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A Case of Myotonic Dystrophy with Electrolyte Imbalance

Ko WJ, Kim KY, Kim SM, Hong SJ, Lee SH, Song R, Yang HI, Lee YA

Type 1 myotonic dystrophy (DM1) is an autosomal-dominant inherited disorder with a multisystem involvement, caused by an abnormal expansion of the CTG sequence of the dystrophic myotonia protein kinase (DMPK)...
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Alternative splicing in 5'-untranslational region of STK-15 gene, encoding centrosome associated kinase, in breast cancer cell lines

Shin SO, Lee KH, Kim JH, Baek SH, Park JW, Gabrielson EW, Kwon TK

  • KMID: 755098
  • Exp Mol Med.
  • 2000 Dec;32(4):193-196.
Centrosomes maintain genomic stability by establishing the bipolar spindles during cell division and, execute accurate segregation of chromosomes during mitosis. In this study, we have demonstrated that there...
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Molecular cloning of the cDNA of canine homeodomain-interacting protein kinase 2

Lee SY, Chung JY, Shin IS, Choi EW, Hwang CY, Youn HY, Han HR

  • KMID: 1114855
  • J Vet Sci.
  • 2005 Jun;6(2):141-145.
The research of p53 is being conducted to find the mechanisms of tumorigenesis and to treat various cancers. Homeodomain-interacting protein kinase2 (HIPK2) is an important factor to regulate p53 and...
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Distal hereditary motor neuropathy in Korean patients with a small heat shock protein 27 mutation

Chung KW, Kim SB, Cho SY, Hwang SJ, Park SW, Kang SH, Kim J, Yoo JH, Choi BO

Distal hereditary motor neuropathy (dHMN) is a heterogeneous disorder characterized by degeneration of motor nerves in the absence of sensory abnormalities. Recently, mutations in the small heat shock protein 27...
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