- Spectrin Cleavage Induced by LLP-1 Lentivirus Lytic Peptide Domain in the Intracytoplasmic Tail of Human Immunodeficiency Virus Type 1 GP41 in Rat Organotypic Hippocampal Slice Cultures
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Lee JH, Lee EO, Chong YH
- KMID: 2055033
- J Bacteriol Virol.
- 2006 Dec;36(4):247-254.
- doi: 10.4167/jbv.2006.36.4.247
We previously demonstrated that the lentivirus lytic peptide 1 (LLP-1) corresponding to the carboxyl terminus of HIV-1 gp41 induced cell death in human neuronal cells. Present study was conducted to... -
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- Kinesin Superfamily KIF5 Proteins Bind to betaIII Spectrin
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Paik JE, Kim N, Yea SS, Jang WH, Chung JY, Lee SK, Park YH, Han J, Seog DH
- KMID: 2285302
- Korean J Physiol Pharmacol.
- 2004 Jun;8(3):167-172.
The kinesin proteins (KIFs) make up a large superfamily of molecular motors that transport cargo such as vesicles, protein complexes, and organelles. KIF5 is a heterotetrameric motor that conveys vesicles... -
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- Hereditary Spherocytosis
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Park ES
- KMID: 2049272
- Clin Pediatr Hematol Oncol.
- 2012 Oct;19(2):57-63.
Hereditary spherocytosis is a hemolytic anemia caused by erythrocyte membrane deficiencies that lead to membrane destabilization and vesiculation. Abnormal spherocytes are trapped and destroyed in the spleen. Mutations in several... -
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- Spectrin Tunis (Sp alpha I/78) in a Korean Family with Hereditary Elliptocytosis
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Han E, Kim A, Park J, Kim M, Kim Y, Han K, Kim YJ
- KMID: 1781350
- Ann Lab Med.
- 2013 Sep;33(5):386-389.
- doi: 10.3343/alm.2013.33.5.386
No abstract available. -
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- A Patient Diagnosed with Spinocerebellar Ataxia Type 5 associated with SPTBN2: Case Report
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Hur MW, Ko A, Lee HJ, Lee JS, Kang HC
- KMID: 2392561
- J Korean Child Neurol Soc.
- 2017 Sep;25(3):200-203.
- doi: 10.26815/jkcns.2017.25.3.200
Spinocerebellar ataxias (SCAs) are autosomal dominant neurodegenerative disorders which disrupt the afferent and efferent pathways of the cerebellum that cause cerebellar ataxia. Spectrin beta non-erythrocytic 2 (SPTBN2) gene encodes the... -
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- Abnormalities of erythrocyte membrane proteins in Korean patients with hereditary spherocytosis
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Lee YK, Cho HI, Park SS, Lee YJ, Ra E, Chang YH, Hur M, Shin HY, Ahn HS
- KMID: 1128625
- J Korean Med Sci.
- 2000 Jun;15(3):284-288.
- doi: 10.3346/jkms.2000.15.3.284
Hereditary spherocytosis (HS) is a common inherited erythrocyte membrane disorder characterized by chronic hemolytic anemia. Clinical manifestations and biochemical abnormalities of HS are heterogeneous. In this study, we investigated erythrocyte... -
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- Splenectomy in Hereditary Spherocytosis in Childhood
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Heo YS, Kim CS, Do BS, Suh BY, Hah JO
- KMID: 2352262
- Yeungnam Univ J Med.
- 1994 Jun;11(1):42-48.
- doi: 10.12701/yujm.1994.11.1.42
Among the erythrocyte membrane defects, hereditary spherocytosis is the most common. The erythrocyte membrane defect results from a deficiency of spectrin, the most important structural protein in red cell. Hereditary spherocytosis... -
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- Hypoxia-inducible factor: role in cell survival in superoxide dismutase overexpressing mice after neonatal hypoxia-ischemia
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Jeon GW, Sheldon RA, Ferriero D
- KMID: 2469014
- Korean J Pediatr.
- 2019 Dec;62(12):444-449.
- doi: 10.3345/kjp.2019.00850
BACKGROUND: Sixty percent of infants with severe neonatal hypoxic-ischemic encephalopathy die, while most survivors have permanent disabilities. Treatment for neonatal hypoxic-ischemic encephalopathy is limited to therapeutic hypothermia, but it does... -
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- Associations between Lead Exposure and Dose and Protein Kinase C Activation in Erythrocytes Among Lead Workers
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Hwang KY, Hwangbo Y, Ahn HC, Kim YB, Lee GS, Lee SS, Ahn KD, Lee BK
- KMID: 2028161
- Korean J Occup Environ Med.
- 2001 Dec;13(4):369-375.
OBJECTIVES: Protein kinase C(PKC), a calcium and phospholipid dependent enzyme, is activated by lead in vitro at picomolar concentrations. However, the effect of lead on PKC has never been studied... -
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- Erythrocyte Membrane Protein Alterations by SDS-PAGE and Underlying Clinical Heterogeneity in Hereditary Spherocytosis
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Yoo ES, Choi HS, Shin HY, Ahn HS, Lee YK, Cho HI
- KMID: 1979968
- Korean J Pediatr Hematol Oncol.
- 1997 Oct;4(2):261-272.
BACKGROUND: Hereditary spherocytosis(HS) is a clinically and biochemically very heterogeneous disorder The purpose of this study is to detect erythrocyte membrane protein abnormalities by SDS-PAGE and to investigate the frequency... -
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- Purification of Band 3 from the Human Erythrocyte Membrane and its Incorporation into Liposome
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Kim JR, Kim JH, Lee KY
- KMID: 2373862
- Yeungnam Univ J Med.
- 1986 Dec;3(1):41-48.
- doi: 10.12701/yujm.1986.3.1.41
Band 3, the predominant 95,000 dalton anion transport protein, is the major intrinsic glycoprotein of the human erythrocyte membrane. This anion carrier exists as a dimer and binds the cytoskeletons... -
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- SDS-PAGE Analysis of Red Cell Membrane Proteins in Hereditary Hemolytic Anemia
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Lee YK, Cho HI, Park SS, Ra E, Chang YH, Hur M, Lee YJ, Shin HY, Ahn HS
- KMID: 1533972
- Korean J Hematol.
- 1999 Nov;34(4):559-567.
BACKGROUND: Red cell membrane is a lipid bilayer laminated by the membrane cytoskeleton at the surface of inner monolayer. A class of hemolytic anemia, such as hereditary spherocytosis (HS) or... -
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