Published in Am J Med Genet on December 22, 1999
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Search for imprinted regions on chromosome 14: comparison of maternal and paternal UPD cases with cases of chromosome 14 deletion. Am J Med Genet (2000) 1.36
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Cutaneous photodamage in Koreans: influence of sex, sun exposure, smoking, and skin color. Arch Dermatol (2001) 1.28
DNA rearrangements on both homologues of chromosome 17 in a mildly delayed individual with a family history of autosomal dominant carpal tunnel syndrome. Am J Hum Genet (1999) 1.28
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Circadian rhythm abnormalities of melatonin in Smith-Magenis syndrome. J Med Genet (2000) 1.26
The human homologue of the Drosophila melanogaster flightless-I gene (flil) maps within the Smith-Magenis microdeletion critical region in 17p11.2. Am J Hum Genet (1995) 1.26
Further evidence that CENP-C is a necessary component of active centromeres: studies of a dic(X; 15) with simultaneous immunofluorescence and FISH. Hum Mol Genet (1995) 1.26
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Acid-induced structural changes in human rhinovirus 14: possible role in uncoating. Proc Natl Acad Sci U S A (1992) 1.25
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Activation of multiple effector pathways of immune system by the antineoplastic immunostimulator acidic polysaccharide ginsan isolated from Panax ginseng. Anticancer Res (1997) 1.24
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Evaluation of rapid immunocapture assays for diagnosis of Plasmodium vivax in Korea. Parasitol Res (2001) 1.23
A case of abdominal cocoon. J Korean Med Sci (1995) 1.23
Enhanced solubility and dissolution rate of itraconazole by a solid dispersion technique. Int J Pharm (1999) 1.23
Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11. Am J Hum Genet (1996) 1.23
Evidence for an anaplerotic/malonyl-CoA pathway in pancreatic beta-cell nutrient signaling. Diabetes (1996) 1.22
Obese gene expression alters the ability of 30A5 preadipocytes to respond to lipogenic hormones. J Biol Chem (1996) 1.22
The promise and pitfalls of telomere region-specific probes. Am J Hum Genet (2000) 1.21
Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomy. Am J Med Genet (1999) 1.21
A role for apoptosis in the pathogenesis of AIDS-related idiopathic esophageal ulcers. J Infect Dis (1997) 1.20
Heterogeneity in the processing defect of SLC26A4 mutants. J Med Genet (2008) 1.20
The roles of the red clover necrotic mosaic virus capsid and cell-to-cell movement proteins in systemic infection. Virology (1993) 1.20
Regulatory interaction between the cystic fibrosis transmembrane conductance regulator and HCO3- salvage mechanisms in model systems and the mouse pancreatic duct. J Biol Chem (2001) 1.19
Dephosphorylation of Sp1 by protein phosphatase 1 is involved in the glucose-mediated activation of the acetyl-CoA carboxylase gene. J Biol Chem (1996) 1.19
Exercise diminishes the activity of acetyl-CoA carboxylase in human muscle. Diabetes (2000) 1.18
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Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndrome. Am J Hum Genet (2001) 1.17
Metallic stents in malignant biliary obstruction: prospective long-term clinical results. AJR Am J Roentgenol (1997) 1.17
High current-carrying capability in c-axis-oriented superconducting MgB2 thin films. Phys Rev Lett (2001) 1.16
Glucose regulates acetyl-CoA carboxylase gene expression in a pancreatic beta-cell line (INS-1). J Biol Chem (1993) 1.16
Epigenetic detection of human chromosome 14 uniparental disomy. Hum Mutat (2003) 1.15
Poly(ADP-ribose) polymerase at active centromeres and neocentromeres at metaphase. Hum Mol Genet (2000) 1.15
Structural studies on human rhinovirus 14 drug-resistant compensation mutants. J Mol Biol (1995) 1.15
A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation. Am J Hum Genet (1999) 1.15
Ultraviolet irradiation induces the production of multiple cytokines by human corneal cells. Invest Ophthalmol Vis Sci (1997) 1.15
Population data suggest that deletions of 1p36 are a relatively common chromosome abnormality. Clin Genet (2003) 1.15
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Simultaneous, multilocus FISH analysis for detection of microdeletions in the diagnostic evaluation of developmental delay and mental retardation. Am J Hum Genet (1997) 1.13
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