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  1. Article ; Online: Rationale and Design of the SOTA-P-CARDIA Trial (ATRU-V): Sotagliflozin in HFpEF Patients Without Diabetes.

    Pérez, Maeve Soto / Rodríguez-Capitán, Jorge / Requena-Ibáñez, Juan Antonio / Santos-Gallego, Carlos G / Urooj Zafar, M / Escolar, Ginés / Mancini, Donna / Mitter, Sumeet / Lam, David / Contreras, Johanna P / Fergus, Icilma / Atallah-Lajam, Farah / Abascal, Vivian / Lala, Anu / Moreno, Pedro / Moss, Noah / Lerakis, Stamatios / Sanz, Javier / Fuster, Valentin /
    Badimon, Juan José

    Cardiovascular drugs and therapy

    2023  

    Abstract: ... Fraction Patients (SOTA-P-CARDIA) trial (NCT05562063) is to investigate whether the observed cardiorenal ... The SOTA-P-CARDIA is a prospective, randomized, double-blinded, placebo-controlled study ...

    Abstract Heart failure with preserved ejection fraction (HFpEF) is now the most common form of heart failure (HF). This syndrome is associated with an elevated morbi-mortality, and effective therapies are urgently needed. Sodium-glucose co-transporter 2 inhibitors (SGLT2i) are the first pharmacological class that has demonstrated to reduce hospitalization and cardiovascular mortality in large clinical trials in HFpEF. Furthermore, the dual SGLT 1/2 inhibitor sotagliflozin has shown a reduction in cardiovascular outcomes in diabetic HF patients, regardless of ejection fraction Sotagliflozin on Cardiovascular Events in Patients with Type 2 Diabetes Post Worsening Heart Failure (SOLOIST-WHF) Trial, and prevents the development of HF in patients with diabetes and chronic kidney disease Sotagliflozin on Cardiovascular and Renal Events in Patients with Type 2 Diabetes and Moderate Renal Impairment Who Are at Cardiovascular Risk (SCORED) trial. The major objective of the Sotagliflozin in Heart Failure With Preserved Ejection Fraction Patients (SOTA-P-CARDIA) trial (NCT05562063) is to investigate whether the observed cardiorenal benefits of sotagliflozin in HF patients with diabetes can be extended to a non-diabetic population. The SOTA-P-CARDIA is a prospective, randomized, double-blinded, placebo-controlled study that will randomize non-diabetic patients with the universal definition of HFpEF (ejection fraction > 50% assessed the day of randomization). Qualifying patients will be randomized, in blocks of 4, to receive either sotagliflozin or placebo for a period of 6 months. The primary outcome is changes in left ventricular mass by cardiac magnetic resonance from randomization to end of the study between the groups. Secondary end points include changes in peak VO
    Language English
    Publishing date 2023-06-15
    Publishing country United States
    Document type Journal Article
    ZDB-ID 639068-7
    ISSN 1573-7241 ; 0920-3206
    ISSN (online) 1573-7241
    ISSN 0920-3206
    DOI 10.1007/s10557-023-07469-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: A refutation to 'A new A-P compartment boundary and organizer in holometabolous insect wings'.

    Lawrence, Peter A / Casal, José / Celis, José F de / Morata, Ginés

    Scientific reports

    2019  Volume 9, Issue 1, Page(s) 7049

    Abstract: We respond to a recent report by Abbasi and Marcus who present two main findings: first they argue that there is an organiser and a compartment boundary within the posterior compartment of the butterfly wing. Second, they present evidence for a ... ...

    Abstract We respond to a recent report by Abbasi and Marcus who present two main findings: first they argue that there is an organiser and a compartment boundary within the posterior compartment of the butterfly wing. Second, they present evidence for a previously undiscovered lineage boundary near wing vein 5 in Drosophila, a boundary that delineates a "far posterior" compartment. Clones of cells were marked with the yellow mutation and they reported that these clones always fail to cross a line close to vein 5 on the Drosophila wing. In our hands yellow proved an unusable marker for clones in the wing blade and therefore we reexamined the matter. We marked clones of cells with multiple wing hairs or forked and found a substantial proportion of these clones cross the proposed lineage boundary near vein 5, in conflict with their findings and conclusion. As internal controls we showed that these same clones respect the other two well established compartment boundaries: the anteroposterior compartment boundary is always respected. The dorsoventral boundary is mostly respected, and is crossed only by clones that are induced early in development, consistent with many reports. We question the validity of Abbasi and Marcus' conclusions regarding the butterfly wing but present no new data.Arising from: R. Abbasi and J. M. Marcus Sci. Rep. 7, 16337 (2017); https://doi.org/10.1038/s41598-017-16553-5 .
    MeSH term(s) Animals ; Butterflies ; Drosophila ; Drosophila Proteins ; Mutation ; Wings, Animal
    Chemical Substances Drosophila Proteins
    Language English
    Publishing date 2019-05-07
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Comment
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-019-42668-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: A refutation to ‘A new A-P compartment boundary and organizer in holometabolous insect wings’

    Peter A. Lawrence / José Casal / José F. de Celis / Ginés Morata

    Scientific Reports, Vol 9, Iss 1, Pp 1-

    2019  Volume 6

    Abstract: Abstract We respond to a recent report by Abbasi and Marcus who present two main findings: first they argue that there is an organiser and a compartment boundary within the posterior compartment of the butterfly wing. Second, they present evidence for a ... ...

