- The molecular mechanism for nuclear transport and its application
-
Kim YH, Han ME, Oh SO
- KMID: 2451231
- Anat Cell Biol.
- 2017 Jun;50(2):77-85.
- doi: 10.5115/acb.2017.50.2.77
Transportation between the cytoplasm and the nucleoplasm is critical for many physiological and pathophysiological processes including gene expression, signal transduction, and oncogenesis. So, the molecular mechanism for the transportation needs... -
- CITED
-
- Close
- SHARE
-
- Close
- Impaired Nucleoporins Are Present in Sporadic Amyotrophic Lateral Sclerosis Motor Neurons that Exhibit Mislocalization of the 43-kDa TAR DNA-Binding Protein
-
Aizawa H, Yamashita , Kato H, Kimura T, Kwak S
- KMID: 2451146
- J Clin Neurol.
- 2019 Jan;15(1):62-67.
- doi: 10.3988/jcn.2019.15.1.62
BACKGROUND AND PURPOSE: Disruption of nucleoporins has been reported in the motor neurons of patients with sporadic amyotrophic lateral sclerosis (sALS). However, the precise changes in the morphology of nucleoporins... -
- CITED
-
- Close
- SHARE
-
- Close
- Survive or thrive: tradeoff strategy for cellular senescence
-
Park SC
- KMID: 2386962
- Exp Mol Med.
- 2017 Jun;49(6):e342.
- doi: 10.1038/emm.2017.94
Aging-dependent cellular behaviors toward extrinsic stress are characterized by the confined localization of certain molecules to either nuclear or perinuclear regions. Although most growth factors can activate downstream signaling in... -
- CITED
-
- Close
- SHARE
-
- Close
- The First Korean Case of Childhood Acute Myeloid Leukemia with Inv(11)(p15q22)/NUP98-DDX10 Rearrangement: A Rare but Recurrent Genetic Abnormality
-
Choi R, Jang MA, Yoo KH, Lee ST, Kim HJ, Kim SH
- KMID: 2129577
- Ann Lab Med.
- 2014 Nov;34(6):478-480.
- doi: 10.3343/alm.2014.34.6.478
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- Tissue-specific expression and subcellular localization of ALADIN, the absence of which causes human triple A syndrome
-
Cho AR, Yang KJ, Bae Y, Bahk YY, Kim E, Lee H, Kim JK, Park W, Rhim H, Choi SY, Imanaka T, Moon S, Yoon J, Yoon SK
- KMID: 756230
- Exp Mol Med.
- 2009 Jun;41(6):381-386.
- doi: 10.3858/emm.2009.41.6.043
Triple A syndrome is a rare genetic disorder caused by mutations in the achalasia-addisonianism-alacrima syndrome (AAAS) gene which encodes a tryptophan aspartic acid (WD) repeat-containing protein named alacrima-achalasia-adrenal insufficiency neurologic... -
- CITED
-
- Close
- SHARE
-
- Close
- Detection of Autoantibodies Against Nucleoporin p62 in Sera of Patients With Primary Biliary Cholangitis
-
Bauer A, Habior A
- KMID: 2431607
- Ann Lab Med.
- 2019 May;39(3):291-298.
- doi: 10.3343/alm.2019.39.3.291
BACKGROUND: Primary biliary cholangitis (PBC) is an autoimmune liver disease characterized by specific autoantibodies. We evaluated the prevalence of autoantibodies against nucleoporin p62 (anti-p62) in PBC patients' sera to determine... -
- CITED
-
- Close
- SHARE
-
- Close
- Microarray Analysis of Gene Expression in Rat Glioma after Ethanol Treatment
-
Lee SH, Oh DY, Han JH, Choi IG, Jeon YW, Lee JN, Lee TK, Jeong JH, Jung KH, Chai YG
- KMID: 2249214
- Korean J Biol Psychiatry.
- 2007 May;14(2):115-121.
Objetives: Identification of target genes for ethanol in neurons is important for understanding its molecular and cellular mechanism of action and the neuropathological changes seen in alcoholics. The purpose of... -
- CITED
-
- Close
- SHARE
-
- Close
