نتایج جستجو برای: hsp40 gene family

تعداد نتایج: 1463774  

2017
Seung-Hoon Baek Kang-Il Kim Kyung-Sik Yoon Tae-Ho Kim Shin-Yoon Kim

Osteonecrosis of the femoral head (ONFH) is a multifactorial disease and is associated with genetic predisposition, and exposure to certain risk factors. In particular, idiopathic ONFH in twins and the clustering of cases in families have indicated that genetic factors are involved. However, the majority of cases of ONFH are sporadic and various studies have demonstrated that differences in the...

Journal: :Infection and immunity 2004
Hiroko Ohnishi Yoshimitsu Mizunoe Akemi Takade Yoshitaka Tanaka Hiroshi Miyamoto Mine Harada Shin-ichi Yoshida

Legionella dumoffii is one of the common causes of Legionnaires' disease and is capable of replicating in macrophages. To understand the mechanism of survival within macrophages, transposon mutagenesis was employed to isolate the genes necessary for intracellular growth. We identified four defective mutants after screening 790 transposon insertion mutants. Two transposon insertions were in gene...

2011
Francesco Cappello Gaetano Caramori Claudia Campanella Chiara Vicari Isabella Gnemmi Andrea Zanini Antonio Spanevello Armando Capelli Giampiero La Rocca Rita Anzalone Fabio Bucchieri Silvestro Ennio D'Anna Fabio L. M. Ricciardolo Paola Brun Bruno Balbi Mauro Carone Giovanni Zummo Everly Conway de Macario Alberto J. L. Macario Antonino Di Stefano

BACKGROUND It is increasingly clear that some heat shock proteins (Hsps) play a role in inflammation. Here, we report results showing participation of Hsp60 in the pathogenesis of chronic obstructive pulmonary diseases (COPD), as indicated by data from both in vivo and in vitro analyses. METHODS AND RESULTS Bronchial biopsies from patients with stable COPD, smoker controls with normal lung fu...

Journal: :journal of arthropod-borne diseases 0
g eslami department of parasitology and mycology, school of medicine, isfahan university of medical sciences, isfahan, iran r salehi department of genetics and molecular biology, school of medicine, isfahan university of medical sci- ences, isfahan, iran h hejazi department of parasitology and mycology, school of medicine, isfahan university of medical sciences, isfahan, iran a khamesipour center for research and training in skin diseases and leprosy, tehran university of medical sciences, tehran, iran b kazemi cellular and molecular biology research center, department of parasitology, school of medicine, sha- heed beheshti university of medical sciences, tehran, iran

background: leishmania, needs to detoxify the macrophage derived potent peroxides (h2o2). tryparedoxin path­way contains tryparedoxin peroxidase (tsa or tryp). the aim of the study was to detect the full-length gene se­quence and its encoded protein of the lmtryp6 gene (eu251502), and comparison the gene sequence with lmtryp6 (lmjf15.1140), another previously reported member of this gene family...

Journal: :Current opinion in genetics & development 2017
James Shorter

Protein misfolding and aggregation unify several devastating neurodegenerative disorders, including Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis. There are no effective therapeutics for these disorders and none that target the reversal of the aberrant protein misfolding and aggregation that cause disease. Here, I showcase important advances to define, engineer, an...

Journal: :Journal of molecular biology 2004
Georgeta L Dumitru Yvonne Groemping Dagmar Klostermeier Tobias Restle Elke Deuerling Jochen Reinstein

DafA is encoded by the dnaK operon of Thermus thermophilus and mediates the formation of a highly stable complex between the chaperone DnaK and its co-chaperone DnaJ under normal growth conditions. DafA(Tth) contains 87 amino acid residues and is the only member of the DnaK(Tth) chaperone system for which no corresponding protein has yet been identified in other organisms and whose particular f...

1999
A.J.L. Macario E. Conway de Macario

The purpose of this article is to provide an introductory overview of stress-gene transcription in archaea for those unfamiliar with the topic. Archaea are diverse and inhabit disparate ecosystems (very cold or hot, temperate, etc.). The study of their stress genes should reveal a variety of strategies for cell survival and suggest manifold applications. Survival relies on the mechanisms of tra...

2011
Raffaella Pantile Nicole Webster

In light of increasing sea surface temperatures, quantifying the expression of stressinducible genes in coastal organisms is imperative to identify early biomarkers of thermal stress. In the present study we developed a quantitative PCR (qPCR) assay to test the molecular response to heat stress in the Great Barrier Reef sponge Rhopaloeides odorabile. Suitable reference genes (coding for α-tubul...

Journal: :iranian journal of basic medical sciences 0
somayeh reiisi department of genetics, faculty of basic sciences, university of shahrekord, shahrekord, iran mohammad amin tabatabaiefar medical genetics dept., isfahan university of medical sciences, medical genetics dept., national institute of genetic engineering and biotechnology (nigeb), isfahan, iran mohammad hosein sanati medical genetics dept., national institute of genetic engineering and biotechnology (nigeb) morteza hashemzadeh chaleshtori cellular and molecular research center, shahrekord university of medical sciences, shahrekord, iran

objective(s): non-syndromic sensorineural hearing loss (nshl) is a common disorder affecting approximately 1 in 500 newborns. this type of hearing loss is extremely heterogeneous and includes over 100 loci. mutations in the gjb2 gene have been implicated in about half of autosomal recessive nshl (arnshl) cases, making this the most common cause of arnshl. for the latter form of deafness, most f...

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