávání: '"35"'
Publikováno v:
Andrologia. 35:263-265
Our study was designed to establish the necessity of routine evaluation of patients with inflammatory (IIIA) and noninflammatory (IIIB) types of nonbacterial prostatitis (NBP) for chlamydial and ureaplasmal infections. From 1999 to 2001, 165 patients
Publikováno v:
Journal of Biomedicine and Biotechnology, Vol 2012 (2012)
Journal of Biomedicine and Biotechnology
Journal of Biomedicine and Biotechnology
AttenuatedSalmonellahas been used as a carrier for DNA vaccine. However,in vitroandin vivostudies on the bacteria following transfection of plasmid DNA were poorly studied. In this paper, eukaryotic expression plasmids encoding avian influenza virus
Autor:
Agnieszka Blachnio-Zabielska, Adrian Chabowski, Slawomir Wolczynski, Katarzyna Jarząbek, Paweł Knapp
Publikováno v:
PPAR Research, Vol 2012 (2012)
PPAR Research
PPAR Research
Peroxisome proliferator-activated receptors (PPARs) belong to a family of nuclear hormone receptors acting as transcriptional factors, recently involved also in carcinogenesis. Present study was undertaken to evaluate the presence and subcellular loc
Publikováno v:
Journal of Biomedicine and Biotechnology, Vol 2010 (2010)
Journal of Biomedicine and Biotechnology
Journal of Biomedicine and Biotechnology
Molecular analysis of MalaysianVibrio choleraewas carried out using a multiple-locus variable-number tandem repeat analysis (MLVA) assay based on 7 loci ofV. cholerae. The discriminatory ability of the assay was compared with pulsed-field gel electro
Autor:
U. Waller
Publikováno v:
Journal of Applied Ichthyology. 8:62-71
ummary Routine oxygen consumption of turbot, Scophthalmus maximus, was determined in relation to temperature, salinity, body wet weight, and time of day. The highest routine oxygen consumption rates measured roughly followed a arabolic curve over the
Autor:
Shirley Cohen, Dorit Lev, Liat Ries-Levavi, Tsofia Ish-Shalom, Peter H. Byers, Boleslaw Goldman, Moshe Frydman, Eitan Friedman, Gad Barkai
Publikováno v:
Scopus-Elsevier
Osteogenesis imperfecta (OI) is clinically characterized by abnormal bone fragility, with most patients harboring heterozygote germline mutations in the COL1A1 or COL1A2 genes that encode the chains of type I procollagen, the major protein in bone. M
Autor:
Beat Steinmann, Erik Harms, Andrea Superti-Furga, J. Schickel, Bärbel von der Gönne, Hans-Georg Koch, Michael Kiehntopf, Thomas Deufel
Publikováno v:
Human Mutation. 20:237-237
The autosomal recessive lysosomal storage disorder, nephropathic cystinosis is characterized by impaired transport of free cystine out of lysosomes. The gene responsible for cystinosis, CTNS, consists of 12 exons and encodes a 55 kDa putative lysosom
Publikováno v:
Human Mutation. 13:258-258
The beta-thalassemia mutations of 13 unrelated heterozygous Germans who remained unidentified in a previous study of 40 subjects were investigated at the DNA level. Two Mediterranean, one Asian and three novel mutations (CD6 -G, CDs 108 /112-12nt, CD
Autor:
Eva Machackova, Kathleen Claes, Anne De Paepe, Geert Mortier, Ludwine Messiaen, Michel De Vos
Publikováno v:
Human Mutation. 13:256-256
Since the identification of the BRCA1 and BRCA2 genes (MIM#s 113705 and 600185), more than hundred different mutations throughout both genes have been reported. Recurrent mutations are rare and mainly due to founder effects. We analyzed 12 sporadic f