    Abstract Abstract We respond to a recent report by Abbasi and Marcus who present two main findings: first they argue that there is an organiser and a compartment boundary within the posterior compartment of the butterfly wing. Second, they present evidence for a previously undiscovered lineage boundary near wing vein 5 in Drosophila, a boundary that delineates a “far posterior” compartment. Clones of cells were marked with the yellow mutation and they reported that these clones always fail to cross a line close to vein 5 on the Drosophila wing. In our hands yellow proved an unusable marker for clones in the wing blade and therefore we reexamined the matter. We marked clones of cells with multiple wing hairs or forked and found a substantial proportion of these clones cross the proposed lineage boundary near vein 5, in conflict with their findings and conclusion. As internal controls we showed that these same clones respect the other two well established compartment boundaries: the anteroposterior compartment boundary is always respected. The dorsoventral boundary is mostly respected, and is crossed only by clones that are induced early in development, consistent with many reports. We question the validity of Abbasi and Marcus’ conclusions regarding the butterfly wing but present no new data. Arising from: R. Abbasi and J. M. Marcus Sci. Rep. 7, 16337 (2017); https://doi.org/10.1038/s41598-017-16553-5.
    Keywords Medicine ; R ; Science ; Q
    Subject code 590
    Language English
    Publishing date 2019-05-01T00:00:00Z
    Publisher Nature Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  4. Article ; Online: EASL International Recognition Award Recipient 2022: Prof. Patrick S. Kamath.

    Ginès, Pere

    Journal of hepatology

    2022  Volume 77, Issue 2, Page(s) 285–286

    MeSH term(s) Awards and Prizes ; Gastroenterology
    Language English
    Publishing date 2022-06-22
    Publishing country Netherlands
    Document type Editorial
    ZDB-ID 605953-3
    ISSN 1600-0641 ; 0168-8278
    ISSN (online) 1600-0641
    ISSN 0168-8278
    DOI 10.1016/j.jhep.2022.05.007
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Book ; Conference proceedings: Autoimmune diseases of the liver

    Ginès, Pere

    official congress report

    (Digestive diseases ; 33, Suppl. 2)

    2015  

    Event/congress Falk Symposium (197., 2015, Lissabon)
    Author's details Falk Symposium 197, Lisbon, May 8 - 9, 2015. Ed. P. Ginès
    Series title Digestive diseases ; 33, Suppl. 2
    Collection
    Keywords Gastroenterology ; Leberkrankheit ; Autoaggressionskrankheit
    Subject Autoantikörperkrankheit ; Autoimmunkrankheit ; Autoimmunopathie ; Autoimmunerkrankung ; Lebererkrankung ; Leber ; Hepatopathie ; Hepatopathia
    Language English
    Size IV, 191 S. : Ill., graph. Darst.
    Publisher Karger
    Publishing place Basel u.a.
    Publishing country Switzerland
    Document type Book ; Conference proceedings
    HBZ-ID HT018842586
    ISBN 978-3-318-05561-0 ; 978-3-318-05562-7 ; 3-318-05561-1 ; 3-318-05562-X
    Database Catalogue ZB MED Medicine, Health

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  6. Article ; Online: Robert W Schrier, an influential observer from outside Hepatology (1936-2021).

    Ginès, Pere

    Journal of hepatology

    2021  

    Language English
    Publishing date 2021-04-20
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 605953-3
    ISSN 1600-0641 ; 0168-8278
    ISSN (online) 1600-0641
    ISSN 0168-8278
    DOI 10.1016/j.jhep.2021.03.008
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Simulation of P systems with active membranes on CUDA.

    Cecilia, José M / García, José M / Guerrero, Ginés D / Martínez-del-Amor, Miguel A / Pérez-Hurtado, Ignacio / Pérez-Jiménez, Mario J

    Briefings in bioinformatics

    2010  Volume 11, Issue 3, Page(s) 313–322

    Abstract: P systems or Membrane Systems provide a high-level computational modelling framework that combines ... design principles and key of the implementation of a simulator for the class of recognizer P systems with active ... for a single central processing unit (CPU), showing that GPUs are better suited than CPUs to simulate P systems ...

