نتایج جستجو برای: .csge

تعداد نتایج: 76  

Journal: :Haematologica 2007
Mohammad Hashemi Soteh Ian R Peake Luke Marsden John Anson Javier Batlle Dominique Meyer Edith Fressinaud Claudine Mazurier Jenny Goudemand Jeroen Eikenboom Anne Goodeve

Two versions of conformation sensitive gel electrophoresis, fluorescent (F-CSGE) and manual (M-CSGE) techniques, were compared for mutation analysis of the von Willebrand factor gene. 56 PCRs were used to amplify all 52 exons of the gene in seven type 1 von Willebrand disease cases, plus a healthy control. One hundred and ninety-two samples were analyzed on each F-CSGE gel, compared with 40 on ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2016
Qin Shu Andrzej M Krezel Zachary T Cusumano Jerome S Pinkner Roger Klein Scott J Hultgren Carl Frieden

Curli, consisting primarily of major structural subunit CsgA, are functional amyloids produced on the surface of Escherichia coli, as well as many other enteric bacteria, and are involved in cell colonization and biofilm formation. CsgE is a periplasmic accessory protein that plays a crucial role in curli biogenesis. CsgE binds to both CsgA and the nonameric pore protein CsgG. The CsgG-CsgE com...

Journal: :Molecular microbiology 2011
Ashley A Nenninger Lloyd S Robinson Neal D Hammer Elisabeth Ashman Epstein Matthew P Badtke Scott J Hultgren Matthew R Chapman

Curli are extracellular amyloid fibres produced by Escherichia coli that are critical for biofilm formation and adhesion to biotic and abiotic surfaces. CsgA and CsgB are the major and minor curli subunits, respectively, while CsgE, CsgF and CsgG direct the extracellular localization and assembly of curli subunits into fibres. The secretion and stability of CsgA and CsgB are dependent on the ou...

Journal: :Arquivos brasileiros de endocrinologia e metabologia 2007
Marcelo A C G dos Santos Elisangela Pereira de S Quedas Rodrigo de Almeida Toledo Delmar M Lourenço Sergio Pereira de A Toledo

Multiple endocrine neoplasia type 2 (MEN2) is an autosomal dominant inherited tumor syndrome caused by RET proto-oncogene germline mutations (RET). Here we tested the Conformation Sensitive Gel Electrophoresis (CSGE) as a screening method for RET hot-spot mutations. Seven MEN2 families were studied by direct sequencing analysis, CSGE and Single Strand Conformational Polymorphism (SSCP). Using C...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1998
J Körkkö S Annunen T Pihlajamaa D J Prockop L Ala-Kokko

Previously, an assay called conformation sensitive gel electrophoresis (CSGE) was developed for scanning PCR products for the presence of single-base and larger base mismatches in DNA. The assay was based on the assumption that mildly denaturing solvents in an appropriate buffer can accentuate the conformational changes produced by single-base mismatches in double-stranded DNA and thereby incre...

Journal: :Iranian biomedical journal 2008
Hamid Reza Khorram Khorshid Raymond Dalgleish

BACKGROUND Several methods have been developed for detection of sequence variation in genes and each has its advantages and disadvantages. A disadvantage of them is that the simpler, cost-effective methods are commonly perceived as being less sensitive in their detection of sequence variation, whereas those with proven sensitivity have a requirement for complex or expensive laboratory equipment...

2015
Erik Chorell Emma Andersson Margery L. Evans Neha Jain Anna Götheson Jörgen Åden Matthew R. Chapman Fredrik Almqvist Pernilla Wittung-Stafshede Ilia V Baskakov

Amyloid formation is historically associated with cytotoxicity, but many organisms produce functional amyloid fibers (e.g., curli) as a normal part of cell biology. Two E. coli genes in the curli operon encode the chaperone-like proteins CsgC and CsgE that both can reduce in vitro amyloid formation by CsgA. CsgC was also found to arrest amyloid formation of the human amyloidogenic protein α-syn...

هاشمی سوته , سیدمحمدباقر, گودیو , آن,

Background and purpose: Von Willebrand Disease (VWD) type 1, is the most common inherited bleeding disorder caused by defect in Von Willebrand Factor (VWF) gene with 178000 nucleotide length. Different methods are available to detect unknown mutations in a genetic study. The fluorescent conformation sensitive gel electrophoresis (F-CSGE) was designed for the VWF gene by using fluorescent dyes...

2011
R Alizadeh H Hooshyar M Bandehpor M Arbabi F Kazemi A Talari B Kazemi

BACKGROUND Cutaneous leishmaniasis is still a health problem in many rural and urban regions of Iran and drug resistance has emerged as a major impediment in the treatment of leishmaniasis. This study aims to determine the drug resistance gene in cutaneous leishmaniasis by PCR in some endemic areas of Iran. METHODS Ninety seven samples were collected from ulcers of leishmaniasis patients from...

Journal: :Medical science monitor : international medical journal of experimental and clinical research 2007
Santhosh Sundaresan Chundamannil Eapen Eapen Ramachandran Velayutham Shaji Mammen Chandy George Kurian George Chandy

BACKGROUND Wilson's disease (WD) is an autosomal recessive disorder leading to copper overload, mainly in the liver and brain, due to mutations in the ATP7B gene. About 10% of heterozygous carriers of ATP7B gene mutations have decreased serum ceruloplasmin, posing diagnostic difficulties. CASE REPORT We report a four-member family wherein the 11-year-old daughter was diagnosed as having WD ba...

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