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  1. Book: Economic and social rights after the global financial crisis

    Nolan, Aoife

    2016  

    Author's details Aoife Nolan
    Language English
    Publisher Cambridge Univ Press
    Publishing place S.l.
    Document type Book
    ISBN 1107618428 ; 9781107618428
    Database ECONomics Information System

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  2. Book: Economic and social rights after the global financial crises

    Nolan, Aoife

    2014  

    Author's details ed. by Aoife Nolan
    Keywords Basic needs/Law and legislation ; Economic policy ; Global Financial Crisis, 2008-2009 ; Human rights/Economic aspects ; Social rights
    Language English
    Size XXXIV, 378 S
    Publisher Cambridge Univ. Press
    Publishing place Cambridge
    Document type Book
    Note Includes bibliographical references and index
    ISBN 9781107043251 ; 1107043255
    Database Former special subject collection: coastal and deep sea fishing

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  3. Book: Economic and social rights after the global financial crises

    Nolan, Aoife

    2014  

    Author's details ed. by Aoife Nolan
    Keywords Basic needs/Law and legislation ; Economic policy ; Global Financial Crisis, 2008-2009 ; Human rights/Economic aspects ; Social rights ; Finanzkrise ; Menschenrechte ; Sozialstandards ; Global Governance ; Welt
    Language English
    Size XXXIV, 378 S., graph. Darst.
    Publisher Cambridge Univ. Press
    Publishing place Cambridge
    Document type Book
    Note Enthält 11 Beiträge ; Hier auch später erschienene, unveränderte Nachdrucke ; Includes bibliographical references and index
    ISBN 1107618428 ; 9781107043251 ; 9781107618428 ; 1107043255
    Database ECONomics Information System

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  4. Article: Proteomic Mapping of the Interactome of KRAS Mutants Identifies New Features of RAS Signalling Networks and the Mechanism of Action of Sotorasib.

    Nolan, Aoife / Raso, Cinzia / Kolch, Walter / Kriegsheim, Alex von / Wynne, Kieran / Matallanas, David

    Cancers

    2023  Volume 15, Issue 16

    Abstract: RAS proteins are key regulators of cell signalling and control different cell functions including cell proliferation, differentiation, and cell death. Point mutations in the genes of this family are common, particularly ... ...

    Abstract RAS proteins are key regulators of cell signalling and control different cell functions including cell proliferation, differentiation, and cell death. Point mutations in the genes of this family are common, particularly in
    Language English
    Publishing date 2023-08-17
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2527080-1
    ISSN 2072-6694
    ISSN 2072-6694
    DOI 10.3390/cancers15164141
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Hidden Targets in RAF Signalling Pathways to Block Oncogenic RAS Signalling.

    Nolan, Aoife A / Aboud, Nourhan K / Kolch, Walter / Matallanas, David

    Genes

    2021  Volume 12, Issue 4

    Abstract: Oncogenic RAS (Rat sarcoma) mutations drive more than half of human cancers, and RAS inhibition is the holy grail of oncology. Thirty years of relentless efforts and harsh disappointments have taught us about the intricacies of oncogenic RAS signalling ... ...

    Abstract Oncogenic RAS (Rat sarcoma) mutations drive more than half of human cancers, and RAS inhibition is the holy grail of oncology. Thirty years of relentless efforts and harsh disappointments have taught us about the intricacies of oncogenic RAS signalling that allow us to now get a pharmacological grip on this elusive protein. The inhibition of effector pathways, such as the RAF-MEK-ERK pathway, has largely proven disappointing. Thus far, most of these efforts were aimed at blocking the activation of ERK. Here, we discuss RAF-dependent pathways that are regulated through RAF functions independent of catalytic activity and their potential role as targets to block oncogenic RAS signalling. We focus on the now well documented roles of RAF kinase-independent functions in apoptosis, cell cycle progression and cell migration.
    MeSH term(s) Animals ; Antineoplastic Agents/pharmacology ; Carcinogenesis/drug effects ; Carcinogenesis/genetics ; Carcinogenesis/metabolism ; Carcinogenesis/pathology ; Humans ; Neoplasms/drug therapy ; Neoplasms/genetics ; Neoplasms/metabolism ; Neoplasms/pathology ; Signal Transduction ; raf Kinases/genetics ; raf Kinases/metabolism ; ras Proteins/antagonists & inhibitors
    Chemical Substances Antineoplastic Agents ; raf Kinases (EC 2.7.11.1) ; ras Proteins (EC 3.6.5.2)
    Language English
    Publishing date 2021-04-10
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2527218-4
    ISSN 2073-4425 ; 2073-4425
    ISSN (online) 2073-4425
    ISSN 2073-4425
    DOI 10.3390/genes12040553
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Book ; Online: Economic and Social Rights after the Global Financial Crisis

    Nolan, Aoife

    2014  

    Abstract: This book addresses the interrelationship between economic and financial crises, the responses thereto, and economic and social ... ...

