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# Judul Penulis Tahun Akses
Repositori Institusi

Modul teknik pengoperasian laboratorium bioteknologi

Seameo Biotrop, 2020
Perkembangan teknologi, khususnya bidang biologi molekuler, semakin meningkat pesat pada beberapa tahun ini. Manfaat cabang ilmu tersebut sangatlah besar bagi kesejahteraan manusia, seperti dalam bidang kedokteran, peternakan, perikanan, pertanian b...
Jurnal Institusi

A Rapid and Sensitive Diagnosis of Typhoid Fever Based On Nested PCR-Voltammetric DNA Biosensor Using Flagellin Gene Fragment

Indonesian Journal of Chemistry; Vol 16, No 1 (2016); 87-91
Universitas Gadjah Mada, 2018DOI: 10.22146/ijc.21182http://creativecommons.org/licenses/by-nc-nd/4.0
Typhoid fever caused by Salmonella typhi is an important issue for public health in the world. Laboratory methods for rapid and sensitive diagnosis are very important for disease management. The purpose of this study was to determine the performance ...
PubMed

Discrepancy of Breast and Axillary Pathologic Complete Response and Outcomes in Different Subtypes of Node-positive Breast Cancer after Neoadjuvant Chemotherapy

J Cancer
Ivyspring International Publisher, 2021DOI: 10.7150/jca.62830https://creativecommons.org/licenses/by/4.0/
Few studies have analyzed the discrepancy between breast pathologic complete response (B-pCR) and axillary node pCR (N-pCR) rates and their impact on survival outcomes in different intrinsic subtypes of early breast cancer after neoadjuvant chemother...
PubMed

Evaluation of Altona Diagnostics RealStar Zika Virus Reverse Transcription-PCR Test Kit for Zika Virus PCR Testing

J Clin Microbiol
American Society for Microbiology (ASM), 2017DOI: 10.1128/JCM.02153-16Copyright © 2017 American Society for Microbiology. All Rights Reserved.
With the emerging Zika virus (ZIKV) epidemic, accessible real-time reverse transcription-PCR (rRT-PCR) assays are needed to streamline testing. The commercial Altona Diagnostics RealStar ZIKV rRT-PCR test kit (Altona PCR) has been approved for emerge...
PubMed

Determination of PCR efficiency in chelex-100 purified clinical samples and comparison of real-time quantitative PCR and conventional PCR for detection of Chlamydia pneumoniae

BMC Microbiol
BMC, 2002DOI: 10.1186/1471-2180-2-17Copyright © 2002 Mygind et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
BACKGROUND: Chlamydia pneumoniae infection has been detected by serological methods, but PCR is gaining more interest. A number of different PCR assays have been developed and some are used in combination with serology for diagnosis. Real-time PCR co...
PubMed

Comparison of a Miniaturized Cassette PCR System with a Commercially Available Platform for Detecting Escherichia coli in Beef Carcass Swabs

Micromachines (Basel)
Multidisciplinary Digital Publishing Institute (MDPI), 2021DOI: 10.3390/mi12080959https://creativecommons.org/licenses/by/4.0/
Detection sensitivity of cassette PCR was compared with a commercial BAX(®) PCR system for detection of eae and stx genes in Escherichia coli from 806 beef carcass swabs. Cassette PCR detects multiple genetic markers on multiple samples using PCR an...
PubMed

Comparison of six different PCR methods for detection of Pneumocystis carinii.

J Clin Microbiol
American Society for Microbiology (ASM), 1995DOI: 10.1128/jcm.33.10.2785-2788.1995
We have recently developed a nested PCR method which amplifies internal transcribed spacers (ITS) of the ribosomal RNA genes of Pneumocystis carinii. To determine whether this PCR method can be used to diagnose P. carinii infections, we examined 30 b...
PubMed

Enhancing the efficiency of a PCR using gold nanoparticles

Nucleic Acids Res
Oxford University Press, 2005DOI: 10.1093/nar/gni183© The Author 2005. Published by Oxford University Press. All rights reserved The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and Oxford University Press are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions@oxfordjournals.org
We found that the PCR could be dramatically enhanced by Au nanoparticles. With the addition of 0.7 nM of 13 nm Au nanoparticles into the PCR reagent, the PCR efficiency was increased. Especially when maintaining the same or higher amplification yield...
PubMed

Application of Coamplification at Lower Denaturation Temperature-PCR Sequencing for Early Detection of Antiviral Drug Resistance Mutations of Hepatitis B Virus

J Clin Microbiol
American Society for Microbiology (ASM), 2014DOI: 10.1128/JCM.00343-14Copyright © 2014, American Society for Microbiology. All Rights Reserved.
Nucleoside/nucleotide analogue for the treatment of chronic hepatitis B virus (HBV) infection is hampered by the emergence of drug resistance mutations. Conventional PCR sequencing cannot detect minor variants of <20%. We developed a modified co-a...
PubMed

Comparison of a Commercially Available Repetitive-Element PCR System (DiversiLab) with PCR Ribotyping for Typing of Clostridium difficile Strains

J Clin Microbiol
American Society for Microbiology (ASM), 2011DOI: 10.1128/JCM.00324-11Copyright © 2011, American Society for Microbiology. All Rights Reserved.
This study compared a repetitive-element PCR (rep-PCR) method (DiversiLab system) to PCR ribotyping. The discriminatory power of rep-PCR was 0.997. Among the PCR ribotype 027 isolates tested, different rep types could be distinguished. rep-PCR showed...
PubMed

