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De novo transcriptome sequencing and gene expression profiling with/without B-chromosome plants of Lilium amabile

Park D, Kim JH, Kim NS

Supernumerary B chromosomes were found in Lilium amabile (2n = 2x = 24), an endemic Korean lily that grows in the wild throughout the Korean Peninsula. The extra B chromosomes...
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Long-term follow-up of Fanconi anemia: clinical manifestation and treatment outcome

Yoon BG, Kim HN, Han UJ, Jang HI, Han DK, Baek HJ, Hwang TJ, Kook H

PURPOSE: The aim of this study was to characterize Korean patients with Fanconi anemia (FA), which is a rare but very challenging genetic disease. METHODS: The medical records of 12 FA...
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A Case of Fanconi Anemia Diagnosed by a Chromosome Breakage Test with Skin Fibroblasts

Lee JJ, Yun KB, Kim SY, Lee MJ, Jung HJ, Park JE, Kim HJ

Fanconi anemia is an autosomal recessive disease that's characterized by congenital anomalies, defective hematopoiesis and a high risk of developing acute myeloid leukemia and certain solid tumors. The clinical phenotype...
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Primary Pulmonary Ewing's Sarcoma/Primitive Neuroectodermal Tumor in a 67-year-old Man

Lee YY, Kim DH, Lee JH, Choi JS, In KH, Oh YW, Cho KH, Roh YK

Extraskeletal Ewing's sarcoma (EES) is a branch of neuroectodermal tumor (PNET), which is very rare soft tissue sarcoma. We report a case of EES/PNET arising is the lung of a...
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Triplication of 1q in a Patient with Myelodysplastic Syndrome

Cho HS, Kim MK, Hyun MS

Triplication of 1q is a very rare chromosomal abnormality in hematologic malignancies, and it has been related to Fanconi anemia. The clinical significance of this abnormality is unknown. We report...
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Abnormal Fragile Histidine Triad (FHIT) Expression in Cervical Carcinomas

Tong SY, Lee SK, Ji SG

  • KMID: 2272360
  • Korean J Obstet Gynecol.
  • 2004 Jun;47(6):1093-1099.
OBJECTIVE: The fragile histidine triad (FHIT) gene is located at chromosome 3p14.2 and encompasses the common fragile site, FRA3B, which may contribute to chromosome breakage and rearrangement of cancer cells....
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1-beta-D-Arabinofuranosyl-cytosine Induces Chromosomal Breaks in vitro

Jeon IS

  • KMID: 2335789
  • J Korean Pediatr Soc.
  • 2003 Dec;46(12):1186-1193.
PURPOSE: Fragile sites are points on chromosomes which tend to break non-randomly when exposed to specific chemical agents or conditions of tissue culture. The chromosomal break induced by the antineoplastic...
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Chromosomal Assay after In-vitro Irradiation of Lymphocytes in Ataxia Telangiectasia

Kim JS, Lee JY, Park SK, Kim YI, Song MY, Choi BO

  • KMID: 2342929
  • J Korean Neurol Assoc.
  • 2001 Sep;19(5):509-513.
BACKGROUND: Hypersensitivity to both cell-killing and chromosome-damaging effects of ionizing radiation is a consistent feature of cells from individuals with ataxia-telangiectasia (AT). This radiobiological behavior of AT cells is a...
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Expression of FHIT protein and allelic deletion at FHIT locus in primary cervical carcinoma tissues

Kim SY, Seong YS

  • KMID: 2261902
  • Korean J Obstet Gynecol.
  • 2000 Apr;43(4):694-703.
Allelic deletions involving the short arm of chromosome 3(3p13-21.1) have been observed frequently in cervical carcinomas. Recently the fragile histidine triad(FHIT) gene was cloned and mapped to this chromosomal region(3p14.2). From various...
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Fragile sites induced by aphidicolin in lymphocytes, HaCat cells and MRC-5 cells

Park KR, Goo DE, Lee JH, Kim WS, Lee YH, Kwon OY, Chang SI

  • KMID: 1937889
  • Korean J Anat.
  • 1998 Oct;31(5):785-790.
To investigate fragile sites induced by aphidicolin which is a specific inhibitor of eukaryotic DNA polymerase a which is primarily associated with chromosomal DNA replication in human lymphocytes, HaCat cells...
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Chromosome Breakage Test for the Diagnosis of Fanconi's Anemia

Ryang DW, Cho D, Hong WP, Kook H, Hwang TJ

  • KMID: 1863298
  • Korean J Clin Pathol.
  • 1998 Mar;18(1):101-106.
BACKGROUND: Fanconi's anemia (FA) is an autosomal recessive disease characterized by aplastic anemia, pre-malignancy, congenital malformations and chromosome breakage syndromes. As up to 30% of patients have no detectable congenital...
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Chromosomal Abnormalities and p53 Mutation in Metastatic Hepatoblastoma Cell Line (KPH1)

No authors listed

  • KMID: 2146217
  • Korean J Clin Pathol.
  • 1997 Dec;17(6):1157-1175.
BACKGROUND: Hepatoblastoma is the most common primary liver tumor in childhood, mostly occurring at the age of 2. Primary culture of the tumor cells (KPH1-P) was performed from the pleural...
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A Clinical Study of Fanconi's Anemia

Cho SH, Kook H, Kim GM, Yoon WS, Cho TH, Hwang TJ

  • KMID: 2072456
  • Korean J Pediatr Hematol Oncol.
  • 1997 Apr;4(1):70-77.
BACKGROUND: Fanconi's anemia(FA) is an autosomal recessive disease characterized by aplastic anemia and congenital malformations. As up to 30% of patients have no physical stigmata, the modern diagnosis of FA...
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Effect of Radiotherapy on Chromosomal Aberration in Cancer Patients

Chun H, Lee MZ, Yoo MS

  • KMID: 2196899
  • J Korean Soc Ther Radiol.
  • 1993 Jun;11(1):43-50.
We evaluated frequency and types of chromosomal aberrations by ionizing radiation in cancer patients treated with radiotherapy in our institution. Twenty-five patients with various types of carcinomas such as lung,...
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Effects of Nickel Compounds on Sister Chromatid Exchanges and Chromosome Aberrations in Human Cultured Lymphocytes

Hwang ID, Ki NS, Lee JS, Lee SK

  • KMID: 2027835
  • Korean J Occup Environ Med.
  • 1989 Feb;1(1):46-51.
Nickel is a carcinogen in nickel refinery workers. Few chromosome studies have been performed on nickel toxicity. Therefore, this study was performed to investigate cytogenetic toxicity of nickel in human...
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An Effect of benzene on Chromosomes in Bone Marrow Cells of Rats

Kim KH, Oh SH, Shin TS

The toxic action of benzene on erythropoiesis and myelopciesis, has been recognized since the early years of the present century. With the advance in high civilization and modern covenience, benzene...
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