961 resultados para Browne, Edward, d.1730.


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Signed: T.R.

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Mode of access: Internet.

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Title-pages of v. 3-4 read "A history of Persian literature".

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Mode of access: Internet.

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Added t.p.: The book of common prayer ... according to the use of the United Church of England and Ireland ... Cambridge : C.J. Clay, 1866.

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Front Row: John C. Smith, Theodore C. Reissing, Richard D. Hanley, Cyrus C. Hopkins, Anthony Tashnick, Carl T. Woolley, Peter H. Fries

Middle Row: Thomas W. Prunk, M. Allen Maten, Jr., Myril Kaplan, Brian L. Browne, Edward R. Pongracz, Jim Tanner, E. Lee Fitzhugh.

Back Row: diving coach Bruce Harlan, head coach Gus Stager, manager Ray Haselby, Tony A. Turner, Edward W. Cole, Richard J. Kimball, Alvaro Gaxiola, Theodore Pong.

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Genome-wide association studies (GWAS) have identified 76 variants associated with prostate cancer risk predominantly in populations of European ancestry. To identify additional susceptibility loci for this common cancer, we conducted a meta-analysis of > 10 million SNPs in 43,303 prostate cancer cases and 43,737 controls from studies in populations of European, African, Japanese and Latino ancestry. Twenty-three new susceptibility loci were identified at association P < 5 × 10(-8); 15 variants were identified among men of European ancestry, 7 were identified in multi-ancestry analyses and 1 was associated with early-onset prostate cancer. These 23 variants, in combination with known prostate cancer risk variants, explain 33% of the familial risk for this disease in European-ancestry populations. These findings provide new regions for investigation into the pathogenesis of prostate cancer and demonstrate the usefulness of combining ancestrally diverse populations to discover risk loci for disease.

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Human somatic angiotensin I-converting enzyme (ACE), a zinc-dependent dipeptidyl carboxypeptidase, is central to the regulation of the renin-angiotensin aldosterone system. It is a well-known target for combating hypertension and related cardiovascular diseases. In a recent study by Bhuyan and Mugesh [Org. Biomol. Chem. (2011) 9, 1356-1365], it was shown that the selenium analogues of captopril (a well-known clinical inhibitor of ACE) not only inhibit ACE, but also protect against peroxynitrite-mediated nitration of peptides and proteins. Here, we report the crystal structures of human testis ACE (tACE) and a homologue of ACE, known as AnCE, from Drosophila melanogaster in complex with the most promising selenium analogue of captopril (SeCap) determined at 2.4 and 2.35 angstrom resolution, respectively. The inhibitor binds at the active site of tACE and AnCE in an analogous fashion to that observed for captopril and provide the first examples of a protein-selenolate interaction. These new structures of tACE-SeCap and AnCE-SeCap inhibitor complexes presented here provide important information for further exploration of zinc coordinating selenium-based ACE inhibitor pharmacophores with significant antioxidant activity.