نتایج جستجو برای: rare codon

تعداد نتایج: 260293  

Journal: : 2023

An expression vector containing the gene encoding most common isoform Bet v 1.0101 of 1 protein, major birch pollen allergen, was created for a subsequent in prokaryotic system Escherichia coli. Total RNA from collected Belarus used as matrix. The pJC40-Веt obtained using molecular-genetic methods: cloning, ligation, transformation. specificity cloned fragment confirmed by sequencing. During st...

2014
Cristina Pop Silvi Rouskin Nicholas T Ingolia Lu Han Eric M Phizicky Jonathan S Weissman Daphne Koller

Ribosome profiling data report on the distribution of translating ribosomes, at steady-state, with codon-level resolution. We present a robust method to extract codon translation rates and protein synthesis rates from these data, and identify causal features associated with elongation and translation efficiency in physiological conditions in yeast. We show that neither elongation rate nor trans...

Journal: :Journal of medical genetics 1995
S A Gayther R Sud D Wells K Tsioupra J D Delhanty

During the course of screening the 5' half of exon 15 of the APC gene for germline and somatic mutations in two groups of patients, those with the inherited cancer prone syndrome adenomatous polyposis coli (APC) or with sporadic colorectal cancer, we have identified a number of intragenic changes that are not associated with the disease phenotype. Four of these changes are rare variants, each c...

Codon bias refers to the differences in the frequency of occurrence of synonymous codons in coding DNA. Pattern of codon and optimum codon utilization is significantly different between the lives. This difference is due to the long term function of natural selection and evolution process. Genetics drift, mutation and regulation of gene expression are the main reasons for codon bias. In this stu...

Journal: :Current problems in dermatology 1990
Y Nordmann J C Deybach H de Verneuil S Boulechfar B Grandchamp

Congenital erythropoietic porphyria (Günther's disease) is a rare disorder of heme biosynthesis inherited in an autosomal recessive fashion. The molecular abnormality responsible for the characteristic defect in uroporphyrinogen III synthase activity was investigated in two patients. For the first patient, complementary DNA was specifically amplified using the polymerase chain reaction and subs...

2016
Kangxin Li Fang Yang A. Y. Abdullahi Meiran Song Xianli Shi Minwei Wang Yeqi Fu Weida Pan Fang Shan Wu Chen Guoqing Li

Toxascaris leonina is a common parasitic nematode of wild mammals and has significant impacts on the protection of rare wild animals. To analyze population genetic characteristics of T. leonina from South China tiger, its mitochondrial (mt) genome was sequenced. Its complete circular mt genome was 14,277 bp in length, including 12 protein-coding genes, 22 tRNA genes, 2 rRNA genes, and 2 non-cod...

2014
Justin Gardin Rukhsana Yeasmin Alisa Yurovsky Ying Cai Steve Skiena Bruce Futcher

Most amino acids can be encoded by several synonymous codons, which are used at unequal frequencies. The significance of unequal codon usage remains unclear. One hypothesis is that frequent codons are translated relatively rapidly. However, there is little direct, in vivo, evidence regarding codon-specific translation rates. In this study, we generate high-coverage data using ribosome profiling...

Journal: :Sheng wu hua xue yu sheng wu wu li xue bao Acta biochimica et biophysica Sinica 1983
Rene Devos Geert Plaetinck Hilde Cheroutre Guus Simons Wim M. Degrave Jan Tavernier Erik Remaut Walter Fiers

hIL-5 cDNA was amplified through reverse transcription-polymerase chain reaction from peripheral blood lymphocytes induced with PMA and calcium ionophore A23187. The hIL-5 fragment was cloned into pUC18 and its sequence was identified to be hIL-5 cDNA sequence. The fragment which encodes hIL-5 mature polypeptide was amplified and cloned into pBV220 to express hIL-5 recombinant protein in E. col...

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