نتایج جستجو برای: respectively three different genotypic variants including aa

تعداد نتایج: 3886708  

Journal: :FEMS microbiology letters 2006
Renu Bhardwaj Siddhartha Majumdar Nirmal K Ganguly Neelam Taneja Shanta Dutta Thanadavarayan Ramamurthy Anuradha Chakraborti

Enteroaggregative Escherichia coli (EAEC) are causative agents of diarrhea, being characterized by aggregative adherence to cultured epithelial cells. In this study, phenotypic properties of EAEC were analyzed with respect to AA, hemagglutination, clump and biofilm formation, all of which are mediated by aggregative adherence fimbriae (AAF). The strains were also screened for AAF types, AAF adh...

Bacterial wilt caused by Ralstonia solanacearum is one of the most destructive diseases which negatively affect the tomato production worldwide. Considering the importance of the disease, using biological control agents could be effective approaches in reducing the damage of the pathogen. Tomato samples of suspected bacterial wilt disease were gathered from different regions of East Azarbayjan....

2012
John A. Byers Qing-He Zhang

Studies have shown that the bark beetle Pityogenes bidentatus (Coleoptera, Curculionidae, Scolytinae) avoids volatiles of nonhost trees (Norway Spruce, birch, and oak) and healthy host Scotch Pine when orienting to aggregation pheromone. A population genetic model of two behavioral genes was hypothesized where AA, Aa, and aa were allele combinations regulating orientation to host tree and phero...

Journal: :Archives of biochemistry and biophysics 2015
B Simões N Conceição A C Matias J Bragança R N Kelsh M L Cancela

The CBFβ gene encodes a transcription factor that, in combination with CBFα (also called Runx, runt-related transcription factor) regulates expression of several target genes. CBFβ interacts with all Runx family members, such as RUNX2, a regulator of bone-related gene transcription that contains a conserved DNA-binding domain. CBFβ stimulates DNA binding of the Runt domain, and is essential for...

Journal: :Gene 1995
J J Michaille M Gouy S Blanchet L Duret

We report the isolation and characterization of a chicken cDNA which putatively encodes an actin-like protein (chACTL). This 394-amino-acid (aa) polypeptide shares sequence homology (81, 70 and 67% identical aa, respectively) with three actin-related proteins (ARP) described for Drosophila melanogaster (ARP14D), Caenorhabditis elegans (ACTL) and Saccharomyces cerevisiae (ACT2). At least six chA...

2014
Jyoti P Sutar Varsha S Padwal Shilpa M Velhal Atmaram H Bandivdekar

Background Several studies have shown that detectable levels of HIV are observed in semen in spite of undetectable viral load in blood following antiretroviral therapy (ART). Also, different HIV variants have been detected in blood and semen of the same individual, suggesting that drugs may not be uniformly effective to control the viral load and infectivity in different tissues and secretions,...

2015
Sheng Chih Jin Bruno A. Benitez Tara Skorupa David Carrell Dwani Patel Alison M. Goate Carlos Cruchaga Nilufer Ertekin-Taner Minerva M Carrasquillo Bruno A Benitez Sarah Lincoln Siddharth Krishnan Michaela Kachadoorian Christiane Reitz Richard Mayeux Thomas S Wingo James J Lah Allan I Levey Jill Murrell Hugh Hendrie Tatiana Foroud Neill R Graff-Radford Alison M Goate Nilüfer Ertekin-Taner

Background: TREM2 encodes for triggering receptor expressed on myeloid cells 2 and has rare, coding variants that associate with risk for late-onset Alzheimer’s disease (LOAD) in Caucasians of European and North-American origin. This study evaluated the role of TREM2 in LOAD risk in African-American (AA) subjects. We performed exonic sequencing and validation in two independent cohorts of >800 ...

Journal: :Journal of the American Academy of Dermatology 2010
Abdullah Alkhalifah Adel Alsantali Eddy Wang Kevin J McElwee Jerry Shapiro

UNLABELLED Alopecia areata (AA) is an autoimmune disease that presents as nonscarring hair loss, although the exact pathogenesis of the disease remains to be clarified. Disease prevalence rates from 0.1% to 0.2% have been estimated for the United States. AA can affect any hair-bearing area. It often presents as well demarcated patches of nonscarring alopecia on skin of overtly normal appearance...

Journal: : 2023

Background. The vitamin D receptor (VDR) gene is localized in the chromosome 12 (region 12q13). Its polymorphic variants BsmI and FokI are most promising clinical diagnostic terms. During normal ontogenesis, VDR affects total bone content body its resulting length determined by development of skeleton. aim study was to assess genotypic features children with idiopathic short stature. Materials ...

Journal: :Molecules 2016
Xing Liu Zhi-Biao Wang Ya-Nan Wang Jian-Qiang Kong

M01A82W, M11A82W and M01A82WS72I are three cytochrome P450 BM3 (CYP102A1) variants. They can catalyze the hydroxylation of testosterone (TES) and norethisterone at different positions, thereby making them promising biocatalysts for steroid hydroxylation. With the aim of obtaining more hydroxylated steroid precursors it is necessary to probe the steroidal substrate diversity of these BM3 variant...

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