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Items: 1 to 20 of 21

1.
miR-328-3p Affects Axial Length Via Multiple Routes and Anti-miR-328-3p Possesses a Potential to Control Myopia Progression
Chung-Ling Liang, Ku-Chung Chen, Edward Hsi, Jui-Yu Lin, Chien-Yuan Chen, Jung-Kai Tseng, Suh-Hang H. Juo
Invest Ophthalmol Vis Sci. 2022 Nov; 63(12): 11. Published online 2022 Nov 9. doi: 10.1167/iovs.63.12.11
PMCID:
PMC9652717
AbstractArticlePDF–3.0M
2.
MicroRNA miR-328 Regulates Zonation Morphogenesis by Targeting CD44 Expression
Chia-Hui Wang, Daniel Y. Lee, Zhaoqun Deng, Zina Jeyapalan, Shao-Chen Lee, Shireen Kahai, Wei-Yang Lu, Yaou Zhang, Burton B. Yang
PLoS One. 2008; 3(6): e2420. Published online 2008 Jun 18. doi: 10.1371/journal.pone.0002420
PMCID:
PMC2409976
AbstractArticlePDF–1.2M
3.
Long noncoding RNA Glis2 regulates podocyte mitochondrial dysfunction and apoptosis in diabetic nephropathy via sponging miR‐328‐5p
Ting Wang, Yanxia Chen, Zhihong Liu, Jing Zhou, Na Li, Yue Shan, Yinxi He
J Cell Mol Med. 2024 Apr; 28(7): e18204. Published online 2024 Mar 20. doi: 10.1111/jcmm.18204
PMCID:
PMC10951868
AbstractArticlePDF–18M
4.
Long Non-Coding RNA TUG1 Attenuates Insulin Resistance in Mice with Gestational Diabetes Mellitus via Regulation of the MicroRNA-328-3p/SREBP-2/ERK Axis
Xuwen Tang, Qingxin Qin, Wenjing Xu, Xuezhen Zhang
Diabetes Metab J. 2023 Mar; 47(2): 267–286. Published online 2023 Jan 19. doi: 10.4093/dmj.2021.0216
PMCID:
PMC10040623
AbstractArticlePDF–4.6M
5.
Long Noncoding RNA-Maternally Expressed Gene 3 Contributes to Hypoxic Pulmonary Hypertension
Yan Xing, Xiaodong Zheng, Yao Fu, Jing Qi, Minghui Li, Mingfei Ma, Shuang Wang, Shuzhen Li, Daling Zhu
Mol Ther. 2019 Dec 4; 27(12): 2166–2181. Published online 2019 Aug 22. doi: 10.1016/j.ymthe.2019.07.022
Correction in:
Mol Ther. 2022 Jan 5; 30(1): 501.
PMCID:
PMC6904813
AbstractArticlePDF–4.3M
6.
Genome-Wide Analysis of Differentially Expressed miRNAs and Their Associated Regulatory Networks in Lenses Deficient for the Congenital Cataract-Linked Tudor Domain Containing Protein TDRD7
Deepti Anand, Salma Al Saai, Sanjaya K. Shrestha, Carrie E. Barnum, Shinichiro Chuma, Salil A. Lachke
Front Cell Dev Biol. 2021; 9: 615761. Published online 2021 Feb 16. doi: 10.3389/fcell.2021.615761
PMCID:
PMC7921330
AbstractArticlePDF–6.7M
7.
miR-328 Functions as an RNA Decoy to Modulate hnRNP E2 Regulation of mRNA Translation in Leukemic Blasts
Anna M. Eiring, Jason G. Harb, Paolo Neviani, Christopher Garton, Joshua J. Oaks, Riccardo Spizzo, Shujun Liu, Sebastian Schwind, Ramasamy Santhanam, Christopher J. Hickey, Heiko Becker, Jason C. Chandler, Raul Andino, Jorge Cortes, Peter Hokland, Claudia S. Huettner, Ravi Bhatia, Denis C. Roy, Stephen A. Liebhaber, Michael A. Caligiuri, Guido Marcucci, Ramiro Garzon, Carlo M. Croce, George A. Calin, Danilo Perrotti
Cell. Author manuscript; available in PMC 2010 Aug 20.
Published in final edited form as: Cell. 2010 Mar 5; 140(5): 652–665. doi: 10.1016/j.cell.2010.01.007
PMCID:
PMC2924756
AbstractArticlePDF–3.7M
8.
