Search Results - "FERRARIS, V"

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    The Metabolic Profile of Tumors Depends on Both the Responsible Genetic Lesion and Tissue Type by Yuneva, Mariia O., Fan, Teresa W.M., Allen, Thaddeus D., Higashi, Richard M., Ferraris, Dana V., Tsukamoto, Takashi, Matés, José M., Alonso, Francisco J., Wang, Chunmei, Seo, Youngho, Chen, Xin, Bishop, J. Michael

    Published in Cell metabolism (08-02-2012)
    “…The altered metabolism of tumors has been considered a target for anticancer therapy. However, the relationship between distinct tumor-initiating lesions and…”
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    Recent advances in the discovery of D-amino acid oxidase inhibitors and their therapeutic utility in schizophrenia by Ferraris, Dana V, Tsukamoto, Takashi

    Published in Current pharmaceutical design (2011)
    “…D-amino acid oxidase (DAAO) catalyzes the oxidative metabolism of D-amino acids including D-serine, a full agonist at the allosteric glycine binding site of…”
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    Novel mechanism of inhibition of rat kidney-type glutaminase by bis-2-(5-phenylacetamido-1,2,4-thiadiazol-2-yl)ethyl sulfide (BPTES) by Robinson, Mary M, McBryant, Steven J, Tsukamoto, Takashi, Rojas, Camilo, Ferraris, Dana V, Hamilton, Sean K, Hansen, Jeffrey C, Curthoys, Norman P

    Published in Biochemical journal (15-09-2007)
    “…The release of GA (mitochondrial glutaminase) from neurons following acute ischaemia or during chronic neurodegenerative diseases may contribute to the…”
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    Structure-activity relationships of glutamate carboxypeptidase II (GCPII) inhibitors by Ferraris, D V, Shukla, K, Tsukamoto, T

    Published in Current medicinal chemistry (01-03-2012)
    “…Glutamate carboxypeptidase II (GCPII, EC 3.4.17.21) is a zinc metallopeptidase that hydrolyzes N-acetylaspartylglutamate (NAAG) into N-acetylaspartate (NAA)…”
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    Recent development in the discovery of PARP inhibitors as anticancer agents: a patent update (2016-2020) by Velagapudi, Uday Kiran, Patel, Bhargav A, Shao, Xuwei, Pathak, Sanjai Kumar, Ferraris, Dana V, Talele, Tanaji T

    Published in Expert opinion on therapeutic patents (03-07-2021)
    “…Discovery of small molecules that impede the activity of single-strand DNA repair enzyme, PARP1, has led to four marketed drugs for the treatment of…”
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    Kinetic characterization of ebselen, chelerythrine and apomorphine as glutaminase inhibitors by Thomas, Ajit G., Rojas, Camilo, Tanega, Cordelle, Shen, Min, Simeonov, Anton, Boxer, Matthew B., Auld, Douglas S., Ferraris, Dana V., Tsukamoto, Takashi, Slusher, Barbara S.

    “…•Ebselen, chelerythrine and apomorphine were identified as glutaminase inhibitors.•These had greater affinities and efficiency of inhibition than known…”
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    Activation of the alternative pathway of complement during the acute phase of typical haemolytic uraemic syndrome by Ferraris, J. R., Ferraris, V., Acquier, A. B., Sorroche, P. B., Saez, M. S., Ginaca, A., Mendez, C. F.

    Published in Clinical and experimental immunology (01-07-2015)
    “…Summary Haemolytic uraemic syndrome (HUS) is characterized by haemolytic anaemia, thrombocytopenia and acute renal failure. We studied the activation state of…”
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    D-DOPA Is a Potent, Orally Bioavailable, Allosteric Inhibitor of Glutamate Carboxypeptidase II by Gori, Sadakatali S, Thomas, Ajit G, Pal, Arindom, Wiseman, Robyn, Ferraris, Dana V, Gao, Run-Duo, Wu, Ying, Alt, Jesse, Tsukamoto, Takashi, Slusher, Barbara S, Rais, Rana

    Published in Pharmaceutics (23-09-2022)
    “…Glutamate carboxypeptidase-II (GCPII) is a zinc-dependent metalloenzyme implicated in numerous neurological disorders. The pharmacophoric requirements of…”
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    Inhibition of Glutaminase Preferentially Slows Growth of Glioma Cells with Mutant IDH1 by SELTZER, Meghan J, BENNETT, Bryson D, DANG, Chi V, RIGGINS, Gregory J, JOSHI, Avadhut D, PING GAO, THOMAS, Ajit G, FERRARIS, Dana V, TSUKAMOTO, Takashi, ROJAS, Camilo J, SLUSHER, Barbara S, RABINOWITZ, Joshua D

    Published in Cancer research (Chicago, Ill.) (15-11-2010)
    “…Mutation at the R132 residue of isocitrate dehydrogenase 1 (IDH1), frequently found in gliomas and acute myelogenous leukemia, creates a neoenzyme that…”
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    Synthesis of substituted 5[ H]phenanthridin-6-ones as potent poly(ADP-ribose)polymerase-1 (PARP1) inhibitors by Li, Jia-He, Serdyuk, Larisa, Ferraris, Dana V., Xiao, Ge, Tays, Kevin L., Kletzly, Paul W., Li, Weixing, Lautar, Susan, Zhang, Jie, Kalish, Vincent J.

    Published in Bioorganic & medicinal chemistry letters (09-07-2001)
    “…1-, 2-, 3-, 4-, 8-, or 10-Substituted 5( H)phenanthridin-6-ones were synthesized and found to be potent PARP1 inhibitors. Among the 28 compounds prepared, some…”
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    Isolated and complete traumatic rupture of the pancreas: A case report and a review of the literature by Viti, M, Papis, D, Ferraris, V, Fiori, F, D’Urbano, C

    “…Abstract INTRODUCTION Pancreatic trauma without injuries to other organs is uncommon, as reported in the reviewed literature. Diagnosis of pancreatic trauma…”
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    Operative Outcome And Hospital Cost by Ferraris, Victor A., Ferraris, Suellen P., Singh, Amandeep

    “…Introduction: Because of concern about increasing health care costs, we undertook a study to find patient risk factors associated with increased hospital costs…”
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    δ‑Thiolactones as Prodrugs of Thiol-Based Glutamate Carboxypeptidase II (GCPII) Inhibitors by Ferraris, Dana V, Majer, Pavel, Ni, Chiyou, Slusher, C. Ethan, Rais, Rana, Wu, Ying, Wozniak, Krystyna M, Alt, Jesse, Rojas, Camilo, Slusher, Barbara S, Tsukamoto, Takashi

    Published in Journal of medicinal chemistry (09-01-2014)
    “…δ-Thiolactones derived from thiol-based glutamate carboxypeptidase II (GCPII) inhibitors were evaluated as prodrugs. In rat liver microsomes,…”
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