نتایج جستجو برای: gtg

تعداد نتایج: 638  

Journal: :Journal of animal science 2002
S Maak S Jaesert K Neumann G von Lengerken

Name of the Sequence. Cyclin-dependent kinase inhibitor 3 (CDKN3; CDK2-associated dual specificity phosphatase). Genus and Species. Sus scrofa. Origin of Clone. We used the differential display/reverse transcriptase PCR (DD/RT) approach to isolate potential candidate genes for congenital splay leg in piglets. A total of 16 cDNA fragments with apparent differential expression in skeletal muscle ...

2006
Jennifer Abernethy Elizabeth Bradley Robert Sharman

The main challenges in predicting the weather are insufficient computational power and gaps in our understanding of the complex dynamics of atmospheric phenomena. There are comparatively straightforward solutions to these problems: enough teraflops, the right equations. But what happens when you have neither? This is the problem facing aviation turbulence forecasters, who are charged with the t...

2013
Yidan Huang Martin Runge Geovana Brenner Michael Stefan Schwarz Arne Jung Dieter Steinhagen

BACKGROUND Enteric Redmouth Disease (ERM), caused by Yersinia ruckeri, is one of the most important infectious diseases in rainbow trout (Oncorhynchus mykiss) aquaculture in Europe. More recently, non-motile vaccine resistant isolates appear to have evolved and are causing disease problems throughout Europe, including Germany. The aim of this study was to analyse the variation of biochemical an...

Journal: :Nucleic Acids Research 2005
C. P. Diggle J. Bentley M. A. Knowles A. E. Kiltie

The effect of cis-diaminedichloroplatinum(II) (cisplatin) DNA damage on the repair of double-strand breaks by non-homologous end-joining (NHEJ) was determined using cell-free extracts. NHEJ was dramatically decreased when plasmid DNA was damaged to contain multiple types of DNA adducts, along the molecule and at the termini, by incubation of DNA with cisplatin; this was a cisplatin concentratio...

2016
F. Fardsanei F. Nikkhahi B. Bakhshi T.Z. Salehi I.A. Tamai M.M. Soltan Dallal

In recent years, Salmonella enterica serovar Enteritidis has been a primary cause of human salmonellosis in many countries. The major objective of this study was to investigate genetic diversity among Salmonella Enteritidis strains from different origins (food and human) by Enterobacterial Repetitive Intergenic Consensus (ERIC) -PCR, as well as to assess their plasmid profiling and antimicrobia...

2013
Selvi R Mukunda Priyanka A

UNLABELLED Objective(s : Cleft lip/palate are common congenital anomalies, affecting approximately 2/1000 live births. Pierre Robin Sequence is a subgroup of the cleft palate population. Chromosomal abnormalities near the SOX9 gene disrupt the regulation of this gene and prevent the SOX9 protein from properly controlling the development of facial structures, which leads to isolated PRS. The pre...

Journal: :The Journal of Positive Psychology 2023

Welcoming accountability is a responsive and responsible virtue that can be shown in relation to people or God, higher power, transcendent guide. Our interdisciplinary team defined (TA) developed 10-item scale using classical item response theory methods. Across diverse US samples (total N = 990) the exhibited internal consistency, construct validity, incremental known-groups test-retest reliab...

Aghil Esmaeili-Bandboni, Alireza Sharafshah, Arash Davoudi, Fereshteh Fallahabadi, Forozan Milani, Parvaneh Keshavarz, Sara Afzali,

The common causes of 18p deletion syndrome are spontaneous errors in the chromosomal structure in the early stages of human embryonic development. In this study, a 29-year-old girl was introduced with the features of deletion of chromosome 18. In addition, GTG banding karyotype revealed that this case had a deletion involving the short arm of chromosome 18. In comparison with the usual phenotyp...

1998
M Thornley J E Wraith

Genomic DNA from 57 unrelated MPS II (Hunter’s disease) patients was analysed for mutations of the iduronate sulphatase (IDS) gene. The aim of the study was threefold: to identify the primary genetic lesion in patients, to investigate the correlation between genotype and phenotype, and most importantly, to provide reliable carrier testing for female members once the family mutation was identifi...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید