- Home
- Publications
- Publication Search
- Publication Details
Title
Helicases and human diseases
Authors
Keywords
-
Journal
Frontiers in Genetics
Volume 6, Issue -, Pages -
Publisher
Frontiers Media SA
Online
2015-02-13
DOI
10.3389/fgene.2015.00039
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- RECQL1 and WRN DNA repair helicases: potential therapeutic targets and proliferative markers against cancers
- (2015) Kazunobu Futami et al. Frontiers in Genetics
- Werner Syndrome-specific induced pluripotent stem cells: recovery of telomere function by reprogramming
- (2015) Akira Shimamoto et al. Frontiers in Genetics
- Truncating and Missense Mutations in IGHMBP2 Cause Charcot-Marie Tooth Disease Type 2
- (2014) Ellen Cottenie et al. AMERICAN JOURNAL OF HUMAN GENETICS
- The level of RECQL1 expression is a prognostic factor for epithelial ovarian cancer
- (2014) Yoko Matsushita et al. Journal of Ovarian Research
- An appraisal of RECQ1 expression in cancer progression
- (2014) Sudha Sharma Frontiers in Genetics
- Dysregulation of antiviral helicase pathways in systemic lupus erythematosus
- (2014) Luciana Oliveira et al. Frontiers in Genetics
- Molecular and cellular functions of the FANCJ DNA helicase defective in cancer and in Fanconi anemia
- (2014) Robert M. Brosh et al. Frontiers in Genetics
- Multiple functions of DDX3 RNA helicase in gene regulation, tumorigenesis, and viral infection
- (2014) Yasuo Ariumi Frontiers in Genetics
- Structural mechanisms of human RecQ helicases WRN and BLM
- (2014) Ken Kitano Frontiers in Genetics
- Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenita
- (2013) Bari J. Ballew et al. HUMAN GENETICS
- MCM4 mutation causes adrenal failure, short stature, and natural killer cell deficiency in humans
- (2012) Claire R. Hughes et al. JOURNAL OF CLINICAL INVESTIGATION
- Unique and important consequences of RECQ1 deficiency in mammalian cells
- (2011) Sudha Sharma et al. CELL CYCLE
- Autoimmune Disease Risk Variant of IFIH1 Is Associated with Increased Sensitivity to IFN- and Serologic Autoimmunity in Lupus Patients
- (2011) T. Robinson et al. JOURNAL OF IMMUNOLOGY
- Warsaw Breakage Syndrome, a Cohesinopathy Associated with Mutations in the XPD Helicase Family Member DDX11/ChlR1
- (2010) Petra van der Lelij et al. AMERICAN JOURNAL OF HUMAN GENETICS
- The RecQ DNA Helicases in DNA Repair
- (2010) Kara A. Bernstein et al. Annual Review of Genetics
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now