ExLibris header image
SFX Logo
Title: Generation of an epigenetic signature by chronic hypoxia in prostate cells
Source:

Human Molecular Genetics [0964-6906] Watson, J A yr:2009


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. Wu, Z. "Pantothenate Kinase-Associated Neurodegeneration: insights from a Drosophila model." Human Molecular Genetics 18.19 (2009): 3659-3672. Link to SFX for this item
2. Luo, M. "Redox regulation of DNA repair: implications for human health and cancer therapeutic development." Antioxidants & redox signaling 12.11 (2010): 1247-1269. Link to SFX for this item
3. Hsiao, Y. "Ahi1, whose human ortholog is mutated in Joubert syndrome, is required for Rab8a localization, ciliogenesis and vesicle trafficking." Human Molecular Genetics 18.20 (2009): 3926-41. Link to SFX for this item
4. Hurdle, A. "A NOVEL ULTRASOUND-GUIDED PROXIMAL SAPHENOUS NERVE CONDUCTION STUDY." Muscle & nerve 40.4 (2009): 731-731. Link to Full Text for this item Link to SFX for this item
5. Zhong, J.-J. J. "Effect of mixing time on taxoid production using suspension cultures of Taxus chinensis in a centrifugal impeller bioreactor." Journal of bioscience and bioengineering 94.3 (2002): 244-250. Link to Full Text for this item Link to SFX for this item
6. Schneider, S A. "Iron accumulation in syndromes of neurodegeneration with brain iron accumulation 1 and 2 : Causative or consequential?" Journal of Neurology, Neurosurgery and Psychiatry 80.6 (2009): 589-590. Link to SFX for this item
7. Piazza, N. "Multiple measures of functionality exhibit progressive decline in a parallel, stochastic fashion in Drosophila Sod2 null mutants." Biogerontology 10.5 (2009): 637-648. Link to SFX for this item
8. Nagaraj, K. "Pathogenic human L1-CAM mutations reduce the adhesion-dependent activation of EGFR." Human Molecular Genetics 18.20 (2009): 3822-31. Link to SFX for this item
9. Chern, Y. "The A2A adenosine receptor rescues the urea cycle deficiency of Huntington's disease by enhancing the activity of the ubiquitin-proteasome system." Human Molecular Genetics 18.16: 2929-2942. Link to SFX for this item
10. Kuo, Y M M. "Deprivation of pantothenic acid elicits a movement disorder and azoospermia in a mouse model of pantothenate kinase-associated neurodegeneration." Journal of inherited metabolic disease 30.3 (2007): 310-317. Link to Full Text for this item Link to SFX for this item
11. Blessing, H. "Interaction of selenium compounds with zinc finger proteins involved in DNA repair." European journal of biochemistry 271.15 (2004): 3190-9. Link to Full Text for this item Link to SFX for this item
12. Schrer, Orlando D. "Using synthetic DNA interstrand crosslinks to elucidate repair pathways and identify new therapeutic targets for cancer chemotherapy." Cellular and molecular life sciences 67.21 (2010): 3683-3697. Link to Full Text for this item Link to SFX for this item
13. Durackova, Z. "Some current insights into oxidative stress." Physiological Research 59.4 (2009): 459-469. Link to Full Text for this item Link to SFX for this item
14. Inga, J. "A functional genetic study identifies HAND1 mutations in septation defects of the human heart." Human Molecular Genetics 18.19 (2009): 3567-3578. Link to SFX for this item
15. Huang, S.-Y. Y. "Development of a bioreactor operation strategy for L-DOPA production using Stizolobium hassjoo suspension culture." Enzyme and microbial technology 30.6 (2002): 779-791. Link to Full Text for this item Link to SFX for this item
16. Sajc, L. "Bioreactors for plant engineering: an outlook for further research." Biochemical engineering journal 4.2 (2000): 89-99. Link to Full Text for this item Link to SFX for this item
17. Bertram, Kelly L. "Diagnosis of dystonic syndromes-a new eight-question approach." Nature reviews. Neurology 8.5 (2012): 275-283. Link to SFX for this item
18. Schneider, Susanne A. "ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation." Movement disorders 25.8 (2010): 979-84. Link to Full Text for this item Link to SFX for this item
19. Appenzeller, S. "Quantitative Magnetic Resonance Imaging Analyses and Clinical Significance of Hyperintense White Matter Lesions in Systemic Lupus Erythematosus Patients." Annals of neurology 64.6 (2008): 635-643. Link to Full Text for this item Link to SFX for this item
20. van Rooden, Jacobus M. "Motor patterns in Parkinson's disease: A data-driven approach." Movement disorders 24.7 (2009): 1042-1047. Link to Full Text for this item Link to SFX for this item
View More...
View Less...
Select All Clear All

Expand list of advanced services Advanced