- Errol Flynn
- Iterative Anagram Solver
- Multi-Disciplinary Approach to the Study of Chronic Pelvic Pain
- Ronald R. Magness, PHD | Faculty | USF Health
Chronic prostatitis and comorbid non-urological overlapping pain conditions: A co-twin control study. J Psychosom Res. Epub Sep 6.
Brain signature and functional impact of centralized pain: a multidisciplinary approach to the study of chronic pelvic pain MAPP network study. Wolters Kluwer on OvidInsights. Epub Jun Resting-state functional connectivity predicts longitudinal pain symptom change in urologic chronic pelvic pain syndrome: A MAPP Network Study. Brain white matter changes associated with urological chronic pelvic pain syndrome: Multi-site neuroimaging from a MAPP case-control study.
- Recent Publications - Biochemistry and Molecular Biology.
- The Divine Ryans.
- GEO Accession viewer.
- Graduating From Guilt: Six Steps to Overcome Guilt and Reclaim Your Life.
Evidence for the role of mast cells in cystitis-associated lower urinary tract dysfunction: A multidisciplinary approach to the study of chronic pelvic pain research network animal model study. Symptom variability and early symptom regression in the MAPP study, a prospective study of urologic chronic pelvic pain syndrome. Heritability of lower urinary tract symptoms in men: A Twin Study.
Iterative Anagram Solver
Bladder distension increases blood flow in pain-related brain structures in subjects with Interstitial Cystitis. Transgenic mice expressing MCP-1 by the urothelium demonstrate bladder hypersensitivity, pelvic pain and voiding dysfunction: A multidisciplinary approach to the study of chronic pelvic pain research network animal model study. Pain and urinary symptoms should not be combined into a single score: psychometric findings from the MAPP research network.
Inflammation and symptom change in interstitial cystitis or bladder pain syndrome: a multidisciplinary approach to the study of chronic pelvic pain research network study. Schrepf A. Epub Jan 6. Alterations in connectivity on functional magnetic resonance imaging with provocation of lower urinary tract symptoms: a MAPP research network feasibility study of urological chronic pelvic pain syndromes.
Epub Oct Assessment of the lower urinary tract microbiota during symptom flare in women with urologic chronic pelvic pain syndrome: a MAPP Network Study. Epub Sep Multisite, multimodal neuroimaging of chronic urological pelvic pain: methodology of the MAPP research network. Painful bladder filling and painful urgency are distinct characteristics in men and women with urological chronic pelvic pain syndromes: a MAPP research network study.
Epub Jul Brain Behav Immun. Unique microstructural changes in the brain associated with urological chronic pelvic pain syndrome UCPPS revealed by diffusion tensor MRI, super-resolution track density imaging, and statistical parameter mapping: a MAPP Network neuroimaging study. The posterior medial cortex in urologic chronic pelvic pain syndrome: detachment from default mode network. A resting-state study from the MAPP research network. PMC Wolters Kluwer. Epub Feb Urological chronic pelvic pain syndrome flares and their impact: qualitative analysis in the MAPP network.
Int Urogynecol J. Sharma; Weizhong Zheng; Alummoottil V. Joshua; Douglas N. Abrams; Alexander J.
McEwan Synthesis of 4-amino-4,6-androstadiene-3,dione 7 , an analog of formestane used in breast cancer therapy as an aromatase inhibitor, from 4-acetoxyandrostene-3,dione 2 is described. This is the first report of a 4-amino diene 4,6 system in this series of molecules. Compound 7 showed best activity against breast cancer cell line MCF Molecule 7 showed best activity against breast cancer cell line MCF Effect of B-ring substitution pattern on binding mode of propionamide selective androgen receptor modulators by Casey E.
Miller; Charles E. Bell; James T. Dalton Selective androgen receptor modulators SARMs are essentially prostate sparing androgens, which provide therapeutic potential in osteoporosis, male hormone replacement, and muscle wasting. Herein we report crystal structures of the androgen receptor AR ligand-binding domain LBD complexed to a series of potent synthetic nonsteroidal SARMs with a substituted pendant arene referred to as the B-ring.
