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Items: 1 to 20 of 23

1.
LncRNA SNHG14 silencing attenuates the progression of diabetic nephropathy via the miR‐30e‐5p/SOX4 axis
YunXia Wang, JiaJia Yang, Chun Wu, Yuqin Guo, Yuan Ding, Xiujuan Zou
J Diabetes. 2024 Jun; 16(6): e13565. Published online 2024 May 16. doi: 10.1111/1753-0407.13565
PMCID:
PMC11096814
AbstractArticlePDF–32M
2.
LncRNA SNHG14 activates autophagy via regulating miR-493-5p/Mef2c axis to alleviate osteoporosis progression
Jingbo Xue, Lulu Liu, Hao Liu, Zepeng Li
Commun Biol. 2023; 6: 1120. Published online 2023 Nov 4. doi: 10.1038/s42003-023-05493-8
PMCID:
PMC10625635
AbstractArticlePDF–2.9M
3.
Analysis of SNHG14: A Long Non-Coding RNA Hosting SNORD116, Whose Loss Contributes to Prader–Willi Syndrome Etiology
Shadi Ariyanfar, Deborah J. Good
Genes (Basel) 2023 Jan; 14(1): 97. Published online 2022 Dec 29. doi: 10.3390/genes14010097
PMCID:
PMC9858946
AbstractArticlePDF–3.4M
4.
CRISPR/Cas9 directed to the Ube3a antisense transcript improves Angelman syndrome phenotype in mice
Ralf S. Schmid, Xuefeng Deng, Priyalakshmi Panikker, Msema Msackyi, Camilo Breton, James M. Wilson
J Clin Invest. 2021 Mar 1; 131(5): e142574. Published online 2021 Mar 1. doi: 10.1172/JCI142574
PMCID:
PMC7919720
AbstractArticlePDF–2.8M
5.
SP1‐induced SNHG14 aggravates hypertrophic response in in vitro model of cardiac hypertrophy via up‐regulation of PCDH17
Yadong Long, Lin Wang, Zhiqiang Li
J Cell Mol Med. 2020 Jul; 24(13): 7115–7126. Published online 2020 May 21. doi: 10.1111/jcmm.15073
PMCID:
PMC7339172
AbstractArticlePDF–2.4M
6.
Dopaminergic neuron injury in Parkinson’s disease is mitigated by interfering lncRNA SNHG14 expression to regulate the miR-133b/ α-synuclein pathway
Li-Min Zhang, Meng-Han Wang, He-Cheng Yang, Tian Tian, Gui-Fang Sun, Yang-Fei Ji, Wen-Tao Hu, Xi Liu, Jian-Ping Wang, Hong Lu
Aging (Albany NY) 2019 Nov 15; 11(21): 9264–9279. Published online 2019 Nov 4. doi: 10.18632/aging.102330
PMCID:
PMC6874444
AbstractArticlePDF–6.4M
7.
Widespread and dynamic translational control of red blood cell development
Juan R. Alvarez-Dominguez, Xu Zhang, Wenqian Hu
Blood. 2017 Feb 2; 129(5): 619–629. Prepublished online 2016 Nov 29. doi: 10.1182/blood-2016-09-741835
PMCID:
PMC5290990
AbstractArticle
8.
Global discovery of erythroid long noncoding RNAs reveals novel regulators of red cell maturation
Juan R. Alvarez-Dominguez, Wenqian Hu, Bingbing Yuan, Jiahai Shi, Staphany S. Park, Austin A. Gromatzky, Alexander van Oudenaarden, Harvey F. Lodish
Blood. 2014 Jan 23; 123(4): 570–581. Prepublished online 2013 Nov 7. doi: 10.1182/blood-2013-10-530683
PMCID:
PMC3901070
AbstractArticle
9.
Truncation of Ube3a-ATS Unsilences Paternal Ube3a and Ameliorates Behavioral Defects in the Angelman Syndrome Mouse Model
Linyan Meng, Richard Erwin Person, Wei Huang, Ping Jun Zhu, Mauro Costa-Mattioli, Arthur L. Beaudet
PLoS Genet. 2013 Dec; 9(12): e1004039. Published online 2013 Dec 26. doi: 10.1371/journal.pgen.1004039
PMCID:
PMC3873245
AbstractArticlePDF–5.7M
10.
Ube3a-ATS is an atypical RNA polymerase II transcript that represses the paternal expression of Ube3a
Linyan Meng, Richard E. Person, Arthur L. Beaudet
Hum Mol Genet. 2012 Jul 1; 21(13): 3001–3012. Published online 2012 Apr 5. doi: 10.1093/hmg/dds130
PMCID:
PMC3465693
AbstractArticlePDF–559K
11.
Topoisomerase inhibitors unsilence the dormant allele of Ube3a in neurons
Hsien-Sung Huang, John A. Allen, Angela M. Mabb, Ian F. King, JayaLakshmi Miriyala, Bonnie Taylor-Blake, Noah Sciaky, J. Walter Dutton, Jr, Hyeong-Min Lee, Xin Chen, Jian Jin, Arlene S. Bridges, Mark J. Zylka, Bryan L. Roth, Benjamin D. Philpot
Nature. Author manuscript; available in PMC 2012 Jul 12.
Published in final edited form as: Nature. 2012 Jan 12; 481(7380): 185–189. Published online 2011 Dec 21. doi: 10.1038/nature10726
PMCID:
PMC3257422
AbstractArticlePDF–1.3M
12.
