نتایج جستجو برای: haeiii

تعداد نتایج: 400  

Journal: :The Journal of clinical investigation 2015
Jenny Björkqvist Steven de Maat Urs Lewandrowski Antonio Di Gennaro Chris Oschatz Kai Schönig Markus M Nöthen Christian Drouet Hal Braley Marc W Nolte Albert Sickmann Con Panousis Coen Maas Thomas Renné

Hereditary angioedema type III (HAEIII) is a rare inherited swelling disorder that is associated with point mutations in the gene encoding the plasma protease factor XII (FXII). Here, we demonstrate that HAEIII-associated mutant FXII, derived either from HAEIII patients or recombinantly produced, is defective in mucin-type Thr309-linked glycosylation. Loss of glycosylation led to increased cont...

Journal: :Journal of clinical microbiology 1984
A R Torres M K Li D C Ward S C Edberg

We used the restriction endonuclease HaeIII to differentiate Neisseria gonorrhoeae from other Neisseria species and Branhamella catarrhalis. A total of 16 clinical isolates and four American Type Culture Collection strains of N. gonorrhoeae were resistant to HaeIII digestion, whereas 17 isolates and four American Type Culture Collection strains from eight different bacterial species were suscep...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1975
K Horiuchi N D Zinder

Single-stranded viral DNA of bacteriophage f1 is cleaved into specific fragments by endo R-HaeIII, a restriction endonuclease isolated from Hemophilus aegyptius. The sites of the single strand cleavage correspond to those of the double strand cleavage. A single-stranded DNA fragment containing only one HaeIII site is also cleaved by this enzyme. This observation suggests that the reaction of si...

Journal: :Genome 2004
A Leitão R Chaves S Santos H Guedes-Pinto P Boudry

Reliable banding techniques are a major necessity for genetic research in oysters. In this study, we carried out the cytogenetic characterization of four oyster species (family Ostreidae) using restriction endonuclease treatments. Chromosomes were treated with three different restriction enzymes, stained with Giemsa, and examined for banding patterns. The following species were studied: Crassos...

Journal: :Journal of virology 2004
Gary Quinn James Wood Kristen Suling Scott Arn David H Sachs Henk-Jan Schuurman Clive Patience

The identification of animals in an inbred miniature swine herd that consistently fail to produce replication- competent humantropic porcine endogenous retrovirus (PERV) has prompted studies on the biology of PERV in transmitter and nontransmitter animals. We analyzed PERV RNA transcript profiles in a family of inbred miniature swine (SLA(d/d) haplotype) in which individual members differed in ...

Journal: :Pathophysiology of haemostasis and thrombosis 2003
Mojca Bozic Natasa Teran Borut Peterlin Mojca Stegnar

High fibrinogen is recognised as a risk factor for atherosclerosis. It seems that high fibrinogen is also a risk factor for deep vein thrombosis (DVT). It has been shown that certain polymorphisms in fibrinogen genes can influence the fibrinogen level. In this study, fibrinogen levels and the frequency of the polymorphisms TaqI, HaeIII and BclI were studied in 114 patients with DVT and 244 heal...

2011
Yongju Zhao Huizhong Xu Lixiang Shi Jiahua Zhang

Polymorphism of the second exon of the caprine leukocyte antigen-DRB3 gene (CLA-DRB3*02) was investigated in this study. The 285 bp PCR product of 258 individuals from 10 domestic goat breeds in Southwest China was digested with restriction endonucleases PstI and HaeIII and then genotyped. Three alleles and 4 restriction digestion profiles were distinguished by digestion of the PCR fragment by ...

Journal: :Acta Scientiarum. Animal Sciences 2022

The study characterized the lactoferrin (Lf) mRNA gene in different goat breeds Philippines and determined its association with subclinical mastitis (SCM). involved collection of milk at second week lactation (n=75) blood samples (n=5) to obtain extracted RNA using cDNA amplify Lf through polymerase chain reaction. nucleotide amino acid sequences were used as reference evaluation phylogenetic r...

Journal: :Genetics 1992
A Torroni T G Schurr C C Yang E J Szathmary R C Williams M S Schanfield G A Troup W C Knowler D N Lawrence K M Weiss

Mitochondrial DNAs (mtDNAs) from 167 American Indians including 87 Amerind-speakers (Amerinds) and 80 Nadene-speakers (Nadene) were surveyed for sequence variation by detailed restriction analysis. All Native American mtDNAs clustered into one of four distinct lineages, defined by the restriction site variants: HincII site loss at np 13,259, AluI site loss at np 5,176, 9-base pair (9-bp) COII-t...

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