We found that hydrophilic B-ring para -substituted analogs exhibit an additional region of hydrogen bonding not seen with steroidal compounds and that multiple halogen substitutions affect the B-ring conformation and aromatic interactions with Trp This information elucidates interactions important for high AR binding affinity and provides new insight for structure-based drug design.
The synthesis and SAR of a group of apoptosis inducing 4-aryloxo-2 H -chromenes with modifications at the 4-aryl, 7- and 8-positions is reported. As a continuation of our efforts to discover and develop the apoptosis inducing 4-aryl-4 H -chromenes as potential anticancer agents, we explored the removal of the chiral center at the 4-position and prepared a series of 4-aryloxo-2 H -chromenes. It was found that, in general, removal of the chiral center and replacement of the 2-amino group with a 2-oxo group were tolerated and 4-aryloxo-2 H -chromenes exhibited SAR similar to 4-arylamino-4 H -chromenes.
It was found that an OMe group was preferred at the 7-positon. These 4-aryloxo-2 H -chromenes are a series of potent apoptosis inducers with potential advantage over the 4-arylamino-4 H -chromenes series via elimination of the chiral center at the 4-position. Keywords: Apoptosis inducers; Anticancer agents;.
Multi-Disciplinary Approach to the Study of Chronic Pelvic Pain
It is demonstrated that certain G-quadruplex structures formed by human telomeric repeats could perform site-specific self-cleaving actions. It is demonstrated in our investigations that certain G-quadruplex structures formed by human telomeric repeats could perform self-cleaving actions. Our further studies verify that these reactions are site-specific and undergo hydrolytic pathways.
Keywords: G-quadruplex; Self-cleavage; Telomere;. Serafinowska; Frank E. Blaney; Peter J.
Lovell; Giancarlo G. Merlo; Claire M.
Ronald R. Magness, PHD | Faculty | USF Health
Scott; Paul W. Smith; Kathryn R. Starr; Jeannette M. Watson Compound 13c exhibited potent hypoglycemic and lipid lowering activity and high oral bioavailability. Both compounds were selected as promising candidates for further biological evaluation.
Synthesis, mitochondriotropic behavior, and cytotoxicity of resveratrol-triphenylphosphonium conjugates. They provide a powerful potential tool to intervene on mitochondrial and cellular redox processes of pathophysiological relevance. Synthesis and biological activity of enantiomeric pairs of 5-[ E -cycloalkenylidenemethyl]thiolactomycin congeners by Kohei Ohata; Shiro Terashima While all the synthesized congeners lacked in vitro antibacterial activity, some of the congeners ent - 4b , 5b and ent - 4c were found to exhibit more potent mammalian type I FAS inhibitory activity than S demethylthiolactomycin ent - 2 having an unnatural configuration.
The title congeners were synthesized by employing our efficient synthetic route previously explored for preparing enantiomeric pairs of thiolactomycin and its 3-demethyl derivative. While all the synthesized congeners lacked in vitro antibacterial activity, some of the congeners bearing an E -cycloheptenylidenemethyl or an E -cyclooctenylidenemethyl group were found to exhibit more potent type I FAS inhibitory activity than S demethylthiolactomycin having an unnatural configuration.
Keywords: Antibiotic; Inhibitor of mammalian type I fatty acid synthase; 5-[ E -Cycloalkenylidenemethyl]thiolactomycin;. The optimisation of a series of amides for C5a receptor binding and functional activity, and physicochemical properties is described. Keywords: C5a receptor; Complement; Inflammation; Antagonist;. Attempts to increase the polarity of these compounds through the introduction of basic centres or incorporation into weakly basic heterocycles is described.
Westaway; Mervyn Thompson; Harshad K. Rami; Geoffrey Stemp; Leontine S. Trouw; Darren J. Mitchell; Jon T.