Global deficits in development, function, and gene expression in the endocrine pancreas in a deletion mouse model of Prader-Willi syndrome
Mihaela Stefan, Rebecca A. Simmons, Suzanne Bertera, Massimo Trucco, Farzad Esni, Peter Drain, Robert D. Nicholls
Am J Physiol Endocrinol Metab. 2011 May; 300(5): E909–E922. Published online 2011 Feb 22. doi: 10.1152/ajpendo.00185.2010
PMCID:
PMC3093973
AbstractArticle
13.
Highly parallel SNP genotyping reveals high-resolution landscape of mono-allelic Ube3a expression associated with locus-wide antisense transcription
Koji Numata, Chihiro Kohama, Kuniya Abe, Hidenori Kiyosawa
Nucleic Acids Res. 2011 Apr; 39(7): 2649–2657. Published online 2010 Dec 3. doi: 10.1093/nar/gkq1201
PMCID:
PMC3074135
AbstractArticlePDF–4.4M
14.
Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size
Karen N. Leung, Roxanne O. Vallero, Amanda J. DuBose, James L. Resnick, Janine M. LaSalle
Hum Mol Genet. 2009 Nov 15; 18(22): 4227–4238. Published online 2009 Aug 5. doi: 10.1093/hmg/ddp373
PMCID:
PMC2766290
AbstractArticlePDF–443K
15.
Loss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT2CR-mediated behaviour
Christine M. Doe, Dinko Relkovic, Alastair S. Garfield, Jeffrey W. Dalley, David E.H. Theobald, Trevor Humby, Lawrence S. Wilkinson, Anthony R. Isles
Hum Mol Genet. 2009 Jun 15; 18(12): 2140–2148. Published online 2009 Mar 20. doi: 10.1093/hmg/ddp137
PMCID:
PMC2685753
AbstractArticlePDF–267K
16.
Deletion of the MBII-85 snoRNA Gene Cluster in Mice Results in Postnatal Growth Retardation
Boris V Skryabin, Leonid V Gubar, Birte Seeger, Jana Pfeiffer, Sergej Handel, Thomas Robeck, Elena Karpova, Timofey S Rozhdestvensky, Jürgen Brosius
PLoS Genet. 2007 Dec; 3(12): e235. Published online 2007 Dec 28. doi: 10.1371/journal.pgen.0030235
PMCID:
PMC2323313
AbstractArticlePDF–695K
17.
SnoRNA Snord116 (Pwcr1/MBII-85) Deletion Causes Growth Deficiency and Hyperphagia in Mice
Feng Ding, Hong Hua Li, Shengwen Zhang, Nicola M. Solomon, Sally A. Camper, Pinchas Cohen, Uta Francke
PLoS One. 2008; 3(3): e1709. Published online 2008 Mar 5. doi: 10.1371/journal.pone.0001709
PMCID:
PMC2248623
AbstractArticlePDF–1.6M
18.
Small Evolutionarily Conserved RNA, Resembling C/D Box Small Nucleolar RNA, Is Transcribed from PWCR1, a Novel Imprinted Gene in the Prader-Willi Deletion Region, Which Is Highly Expressed in Brain
Tala de los Santos, Johannes Schweizer, Christian A. Rees, Uta Francke
Am J Hum Genet. 2000 Nov; 67(5): 1067–1082. Published online 2000 Sep 26. doi: 10.1086/303106
PMCID:
PMC1288549
AbstractArticlePDF–2.2M
19.
Regulation of the large (∼1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn
Miguel Landers, Daria L. Bancescu, Elodie Le Meur, Claire Rougeulle, Heather Glatt-Deeley, Camilynn Brannan, Françoise Muscatelli, Marc Lalande
Nucleic Acids Res. 2004; 32(11): 3480–3492. Published online 2004 Jun 29. doi: 10.1093/nar/gkh670
PMCID:
PMC443545
AbstractArticlePDF–853K
20.
RIKEN Integrated Sequence Analysis (RISA) System—384-Format Sequencing Pipeline with 384 Multicapillary Sequencer
Kazuhiro Shibata, Masayoshi Itoh, Katsunori Aizawa, Sumiharu Nagaoka, Nobuya Sasaki, Piero Carninci, Hideaki Konno, Junichi Akiyama, Katsuo Nishi, Tokuji Kitsunai, Hideo Tashiro, Mari Itoh, Noriko Sumi, Yoshiyuki Ishii, Shin Nakamura, Makoto Hazama, Tsutomu Nishine, Akira Harada, Rintaro Yamamoto, Hiroyuki Matsumoto, Sumito Sakaguchi, Takashi Ikegami, Katsuya Kashiwagi, Syuji Fujiwake, Kouji Inoue, Yoshiyuki Togawa, Masaki Izawa, Eiji Ohara, Masanori Watahiki, Yuko Yoneda, Tomokazu Ishikawa, Kaori Ozawa, Takumi Tanaka, Shuji Matsuura, Jun Kawai, Yasushi Okazaki, Masami Muramatsu, Yorinao Inoue, Akira Kira, Yoshihide Hayashizaki
Genome Res. 2000 Nov; 10(11): 1757–1771. doi: 10.1101/gr.152600
PMCID:
PMC310992
AbstractArticlePDF–3.4M

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