Identification of differentially expressed circular RNAs in HeLa cells infected with Chlamydia trachomatis
Published 2019 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Identification of differentially expressed circular RNAs in HeLa cells infected with Chlamydia trachomatis
Authors
Keywords
-
Journal
Pathogens and Disease
Volume 77, Issue 7, Pages -
Publisher
Oxford University Press (OUP)
Online
2019-10-28
DOI
10.1093/femspd/ftz062
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Screening differential circular RNA expression profiles reveal that hsa_circ_0128298 is a biomarker in the diagnosis and prognosis of hepatocellular carcinoma
- (2018) Dawei Chen et al. Cancer Management and Research
- Chlamydia trachomatis paralyses neutrophils to evade the host innate immune response
- (2018) Karthika Rajeeve et al. Nature Microbiology
- Acquisition of Rab11 and Rab11-Fip2—A novel strategy for Chlamydia pneumoniae early survival
- (2017) Katja Mölleken et al. PLoS Pathogens
- Circular RNA Expression Profile of Pancreatic Ductal Adenocarcinoma Revealed by Microarray
- (2016) Haimin Li et al. CELLULAR PHYSIOLOGY AND BIOCHEMISTRY
- Comprehensive profile of differentially expressed circular RNAs reveals that hsa_circ_0000069 is upregulated and promotes cell proliferation, migration, and invasion in colorectal cancer
- (2016) Jia-ni Guo et al. OncoTargets and Therapy
- The Circular RNA Cdr1as Act as an Oncogene in Hepatocellular Carcinoma through Targeting miR-7 Expression
- (2016) Lei Yu et al. PLoS One
- Circular RNA: A new star of noncoding RNAs
- (2015) Shibin Qu et al. CANCER LETTERS
- Murine MicroRNA-214 regulates intracellular adhesion molecule (ICAM1) gene expression in genitalChlamydia muridaruminfection
- (2015) Tanvi Arkatkar et al. IMMUNOLOGY
- Identification of Plasmid-Free Chlamydia muridarum Organisms Using a Pgp3 Detection-Based Immunofluorescence Assay
- (2015) Chaoqun Chen et al. JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY
- Regulation of circRNA biogenesis
- (2015) Ling-Ling Chen et al. RNA Biology
- Plasmid-Encoded Pgp3 Is a Major Virulence Factor for Chlamydia muridarum To Induce Hydrosalpinx in Mice
- (2014) Yuanjun Liu et al. INFECTION AND IMMUNITY
- Chlamydia inhibit host cell apoptosis by inducing Bag-1 via the MAPK/ERK survival pathway
- (2013) Du Kun et al. APOPTOSIS
- Transformation of Chlamydia muridarum Reveals a Role for Pgp5 in Suppression of Plasmid-Dependent Gene Expression
- (2013) Y. Liu et al. JOURNAL OF BACTERIOLOGY
- Natural RNA circles function as efficient microRNA sponges
- (2013) Thomas B. Hansen et al. NATURE
- pORF5 plasmid protein of Chlamydia trachomatis induces MAPK-mediated pro-inflammatory cytokines via TLR2 activation in THP-1 cells
- (2013) Hui Zhou et al. Science China-Life Sciences
- Conjunctival MicroRNA Expression in Inflammatory Trachomatous Scarring
- (2013) Tamsyn Derrick et al. PLoS Neglected Tropical Diseases
- Circular RNA (circRNA) in Alzheimer's disease (AD)
- (2013) Walter J. Lukiw Frontiers in Genetics
- Rab11 proteins in health and disease
- (2012) Eoin E. Kelly et al. BIOCHEMICAL SOCIETY TRANSACTIONS
- Rab11-Family of Interacting Protein 2 associates with chlamydial inclusions through its Rab-binding domain and promotes bacterial multiplication
- (2012) Natalia Leiva et al. CELLULAR MICROBIOLOGY
- Chlamydia trachomatis protein GrgA activates transcription by contacting the nonconserved region of 66
- (2012) X. Bao et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- A live-attenuated chlamydial vaccine protects against trachoma in nonhuman primates
- (2011) Laszlo Kari et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Rab6 and Rab11 Regulate Chlamydia trachomatis Development and Golgin-84-Dependent Golgi Fragmentation
- (2009) Anette Rejman Lipinski et al. PLoS Pathogens
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started