نتایج جستجو برای: silver mutation

تعداد نتایج: 336478  

2015
Christopher P. Randall Arya Gupta Nicole Jackson David Busse Alex J. O'Neill

OBJECTIVES To gain a more detailed understanding of endogenous (mutational) and exogenous (horizontally acquired) resistance to silver in Gram-negative pathogens, with an emphasis on clarifying the genetic bases for resistance. METHODS A suite of microbiological and molecular genetic techniques was employed to select and characterize endogenous and exogenous silver resistance in several Gram-...

2013
Lisa S. Andersson Maria Wilbe Agnese Viluma Gus Cothran Björn Ekesten Susan Ewart Gabriella Lindgren

Equine Multiple Congenital Ocular Anomalies (MCOA) syndrome is a heritable eye disorder mainly affecting silver colored horses. Clinically, the disease manifests in two distinct classes depending on the horse genotype. Horses homozygous for the mutant allele present with a wide range of ocular defects, such as iris stromal hypoplasia, abnormal pectinate ligaments, megaloglobus, iridociliary cys...

Journal: :Iranian journal of pharmaceutical research : IJPR 2015
Masomeh Heshmati Sepideh ArbabiBidgoli Samideh Khoei Seyed Mahdi Rezayat Kazem Parivar

Serious concerns have been expressed about potential health risks of Nano silver containing consumer products (AgNPs) therefore regulatory health risk assessment on such nanoparticles has become mandatory for the safe use of AgNPsinbiomedicalproducts with special concerns to the mutagenic potentials. In this study, we examined the inhibitory and mutagenicity effects of AgNPs in three different ...

Journal: :Clinical chemistry 1994
T Arai T Tsukada T Nakayama

We developed a polymerase chain reaction (PCR)-single-strand conformation polymorphism (SSCP) analysis technique by using silver staining to detect the G-->A point mutation of intron 14 of the cholesteryl ester transfer protein (CETP) gene, which is a common mutation in CETP deficiency. After conventional PCR, amplified DNA was heated and subjected to electrophoresis in polyacrylamide gel conta...

Members the DNA Methyltransferases (DNMT) gene family have been shown to play fundamental roles in regulating embryonic growth and development from embryonic fertilization to postnatal life; through regulating the establishment and/or maintenance of specific epigenetic marks. The present study was conducted to identify potential reported mutations within the exon 33 of DNMT-1, intron 4 of DNMT-...

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 Background: Breast cancer is one of the most common cancer of women in the world.  Although different genetic alteration has been reported in this malignancy, but P 53 gene  mutations has more frequency. P 53 gene is one of the most important suppressor genes and it  play a central role in breast cancer and detecting of mutations in this gene would be very helpful in understanding of genetic m...

2016
Alejandro Horga Pedro J. Tomaselli Michael A. Gonzalez Matilde Laurà Francesco Muntoni Adnan Y. Manzur Michael G. Hanna Julian C. Blake Henry Houlden Stephan Züchner Mary M. Reilly

OBJECTIVE To describe the genetic and clinical features of a simplex patient with distal hereditary motor neuropathy (dHMN) and lower limb spasticity (Silver-like syndrome) due to a mutation in the sigma nonopioid intracellular receptor-1 gene (SIGMAR1) and review the phenotypic spectrum of mutations in this gene. METHODS We used whole-exome sequencing to investigate the proband. The variants...

Journal: :Journal of occupational health 2009
Keiko Asakura Hiroshi Satoh Momoko Chiba Masahide Okamoto Koji Serizawa Makiko Nakano Kazuyuki Omae

OBJECTIVES Many kinds of heavy metals are used in industry; thus, it is important for us to clarify their toxicity. For example, lead, which is a component of solder, is notorious for its neurotoxicity, and substitute materials have been sought for many years. Therefore, we examined the genotoxicity of lead and also those of metallic bismuth, indium, silver and antimony which are possible subst...

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