Ara
Toplam kayıt 82, listelenen: 1-20
Bilgi Toplumu ve Bilgi Teknolojisi
(TKD, 1999)
Oxa-17, A Further Extended-Spectrum Variant Of Oxa-10 Beta-Lactamase, Isolated From Pseudomonas Aeruginosa
(Amer Soc Microbiology, 1999)
Pseudomonas aeruginosa isolates 871 and 873 were isolated at Hacettepe University Hospital in Ankara and were highly resistant to ceftazidime (MIC, 128 mu g/ml). Each produced three beta-lactamases, with pIs of 5.3, 6.1, ...
Antioxidant Action of the Antiarrhythmic Drug Mexiletine in Brain Membranes
(Japanese Pharmacological Soc, 1999)
Mexiletine is a class Ib antiarrhythmic drug used in the treatment of ventricular arrhythmias. The Naf channel blocker mexiletine inhibits calcium influx in cells via decreasing reverse operation of the Na+-Ca2+ exchanger. ...
Sosyal ve İnsan Bilimleri Alanlarında Bilgi Gereksinimi ve Kullanımı
(1999)
Information need and information seeking behaviour are effected by many factorso One
of the most important factors is the occupation of the individual, especially if the individual is
a scholar. In other words, information ...
Evaluation Of Apical Root Resorption Following Extraction Therapy In Subjects With Class I And Class Ii Malocclusions
(Oxford Univ Press, 1999)
The purpose of this study was to determine the amount of root resorption during orthodontic treatment, and to examine the relationship between tooth movement and apical root resorption. Twenty-seven Class I and 27 Class ...
Altered Apoptotic Profiles in Irradiated Patients with Increased Toxicity
(Elsevier Science Inc, 1999)
Purpose: A retrospective study of radiation-induced apoptosis in CD4 and CD8 T-lymphocytes, from 12 cancer patients who displayed enhanced toxicity to radiation therapy and 9 ataxia telangiectasia patients, was performed ...
Heterogeneous Spectrum Of Mutations In The Fanconi Anaemia Group A Gene
(Stockton Press, 1999)
Fanconi anaemia (FA) is a genetically heterogeneous autosomal recessive disorder associated with chromosomal fragility, bone-marrow failure, congenital abnormalities and cancer. The gene for complementation group A (FAA), ...
Effect of Formoterol on Clinical Parameters and Lung Functions in Patients With Bronchial Asthma: A Randomised Controlled Trial
(British Med Journal Publ Group, 1999)
Aims-To determine the role of formoterol in the treatment of children with bronchial asthma who are symptomatic despite regular use of inhaled corticosteroids. Methods-A randomised, double blind, parallel group, placebo ...
Fish Studies In 45 Patients With Rubinstein-Taybi Syndrome: Deletions Associated With Polysplenia, Hypoplastic Left Heart And Death In Infancy
(Nature Publishing Group, 1999)
Rubinstein-Taybi syndrome (RTS) is a dominant Mendelian disorder characterised by mental retardation, a typical facies, broad thumbs and short stature. Previous reports indicated that 4-25% of RTS patients have a submicroscopic ...
Calpainopathy - A Survey of Mutations and Polymorphisms
(Cell Press, 1999)
Limb-girdle muscular dystrophy-type 2A (LGMD2A) is an autosomal recessive disorder characterized mainly by symmetrical and selective atrophy of the proximal limb muscles. It derives, from defects in the, human CAPN3 gene, ...
Assignment of the Muscle-Eye-Brain Disease Gene to 1P32-P34 by Linkage Analysis and Homozygosity Mapping
(Univ Chicago Press, 1999)
Muscle-eye-brain disease (MEB) is an autosomal recessive disease of unknown etiology characterized by severe mental retardation, ocular abnormalities, congenital muscular dystrophy, and a polymicrogyria-pachygyria-type ...
Penetration of Topical, Oral, and Combined Administered Ofloxacin into the Subretinal Fluid
(Bmj Publishing Group, 1999)
Aims-To assess the subretinal fluid (SRF) levels of ofloxacin following topical, oral or combined administration. Methods-31 patients undergoing conventional retinal reattachment surgery were randomly assigned to three ...
Splicing Defects In The Ataxia-Telangiectasia Gene, Atm: Underlying Mutations And Consequences
(Cell Press, 1999)
Mutations resulting in defective splicing constitute a significant proportion (30/62 [48%]) of a new series of mutations in the ATM gene in patients with ataxia-telangiectasia (AT) that were detected by the protein-truncation ...