ExLibris header image
SFX Logo
Title: Use of the HPRT gene to study nuclease-induced DNA double-strand break repair
Source:

Human Molecular Genetics [0964-6906] Gravells, P yr:2015


Collapse list of basic services Basic
Sorry, no full text available...
Please use the document delivery service (see below)  
Holding information
Holdings in library search engine ALBERT GO
Document delivery
Request document via Library/Bibliothek GO
Users interested in this article also expressed an interest in the following:
1. Hira, A. "Mutations in the gene encoding the E2 conjugating enzyme UBE2T cause Fanconi anemia." American journal of human genetics 96.6 (2015): 1001-7. Link to Full Text for this item Link to SFX for this item
2. Whitworth. "A clinical and genetic analysis of multiple primary cancer referrals to genetics services." European Journal of Human Genetics : EJHG 23.5 (2015): 581-7. Link to Full Text for this item Link to SFX for this item
3. Rickman, Kimberly A. "Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia." Cell Reports 12.1 (2015): 35-41. Link to SFX for this item
4. Ellison, G. "A reliable method for the detection of BRCA1 and BRCA2 mutations in fixed tumour tissue utilising multiplex PCR-based targeted next generation sequencing." BMC Clinical Pathology 15.1 (2015): 5-5. Link to Full Text for this item Link to SFX for this item
5. Walden, H. "Structure of the human FANCL RING-Ube2T complex reveals determinants of cognate E3-E2 selection." Structure 22.2 (2014): 337-44. Link to SFX for this item
6. Kelsall, Ian R. "The Fanconi Anaemia Components UBE2T and FANCM Are Functionally Linked to Nucleotide Excision Repair." PLoS ONE 7.5 (2012). Link to Full Text for this item Link to SFX for this item
7. Burghel, George J. "Towards a Next-Generation Sequencing Diagnostic Service for Tumour Genotyping: A Comparison of Panels and Platforms." BioMed Research International 2015 (2015): 1-6. Link to Full Text for this item Link to SFX for this item
8. Gorokhova, S. "Clinical massively parallel sequencing for the diagnosis of myopathies." Revue neurologique 171.6-7 (2015): 558-71. Link to SFX for this item
9. Vrijenhoek, T. "Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects." European journal of human genetics 23.9 (2015): 1142-1150. Link to Full Text for this item Link to SFX for this item
10. Getz, G. "Discovery and saturation analysis of cancer genes across 21 tumour types." Nature 505.7484 (2014): 495-501. Link to Full Text for this item Link to SFX for this item
11. Kutler, D. "A 20-year perspective on the International Fanconi Anemia Registry (IFAR)." Blood 101.4 (2003): 1249-1256. Link to SFX for this item
12. Barrois, M. "Real-time PCR-based gene dosage assay for detecting BRCA1 rearrangements in breast-ovarian cancer families." Clinical genetics 65.2 (2004): 131-6. Link to Full Text for this item Link to SFX for this item
13. Markoulatos, P. "Multiplex polymerase chain reaction: a practical approach." Journal of clinical laboratory analysis 16.1 (2002): 47-51. Link to Full Text for this item Link to SFX for this item
14. Chen, H. "Fanconi anemia pathway defects in inherited and sporadic cancers." Translational Pediatrics 3.4 (2014): 300-304. Link to Full Text for this item Link to SFX for this item
15. Walden, H. "The Fanconi Anemia DNA Repair Pathway: Structural and Functional Insights into a Complex Disorder." Annual review of biophysics 43.1 (2014): 257-278. Link to Full Text for this item Link to SFX for this item
16. Luo, Li Z. "Correction: DNA Repair in Human Pluripotent Stem Cells Is Distinct from That in Non-Pluripotent Human Cells." PLoS ONE (2012). Link to Full Text for this item Link to SFX for this item
17. Castella, M. "Chromosome fragility in patients with Fanconi anaemia: diagnostic implications and clinical impact." Journal of medical genetics 48.4 (2011): 242-250. Link to SFX for this item
18. Alpi, A. "Mechanistic Insight into Site-Restricted Monoubiquitination of FANCD2 by Ube2t, FANCL, and FANCI." Molecular cell 32.6 (2008): 767-777. Link to SFX for this item
View More...
View Less...
Select All Clear All

Expand list of advanced services Advanced
A service provided by the Library of the Wissenschaftspark Albert Einstein, Potsdam, Germany.
© 2005 SFX by Ex Libris Inc.