- Determination of angiotensin I-converting enzyme activity in equine blood: lack of agreement between methods of analysis
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Costa MF, Carmona AK, Alves MF, Ryan TM, Davies HM, Anderson G, Slocombe R
- KMID: 1067333
- J Vet Sci.
- 2011 Mar;12(1):21-25.
- doi: 10.4142/jvs.2011.12.1.21
Angiotensin-I converting enzyme (ACE) is a key regulator of blood pressure, electrolytes and fluid homeostasis through conversion of angiotensin I into angiotensin II. Recently, a genetic polymorphism of the ACE... -
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- Characterization of Two Novel mAbs Recognizing Different Epitopes on CD43
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Kim S, Hong JW, Cho WD, Moon YR, Yoon SS, Kim MY, Hong KP, Lee YM, Yi JH, Ham YJ, Rah HC, Kim SR, Song HG
- KMID: 2168028
- Immune Netw.
- 2014 Jun;14(3):164-170.
- doi: 10.4110/in.2014.14.3.164
JL1, a specific epitope on CD43, is a potential biomarker for the diagnosis of acute leukemia. Although qualitative assays for detecting leukemia-specific CD43 exist, there is a need to develop... -
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- Genetic and Biochemical Characterization of Monokaryotic Progeny Strains of Button Mushroom (Agaricus bisporus)
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Kwon HW, Choi MA, Yun YH, Oh YL, Kong WS, Kim SH
- KMID: 2312798
- Mycobiology.
- 2015 Mar;43(1):81-86.
- doi: 10.5941/MYCO.2015.43.1.81
To promote the selection of promising monokaryotic strains of button mushroom (Agaricus bisporus) during breeding, 61 progeny strains derived from basidiospores of two different lines of dikaryotic parental strains, ASI1038... -
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- Use of Tandem Mass Spectrometry for Newborn Screening of 6 Lysosomal Storage Disorders in a Korean Population
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Han M, Jun SH, Song SH, Park KU, Kim JQ, Song J
- KMID: 1781688
- Korean J Lab Med.
- 2011 Oct;31(4):250-256.
- doi: 10.3343/kjlm.2011.31.4.250
BACKGROUND: We evaluated the performance of multiplex tandem mass spectrometry (MS/MS) in newborn screening for detection of 6 lysosomal storage disorders (LSDs), namely, Niemann-Pick A/B, Krabbe, Gaucher, Fabry, and Pompe... -
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- Identification and Characterization of Fungi Contaminated in the Built-In Furniture of an Apartment Home
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Choi MA, Ahn GR, Kim SH
- KMID: 2470175
- Mycobiology.
- 2019 Dec;47(4):430-440.
- doi: 10.1080/12298093.2019.1703529
Fungal contamination of built-in furniture is a frequent problem in Korea when new apartment is built. However, domestic information on the contaminating fungi is very limited. This study was conducted... -
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- Ascorbate Oxidase Minimizes Interference by High-Concentration Ascorbic Acid in Total Cholesterol Assays
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Nah H, Yim J, Lee SG, Lim JB, Kim JH
- KMID: 2373524
- Ann Lab Med.
- 2016 Mar;36(2):188-190.
- doi: 10.3343/alm.2016.36.2.188
No abstract available. -
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- A Case of Metachromatic Leukodystrophy Confirmed by Molecular Genetic Analysis
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Lee JH, Min KB, Lee YM, Kang HC, Lee JS, Kim HD
- KMID: 2329492
- J Korean Child Neurol Soc.
- 2011 Dec;19(3):272-276.
Metachromatic leukodystrophy (MLD) is the rare neurometabolic disease caused by the deficiency of the enzyme arylsulfatase A resulting in a deficiency of sulfatide degradation and the target gene is ARSA... -
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- Ultrastructural Changes in Skeletal Muscle of Infants with Mitochondrial Respiratory Chain Complex I Defects
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Mun JY, Jung MK, Kim SH, Eom S, Han SS, Lee YM
- KMID: 2392131
- J Clin Neurol.
- 2017 Oct;13(4):359-365.
- doi: 10.3988/jcn.2017.13.4.359
BACKGROUND AND PURPOSE: The pathogenesis of mitochondrial disease (MD) involves the disruption of cellular energy metabolism, which results from defects in the mitochondrial respiratory chain complex (MRC). We investigated whether... -
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- Electrocardiography as an early cardiac screening test in children with mitochondrial disease
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Baik R, Chae JH, Lee YM, Kang HC, Lee JS, Kim HD
- KMID: 2042068
- Korean J Pediatr.
- 2010 May;53(5):644-647.
- doi: 10.3345/kjp.2010.53.5.644
PURPOSE: To evaluate myocardial conductivity to understand cardiac involvement in patients with mitochondrial disease. METHODS: We performed retrospective study on fifty-seven nonspecific mitochondrial encephalopathy patients with no clinical cardiac manifestations. The... -
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- Salivary alpha-amylase as a stress biomarker in diseased dogs
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Hong HR, Oh YI, Kim YJ, Seo KW
- KMID: 2464092
- J Vet Sci.
- 2019 Sep;20(5):e46.
- doi: 10.4142/jvs.2019.20.e46
Salivary alpha-amylase (sAA) is a stress biomarker in human diseases, but there are no reports of sAA measurements in diseased dogs. This study measured the sAA and serum alpha-amylase (AA)... -
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- Sucrase to Lactase Activities Ratio in Duodenal Mucosa as a Diagnostic Method of Lactase Deficiency
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Kim BG, Kim SM, Kim YS, Moon SH, Lee KL, Jung HC, Song IS, Kim CY
- KMID: 2084725
- Korean J Gastroenterol.
