نتایج جستجو برای: 9 bp deletion

تعداد نتایج: 604247  

2017
Zi WANG Ling-Cong KONG Bo-Yan JIA Shu-Ming LIU Xiu-Yun JIANG Hong-Xia MA

Twenty-three isolates of Pasteurella multocida were tested for susceptibility to six aminoglycoside agents and screened by polymerase chain reaction for the presence of aminoglycoside resistance genes. In addition, mutations in the resistance-determining region of strains showing a high level of induced resistance to spectinomycin strains were examined. Susceptibility testing showed that all of...

Journal: :Genetics 2000
L Markovtsova P Marjoram S Tavaré

We develop a Markov chain Monte Carlo approach for estimating the distribution of the age of a mutation that is assumed to have arisen just once in the history of the population of interest. We assume that in addition to the presence or absence of this mutation in a sample of chromosomes, we have DNA sequence data from a region completely linked to the mutant site. We apply our method to a mito...

Journal: :BMC Genomics 2021

Abstract Background Cannabis sativa L., a dioecious plant derived from China, demonstrates important medicinal properties and economic value worldwide. have been usually harnessed depending on the sex of plant. To analyse genetic structure Chinese identify sex-linked makers, genome-wide insertion-deletion (InDel) markers were designed used. Results In this study, analysis polymorphisms was perf...

Journal: :Blood 2000
F F Wagner W A Flegel

The Rh blood group antigens derive from 2 genes, RHD and RHCE, that are located at chromosomal position 1p34.1-1p36 (chromosome 1, short arm, region 3, band 4, subband 1, through band 6). In whites, a cde haplotype with a deletion of the whole RHD gene occurs with a frequency of approximately 40%. The relative position of the 2 RH genes and the location of the RHD deletion was previously unknow...

Journal: :Haematologica 2007
Carolina Mordillo Elisabeth Martinez-Marchán Jordi Fontcuberta José Manuel Soria

We studied 3 Spanish patients with <1% FXII levels. DNA sequencing of the whole F12 gene identified 15 genetic variants. Molecular analyses of F12 mRNA demonstrated that the deficiency was caused by 5281delG in exon 9 of Patient 1 (in the homozygous state) and the 6306delG in exon 12 and another deletion of 23 bp in intron 8 of Patient 2 (both in the heterozygous state). Finally, a G-8C transve...

Journal: :Agriculture 2023

The objective of this study was to determine the ideal amino acid ratio for Japanese quail based on egg quality. In total, 120 were used. A completely randomized design used with 12 treatments and 10 replicates per treatment. consisted a balanced protein (BP) subsequent 11 diets obtained by 40% deletion BP specific test Lys, Met + Cys, Thr, Trp, Arg, Gly Ser, Val, Ile, Leu, His, Phr Tyr. trial ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2006
Alexander Eckehart Urban Jan O Korbel Rebecca Selzer Todd Richmond April Hacker George V Popescu Joseph F Cubells Roland Green Beverly S Emanuel Mark B Gerstein Sherman M Weissman Michael Snyder

Deletions and amplifications of the human genomic sequence (copy number polymorphisms) are the cause of numerous diseases and a potential cause of phenotypic variation in the normal population. Comparative genomic hybridization (CGH) has been developed as a useful tool for detecting alterations in DNA copy number that involve blocks of DNA several kilobases or larger in size. We have developed ...

Journal: :Genetics 1995
M Zahn-Zabal E Lehmann J Kohli

The M26 mutation in the ade6 gene of Schizosaccharomyces pombe creates a hot spot of meiotic recombination. A single base substitution, the M26 mutation is situated within the open reading frame, near the 5' end. It has previously been shown that the heptanucleotide sequence 5' ATGACGT 3', which includes the M26 mutation, is required for hot spot activity. The 510-bp ade6-delXB deletion encompa...

Journal: :Acta medica Iranica 2014
Ebrahim Eskandari-Nasab Eslam Kharazi-Nejad Alireza Nakhaee Masoumeh Afzali Seyed Payman Tabatabaei Kourosh Tirgar-Fakheri Mohammad Hashemi

Compelling evidence suggests that the oxidative stress plays a key role in the pathophysiology of cardiovascular disease (CVD). Superoxide dismutase (SOD) enzymes play a major role in detoxification of reactive oxygen species and protection against oxidative stress. We examined the possible association between a 50-bp insertion/deletion in the SOD1 promoter 1684-bp upstream of the SOD1 ATG with...

Ebrahim Eskandari-Nasab, Mohammad Ali Mashhadi, Mohammad Hashemi, Mohsen Omrani, Mohsen Taheri, Seyed-Shahaboddin Hasani,

Background: MDM2 (Murine Double Minute2) is an oncoprotein that inhibits the P53 activity. Overexpression of MDM2 gene has been reported in several human tumors. In the present study, we aimed to evaluate the impact of 40-bp insertion/deletion (ins/del) polymorphism on the promoter of MDM2 and susceptibility to breast cancer in a sample of Iranian population. Methods: This case-control study wa...

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