scholarly journals Transcriptional Regulation of Human GD3 Synthase (hST8Sia I) by Fenretinide in Human Neuroblastoma SH-SY-5Y Cells

2010 ◽  
Vol 20 (9) ◽  
pp. 1332-1338
Author(s):  
Nam-Young Kang ◽  
Haw-Young Kwon ◽  
Young-Choon Lee
2013 ◽  
Vol 46 (1) ◽  
pp. 65-71 ◽  
Author(s):  
J.-S. Baik ◽  
K.-S. Kim ◽  
H.-I. Moon ◽  
H.-K. An ◽  
S.-J. Park ◽  
...  

2008 ◽  
Vol 29 (9) ◽  
pp. 999-1005 ◽  
Author(s):  
Haw-young KWON ◽  
Nam-young KANG ◽  
Hyun-mi DAE ◽  
Kyoung-sook KIM ◽  
Cheorl-ho KIM ◽  
...  

1992 ◽  
Vol 12 (5) ◽  
pp. 2193-2202
Author(s):  
M Taiji ◽  
K Taiji ◽  
K L Deyerle ◽  
M Bothwell

The human neuroblastoma cell line CHP100 provides a useful model system in which to study the molecular mechanisms of transcriptional regulation of the low-affinity nerve growth factor receptor (NGFR) gene during neuronal development. Basic fibroblast growth factor (bFGF) induced morphological changes in CHP100 cells, including flattening of cell bodies and neurite outgrowth. bFGF also increased p75NGFR immunoreactivity, as assessed by immunocytochemistry, and increased p75NGFR mRNA levels, as assessed by Northern (RNA) blot analysis. A chimeric gene consisting of 6.7 kb of the 5'-flanking region of the human NGFR gene linked to the chloramphenicol acetyltransferase gene was constructed. In stable transformants of CHP100 cells, 10 ng of bFGF per ml induced an eightfold increase in chloramphenicol acetyltransferase activity. These results indicate that upstream elements of the NGFR gene mediate transcriptional regulation by bFGF.


2008 ◽  
Vol 27 (1) ◽  
pp. 113-118 ◽  
Author(s):  
Haw-Young Kwon ◽  
Hyun-Mi Dae ◽  
Na-Ri Song ◽  
Kyoung-Sook Kim ◽  
Cheorl-Ho Kim ◽  
...  

2020 ◽  
Vol 100 (12) ◽  
pp. 1551-1563
Author(s):  
Ikumi Kitazono ◽  
Taiji Hamada ◽  
Takuya Yoshimura ◽  
Mari Kirishima ◽  
Seiya Yokoyama ◽  
...  

1992 ◽  
Vol 12 (5) ◽  
pp. 2193-2202 ◽  
Author(s):  
M Taiji ◽  
K Taiji ◽  
K L Deyerle ◽  
M Bothwell

The human neuroblastoma cell line CHP100 provides a useful model system in which to study the molecular mechanisms of transcriptional regulation of the low-affinity nerve growth factor receptor (NGFR) gene during neuronal development. Basic fibroblast growth factor (bFGF) induced morphological changes in CHP100 cells, including flattening of cell bodies and neurite outgrowth. bFGF also increased p75NGFR immunoreactivity, as assessed by immunocytochemistry, and increased p75NGFR mRNA levels, as assessed by Northern (RNA) blot analysis. A chimeric gene consisting of 6.7 kb of the 5'-flanking region of the human NGFR gene linked to the chloramphenicol acetyltransferase gene was constructed. In stable transformants of CHP100 cells, 10 ng of bFGF per ml induced an eightfold increase in chloramphenicol acetyltransferase activity. These results indicate that upstream elements of the NGFR gene mediate transcriptional regulation by bFGF.


2003 ◽  
Vol 85 (4) ◽  
pp. 957-968 ◽  
Author(s):  
Melisa J. Baptista ◽  
Casey O'Farrell ◽  
Sneha Daya ◽  
Rili Ahmad ◽  
David W. Miller ◽  
...  

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