Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

121 results
Display

Histologic and Molecular Pathogenesis of Gallbladder Cancer

Lee KB

Adenocarcinoma is the major histology of gallbladder cancer. There are three subtypes of adenocarcinoma of the gallbladder: biliary, intestinal, and gastric foveolar subtypes. Also, there are three premalignant lesions of...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
An appraisal of pancreatic cyst fluid molecular markers

Modi RM, Pavurala R, Krishna SG

Pancreatic malignancy is the third leading cause of cancer related death in the United States with limited viable screening options. By the end of this decade, cancers are poised to...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Nevus Vascularis Mixtus

Park SM, Kim JM, Kim GW, Kim HS, Kim BS, Kim MB, Ko HC

  • KMID: 2373105
  • Korean J Dermatol.
  • 2017 Mar;55(3):203-207.
The concept of mosaicism has been used to explain different cutaneous patterns, such as the lines of Blaschko, the checkerboard pattern, the phylloid pattern, and a patchy pattern. Many mosaic...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Unique Mutational Spectrum of MLC1 in Korean Patients With Megalencephalic Leukoencephalopathy With Subcortical Cysts: p.Ala275Asp Founder Mutation and Maternal Uniparental Disomy of Chromosome 22

Choi SA, Kim SY, Yoon J, Choi J, Park SS, Seong MW, Kim H, Hwang H, Choi JE, Chae JH, Kim KJ, Kim S, Lee YJ, Nam SO, Lim BC

BACKGROUND: Megalencephalic leukoencephalopathy with subcortical cysts (MLC) is a rare inherited disorder characterized by infantile-onset macrocephaly, slow neurologic deterioration, and seizures. Mutations in the causative gene, MLC1, are found in...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Aberrant Expression of Breast Development-Related MicroRNAs, miR-22, miR-132, and miR-212, in Breast Tumor Tissues

Damavandi , Torkashvand S, Vasei M, Soltani BM, Tavallaei , Mowla SJ

PURPOSE: MicroRNAs (miRNAs) are a major class of small endogenous RNA molecules that posttranscriptionally regulate the expression of most genes in the human genome. miRNAs are often located in chromosomal...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Novel Case of Extreme Thrombocytosis in Acute Myeloid Leukemia Associated With Isochromosome 17q and Copy Neutral Loss of Heterozygosity

You E, Cho SY, Yang JJ, Lee HJ, Lee WI, Lee J, Cho KS, Cho EH, Park TS

No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Clinical Relevance of High-Resolution Single Nucleotide Polymorphism Array in Patients with Relapsed Acute Lymphoblastic Leukemia with Normal Karyotype: A Report of Three Cases

Park SH, Lee SH, Kim SY, Lee SM, Yi J, Kim IS, Kim HH, Chang CL, Lee EY

We report three patients with normal karyotype (NK) ALL, who showed genetic aberrations as determined by high-resolution single nucleotide polymorphism array (SNP-A) analysis at both diagnosis and relapse. We evaluated...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Clinical Significance of Previously Cryptic Copy Number Alterations and Loss of Heterozygosity in Pediatric Acute Myeloid Leukemia and Myelodysplastic Syndrome Determined Using Combined Array Comparative Genomic Hybridization plus Single-Nucleotide Polymorphism Microarray Analyses

Koh KN, Lee JO, Seo EJ, Lee SW, Suh JK, Im HJ, Seo JJ

The combined array comparative genomic hybridization plus single-nucleotide polymorphism microarray (CGH+SNP microarray) platform can simultaneously detect copy number alterations (CNA) and copy-neutral loss of heterozygosity (LOH). Eighteen children with acute...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Hashimoto's Thyroiditis and Papillary Thyroid Cancer

Nam KH

  • KMID: 2325292
  • J Korean Thyroid Assoc.
  • 2014 May;7(1):57-61.
The association of Hashimoto's thyroiditis (HT) with papillary thyroid cancer (PTC) has been still under debate. Some suggest that these two are positively correlated, whereas other studies report no relationship....
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Loss of Heterozygosities in Five Tumor Suppressor Genes (FHIT Gene, p16, pRb, E-Cadherin and p53) in Thyroid Tumors

Kim JH, Choi KY, Lee DJ, Rho YS, Jo SJ

  • KMID: 2278408
  • Clin Exp Otorhinolaryngol.
  • 2014 Mar;7(1):53-58.
OBJECTIVES: To evaluate the loss of heterozygosities (LOH) of chromosomes 3p14 (FHIT gene), 9p21 (p16), 13q21 (pRb), 6q22 (E-cadherin) and 17p13 (p53) in various thyroid tumors. METHODS: Eighty thyroid tumor cases...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Decreased DBC1 Expression Is Associated With Poor Prognosis in Patients With Non-Muscle-Invasive Bladder Cancer

