Search Results - "Drake, Fred H."
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1
Human Osteoclast Cathepsin K Is Processed Intracellularly Prior to Attachment and Bone Resorption
Published in Journal of bone and mineral research (01-03-2001)“…Cathepsin K is a member of the papain superfamily of cysteine proteases and has been proposed to play a pivotal role in osteoclast‐mediated bone resorption. We…”
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2
Clinical Immunogenicity of rHuPH20, a Hyaluronidase Enabling Subcutaneous Drug Administration
Published in The AAPS journal (01-09-2015)“…Recombinant human PH20 hyaluronidase (rHuPH20) is used to facilitate dispersion of subcutaneously delivered fluids and drugs. This report summarizes rHuPH20…”
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3
The Collagenolytic Activity of Cathepsin K Is Unique among Mammalian Proteinases
Published in The Journal of biological chemistry (27-11-1998)“…Type I collagen fibers account for 90% of the organic matrix of bone. The degradation of this collagen is a major event during bone resorption, but its…”
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4
The new partnership of genomics and chemistry for accelerated drug development
Published in Current opinion in chemical biology (01-08-1997)“…Genomics and combinatorial chemistry are two methods that are revolutionizing drug discovery efforts. Analysis of gene sequences allows identification of novel…”
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5
Erratum to: Clinical Immunogenicity of rHuPH20, a Hyaluronidase Enabling Subcutaneous Drug Administration
Published in The AAPS journal (01-11-2015)Get full text
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6
Cathepsin K, but Not Cathepsins B, L, or S, Is Abundantly Expressed in Human Osteoclasts (∗)
Published in The Journal of biological chemistry (24-05-1996)“…Random high throughput sequencing of a human osteoclast cDNA library was employed to identify novel osteoclast-expressed genes. Of the 5475 ESTs obtained,…”
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7
Recombinant human hyaluronidase PH20 (rHuPH20) facilitates subcutaneous infusions of large volumes of immunoglobulin in a swine model
Published in Drug delivery and translational research (01-08-2012)“…Many patients with primary immunodeficiency disease (PIDD) require lifelong immunoglobulin (Ig) replacement therapy. Home-based subcutaneous (SC) infusion…”
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8
Peptide Aldehyde Inhibitors of Cathepsin K Inhibit Bone Resorption Both In Vitro and In Vivo
Published in Journal of bone and mineral research (01-09-1997)“…We have shown previously that cathepsin K, a recently identified member of the papain superfamily of cysteine proteases, is expressed selectively in…”
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Biochemical and pharmacological properties of p170 and p180 forms of topoisomerase II
Published in Biochemistry (Easton) (03-10-1989)“…The p170 and p180 forms of topoisomerase II have been compared. The concentration dependence of ATP for catalytic activity of the two forms of the enzyme was…”
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10
Mitoxantrone resistance in HL-60 leukemia cells: reduced nuclear topoisomerase II catalytic activity and drug-induced DNA cleavage in association with reduced expression of the topoisomerase II .beta. isoform
Published in Biochemistry (Easton) (15-10-1991)“…Mitoxantrone-resistant variants of the human HL-60 leukemia cell line are cross-resistant to several natural product and synthetic antineoplastic agents. The…”
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11
Design and characterization of orally active Arg-Gly-Asp peptidomimetic vitronectin receptor antagonist SB 265123 for prevention of bone loss in osteoporosis
Published in The Journal of pharmacology and experimental therapeutics (01-11-1999)“…The Arg-Gly-Asp (RGD)-binding integrin alpha(V)beta(3) is highly expressed on osteoclasts and has been proposed to mediate cell-matrix adhesion required for…”
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12
In vitro and intracellular inhibition of topoisomerase II by the antitumor agent merbarone
Published in Cancer research (Chicago, Ill.) (15-05-1989)“…Merbarone has previously been shown to have antitumor activity of unknown mechanism in P388 and L1210 tumor models (A. D. Brewer et al., Biochem. Pharmacol.,…”
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13
Localization of DNA topoisomerase II in Chinese hamster fibroblasts by confocal and electron microscopy
Published in Experimental cell research (01-01-1993)“…The localization of the 170- and the 180-kDa isoforms of the enzyme DNA topoisomerase II in growing Chinese hamster fibroblasts has been studied by confocal…”
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14
Proteolytic Activity of Human Osteoclast Cathepsin K
Published in The Journal of biological chemistry (24-05-1996)“…Human cathepsin K is a recently identified protein with high primary sequence homology to members of the papain cysteine protease superfamily including…”
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15
Proteolytic activity of human osteoclast cathepsin K. Expression, purification, activation, and substrate identification
Published in The Journal of biological chemistry (24-05-1996)“…Human cathepsin K is a recently identified protein with high primary sequence homology to members of the papain cysteine protease superfamily including…”
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16
Design of Potent and Selective Human Cathepsin K Inhibitors that Span the Active Site
Published in Proceedings of the National Academy of Sciences - PNAS (23-12-1997)“…Potent and selective active-site-spanning inhibitors have been designed for cathepsin K, a cysteine protease unique to osteoclasts. They act by mechanisms that…”
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17
DNA Topoisomerase IIα is the Major Chromosome Protein Recognized by the Mitotic Phosphoprotein Antibody MPM-2
Published in Proceedings of the National Academy of Sciences - PNAS (15-09-1993)“…We have determined that the major mitotic phosphoprotein in chromosomes recognized by the anti-phosphoprotein antibody MPM-2 is the 170-kDa isoform of…”
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18
Characterization and Immunological Identification of cDNA Clones Encoding Two Human DNA Topoisomerase II Isozymes
Published in Proceedings of the National Academy of Sciences - PNAS (01-12-1989)“…Several DNA topoisomerase II (Topo II; EC 5.99.1.3) partial cDNA clones obtained from a human Raji-HN2 cDNA library were sequenced and two classes of…”
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19
Probably, but More Information Is Forthcoming
Published in Journal of bone and mineral research (01-02-1998)Get full text
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Orally bioavailable nonpeptide vitronectin receptor antagonists with efficacy in an osteoporosis model
Published in Bioorganic & medicinal chemistry letters (05-07-1999)“…A new series of potent nonpeptide vitronectin receptor antagonists, based on a novel carbocyclic Gly-Asp mimetic, has been discovered. A representative of this…”
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