نتایج جستجو برای: rare codon

تعداد نتایج: 260293  

Wolfram syndrome (WS) is a rare autosomal recessive neurodegenerative disease with variable symptoms, including neuropsychiatric manifestations. A 26-year-old man was reported with classic symptoms of WS and repetitive psychiatric hospitalizations and at least 16 suicidal attempts. The genetic study demonstrated a novel homozygous stop-codon mutation on the WFS1 gene. This special type of mutat...

جلالی, حسین, خوش آئین, عاطفه, مهدوی, محمدرضا, کوثریان, مهرنوش, روشن, پیام ,

 Background: Beta thalassemia is one of the most common hereditary disorders worldwide. In Iran, it is frequently reported from northern and southern provinces. In order to prevent child birth affected by this complication, prenatal screening and diagnosis is carried out nationwide. However in some instances, this program is unable to identify rare mutations leading to thalassemia. Case ...

A Amiri –Yekta A Zomorodipoor B Abde Emami H Gourabi MN Sanati P Abbasi,

Background Human coagulation factor IX is a 57kDa plasma serine protease made in Liver which plays a vital role in the blood coagulation cascade. FIX deficiency causes severe disorder Hemophilia B or Christmas disease. Nowadays, recombinant proteins have important roles in treatment of diseases. Although, cultivated mammalian cells because of their ability for producing properly folded protein ...

2016
Qing Yan Benjamin Philmus Cedar Hesse Max Kohen Jeff H. Chang Joyce E. Loper

The soil bacterium Pseudomonas protegens Pf-5 can colonize root and seed surfaces of many plants, protecting them from infection by plant pathogenic fungi and oomycetes. The capacity to suppress disease is attributed to Pf-5's production of a large spectrum of antibiotics, which is controlled by complex regulatory circuits operating at the transcriptional and post-transcriptional levels. In thi...

Journal: :PLoS ONE 2008
Rodolfo García-Contreras Xue-Song Zhang Younghoon Kim Thomas K. Wood

We discovered previously that the small Escherichia coli proteins Hha (hemolysin expression modulating protein) and the adjacent, poorly-characterized YbaJ are important for biofilm formation; however, their roles have been nebulous. Biofilms are intricate communities in which cell signaling often converts single cells into primitive tissues. Here we show that Hha decreases biofilm formation dr...

G.M Martin N Levy Y Shafeghati

Two Iranian cases with very rare progeroid syndrome are reported. The first is a 24-year-old girl who has been healthy till her 13th birthday. From that time she has been suffering from a progressive generalized and multi-systemic illness. The cardinal clinical findings were growth retardation, subcutaneous fat loss, skin dryness and wrinkling, scattered focal sclerodermoid-like changes, promin...

Journal: :BioSystems 2021

The X circular code is a set of 20 trinucleotides (codons) that has been identified in the protein-coding genes most organisms (bacteria, archaea, eukaryotes, plasmids, viruses). It shown previously important mathematical property being an error-correcting code. Thus, motifs code, i.e. series codons belonging to and called motifs, allow identification maintenance reading frame genes. are signif...

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