- 1997 Feb;29(2):175-181.
BACKGROUND/AIMS: Jejunal biopsy with direct quantitative analysis of mucosal enzyme activities is the standard diagnostic method of lactase deficiency. But this test is seldom used in the clinical setting, because... -
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- A Case of Glycogen Storage Disease Type Ia Confirmed by Biopsy and Enzyme Assay
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Kim PK, Jeong HJ, Kim MJ, Rho KS, Meen SA, Park YN
- KMID: 2098747
- J Korean Soc Pediatr Nephrol.
- 1998 May;2(1):77-81.
A case of multiple myeloma with massive pleural effusion is reported. A 53 year-old previous known multiple myeloma patient vistited our hospital complaining of cough with sputum. Radiologic study revealed... -
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- Zellweger Syndrome : First Confirmed Neonatal Case in Korea
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Kim SS, An YH, Chang YS, Jin DK, Park WS, Lee MH, Kim JW, Yoon HK, Kim BK
- KMID: 1606284
- J Korean Pediatr Soc.
- 2001 Jun;44(6):694-698.
We describe below a case of Zellweger syndrome case with facial dysmorphism, profound hypotonia, and hepatomegaly. He died at the age of 2 months. Zellweger syndrome is a disease marked... -
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- A Case of Tay-Sachs Disease in Korea Diagnosed by Enzyme Assay and DNA Analysis
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Jin HS, Choi JH, Yoo HW
- KMID: 2279500
- Korean J Pediatr.
- 2004 Dec;47(12):1360-1363.
Tay-Sachs disease is an autosomal recessive, neurodegenerative disorder that results from excessive storage of the cell membrane glycolipid, and GM2 ganglioside within the lysosomes of cells. This disease is caused... -
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- A case of mucolipidosis II presenting with prenatal skeletal dysplasia and severe secondary hyperparathyroidism at birth
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Heo JS, Choi KY, Sohn SH, Kim C, Kim YJ, Shin SH, Lee JM, Lee J, Sohn JA, Lim BC, Lee JA, Choi CW, Kim EK, Kim HS, Kim BI, Choi JH
- KMID: 1781706
- Korean J Pediatr.
- 2012 Nov;55(11):438-444.
- doi: 10.3345/kjp.2012.55.11.438
Mucolipidosis II (ML II) or inclusion cell disease (I-cell disease) is a rarely occurring autosomal recessive lysosomal enzyme-targeting disease. This disease is usually found to occur in individuals aged between... -
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- Analysis of Usefulness of Biochemical Enzyme Assay and MR Spectroscopy(MRS) in Leigh Syndrome
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Choi BH, Robinson B, Kim JH, Kim HM, Choi CK, Yoo HW, Ko TS
- KMID: 2177130
- J Korean Child Neurol Soc.
- 1998 May;5(2):319-327.
PURPOSE: Leigh syndrome is a kind of mitochondrial disease with a pathological production of lactate and variable clinical manifestations. Recently biochemical assay of the mitochondrial enzyme activity and MRS are... -
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- Nerve Conduction Studies in the Patients with Mucopolysaccharidoses
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Kim SY, Kim HS, Lee KW, Hwang JH, Lee YT, Jung ST, Lee MH, Jin DK
- KMID: 2323673
- J Korean Acad Rehabil Med.
- 2001 Oct;25(5):791-794.
OBJECTIVE: To evaluate the characteristics of peripheral nervous system involvement in patients with mucopolysaccharidoses (MPS). METHOD: Electrophysiologic studies were performed in 26 children with MPS confirmed by semiquantitative MPS study,... -
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- Anti-Apoptotic Effect of Rheum undulatum Water Extract in Pancreatic beta-cell Line, HIT-T15
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Yoon SH, Hong MS, Chung JH, Chung SH
- KMID: 1517037
- Korean J Physiol Pharmacol.
- 2004 Feb;8(1):51-55.
Sopungsungi-won has been used as a traditional medicine for diabetes and it has been proved to be a potential remedy for type 2 diabetes mellitus. We previously reported that water... -
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- The Effects of Sorbic Acid, All-trans-retinoic Acid StructuralAnalog, on Retinoids Metabolism in Squamous Cell CarcinomaAMC-HN-6 Cell Line
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Choi JH, Chung EC, Sung KJ, Moon KC, Koh JK, Kim SY, Han IS
- KMID: 2303339
- Korean J Dermatol.
- 1999 Aug;37(8):992-1000.
BACKGROUND: All-trans-retinoic acid metabolism by cytochrome P450 is one of the major mechanisms that can regulate the level of retinoids in cells. Therefore, enhanced metabolism of all-trans retinoic acid by... -
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- Clinical, Biochemical, and Genetic Characterization of Glycogen Storage Type IX in a Child with Asymptomatic Hepatomegaly
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Kim JA, Kim JH, Lee BH, Kim GH, Shin YS, Yoo HW, Kim KM
- KMID: 2315562
- Pediatr Gastroenterol Hepatol Nutr.
- 2015 Jun;18(2):138-143.
- doi: 10.5223/pghn.2015.18.2.138
Glycogen storage disease type IX (GSD IX) is caused by a defect in phosphorylase b kinase (PhK) that results from mutations in the PHKA2, PHKB, and PHKG2 genes. Patients usually... -
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