    Abstract P systems or Membrane Systems provide a high-level computational modelling framework that combines the structure and dynamic aspects of biological systems in a relevant and understandable way. They are inherently parallel and non-deterministic computing devices. In this article, we discuss the motivation, design principles and key of the implementation of a simulator for the class of recognizer P systems with active membranes running on a (GPU). We compare our parallel simulator for GPUs to the simulator developed for a single central processing unit (CPU), showing that GPUs are better suited than CPUs to simulate P systems due to their highly parallel nature.
    MeSH term(s) Algorithms ; Biology/methods ; Biomimetics/methods ; Computer Simulation ; Models, Biological ; Programming Languages ; Software ; Software Design ; Systems Integration
    Language English
    Publishing date 2010-05
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2068142-2
    ISSN 1477-4054 ; 1467-5463
    ISSN (online) 1477-4054
    ISSN 1467-5463
    DOI 10.1093/bib/bbp064
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Hepatorenal Syndrome in Cirrhosis.

    Pose, Elisa / Piano, Salvatore / Juanola, Adrià / Ginès, Pere

    Gastroenterology

    2024  Volume 166, Issue 4, Page(s) 588–604.e1

    Abstract: Hepatorenal syndrome (HRS) is a form of kidney dysfunction that characteristically occurs in liver cirrhosis. It is characterized by a marked impairment of kidney function in response to circulatory and hemodynamic alterations that occur in advanced ... ...

    Abstract Hepatorenal syndrome (HRS) is a form of kidney dysfunction that characteristically occurs in liver cirrhosis. It is characterized by a marked impairment of kidney function in response to circulatory and hemodynamic alterations that occur in advanced stages of liver cirrhosis, aggravated by systemic inflammation and bacterial translocation. The classical definitions of the types of HRS have been recently revisited and 2 forms of HRS have been redefined: the acute form, referred to as acute kidney injury (HRS-AKI), and the chronic form, referred to as chronic kidney disease. HRS-AKI is one of the most severe forms of AKI in patients with cirrhosis and it consists of an abrupt impairment of kidney function, frequently triggered by an infection, appearing in the setting of advanced decompensated cirrhosis. Differential diagnosis with other causes of AKI is crucial because HRS-AKI requires a specific treatment. Differential diagnosis with AKI-acute tubular necrosis may be challenging and kidney biomarkers may be useful in this setting. Treatment of HRS-AKI is based on the administration of vasoconstrictor drugs in combination with volume expansion with albumin. Prognosis of HRS-AKI is poor, and the ideal definitive treatment consists of liver transplantation or simultaneous liver-kidney transplantation. HRS-AKI has a big impact on patients' quality of life. Management of HRS-AKI remains challenging in specific situations such as alcohol-associated hepatitis or metabolic-associated steatotic liver disease cirrhosis. Developing preventive measures for HRS-AKI, improving its early identification, discovering new biomarkers for differential diagnosis, and improving the response to therapy are some of the unmet needs in the field of HRS-AKI.
    MeSH term(s) Humans ; Hepatorenal Syndrome/diagnosis ; Hepatorenal Syndrome/etiology ; Hepatorenal Syndrome/therapy ; Quality of Life ; Liver Cirrhosis/complications ; Liver Cirrhosis/diagnosis ; Liver Cirrhosis/therapy ; Acute Kidney Injury/diagnosis ; Acute Kidney Injury/etiology ; Acute Kidney Injury/therapy ; Biomarkers
    Chemical Substances Biomarkers
    Language English
    Publishing date 2024-01-19
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 80112-4
    ISSN 1528-0012 ; 0016-5085
    ISSN (online) 1528-0012
    ISSN 0016-5085
    DOI 10.1053/j.gastro.2023.11.306
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Improving Outcome Prediction in Alcohol-Associated Hepatitis: Blood Urea Nitrogen and Albumin Help.

    Pose, Elisa / Ginès, Pere

    Mayo Clinic proceedings

    2022  Volume 97, Issue 3, Page(s) 436–438

    MeSH term(s) Albumins ; Blood Urea Nitrogen ; Hepatitis, Alcoholic/diagnosis ; Humans ; Nitrogen
    Chemical Substances Albumins ; Nitrogen (N762921K75)
    Language English
    Publishing date 2022-03-04
    Publishing country England
    Document type Editorial ; Research Support, Non-U.S. Gov't ; Comment
    ZDB-ID 124027-4
    ISSN 1942-5546 ; 0025-6196
    ISSN (online) 1942-5546
    ISSN 0025-6196
    DOI 10.1016/j.mayocp.2022.01.019
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Terlipressin for hepatorenal syndrome: ready for prime time.

    Ginès, Pere

    The lancet. Gastroenterology & hepatology

    2017  Volume 2, Issue 2, Page(s) 75–76

    Language English
    Publishing date 2017-02
    Publishing country Netherlands
    Document type Journal Article
    ISSN 2468-1253
    ISSN (online) 2468-1253
    DOI 10.1016/S2468-1253(16)30211-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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