about
The mitochondrial permeability transition pore: molecular nature and role as a target in cardioprotectionStructural and biochemical characterization of the human cyclophilin family of peptidyl-prolyl isomerasesCharacterization of Peptidyl-Prolyl Cis-Trans Isomerase- and Calmodulin-Binding Activity of a Cytosolic Arabidopsis thaliana Cyclophilin AtCyp19-3Fragment-based discovery of a new family of non-peptidic small-molecule cyclophilin inhibitors with potent antiviral activitiesImplication of cysteine residues in the selection of oxorhenium inhibitors of cyclophilin hCyp18.Melanocytes from Patients Affected by Ullrich Congenital Muscular Dystrophy and Bethlem Myopathy have Dysfunctional Mitochondria That Can be Rescued with Cyclophilin Inhibitors.A calcineurin-independent mechanism of angiogenesis inhibition by a nonimmunosuppressive cyclosporin A analog.Blocking cyclophilins in the chronic phase of asthma reduces the persistence of leukocytes and disease reactivation.Nuclear cyclophilins affect spliceosome assembly and function in vitro.Identification of ER-000444793, a Cyclophilin D-independent inhibitor of mitochondrial permeability transition, using a high-throughput screen in cryopreserved mitochondria.A cell-impermeable cyclosporine A derivative reduces pathology in a mouse model of allergic lung inflammation.Identification of HIV inhibitors guided by free energy perturbation calculations.Cyclophilin D in mitochondrial pathophysiology.Cyclophilin-CD147 interactions: a new target for anti-inflammatory therapeutics.Exploring the role of host cell chaperones/PPIases during cellular up-take of bacterial ADP-ribosylating toxins as basis for novel pharmacological strategies to protect mammalian cells against these virulence factors.Survey of the year 2009: applications of isothermal titration calorimetry.Enhanced molecular dynamics sampling of drug target conformations.Peptidyl-Proline Isomerases (PPIases): Targets for Natural Products and Natural Product-Inspired Compounds.Synthesis of the C21-C34 fragment of antascomicin B.Cyclophilin40 isomerase activity is regulated by a temperature-dependent allosteric interaction with Hsp90.The spliceosomal proteins PPIH and PRPF4 exhibit bi-partite binding.NIM811, a cyclophilin inhibitor without immunosuppressive activity, is beneficial in collagen VI congenital muscular dystrophy models.
P2860
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P2860
description
2009 nî lūn-bûn
@nan
2009 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Isoform-specific inhibition of cyclophilins
@ast
Isoform-specific inhibition of cyclophilins
@en
type
label
Isoform-specific inhibition of cyclophilins
@ast
Isoform-specific inhibition of cyclophilins
@en
prefLabel
Isoform-specific inhibition of cyclophilins
@ast
Isoform-specific inhibition of cyclophilins
@en
P2093
P2860
P356
P1433
P1476
Isoform-specific inhibition of cyclophilins
@en
P2093
Boris Féaux de Lacroix
Fabian Kruska
Manfred Braun
Michael Schumann
Molly A Balsley
Sebastian Daum
Sebastian Mathea
Stephanie L Constant
Tobias Aumüller
P2860
P304
P356
10.1021/BI9007287
P407
P577
2009-07-01T00:00:00Z