ExLibris header image
SFX Logo
Title: Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans
Source:

Human Molecular Genetics [0964-6906] 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. Eckardt, Kai-Uwe U. "Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management-A KDIGO consensus report." Kidney international 88.4 (2015): 676-683. Link to SFX for this item
2. Kirchhoff, K. "Susceptibility loci associated with prostate cancer progression and mortality." Clinical cancer research 16.10 (2010): 2819-2832. Link to SFX for this item
3. Platz, Elizabeth A. "Polymorphisms influencing prostate-specific antigen concentration may bias genome-wide association studies on prostate cancer." Cancer epidemiology, biomarkers & prevention 24.1 (2015): 88-93. Link to SFX for this item
4. Padmanabhan, S. "Uromodulin, an Emerging Novel Pathway for Blood Pressure Regulation and Hypertension." Hypertension 64.5 (2014): 918-923. Link to SFX for this item
5. Firoozifar, M. "Shiraz guideline for the management of patients with brain death." International journal of organ transplantation medicine 5.1 (2014): 34-7. Link to Full Text for this item Link to SFX for this item
6. Woolf, Adrian S. "Genetics of human congenital urinary bladder disease." Pediatric nephrology 29.3 (2013): 1-8. Link to SFX for this item
7. Han, J. "Common genetic variants of the human uromodulin gene regulate transcription and predict plasma uric acid levels." Kidney international 83.4 (2013): 733-740. Link to SFX for this item
8. Mitsui, Hiroyoshi n. "Two distinct mechanisms of augmented antitumor activity by modulation of immunostimulatory/inhibitory signals." Clinical cancer research 16.10 (2010): 2781-2791. Link to SFX for this item
9. Stadler, Zsofia K. "Absence of genomic BRCA1 and BRCA2 rearrangements in Ashkenazi breast and ovarian cancer families." Breast Cancer Research and Treatment 123.2 (2010): 1-5. Link to Full Text for this item Link to SFX for this item
10. Michos, O. "Kidney development: from ureteric bud formation to branching morphogenesis." Current opinion in genetics & development 19.5 (2009): 484-490. Link to SFX for this item
11. Middeldorp, A. "Enrichment of Low Penetrance Susceptibility Loci in a Dutch Familial Colorectal Cancer Cohort." Cancer epidemiology biomarkers & prevention (2009): 3062-3067. Link to SFX for this item
12. Chen, F. "Genetic and developmental basis for urinary tract obstruction." Pediatric nephrology 24.9 (2008): 1621-32. Link to SFX for this item
13. Costantini, F. "Patterning a complex organ: branching morphogenesis and nephron segmentation in kidney development." Developmental cell 18.5 (2010): 698-712. Link to SFX for this item
14. Shah, Mita M M. "Branching morphogenesis and kidney disease." Development 131.7 (2004): 1449-62. Link to SFX for this item
15. Farren, Matthew R. "The Exportin-1 Inhibitor Selinexor Exerts Superior Antitumor Activity when Combined with T-Cell Checkpoint Inhibitors." Molecular cancer therapeutics 16.3 (2017): 417-427. Link to SFX for this item
16. Falck, John R. "14,15-Epoxyeicosa-5,8,11-trienoic Acid (14,15-EET) Surrogates: Carboxylate Modifications." Journal of medicinal chemistry 57.16 (2014): 6965-6972. Link to Full Text for this item Link to SFX for this item
17. Takeuchi, F. "Genetic impact on uric acid concentration and hyperuricemia in the Japanese population." Journal of Atherosclerosis and Thrombosis 20.4 (2013): 351-367. Link to SFX for this item
18. Jelakovic, B. "Consensus statement on screening, diagnosis, classification and treatment of endemic (Balkan) nephropathy." Nephrology, Dialysis, Transplantation 29.11 (2013): 2020-7. Link to SFX for this item
19. Pickering, Matthew C. "C3 glomerulopathy: consensus report." Kidney international 84.6 (2013): 1079-1089. Link to SFX for this item
20. Richer, J. "R179H mutation in ACTA2 expanding the phenotype to include prune-belly sequence and skin manifestations." American journal of medical genetics. Part A 158A.3 (2012): 664-668. Link to SFX for this item
View More...
View Less...
Select All Clear All

Expand list of advanced services Advanced