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Mapping of the Faded (fe) Gene to a Region between D10mit191 and D10mit44 on Mouse Chromosome 10

Oh SH, Nam Y, Suh JG

The faded mouse is a coat color mutant that shows faded coat color and age-related loss of pigmentation. This mutation is transmitted by an autosomal recessive gene with 100% penetrance....
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A high resolution genetic mapping of the faded (fe) gene to a region between D10mit156 and D10mit193 on mouse chromosome 10

Oh SH, Nam H, Suh JG

The C57BL/6J-fe/fe mouse is a coat color mutant. The coat color of the homozygote mouse becomes progressively lighter with advancing age. The faded gene (fe) of C57BL/6J-fe/fe was mapped in...
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In vivo determination of the gap2 gene promoter activity in Giardia lamblia

Yang HW, Kim J, Yong TS, Park SJ

A shuttle vector for Escherichia coli and Giardia lamblia was modified to produce a reporter plasmid, which monitors the expression of prescribed gene in G. lamblia by measuring its luciferase...
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Duplication and deletion of 21 hydroxylase gene among the normal Korean subjects and in adrenogenital syndrome patients

Jin DK, Beck NS, Oh PS

  • KMID: 1963061
  • J Genet Med.
  • 1997 Sep;1(1):27-32.
Steroid 21 hydroxylase deficiency is a major cause of congenital adrenal hyperplasia(CAH) and is caused by genetic impairment (CYP21B) of this enzyme. In the human genome, CYP21B is located within...
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Genomic Diversity of Helicobacter pylori

Lee WK, Choi SH, Park SG, Choi YJ, Choe MY, Park JW, Jung SA, Byun EY, Song JY, Jung TS, Lee BS, Baik SC, Cho MJ, Youn HS, Ko GH, Kim YS, Park JH, Lee DS, Yoo HS, Ghim SY, Lee KH

  • KMID: 2099312
  • J Korean Soc Microbiol.
  • 1999 Dec;34(6):519-532.
Helicobacter pylori is a causative agent of type B gastritis and plays a central role in the pathogenesis of gastroduodenal ulcer and gastric cancer. To elucidate the host-parasite relationship of...
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Two Cases of Subcutaneous Panniculitis-like T-cell Lymphoma

Chang SE, Lee WS, Lee MW, Sung KJ, Moon KC, Koh JK

  • KMID: 2251033
  • Korean J Dermatol.
  • 2001 Sep;39(9):1037-1040.
Subcutaneous panniculitis-like T-cell lymphoma(SPTCL) is a rare subtype of cutaneous T-cell lymphoma and needs to be differentiated from benign causes of panniculitis and other cutaneous T-cell lymphomas involving subcutis, especially...
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Loss of glucocerebrosidase 1 activity causes lysosomal dysfunction and alpha-synuclein aggregation

Bae EJ, Yang NY, Lee C, Lee HJ, Kim S, Sardi SP, Lee SJ

Lysosomal dysfunction is a common pathological feature of neurodegenerative diseases. GTP-binding protein type A1 (GBA1) encodes beta-glucocerebrosidase 1 (GCase 1), a lysosomal hydrolase. Homozygous mutations in GBA1 cause Gaucher disease,...
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Mycosis Fungoides in Children: Clinical Feature of 14 Patients

Seong JY, Suh KS, Kim ST

  • KMID: 1595174
  • Korean J Dermatol.
  • 2001 Apr;39(4):413-419.
BACKGROUND: Mycosis fungoides(MF) is a representative of cutaneous T cell lymphoma and progresses through clinical stages, such as initial pre-mycotic(macule or patch), plaque, and tumor stage. MF is usually thought...
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Association of Paraoxonase 1 (PON1) polymorphisms with osteoporotic fracture risk in postmenopausal Korean women

Kim BJ, Kim SY, Cho YS, Kim BJ, Han BG, Park EK, Lee SH, Kim HY, Kim GS, Lee JY, Koh JM

There is increasing evidence of a biochemical link between lipid oxidation and bone metabolism. Paraoxonase 1 (PON1) prevents the oxidation of low-density lipoprotein (LDL) and metabolizes biologically active phospholipids in...
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Complete Mitochondrial Genome of Haplorchis taichui and Comparative Analysis with Other Trematodes

Lee D, Choe S, Park H, Jeon HK, Chai JY, Sohn WM, Yong TS, Min DY, Rim HJ, Eom KS

Mitochondrial genomes have been extensively studied for phylogenetic purposes and to investigate intra- and interspecific genetic variations. In recent years, numerous groups have undertaken sequencing of platyhelminth mitochondrial genomes. Haplorchis...
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