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Kim S

No abstract available.
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Duplicate Publication: Copy, Salami, and Imalas

Huh S

  • KMID: 2306592
  • Korean J Med Educ.
  • 2010 Jun;22(2):87-88.
No abstract available.
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Characterization of a Replication Element in the Coat Protein ORF of Turnip Yellow Mosaic Virus

Shin HI, Cho TJ

Turnip yellow mosaic virus (TYMV) is a non-enveloped icosahedral virus that has a single 6.3 kb positive-strand RNA as a genome. Previously, it was observed that the recombinant construct TY-eGFP2,...
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Ethical considerations in publication of medical papers

Bae CW

It is fair to say that there are many ethical issues concerning the publication of medical papers. To define the best practice in the ethics of scientific publishing and a...
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Web-Based Database and Viewer of East Asian Copy Number Variations

Kim JH, Hu HJ, Chung YJ

We have discovered copy number variations (CNVs) in 3,578 Korean individuals with the Affymetrix Genome-Wide SNP array 5.0, and 4,003 copy number variation regions (CNVRs) were defined in a previous...
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The Search for Genetic Variants and Epigenetics Related to Asthma

Lee SH, Park JS, Park CS

For the past two decades, a huge number of genetic studies have been conducted to identify the genetic variants responsible for asthma risk. Several types of genetic and genomic approaches,...
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Array-based Comparative Genomic Hybridization and Its Application to Cancer Genomes and Human Genetics

Cho EK

Microarray comparative genomic hybridization (CGH) has proven to be a specific, sensitive, and rapid technique, with considerable advantages compared to other methods used for analysis of DNA copy number changes....
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Maxillary cement retained implant supported monolithic zirconia prosthesis in a full mouth rehabilitation: a clinical report

Sadid-Zadeh R, Liu PR, Aponte-Wesson R, O'Neal SJ

This clinical report presents the reconstruction of a maxillary arch with a cement retained implant supported fixed prosthesis using a monolithic zirconia generated by CAD/CAM system on eight osseointegrated implants....
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Left Subcortical Infarction Presenting Pure Agraphia

Yun YH, Park SA, Park JH, Lee TK, Seok H, Sung KB

  • KMID: 2191923
  • J Korean Neurol Assoc.
  • 2009 Nov;27(4):393-397.
We report a man who exhibited pure agraphia after suffering a left subcortical infarction involving part of the thalamus and the basal ganglia. His writing difficulty was characterized by stopping,...
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Visual-perceptual Function in Children with Spastic Cerebral Palsy

Kim SW, Shin JB, You S, Bae MS, Jeon HR, Lee HJ

  • KMID: 2176947
  • J Korean Acad Rehabil Med.
  • 2011 Feb;35(1):55-60.
OBJECTIVE: To compare visual-perceptual function between children with bilateral spastic cerebral palsy who have periventricular leukomalacia and unilateral spastic cerebral palsy without periventricular leukomalacia. METHOD: Twenty-one children with spastic cerebral palsy...
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Transposable Elements: No More 'Junk DNA'

Kim YJ, Lee J, Han K

Since the advent of whole-genome sequencing, transposable elements (TEs), just thought to be 'junk' DNA, have been noticed because of their numerous copies in various eukaryotic genomes. Many studies about...
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The EGFR Protein Expression and the Gene Copy Number Changes in Renal Cell Carcinomas

Lee S, An J, Kim A, Kim YS, Kim I, Genitourinary Pathology Study Group

BACKGROUND: The epidermal growth factor receptor (EGFR) is known to be involved in many tumor promoting activities. EGFR inhibition has been tried as a therapeutic modality in many human malignancies. METHODS:...
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A Study on the Recognition and Performance of Nursing Students' Hand Washing

Choi SI, Yoon JW

  • KMID: 2307585
  • Korean J Nosocomial Infect Control.
  • 2008 Dec;13(2):97-104.
BACKGROUND: The purpose of this study is to inquire into the recognition and performance of nursing students' hand washing and propose basic data for upright recognition and performance as reserve...
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Copy Number Variations in the Human Genome: Potential Source for Individual Diversity and Disease Association Studies

Kim TM, Yim SH, Chung YJ

  • KMID: 2166314
  • Genomics Inform.
  • 2008 Mar;6(1):1-7.
The widespread presence of large-scale genomic variations, termed copy number variation (CNVs), has been recently recognized in phenotypically normal individuals. Judging by the growing number of reports on CNVs, it...
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Plagiarism

Huh S

Plagiarism, the use of text and ideas from published works without proper permission or citation, is difficult to detect since the whole text should be searched and compared to literature...
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Awareness Levels and Influencing Factors of Sexual Harassment and Gender Egalitarianism among College Students

Lee YR, Kim KM, Choi SE

PURPOSE: This study was conducted to identify awareness levels and influencing factors of sexual harassment and gender egalitarianism among college students. METHODS: This study was based on a questionnaire survey with...
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Perspectives of Integrative Cancer Genomics in Next Generation Sequencing Era

Kwon SM, Cho H, Choi JH, Jee BA, Jo Y, Woo HG

The explosive development of genomics technologies including microarrays and next generation sequencing (NGS) has provided comprehensive maps of cancer genomes, including the expression of mRNAs and microRNAs, DNA copy numbers,...
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Detection of hydin Gene Duplication in Personal Genome Sequence Data

Kim JI, Ju YS, Kim S, Hong D, Seo JS

  • KMID: 1469575
  • Genomics Inform.
  • 2009 Sep;7(3):159-162.
Human personal genome sequencing can be done with high efficiency by aligning a huge number of short reads derived from various next generation sequencing (NGS) technologies to the reference genome...
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CGHscape: A Software Framework for the Detection and Visualization of Copy Number Alterations

Jeong YB, Kim TM, Chung YJ

  • KMID: 2166408
  • Genomics Inform.
  • 2008 Sep;6(3):126-129.
The robust identification and comprehensive profiling of copy number alterations (CNAs) is highly challenging. The amount of data obtained from high-throughput technologies such as array-based comparative genomic hybridization is often...
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HER2-Positive Breast Carcinomas with Co-amplification or Gain of Chromosome 17 Centromere Locus: Report of Three Cases and an Impact on HER2 Testing

Shin HC, Bae YK, Kim A, Park SJ

  • KMID: 1979073
  • Korean J Pathol.
  • 2011 Dec;45(6):665-669.
Recently we experienced three cases of human epidermal growth factor receptor 2 (HER2)-amplified invasive breast carcinomas associated with co-amplification or gain of chromosome 17 centromere (CEP17) in silver-enhanced in situ...
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