نتایج جستجو برای: editing and encoding

تعداد نتایج: 16842753  

Journal: :iranian journal of parasitology 0
b kazemi department of biotechnology, school of medicine, shahid beheshti university of medical sciences, tehran, iran and cellular and molecular biology research center, shahid beheshti university of medical sciences, tehran, iran

leishmania is a protozoan parasite belonging to the family trypanosomatidae, which is found among 88 different countries. the parasite lives as an amastigote in vertebrate macro­phages and as a promastigote in the digestive tract of sand fly. it can be cultured in the laboratory us­ing appropriate culture media. although the sexual cycle of leishmania has not been observed during the promastigo...

Journal: :international clinical neurosciences journal 0
afsaneh zarghi

eye movement desensitization and reprocessing (emdr) process encompasses several nervous system components such as medulla, pons, midbrain, cerebellum, basal ganglia, parietal, frontal and occipital lobes. the role of eye movement (em) has been documented previously in relation with cognitive processing mechanisms. by emdr we can reach some parts of memory which were inaccessible before and als...

Journal: :The EMBO journal 2005
Liam P Keegan James Brindle Angela Gallo Anne Leroy Robert A Reenan Mary A O'Connell

RNA editing increases during development in more than 20 transcripts encoding proteins involved in rapid synaptic neurotransmission in Drosophila central nervous system and muscle. Adar (adenosine deaminase acting on RNA) mutant flies expressing only genome-encoded, unedited isoforms of ion-channel subunits are viable but show severe locomotion defects. The Adar transcript itself is edited in a...

2017
Angela Gallo Emma Thomson James Brindle Mary A. O'Connell Liam P. Keegan

Post-transcriptional processes such as alternative splicing and RNA editing have a huge impact on the diversity of the proteome. Detecting alternatively spliced transcripts is dif®cult when they are rare. In addition, edited transcripts often differ from the genomic sequence by only a few nucleotides. Denaturing high performance liquid chromatography (DHPLC) is routinely used for single nucleot...

2016
Ignazio Maggio Jin Liu Josephine M. Janssen Xiaoyu Chen Manuel A. F. V. Gonçalves

Mutations disrupting the reading frame of the ~2.4 Mb dystrophin-encoding DMD gene cause a fatal X-linked muscle-wasting disorder called Duchenne muscular dystrophy (DMD). Genome editing based on paired RNA-guided nucleases (RGNs) from CRISPR/Cas9 systems has been proposed for permanently repairing faulty DMD loci. However, such multiplexing strategies require the development and testing of del...

Journal: :Nucleic acids research 2002
Angela Gallo Emma Thomson James Brindle Mary A O'Connell Liam P Keegan

Post-transcriptional processes such as alternative splicing and RNA editing have a huge impact on the diversity of the proteome. Detecting alternatively spliced transcripts is difficult when they are rare. In addition, edited transcripts often differ from the genomic sequence by only a few nucleotides. Denaturing high performance liquid chromatography (DHPLC) is routinely used for single nucleo...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2002
Ilona Gurevich Michael T Englander Mella Adlersberg Nathan B Siegal Claudia Schmauss

Serotonin 2C (5-HT2C) receptor pre-mRNA is a substrate for RNA editing enzymes that convert five adenosines (named A, B, C', C, and D editing sites) to inosines. Editing of two of these sites (C' and C) is crucial for decreasing the efficiency of the receptor to activate G-protein. Nucleotide sequence analysis of mouse forebrain neocortical 5-HT2C mRNA isoforms revealed that editing at these tw...

Journal: :Nucleic acids research 1996
G R Skuse A J Cappione M Sowden L J Metheny H C Smith

A functional mooring sequence, known to be required for apolipoprotein B (apoB) mRNA editing, exists in the mRNA encoding the neurofibromatosis type I (NF1) tumor suppressor. Editing of NF1 mRNA modifies cytidine in an arginine codon (CGA) at nucleotide 2914 to a uridine (UGA), creating an in frame translation stop codon. NF1 editing occurs in normal tissue but was several-fold higher in tumors...

2007
Luis Mateus Rocha Jasleen Kaur

Our agent-based model of genotype editing is defined by two distinct genetic components: a coding portion encoding phenotypic solutions, and a non-coding portion used to edit the coding material. This set up leads to an indirect, stochastic genotype/phenotype mapping which captures essential aspects of RNA editing. We show that, in drastically changing environments, genotype editing leads to qu...

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