Fibroblast Growth Factor 9 Regulation by MicroRNAs Controls Lung Development and Links DICER1 Loss to the Pathogenesis of Pleuropulmonary Blastoma
Yongjun Yin, Angela M. Castro, Marrit Hoekstra, Thomas J. Yan, Ajay C. Kanakamedala, Louis P. Dehner, D. Ashley Hill, David M. Ornitz
PLoS Genet. 2015 May; 11(5): e1005242. Published online 2015 May 15. doi: 10.1371/journal.pgen.1005242
PMCID:
PMC4433140
AbstractArticlePDF–19M
9.
Regulation of mouse stomach development and Barx1 expression by specific microRNAs
Byeong-Moo Kim, Janghee Woo, Chryssa Kanellopoulou, Ramesh A. Shivdasani
Development. 2011 Mar 15; 138(6): 1081–1086. doi: 10.1242/dev.056317
PMCID:
PMC3042866
AbstractArticle
10.
miR-17 family of microRNAs controls FGF10-mediated embryonic lung epithelial branching morphogenesis through MAPK14 and STAT3 regulation of E-Cadherin distribution
Gianni Carraro, Ahmed El-Hashash, Diego Guidolin, Caterina Tiozzo, Gianluca Turcatel, Brittany M. Young, Stijn P. De Langhe, Saverio Bellusci, Wei Shi, Pier Paolo Parnigotto, David Warburton
Dev Biol. Author manuscript; available in PMC 2010 Sep 15.
Published in final edited form as: Dev Biol. 2009 Sep 15; 333(2): 238–250. Published online 2009 Jun 25. doi: 10.1016/j.ydbio.2009.06.020
PMCID:
PMC2735610
AbstractArticlePDF–4.8M
11.
Identification of many microRNAs that copurify with polyribosomes in mammalian neurons
John Kim, Anna Krichevsky, Yonatan Grad, Gabriel D. Hayes, Kenneth S. Kosik, George M. Church, Gary Ruvkun
Proc Natl Acad Sci U S A. 2004 Jan 6; 101(1): 360–365. Published online 2003 Dec 22. doi: 10.1073/pnas.2333854100
PMCID:
PMC314190
AbstractArticlePDF–461K
12.
Profiling of T helper cell-derived small RNAs reveals unique antisense transcripts and differential association of miRNAs with argonaute proteins 1 and 2
Sumanth Polikepahad, David B. Corry
Nucleic Acids Res. 2013 Jan; 41(2): 1164–1177. Published online 2012 Nov 25. doi: 10.1093/nar/gks1098
PMCID:
PMC3553939
AbstractArticlePDF–873K
13.
miR-26a and miR-384-5p are required for LTP maintenance and spine enlargement
Qin-Hua Gu, Danni Yu, Zhonghua Hu, Xing Liu, Yanqin Yang, Yan Luo, Jun Zhu, Zheng Li
Nat Commun. 2015 Apr 10; 6: 6789. Published online 2015 Apr 10. doi: 10.1038/ncomms7789
PMCID:
PMC4403380
AbstractArticlePDF–4.4M
14.
A resource of vectors and ES cells for targeted deletion of microRNAs in mice
Haydn M. Prosser, Hiroko Koike-Yusa, James D. Cooper, Frances C. Law, Allan Bradley
Nat Biotechnol. Author manuscript; available in PMC 2012 Mar 1.
Published in final edited form as: Nat Biotechnol. 2011 Aug 7; 29(9): 840–845. Published online 2011 Aug 7. doi: 10.1038/nbt.1929
PMCID:
PMC3242032
AbstractArticlePDF–2.6M
15.
Maternal microRNAs are essential for mouse zygotic development
Fuchou Tang, Masahiro Kaneda, Dónal O’Carroll, Petra Hajkova, Sheila C. Barton, Y. Andrew Sun, Caroline Lee, Alexander Tarakhovsky, Kaiqin Lao, M. Azim Surani
Genes Dev. 2007 Mar 15; 21(6): 644–648. doi: 10.1101/gad.418707
PMCID:
PMC1820938
AbstractArticlePDF–433K
16.
MicroRNA transcriptome in the newborn mouse ovaries determined by massive parallel sequencing
Hyo Won Ahn, Ryan D. Morin, Han Zhao, Ronald A. Harris, Cristian Coarfa, Zi-Jiang Chen, Aleksandar Milosavljevic, Marco A. Marra, Aleksandar Rajkovic
Mol Hum Reprod. 2010 Jul; 16(7): 463–471. Published online 2010 Mar 9. doi: 10.1093/molehr/gaq017
PMCID:
PMC2882868
AbstractArticlePDF–392K
17.
