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Items: 1 to 20 of 137

1.
Specific expression of lncRNA RP13-650J16.1 and TCONS_00023979 in prostate cancer
Xiaochen Zhou, Qiong Chen, Haolin Wang, Cheng Zhang, Bin Fu, Gongxian Wang
Biosci Rep. 2018 Oct 31; 38(5): BSR20171571. Prepublished online 2018 Oct 2. Published online 2018 Oct 31. doi: 10.1042/BSR20171571
Retraction in:
Biosci Rep. 2024 Feb 29; 44(2): BSR-2017-1571_RET.
PMCID:
PMC6209587
AbstractArticle
2.
Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa.
T. L. Kojis, C. Heinzmann, P. Flodman, J. T. Ngo, R. S. Sparkes, M. A. Spence, J. B. Bateman, J. R. Heckenlively
Am J Hum Genet. 1996 Feb; 58(2): 347–355.
PMCID:
PMC1914553
SummaryPage BrowsePDF–1.2M
3.
A new family linked to the RP13 locus for autosomal dominant retinitis pigmentosa on distal 17p.
E E Tarttelin, C Plant, J Weissenbach, A C Bird, S S Bhattacharya, C F Inglehearn
J Med Genet. 1996 Jun; 33(6): 518–520. doi: 10.1136/jmg.33.6.518
PMCID:
PMC1050642
SummaryPage BrowsePDF–552K
4.
Epigenome-wide scan identifies differentially methylated regions for lung cancer using pre-diagnostic peripheral blood
Naisi Zhao, Mengyuan Ruan, Devin C. Koestler, Jiayun Lu, Carmen J. Marsit, Karl T. Kelsey, Elizabeth A. Platz, Dominique S. Michaud
Epigenetics. 2022; 17(4): 460–472. Published online 2021 May 19. doi: 10.1080/15592294.2021.1923615
PMCID:
PMC8993104
AbstractArticlePDF–653K
5.
Molecular Epidemiology in 591 Italian Probands With Nonsyndromic Retinitis Pigmentosa and Usher Syndrome
Leonardo Colombo, Paolo E. Maltese, Marco Castori, Said El Shamieh, Christina Zeitz, Isabelle Audo, Alessandra Zulian, Carla Marinelli, Sabrina Benedetti, Alisia Costantini, Simone Bressan, Marcella Percio, Paolo Ferri, Andi Abeshi, Matteo Bertelli, Luca Rossetti
Invest Ophthalmol Vis Sci. 2021 Feb; 62(2): 13. Published online 2021 Feb 12. doi: 10.1167/iovs.62.2.13
PMCID:
PMC7884295
AbstractArticlePDF–1.2M
6.
Identification of Long Noncoding RNA Biomarkers for Hepatocellular Carcinoma Using Single-Sample Networks
Xiaoqing Yu, Jingsong Zhang, Rui Yang, Chun Li
Biomed Res Int. 2020; 2020: 8579651. Published online 2020 Nov 14. doi: 10.1155/2020/8579651
PMCID:
PMC7700720
AbstractArticlePDF–1002K
7.
Biallelic RP1-associated retinal dystrophies: Expanding the mutational and clinical spectrum
Rachel M. Huckfeldt, Florin Grigorian, Emily Place, Jason I. Comander, Demetrios Vavvas, Lucy H. Young, Paul Yang, Maria Shurygina, Eric A. Pierce, Mark E. Pennesi
Mol Vis. 2020; 26: 423–433. Published online 2020 Jun 3.
PMCID:
PMC7300197
AbstractArticlePDF–1.0M
8.
In Silico Analysis Identifies Differently Expressed lncRNAs as Novel Biomarkers for the Prognosis of Thyroid Cancer
Yuansheng Rao, Haiying Liu, Xiaojuan Yan, Jianhong Wang
Comput Math Methods Med. 2020; 2020: 3651051. Published online 2020 Apr 23. doi: 10.1155/2020/3651051
PMCID:
PMC7195652
AbstractArticlePDF–4.4M
9.
Application of targeted panel sequencing and whole exome sequencing for 76 Chinese families with retinitis pigmentosa
Handong Dan, Xin Huang, Yiqiao Xing, Yin Shen
Mol Genet Genomic Med. 2020 Mar; 8(3): e1131. Published online 2020 Jan 20. doi: 10.1002/mgg3.1131
PMCID:
PMC7057118
AbstractArticlePDF–1.2M
10.
Selection of housekeeping genes and demonstration of RNAi in cotton leafhopper, Amrasca biguttula biguttula (Ishida)
Satnam Singh, Mridula Gupta, Suneet Pandher, Gurmeet Kaur, Pankaj Rathore, Subba Reddy Palli
PLoS One. 2018; 13(1): e0191116. Published online 2018 Jan 12. doi: 10.1371/journal.pone.0191116
PMCID:
PMC5766320
AbstractArticlePDF–4.3M
11.
Prevalence of Mutations in eyeGENE Probands With a Diagnosis of Autosomal Dominant Retinitis Pigmentosa
Lori S. Sullivan, Sara J. Bowne, Melissa J. Reeves, Delphine Blain, Kerry Goetz, Vida NDifor, Sally Vitez, Xinjing Wang, Santa J. Tumminia, Stephen P. Daiger
Invest Ophthalmol Vis Sci. 2013 Sep; 54(9): 6255–6261. Published online 2013 Sep 19. doi: 10.1167/iovs.13-12605
PMCID:
PMC3778873
AbstractArticlePDF–313K
12.
