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miR than meets the eye: Figure 1.
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Zeitschriftentitel: | Genes & Development |
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Personen und Körperschaften: | , |
In: | Genes & Development, 25, 2011, 16, S. 1663-1667 |
Format: | E-Article |
Sprache: | Englisch |
veröffentlicht: |
Cold Spring Harbor Laboratory
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Schlagwörter: |
author_facet |
Sage, Julien Ventura, Andrea Sage, Julien Ventura, Andrea |
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author |
Sage, Julien Ventura, Andrea |
spellingShingle |
Sage, Julien Ventura, Andrea Genes & Development miR than meets the eye: Figure 1. Developmental Biology Genetics |
author_sort |
sage, julien |
spelling |
Sage, Julien Ventura, Andrea 0890-9369 1549-5477 Cold Spring Harbor Laboratory Developmental Biology Genetics http://dx.doi.org/10.1101/gad.17454011 <jats:p>Retinoblastoma is a rare pediatric cancer that has served as a paradigm to investigate the mechanisms of tumorigenesis. In this issue of <jats:italic>Genes & Development</jats:italic>, Conkrite and colleagues (pp. 1734–1745) found high levels of the <jats:italic>miR-17∼92</jats:italic> and <jats:italic>miR-106b-25</jats:italic> microRNAs in primary retinoblastomas and show that overexpression of <jats:italic>miR-17∼92</jats:italic> accelerates retinoblastoma development in mice by promoting proliferation, in part by reducing expression of the cell cycle inhibitor p21. These experiments identify the <jats:italic>RB/miR-17∼92/p21</jats:italic> axis as a critical regulator of retinoblastoma tumorigenesis and potentially many other cancers.</jats:p> miR than meets the eye: Figure 1. Genes & Development |
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10.1101/gad.17454011 |
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Cold Spring Harbor Laboratory, 2011 |
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Cold Spring Harbor Laboratory |
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title |
miR than meets the eye: Figure 1. |
title_unstemmed |
miR than meets the eye: Figure 1. |
title_full |
miR than meets the eye: Figure 1. |
title_fullStr |
miR than meets the eye: Figure 1. |
title_full_unstemmed |
miR than meets the eye: Figure 1. |
title_short |
miR than meets the eye: Figure 1. |
title_sort |
mir than meets the eye: figure 1. |
topic |
Developmental Biology Genetics |
url |
http://dx.doi.org/10.1101/gad.17454011 |
publishDate |
2011 |
physical |
1663-1667 |
description |
<jats:p>Retinoblastoma is a rare pediatric cancer that has served as a paradigm to investigate the mechanisms of tumorigenesis. In this issue of <jats:italic>Genes & Development</jats:italic>, Conkrite and colleagues (pp. 1734–1745) found high levels of the <jats:italic>miR-17∼92</jats:italic> and <jats:italic>miR-106b-25</jats:italic> microRNAs in primary retinoblastomas and show that overexpression of <jats:italic>miR-17∼92</jats:italic> accelerates retinoblastoma development in mice by promoting proliferation, in part by reducing expression of the cell cycle inhibitor p21. These experiments identify the <jats:italic>RB/miR-17∼92/p21</jats:italic> axis as a critical regulator of retinoblastoma tumorigenesis and potentially many other cancers.</jats:p> |
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author | Sage, Julien, Ventura, Andrea |
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container_issue | 16 |
container_start_page | 1663 |
container_title | Genes & Development |
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description | <jats:p>Retinoblastoma is a rare pediatric cancer that has served as a paradigm to investigate the mechanisms of tumorigenesis. In this issue of <jats:italic>Genes & Development</jats:italic>, Conkrite and colleagues (pp. 1734–1745) found high levels of the <jats:italic>miR-17∼92</jats:italic> and <jats:italic>miR-106b-25</jats:italic> microRNAs in primary retinoblastomas and show that overexpression of <jats:italic>miR-17∼92</jats:italic> accelerates retinoblastoma development in mice by promoting proliferation, in part by reducing expression of the cell cycle inhibitor p21. These experiments identify the <jats:italic>RB/miR-17∼92/p21</jats:italic> axis as a critical regulator of retinoblastoma tumorigenesis and potentially many other cancers.</jats:p> |
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imprint | Cold Spring Harbor Laboratory, 2011 |
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institution | DE-L229, DE-D275, DE-Bn3, DE-Brt1, DE-Zwi2, DE-D161, DE-Gla1, DE-Zi4, DE-15, DE-Pl11, DE-Rs1, DE-105, DE-14, DE-Ch1 |
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spelling | Sage, Julien Ventura, Andrea 0890-9369 1549-5477 Cold Spring Harbor Laboratory Developmental Biology Genetics http://dx.doi.org/10.1101/gad.17454011 <jats:p>Retinoblastoma is a rare pediatric cancer that has served as a paradigm to investigate the mechanisms of tumorigenesis. In this issue of <jats:italic>Genes & Development</jats:italic>, Conkrite and colleagues (pp. 1734–1745) found high levels of the <jats:italic>miR-17∼92</jats:italic> and <jats:italic>miR-106b-25</jats:italic> microRNAs in primary retinoblastomas and show that overexpression of <jats:italic>miR-17∼92</jats:italic> accelerates retinoblastoma development in mice by promoting proliferation, in part by reducing expression of the cell cycle inhibitor p21. These experiments identify the <jats:italic>RB/miR-17∼92/p21</jats:italic> axis as a critical regulator of retinoblastoma tumorigenesis and potentially many other cancers.</jats:p> miR than meets the eye: Figure 1. Genes & Development |
spellingShingle | Sage, Julien, Ventura, Andrea, Genes & Development, miR than meets the eye: Figure 1., Developmental Biology, Genetics |
title | miR than meets the eye: Figure 1. |
title_full | miR than meets the eye: Figure 1. |
title_fullStr | miR than meets the eye: Figure 1. |
title_full_unstemmed | miR than meets the eye: Figure 1. |
title_short | miR than meets the eye: Figure 1. |
title_sort | mir than meets the eye: figure 1. |
title_unstemmed | miR than meets the eye: Figure 1. |
topic | Developmental Biology, Genetics |
url | http://dx.doi.org/10.1101/gad.17454011 |