The aim of this study was to evaluate the use of one of the molecular typing methods such as PCR (polymerase chain reaction) following by RFLP (restriction fragment length polymorphism) analysis in the identification of Candida species and then to differentiate the identified azole susceptible and resistant Candida albicans strains by using AP-PCR (arbitrarily primed-polymerase chain reaction). The identification of Candida species by PCR and RFLP analysis was based on the size and primary structural variation of rDNA intergenic spacer regions (ITS). Forty-four clinical Candida isolates comprising 5 species were included to the study. The amplification products were digested individually with 3 different restriction enzymes: HaeIII, DdeI, a...
PCR amplification of the regions containing the internally transcribed spacers and 5.8S rRNA gene of...
Opportunistic fungal infections including candidiasis have increased dramatically in recent years. M...
A single primer pair amplifying a cytochrome P-450 lanosterol-14 alpha-demethylase (L1A1) gene fragm...
The aim of this study was to evaluate the use of one of the molecular typing methods such as PCR (po...
The aim of this study was to evaluate the use of one of the molecular typing methods such as PCR (po...
Aim: We aimed to identify the distribution of species in candidal strains isolated from clinical sam...
Background and Purpose: The epidemiological alteration in the distribution of Candida species, as we...
INTRODUCTION: Candida albicans is responsible for superficial or systemic infections known as candid...
Restriction fragment length polymorphism analysis was performed with the endonucleases EcoRI, Bglll,...
The aim of this study was to identify 58 Candida sp. strains isolated from animals using the Chromat...
Context: Candida spp. is an emerging cause of bloodstream infections worldwide. Delay in speciation ...
Candida species are the major cause of mortality in both immunocompromised and critically ill patie...
The PCR technique is a promising technique used to establish accurate identification methods to gain...
Candida dubliniensis is an emerging pathogen capable of causing superficial as well as systemic infe...
Abstract- Opportunistic fungal infections including candidiasis have increased dramatically in recen...
PCR amplification of the regions containing the internally transcribed spacers and 5.8S rRNA gene of...
Opportunistic fungal infections including candidiasis have increased dramatically in recent years. M...
A single primer pair amplifying a cytochrome P-450 lanosterol-14 alpha-demethylase (L1A1) gene fragm...
The aim of this study was to evaluate the use of one of the molecular typing methods such as PCR (po...
The aim of this study was to evaluate the use of one of the molecular typing methods such as PCR (po...
Aim: We aimed to identify the distribution of species in candidal strains isolated from clinical sam...
Background and Purpose: The epidemiological alteration in the distribution of Candida species, as we...
INTRODUCTION: Candida albicans is responsible for superficial or systemic infections known as candid...
Restriction fragment length polymorphism analysis was performed with the endonucleases EcoRI, Bglll,...
The aim of this study was to identify 58 Candida sp. strains isolated from animals using the Chromat...
Context: Candida spp. is an emerging cause of bloodstream infections worldwide. Delay in speciation ...
Candida species are the major cause of mortality in both immunocompromised and critically ill patie...
The PCR technique is a promising technique used to establish accurate identification methods to gain...
Candida dubliniensis is an emerging pathogen capable of causing superficial as well as systemic infe...
Abstract- Opportunistic fungal infections including candidiasis have increased dramatically in recen...
PCR amplification of the regions containing the internally transcribed spacers and 5.8S rRNA gene of...
Opportunistic fungal infections including candidiasis have increased dramatically in recent years. M...
A single primer pair amplifying a cytochrome P-450 lanosterol-14 alpha-demethylase (L1A1) gene fragm...