Prevalence of Disease-Causing Mutations in Families with Autosomal Dominant Retinitis Pigmentosa: A Screen of Known Genes in 200 Families
Lori S. Sullivan, Sara J. Bowne, David G. Birch, Dianna Hughbanks-Wheaton, John R. Heckenlively, Richard Alan Lewis, Charles A. Garcia, Richard S. Ruiz, Susan H. Blanton, Hope Northrup, Anisa I. Gire, Robyn Seaman, Hatice Duzkale, Catherine J. Spellicy, Jingya Zhu, Suma P. Shankar, Stephen P. Daiger
Invest Ophthalmol Vis Sci. Author manuscript; available in PMC 2008 Nov 19.
Published in final edited form as: Invest Ophthalmol Vis Sci. 2006 Jul; 47(7): 3052–3064. doi: 10.1167/iovs.05-1443
PMCID:
PMC2585061
AbstractArticlePDF–424K
13.
Hypoxia-regulated components of the U4/U6.U5 tri-small nuclear riboprotein complex: possible role in autosomal dominant retinitis pigmentosa
Rainald Schmidt-Kastner, Hideo Yamamoto, Duco Hamasaki, Hiroko Yamamoto, Jean-Marie Parel, Christoph Schmitz, C. Kathy Dorey, Janet C. Blanks, Markus N. Preising
Mol Vis. 2008; 14: 125–135. Published online 2008 Jan 25.
PMCID:
PMC2263009
AbstractArticlePDF–365K
14.
Crystal structure of the C-terminal domain of splicing factor Prp8 carrying retinitis pigmentosa mutants
Lingdi Zhang, Jingping Shen, Michael T. Guarnieri, Annie Heroux, Kui Yang, Rui Zhao
Protein Sci. 2007 Jun; 16(6): 1024–1031. doi: 10.1110/ps.072872007
PMCID:
PMC2206663
AbstractArticlePDF–492K
15.
Exclusion of CAG repeat expansion as the cause of disease in autosomal dominant retinitis pigmentosa families.
T J Keen, A G Morris, C F Inglehearn
J Med Genet. 1997 Feb; 34(2): 130–132. doi: 10.1136/jmg.34.2.130
PMCID:
PMC1050866
SummaryPage BrowsePDF–624K
16.
Activities of the Combination of Quinupristin-Dalfopristin with Rifampin In Vitro and in Experimental Endocarditis Due to Staphylococcus aureus Strains with Various Phenotypes of Resistance to Macrolide-Lincosamide-Streptogramin Antibiotics
Virginie Zarrouk, Bülent Bozdogan, Roland Leclercq, Louis Garry, Celine Feger, Claude Carbon, Bruno Fantin
Antimicrob Agents Chemother. 2001 Apr; 45(4): 1244–1248. doi: 10.1128/AAC.45.4.1244-1248.2001
Correction in:
Antimicrob Agents Chemother. 2001 Jun; 45(6): 1941.
PMCID:
PMC90450
AbstractArticlePDF–238K
17.
A Drosophila model to study retinitis pigmentosa pathology associated with mutations in the core splicing factor Prp8
Dimitrije Stanković, Ann-Katrin Claudius, Thomas Schertel, Tina Bresser, Mirka Uhlirova
Dis Model Mech. 2020 Jun 1; 13(6): dmm043174. Published online 2020 Jun 26. doi: 10.1242/dmm.043174
PMCID:
PMC7328144
AbstractArticle
18.
Risk Scores Based on Six Survival-Related RNAs in a Competing Endogenous Network Composed of Differentially Expressed RNAs Between Clear Cell Renal Cell Carcinoma Patients Carrying Wild-Type or Mutant Von Hippel–Lindau Serve Well to Predict Malignancy and Prognosis
Rui Zhu, Xiezhao Li, Zhiduan Cai, Siyang Liang, Yaoji Yuan, Yuyu Xu, Dehui Lai, Haibo Zhao, Weiqing Yang, Jun Bian, Leyuan Liu, Guibin Xu
Front Oncol. 2021; 11: 726671. Published online 2021 Oct 25. doi: 10.3389/fonc.2021.726671
PMCID:
PMC8573174
AbstractArticlePDF–3.2M
19.
Identification of a seven-long non-coding RNA signature associated with Jab1/CSN5 in predicting hepatocellular carcinoma
Weijie Ma, Ye Yao, Gang Xu, Xiaoling Wu, Jinghua Li, Ganggang Wang, Xi Chen, Kunlei Wang, Yirang Chen, Yonghua Guo, Yongsheng Li, Deli Tan, Hui Guo, Zhisu Liu, Yufeng Yuan, Francois X. Claret
Cell Death Discov. 2021; 7: 178. Published online 2021 Jul 10. doi: 10.1038/s41420-021-00560-7
PMCID:
PMC8272716
AbstractArticlePDF–3.9M
20.
Genotype-Phenotype Correlations in RP1-Associated Retinal Dystrophies: A Multi-Center Cohort Study in JAPAN
Kei Mizobuchi, Takaaki Hayashi, Noriko Oishi, Daiki Kubota, Shuhei Kameya, Koichiro Higasa, Takuma Futami, Hiroyuki Kondo, Katsuhiro Hosono, Kentaro Kurata, Yoshihiro Hotta, Kazutoshi Yoshitake, Takeshi Iwata, Tomokazu Matsuura, Tadashi Nakano
J Clin Med. 2021 Jun; 10(11): 2265. Published online 2021 May 24. doi: 10.3390/jcm10112265
PMCID:
PMC8197273
AbstractArticlePDF–2.9M

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