    Abstract This book addresses the interrelationship between economic and financial crises, the responses thereto, and economic and social rights
    Language English
    Size Online-Ressource (414 p)
    Publisher Cambridge University Press
    Publishing place Cambridge
    Document type Book ; Online
    Note Description based upon print version of record
    ISBN 9781107043251 ; 1107043255
    Database Library catalogue of the German National Library of Science and Technology (TIB), Hannover

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  7. Article: Hidden Targets in RAF Signalling Pathways to Block Oncogenic RAS Signalling

    Nolan, Aoife A / Aboud, Nourhan K / Kolch, Walter / Matallanas, David

    Genes. 2021 Apr. 10, v. 12, no. 4

    2021  

    Abstract: Oncogenic RAS (Rat sarcoma) mutations drive more than half of human cancers, and RAS inhibition is the holy grail of oncology. Thirty years of relentless efforts and harsh disappointments have taught us about the intricacies of oncogenic RAS signalling ... ...

    Abstract Oncogenic RAS (Rat sarcoma) mutations drive more than half of human cancers, and RAS inhibition is the holy grail of oncology. Thirty years of relentless efforts and harsh disappointments have taught us about the intricacies of oncogenic RAS signalling that allow us to now get a pharmacological grip on this elusive protein. The inhibition of effector pathways, such as the RAF-MEK-ERK pathway, has largely proven disappointing. Thus far, most of these efforts were aimed at blocking the activation of ERK. Here, we discuss RAF-dependent pathways that are regulated through RAF functions independent of catalytic activity and their potential role as targets to block oncogenic RAS signalling. We focus on the now well documented roles of RAF kinase-independent functions in apoptosis, cell cycle progression and cell migration.
    Keywords apoptosis ; catalytic activity ; cell cycle ; cell movement ; humans ; rats ; sarcoma
    Language English
    Dates of publication 2021-0410
    Publishing place Multidisciplinary Digital Publishing Institute
    Document type Article
    Note NAL-AP-2-clean
    ZDB-ID 2527218-4
    ISSN 2073-4425
    ISSN 2073-4425
    DOI 10.3390/genes12040553
    Database NAL-Catalogue (AGRICOLA)

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  8. Book: Human rights and public finance

    Harvey, Colin / Nolan, Aoife / O'Connell, Rory

    budgets and the promotion of economic and social rights

    2013  

    Abstract: This edited collection addresses some of the most important challenges in contemporary human rights law and practice. Its central theme is the linkage between public finance, particularly budget decisions, and the realisation (or not) of economic and ... ...

    Author's details ed. by Aoife Nolan; Rory O'Connell and Colin Harvey
    Abstract "This edited collection addresses some of the most important challenges in contemporary human rights law and practice. Its central theme is the linkage between public finance, particularly budget decisions, and the realisation (or not) of economic and social rights. While much academic and political debate on economic and social rights implementation has focused on the role of the courts, this work places the spotlight squarely on those organs of government that have the primary responsibility and the greatest capacity for giving effect to such rights: namely, the elected branches of government. The major actors considered in this book are politicians, public servants and civil society, with their role in realising economic and social rights the work's key focus. The book thus makes a crucial contribution to remedying the current imbalance in attention paid by economic and social rights scholars to the legislature and executive vis-a-vis the judiciary

    Featuring pioneering work by leading experts in the field of human rights and public finance, this multidisciplinary collection will be of great interest to academics, practitioners, public servants and students working in the areas of law, human rights, economics, development and political science."--Pub. desc
    Keywords Budget/Moral and ethical aspects ; Finance, Public/Moral and ethical aspects ; Human rights/Economic aspects
    Language English
    Size XVI, 257 S., graph. Darst
    Publisher Hart
    Publishing place Oxford u.a.
    Document type Book
    ISBN 1841130117 ; 9781841130118
    Database Former special subject collection: coastal and deep sea fishing

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  9. Article ; Online: Simultaneous pharmacokinetic modeling of unbound and total darunavir with ritonavir in adolescents: a substudy of the SMILE trial.

    Abdalla, Seef / Compagnucci, Alexandra / Riault, Yoann / Chan, Man K / Bamford, Alasdair / Nolan, Aoife / Ramos, José T / Constant, Valentin / Nguyen, Thao-Nguyen / Zheng, Yi / Tréluyer, Jean-Marc / Froelicher-Bournaud, Léo / Neveux, Nathalie / Saidi, Yacine / Cressey, Tim R / Hirt, Déborah

    Antimicrobial agents and chemotherapy

    2023  Volume 68, Issue 2, Page(s) e0100423

    Abstract: Darunavir (DRV) is an HIV protease inhibitor commonly used as part of antiretroviral treatment regimens globally for children and adolescents. It requires a pharmacological booster, such as ritonavir (RTV) or cobicistat. To better understand the ... ...

