نتایج جستجو برای: antitrypsin

تعداد نتایج: 3954  

ژورنال: :iranian red crescent medical journal 0
bita geramizadeh department of pathology, transplant research center, shiraz university of medical sciences, shiraz, ir iran; transplant research center, shiraz university of medical sciences, shiraz, ir iran; department of pathology, transplant research center, shiraz university of medical sciences, shiraz, ir iran. tel: +98-7116474331, fax: +98-7116474331 zahra jowkar department of pathology, transplant research center, shiraz university of medical sciences, shiraz, ir iran leila karami department of pathology, transplant research center, shiraz university of medical sciences, shiraz, ir iran masoum masoumpour department of internal medicine, shiraz university of medical sciences, shiraz, ir iran samrad mehrabi department of internal medicine, shiraz university of medical sciences, shiraz, ir iran mohammad-ali ghayoumi department of internal medicine, shiraz university of medical sciences, shiraz, ir iran

background alpha-1 antitrypsin deficiency is a genetic disease which affects both lung and liver. this disease is a recognized factor for chronic obstructive pulmonary disease (copd). however its importance as the cause of copd in a country such as iran is unclear. objectives this study was conducted to find out the role of α-1 antitrypsin deficiency as a cause of copd in iranian patients. mate...

ژورنال: :hepatitis monthly 0
ignacio blanco the principality of asturias biomedical research office (oib-ficyt), oviedo, spain and alpha1-antitrypsin deficiency spanish registry, spain +34-985252481, [email protected]; uluhqsmoo}yu~yt{iofdew}w{mosyb{mom{ka~ewmsus{ch office (oib-ficyt), oviedo, spain and alpha1-antitrypsin deficiency spanish registry, spain +34-985252481, [email protected]; the principality of asturias biomedical research office (oib-ficyt), oviedo, spain and alpha1-antitrypsin deficiency spanish registry, spain +34-985252481, [email protected] frederick j. de serres national institute of environmental health sciences, research triangle park, nc, usa, usa victoriano cárcaba department of internal medicine, ‘valle del nalón hospital, principado de asturias, spain, spain beatríz lara hospital universitario arnau de vilanova, avda, institut de recerca biomédica de lleida (irb), ciberes instituto salud carlos iii, pneumology service, institut de recerca hospital universitari vall d’hebron, spain enrique fernández-bustillo biostatistics unit, central university hospital of asturias, spain

background currently, there is a remarkable lack of genetic epidemiological studies on alpha 1-antitrypsin (aat) deficiency in about half of the 193 countries of the world. this fact impedes the establishment of a true prevalence pattern of this deleterious hereditary disorder in extensive regions of human population. objectives the aim of the present study was to generate detailed maps of the ...

Journal: :archives of razi institute 2016
b.gh. ghoudarzi a. lotfi a. mesbah a. zare mirakabadi r. bagherian

53 persons suspected to alpha1-antitrypsin deficiency detection (aatd) were investigated for zz, mz, zs, ss, and ms alleles analysis by serum protein electrophoresis (spe), measurement of trypsin inhibiting capacity (tic), isoelectric focusing (ief), polymerase chain reaction (pcr), and ief/pcr-rflp techniques. the result clearly shows by using spe and tic techniques only 35.85 % and 50.08% of ...

Objective(s):Psoriasis is an autoimmune disease that appears on the skin. Although psoriasis is clinically and histologically well characterized, its pathogenesis is unknown in detail. The aims of this study were to evaluate the proteome of psoriatic patients' sera and to compare them with those of normal healthy human to find valuable biomarkers. Materials and Methods: In a case-control study,...

2012
Danielius Serapinas Brigita Sitkauskiene Raimundas Sakalauskas

INTRODUCTION Chronic obstructive pulmonary disease (COPD) has been recently defined as a systemic pulmonary inflammatory disease, and congenital α1 antitrypsin deficiency is one of the well-established genetic risk factors for chronic obstructive pulmonary disease. The aim of our study was to evaluate the possible associations of α1 antitrypsin with inflammatory markers - CRP, sCD14, TNF-α, sTN...

Journal: :The European respiratory journal 1997
D A Lomas P R Elliott R W Carrell

Fractionated plasma alpha1-antitrypsin is widely-used as replacement therapy in patients with Z alpha1-antitrypsin deficiency-related emphysema. We have recently shown that purified antitrypsin may be induced to adopt an inactive latent conformation by heating at high temperatures in stabilizing concentrations of sodium citrate. Such a conformation was predicted to be present in commercial prep...

2014
A. Dickens Dawn L. DeMeo Juan Perez S. Tamir Rashid James Day Adriana Ordoñez J. Marciniak Imran Haq Alan F. Barker Edward J. Campbell Edward Eden Noel G. McElvaney Stephen I. Rennard Robert A. Sandhaus James M. Stocks James K. Stoller Charlie Strange Gerard Turino Farshid N. Rouhani Mark Brantly David A. Lomas

Most individuals carry two wild-type M alleles of the SERPINA1 gene which encodes a1-antitrypsin. 95% of severe deficiency of a1-antitrypsin is associated with the Z allele (Glu342Lys; denoted PiZZ in the homozygote), and with the retention and polymerisation of a1-antitrypsin within hepatocytes [1]. These polymers are contained within periodic acid–Schiff-positive, diastase-resistant inclusion...

Journal: :Lancet 2015
Ronald G Crystal

www.thelancet.com Published online May 28, 2015 http://dx.doi.org/10.1016/S0140-6736(15)60036-8 1 α1 antitrypsin is a serine antiprotease secreted by the liver. Its main function is inhibition of neutrophil elastase, a non-specifi c protease released by activated or dying neutrophils. In individuals with healthy concentrations of α1 antitrypsin, the fragile alveolar structures of the lung paren...

Journal: :The European respiratory journal 2014
Lu Tan Jennifer A Dickens Dawn L Demeo Elena Miranda Juan Perez S Tamir Rashid James Day Adriana Ordoñez Stefan J Marciniak Imran Haq Alan F Barker Edward J Campbell Edward Eden Noel G McElvaney Stephen I Rennard Robert A Sandhaus James M Stocks James K Stoller Charlie Strange Gerard Turino Farshid N Rouhani Mark Brantly David A Lomas

Most individuals carry two wild-type M alleles of the SERPINA1 gene which encodes a1-antitrypsin. 95% of severe deficiency of a1-antitrypsin is associated with the Z allele (Glu342Lys; denoted PiZZ in the homozygote), and with the retention and polymerisation of a1-antitrypsin within hepatocytes [1]. These polymers are contained within periodic acid–Schiff-positive, diastase-resistant inclusion...

Journal: :Journal of clinical pathology 1977
J K Kelly

The finding is recorded of typical a1-antitrypsin globules, confirmed by immunofluorescence and immunoperoxidase methods, in the hepatocytes of a patient shown to have a normal serum antitrypsin level and normal phenotype (TiM) for a1-antitrypsin. The identification of such globules can no longer be regarded as conclusive evidence of an abnormal a1-antitrypsin phenotype.

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