Evaluation of fliC-d based direct blood PCR assays for typhoid diagnosis

BMC Microbiol
BMC, 2016DOI: 10.1186/s12866-016-0723-6http://creativecommons.org/publicdomain/zero/1.0/
BACKGROUND: Typhoid cases need to be diagnosed accurately for early antibiotic therapy and reducing mortality. Identification of Salmonella Typhi (S. Typhi) in blood culture is conclusive, but has poor sensitivity. Detection of S. Typhi by PCR from b...
PubMed

A comparison of MASS-PCR and ARMS-PCR for the detection of lung cancer gene mutation

Transl Cancer Res
AME Publications, 2019DOI: 10.21037/tcr.2019.10.37https://creativecommons.org/licenses/by-nc-nd/4.0/
BACKGROUND: Targeted therapy has been proven to be effective in lung cancer patients with specific driver gene mutations. At present, Sanger sequencing is still the gold standard in clinical practice to detect mutation, and amplification refractory m...
PubMed

Evaluation of enzyme immunoassay for hepatitis B virus DNA based on anti-double-stranded DNA.

J Clin Microbiol
American Society for Microbiology (ASM), 1995DOI: 10.1128/jcm.33.2.413-415.1995
We have evaluated a new enzyme immunoassay technology to detect the products of PCR-based amplification that may be applicable to routine testing of hepatitis B virus (HBV) DNA. Two hundred eight serum samples were studied: 73 were basal samples and ...
PubMed

Clinical usefulness of 16S ribosomal RNA real-time PCR for the diagnosis of scrub typhus

Sci Rep
Nature Publishing Group, 2021DOI: 10.1038/s41598-021-93541-whttps://creativecommons.org/licenses/by/4.0/
Scrub typhus is a major acute febrile disease in the Asia–Pacific region. The purpose of the present study is to investigate the clinical usefulness of real-time PCR (Q-PCR) of 16S rRNA for the diagnosis of scrub typhus. We examined blood specimens...
PubMed

Comparison of different PCR approaches for characterization of Burkholderia (Pseudomonas) cepacia isolates.

J Clin Microbiol
American Society for Microbiology (ASM), 1995DOI: 10.1128/jcm.33.12.3304-3307.1995
In this study, we evaluated three PCR methods for epidemiological typing of Burkholderia (Pseudomonas) cepacia--PCR-ribotyping, arbitrarily primed PCR (AP-PCR) and enterobacterial repetitive intergenic consensus sequence PCR (ERIC-PCR)--and compared ...
PubMed

The usefulness of multiplex PCR for the identification of bacteria in joint infection

J Clin Lab Anal
Wiley, 2010DOI: 10.1002/jcla.20384© 2010 Wiley‐Liss, Inc.
Background: The diagnosis of septic arthritis (SA) relies on synovial analysis and conventional culture. But, these methods lack of sensitivity and culture is time consuming to establish a definite diagnosis. This study evaluated a new multiplex PCR ...
PubMed

Modification of IgH PCR clonal analysis by the addition of sucrose and cresol red directly to PCR reaction mixes.

Mol Pathol
BMJ Publishing Group, 1997DOI: 10.1136/mp.50.3.164
Diagnostic immunoglobulin (Ig) polymerase chain reaction (PCR) clonality analyses need to be simple, reproducible, and rapid. Sucrose and cresol red (gel loading buffer reagents) were added to a routine IgH PCR reaction mix to obviate the need for ad...
PubMed

Realtime PCR Is More Sensitive than Multiplex PCR for Diagnosis and Serotyping in Children with Culture Negative Pneumococcal Invasive Disease

PLoS One
PLOS, 2010DOI: 10.1371/journal.pone.0009282https://creativecommons.org/licenses/by/4.0/
BACKGROUND: Pneumococcal serotyping is usually performed by Quellung reaction, considered the gold standard test. However the method cannot be used on culture-negative samples. Molecular methods can be a useful alternative. The aim of the study was t...
PubMed

Analytical Performance Evaluation of a Digital Real‐Time PCR for Quantifying Major BCR::ABL1 Transcripts

J Clin Lab Anal
Wiley, 2024DOI: 10.1002/jcla.25034https://creativecommons.org/licenses/by-nc-nd/4.0/
BACKGROUND: Accurate quantification of the BCR::ABL1 transcripts is essential for measurable residual disease (MRD) monitoring in chronic myeloid leukemia (CML) after tyrosine kinase inhibitor (TKI) treatment. This study evaluated the newly developed...
PubMed

Comparison of PCR-Ribotyping, Arbitrarily Primed PCR, and Pulsed-Field Gel Electrophoresis for Typing Clostridium difficile

J Clin Microbiol
American Society for Microbiology (ASM), 2000DOI: 10.1128/jcm.38.7.2484-2487.2000Copyright © 2000, American Society for Microbiology
Clostridium difficile is now recognized as the major agent responsible for nosocomial diarrhea in adults. Among the genotyping methods available, arbitrarily primed PCR (AP-PCR), PCR-ribotyping, and pulsed-field gel electrophoresis (PFGE) have been w...