    Abstract Darunavir (DRV) is an HIV protease inhibitor commonly used as part of antiretroviral treatment regimens globally for children and adolescents. It requires a pharmacological booster, such as ritonavir (RTV) or cobicistat. To better understand the pharmacokinetics (PK) of DRV in this younger population and the importance of the RTV boosting effect, a population PK substudy was conducted within SMILE trial, where the maintenance of HIV suppression with once daily integrate inhibitor + darunavir/ritonavir in children and adolescents is evaluated. A joint population PK model that simultaneously used total DRV, unbound DRV, and total RTV concentrations was developed. Competitive and non-competitive models were examined to define RTV's influence on DRV pharmacokinetics. Linear and non-linear equations were tested to assess DRV protein binding. A total of 443 plasma samples from 152 adolescents were included in this analysis. Darunavir PK was best described by a one-compartment model first-order absorption and elimination. The influence of RTV on DRV pharmacokinetics was best characterized by ritonavir area under the curve on DRV clearance using a power function. The association of non-linear and linear equations was used to describe DRV protein binding to alpha-1 glycoprotein and albumin, respectively. In our population, simulations indicate that 86.8% of total and unbound DRV trough concentrations were above 0.55 mg/L [10 times protein binding-adjusted EC
    MeSH term(s) Adult ; Child ; Humans ; Adolescent ; Darunavir/pharmacokinetics ; Ritonavir/therapeutic use ; Anti-HIV Agents/therapeutic use ; Sulfonamides/pharmacology ; HIV Infections/drug therapy ; HIV Protease Inhibitors/therapeutic use
    Chemical Substances Darunavir (YO603Y8113) ; Ritonavir (O3J8G9O825) ; Anti-HIV Agents ; Sulfonamides ; HIV Protease Inhibitors
    Language English
    Publishing date 2023-12-11
    Publishing country United States
    Document type Journal Article
    ZDB-ID 217602-6
    ISSN 1098-6596 ; 0066-4804
    ISSN (online) 1098-6596
    ISSN 0066-4804
    DOI 10.1128/aac.01004-23
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Dietary counselling to reduce moderate sodium intake: effects on cardiovascular and renal biomarkers: primary findings of the COSIP and STICK phase II feasibility randomised controlled trials.

    Smyth, Andrew / Judge, Conor / Kerins, Claire / McDermott, Suzanne / Niland, Aoife / Corcoran, Colette / Dineen, Roisin / Alvarez-Iglesias, Alberto / Nolan, Aoife / Mente, Andrew / Griffin, Matthew D / O'Shea, Paula / Canavan, Michelle / Yusuf, Salim / O'Donnell, Martin

    EClinicalMedicine

    2023  Volume 57, Page(s) 101856

    Abstract: Background: While low sodium intake (<2.3 g/day) is recommended, there is uncertainty about long-term feasibility and effects on cardiorenal biomarkers in populations with moderate intake.: Methods: In two phase IIb, feasibility, randomised, parallel, ...

    Abstract Background: While low sodium intake (<2.3 g/day) is recommended, there is uncertainty about long-term feasibility and effects on cardiorenal biomarkers in populations with moderate intake.
    Methods: In two phase IIb, feasibility, randomised, parallel, open-label, controlled, single-centre trials, individuals aged >40 years with stable blood pressure (BP), without heart failure or postural hypotension were randomised to intensive dietary counselling (target sodium intake <2.3 g/day) or usual care between March 2016 and July 2018. One trial included participants with chronic kidney disease (CKD); the other excluded those with CKD or cardiovascular disease. All participants received healthy eating advice. Primary outcomes were NT-pro B-type natriuretic peptide (NT-proBNP), high sensitivity troponin T (hsTnT), C-reactive protein (CRP), renin, aldosterone and, creatinine clearance (CrCl) at 2-years. These trials are registered with ClinicalTrials.gov, STICK trial (NCT02458248) and COSIP trial (NCT02738736).
    Findings: 373 participants, with mean 24-h urine sodium 3.16 ± 1.47 g/day, were randomised to intervention (n = 187) or usual care (n = 186). At 3-months, the intervention reduced 24-h urine sodium (intervention -0.11 g/day, usual care +0.28 g/day, p = 0.003), BP (systolic -2.52 mmHg, p = 0.05; diastolic -1.92, p = 0.02) and increased renin (+33.35 mIU/L [95%CI 3.78-62.91]). At 2-years, the intervention significantly reduced self-reported salt use (p < 0.001), but not 24-h urine sodium (intervention -0.23 g/day, usual care +0.05 g/day, p = 0.47). At 2-years, there were no significant between-group differences in BP (systolic p = 0.66; diastolic p = 0.09), NT-proBNP (p = 0.68), hsTnT (p = 0.20), CRP (p = 0.56), renin (p = 0.52), aldosterone (p = 0.61), or CrCl (p = 0.68).
    Interpretation: Among individuals with moderate sodium intake, intensive dietary counselling resulted in small short-term reductions in sodium intake and BP, but no significant effect on sodium intake, BP, or cardiorenal biomarkers at two years. Our trial suggests that it may not feasible to reduce sodium sustainably in those with a sodium intake around 3.0 g/day, through an intensive dietary counselling intervention.
    Funding: The STICK trial was funded by the Health Research Board of Ireland and the COSIP trial was funded by the European Research Council.
    Language English
    Publishing date 2023-02-15
    Publishing country England
    Document type Journal Article
    ISSN 2589-5370
    ISSN (online) 2589-5370
    DOI 10.1016/j.eclinm.2023.101856
    Database MEDical Literature Analysis and Retrieval System OnLINE

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