Mammalian microRNAs: experimental evaluation of novel and previously annotated genes
H. Rosaria Chiang, Lori W. Schoenfeld, J. Graham Ruby, Vincent C. Auyeung, Noah Spies, Daehyun Baek, Wendy K. Johnston, Carsten Russ, Shujun Luo, Joshua E. Babiarz, Robert Blelloch, Gary P. Schroth, Chad Nusbaum, David P. Bartel
Genes Dev. 2010 May 15; 24(10): 992–1009. doi: 10.1101/gad.1884710
PMCID:
PMC2867214
AbstractArticlePDF–2.2M
18.
A Mammalian microRNA Expression Atlas Based on Small RNA Library Sequencing
Pablo Landgraf, Mirabela Rusu, Robert Sheridan, Alain Sewer, Nicola Iovino, Alexei Aravin, Sébastien Pfeffer, Amanda Rice, Alice O. Kamphorst, Markus Landthaler, Carolina Lin, Nicholas D. Socci, Leandro Hermida, Valerio Fulci, Sabina Chiaretti, Robin Foà, Julia Schliwka, Uta Fuchs, Astrid Novosel, Roman-Ulrich Müller, Bernhard Schermer, Ute Bissels, Jason Inman, Quang Phan, Minchen Chien, David B. Weir, Ruchi Choksi, Gabriella De Vita, Daniela Frezzetti, Hans-Ingo Trompeter, Veit Hornung, Grace Teng, Gunther Hartmann, Miklos Palkovits, Roberto Di Lauro, Peter Wernet, Giuseppe Macino, Charles E. Rogler, James W. Nagle, Jingyue Ju, F. Nina Papavasiliou, Thomas Benzing, Peter Lichter, Wayne Tam, Michael J. Brownstein, Andreas Bosio, Arndt Borkhardt, James J. Russo, Chris Sander, Mihaela Zavolan, Thomas Tuschl
Cell. Author manuscript; available in PMC 2009 May 13.
Published in final edited form as: Cell. 2007 Jun 29; 129(7): 1401–1414. doi: 10.1016/j.cell.2007.04.040
PMCID:
PMC2681231
AbstractArticlePDF–2.5M
19.
miRBase: integrating microRNA annotation and deep-sequencing data
Ana Kozomara, Sam Griffiths-Jones
Nucleic Acids Res. 2011 Jan; 39(Database issue): D152–D157. Published online 2010 Oct 30. doi: 10.1093/nar/gkq1027
PMCID:
PMC3013655
AbstractArticlePDF–5.1M
20.
A High-Resolution Anatomical Atlas of the Transcriptome in the Mouse Embryo
Graciana Diez-Roux, Sandro Banfi, Marc Sultan, Lars Geffers, Santosh Anand, David Rozado, Alon Magen, Elena Canidio, Massimiliano Pagani, Ivana Peluso, Nathalie Lin-Marq, Muriel Koch, Marchesa Bilio, Immacolata Cantiello, Roberta Verde, Cristian De Masi, Salvatore A. Bianchi, Juliette Cicchini, Elodie Perroud, Shprese Mehmeti, Emilie Dagand, Sabine Schrinner, Asja Nürnberger, Katja Schmidt, Katja Metz, Christina Zwingmann, Norbert Brieske, Cindy Springer, Ana Martinez Hernandez, Sarah Herzog, Frauke Grabbe, Cornelia Sieverding, Barbara Fischer, Kathrin Schrader, Maren Brockmeyer, Sarah Dettmer, Christin Helbig, Violaine Alunni, Marie-Annick Battaini, Carole Mura, Charlotte N. Henrichsen, Raquel Garcia-Lopez, Diego Echevarria, Eduardo Puelles, Elena Garcia-Calero, Stefan Kruse, Markus Uhr, Christine Kauck, Guangjie Feng, Nestor Milyaev, Chuang Kee Ong, Lalit Kumar, MeiSze Lam, Colin A. Semple, Attila Gyenesei, Stefan Mundlos, Uwe Radelof, Hans Lehrach, Paolo Sarmientos, Alexandre Reymond, Duncan R. Davidson, Pascal Dollé, Stylianos E. Antonarakis, Marie-Laure Yaspo, Salvador Martinez, Richard A. Baldock, Gregor Eichele, Andrea Ballabio
PLoS Biol. 2011 Jan; 9(1): e1000582. Published online 2011 Jan 18. doi: 10.1371/journal.pbio.1000582
PMCID:
PMC3022534
AbstractArticlePDF–3.8M

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