Shim UJ, Lee IS, Kang HW, Kim J, Kim WT, Kim IY, Ryu KH, Choi YH, Moon SK, Kim YJ, Yun SJ, Lee SC, Kim WJ

  • KMID: 2316122
  • Korean J Urol.
  • 2013 Sep;54(9):631-637.
PURPOSE: The deleted in bladder cancer 1 (DBC1) gene is located within chromosome 9 (9q32-33), a chromosomal region that frequently shows loss of heterozygosity in bladder cancer (BC). It is...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Bioinformatics Interpretation of Exome Sequencing: Blood Cancer

Kim J, Lee YG, Kim N

We had analyzed 10 exome sequencing data and single nucleotide polymorphism chips for blood cancer provided by the PGM21 (The National Project for Personalized Genomic Medicine) Award program. We had...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Rare Case of Primary Hyperparathyroidism Associated with Primary Aldosteronism, Hurthle Cell Thyroid Cancer and Meningioma

Kim YL, Jang YW, Kim JT, Sung SA, Lee TS, Lee WM, Kim HJ

Multiple endocrine neoplasia type 1 (MEN1) syndrome includes varying combinations of endocrine and non-endocrine tumors. There are also a considerable number of atypical MEN1 syndrome. In this case, a 68-yr-old...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Genetic aberrations on the short arm of chromosome 8 (8p) in tongue carcinomas

Murano A, Ono K, Koike H, Endo Y, Shimada K, Kawasaki K, Nomura H, Shiiba M, Uzawa K, Tanzawa H

Aberrations on the short arm of chromosome 8 (8p) are frequently observed in several human cancers. In this study, 20 squamous cell carcinoma (SCC) specimens from the tongue were examined...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Impact of methylation of the p16INK4a gene on the prognosis ofhead and neck squamous cell carcinoma patients

Lee EH, Hwang DS, Shin SH, Kim UK, Chung IK, Kim YD

OBJECTIVES: The inactivation of the tumor suppressor gene p16INK4a plays an important role in the development of malignant tumors, including oral squamous cell carcinoma. The p16 gene is involved in...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Additional Genomic Aberrations Identified by Single Nucleotide Polymorphism Array-Based Karyotyping in an Acute Myeloid Leukemia Case with Isolated del(20q) Abnormality

Hahm C, Mun YC, Seong CM, Chung WS, Huh J

  • KMID: 2434489
  • Ann Lab Med.
  • 2012 Nov;32(6):445-449.
Prognosis is known to be better in cases with isolated chromosomal abnormalities than in those with complex karyotypes. Accordingly, del(20q) as an isolated abnormality must be distinguished from cases in...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Mutational and Expressional Analysis of DOK2 Gene in Non-small Cell Lung Cancers

Yoo NJ, Kim MS, Lee SH

PURPOSE: Mounting evidence indicates that perturbation of tyrosine phosphorylation is implicated in the development of many human diseases, including cancers. Docking proteins (DOKs) are tyrosine-phosphorylated proteins that negatively regulate tyrosine...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Analysis of copy number abnormality (CNA) and loss of heterozygosity (LOH) in the whole genome using single nucleotide polymorphism (SNP) genotyping arrays in tongue squamous cell carcinoma

Tsukasa K, Nobuharu Y, Takeshi O, Hiroki B, Takashi Y, Akira K, Nobuo T, Takahiko S

Chromosomal loss of heterozygosity (LOH) is a common mechanism for the inactivation of tumor suppressor genes in human epithelial cancers. LOH patterns can be generated through allelotyping using polymorphic microsatellite...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
False Homozygosity Results in HLA Genotyping due to Loss of Chromosome 6 in a Patient with Acute Lymphoblastic Leukemia

Park H, Hyun J, Park SS, Park MH, Song EY

Loss of heterozygosity (LOH) in chromosome 6p has been reported in a number of tumors and some hematologic malignancies, including ALL. LOH in chromosome 6p, on which the HLA genes...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Mixed Endocrine-Exocrine Carcinoma of Gallbladder Derived from Dysplasia

Lhee MJ, Woo JY

A rare case of multiple mixed endocrine-exocrine carcinoma (MEEC) of gallbladder in a 68-year-old man is described. The lesions were two separate nodules (17x13x7 mm and 17 mm in length)...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2021 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr