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  1. AU="Vázquez-Carrera, Manuel"
  2. AU="Tanner, Rikki M"
  3. AU="Daniel H Miller"
  4. AU="Madec, Jean-Yves"
  5. AU=Rahimi Mitra

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  1. Buch ; Online: PPARs as Key Mediators of Metabolic and Inflammatory Regulation

    Vázquez-Carrera, Manuel / Vázquez-Carrera, Manuel / Wahli, Walter

    2022  

    Schlagwörter Research & information: general ; Biology, life sciences ; Biochemistry ; nuclear receptor ; gene transcription ; inflammation ; molecular docking ; PPARβ/δ ; lung ; pulmonary artery ; GW0742 ; GSK3787 ; docking ; lipopolysaccharide (LPS) ; PPARγ ligand ; coumarin ; fluorescent ligand ; screening ; crystal structure ; PPAR ; atopic dermatitis ; psoriasis ; metabolic reprograming ; glucose ; fatty acids ; mycobacteria ; M. tuberculosis ; M. leprae ; PPARs ; lipid droplets ; metabolic alterations ; hepatic damage ; nuclear factors ; pharmacological targets ; AMPK ; GDF15 ; insulin resistance ; type 2 diabetes mellitus ; peroxisome proliferator-activated receptor gamma (PPARγ) ; real-time PCR ; ELISA ; immunohistochemistry ; signaling pathway ; PPAR gamma ; brain ; neural stem cells ; infection ; neuroinflammation ; HIV ; Zika ; cytomegalovirus ; neurogenesis ; microglia ; liver damage ; toll-like receptor 4 ; P2Y2 receptor ; metabolic syndrome ; resveratrol ; quercetin ; PPARα ; peroxisome ; β-oxidation ; PPRE ; ligand ; coregulator ; micronutrients ; PPARα knockout ; adipose tissue ; browning ; lipid metabolism ; depression ; PPARg ; neuropathology ; corticotropin releasing hormone ; norepinephrine ; subgenual prefrontal cortex ; amygdala ; nucleus accumbens ; common carotid artery occlusion ; electroretinography ; fibroblast growth factor 21 ; pemafibrate ; peroxisome proliferator-activated receptor alpha ; retinal ischemia ; skeletal muscle ; substrate metabolism ; nonalcoholic fatty liver disease (NAFLD) ; sex dimorphism ; lipidomics ; hepatic sex-biased gene expression ; PPARγ ; pulmonary arterial hypertension ; TGFβ ; vascular injury ; proliferation ; kidney fibrosis ; pattern-recognition receptors ; phagocytosis ; nitric oxide synthase ; fenofibrate ; oleoylethanolamide ; palmitoylethanolamide ; cancer ; immunity ; obesity ; diabetes ; miRNA ; DNA methylation ; histone modification ; peroxisome-proliferator-activated receptor ; fatty acid oxidation ; doping control ; regulatory T cells ; exercise ; nuclear receptors ; nutrigenomics ; energy homeostasis ; dairy animals ; non-alcoholic fatty liver disease (NAFLD) ; non-alcoholic steatohepatitis (NASH) ; peroxisome proliferator-activated receptors (PPAR) ; bezafibrate ; fenofibric acid ; peroxisome proliferator-activated receptor ; dual/pan agonist ; X-ray crystallography ; n/a
    Sprache 0|e
    Umfang 1 electronic resource (456 pages)
    Verlag MDPI - Multidisciplinary Digital Publishing Institute
    Dokumenttyp Buch ; Online
    Anmerkung English ; Open Access
    HBZ-ID HT021610751
    ISBN 9783036541914 ; 3036541918
    Datenquelle ZB MED Katalog Medizin, Gesundheit, Ernährung, Umwelt, Agrar

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  2. Artikel ; Online: Is Helicobacter pylori a new kid on the block?

    Vázquez-Carrera, Manuel

    Clinica e investigacion en arteriosclerosis : publicacion oficial de la Sociedad Espanola de Arteriosclerosis

    2024  Band 36, Heft 2, Seite(n) 78–79

    Mesh-Begriff(e) Humans ; Helicobacter pylori
    Sprache Spanisch
    Erscheinungsdatum 2024-02-23
    Erscheinungsland Spain
    Dokumenttyp Journal Article
    ISSN 1578-1879
    ISSN (online) 1578-1879
    DOI 10.1016/j.arteri.2024.02.002
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: PPARs as Key Transcription Regulators at the Crossroads of Metabolism and Inflammation.

    Vázquez-Carrera, Manuel / Wahli, Walter

    International journal of molecular sciences

    2024  Band 25, Heft 8

    Abstract: The metabolic and immune systems are complex networks of organs, cells, and proteins that are involved in the extraction of energy from food; this is to run complex cellular processes and defend the body against infections while protecting its own ... ...

    Abstract The metabolic and immune systems are complex networks of organs, cells, and proteins that are involved in the extraction of energy from food; this is to run complex cellular processes and defend the body against infections while protecting its own tissues, respectively [...].
    Mesh-Begriff(e) Humans ; Inflammation/metabolism ; Inflammation/genetics ; Animals ; Peroxisome Proliferator-Activated Receptors/metabolism ; Peroxisome Proliferator-Activated Receptors/genetics ; Gene Expression Regulation
    Chemische Substanzen Peroxisome Proliferator-Activated Receptors
    Sprache Englisch
    Erscheinungsdatum 2024-04-18
    Erscheinungsland Switzerland
    Dokumenttyp Editorial ; Introductory Journal Article
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms25084467
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Buch: New emerging pharmacological targets in metabolic diseases

    Vázquez-Carrera, Manuel

    2007  

    Verfasserangabe ed. in chief: Manuel Vázquez-Carrera
    Sprache Englisch
    Umfang 226 S. : Ill., graph. Darst.
    Verlag Transworld Research Network
    Erscheinungsort Trivandrum
    Erscheinungsland Indien
    Dokumenttyp Buch
    HBZ-ID HT015489042
    ISBN 81-7895-270-X ; 978-81-7895-270-3
    Datenquelle Katalog ZB MED Medizin, Gesundheit

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  5. Artikel ; Online: PPARs as Key Mediators in the Regulation of Metabolism and Inflammation.

    Vázquez-Carrera, Manuel / Wahli, Walter

    International journal of molecular sciences

    2022  Band 23, Heft 9

    Abstract: Nuclear receptors (NRs) form a large family of ligand-dependent transcription factors that control the expression of a multitude of genes involved in diverse, vital biological processes [ ... ]. ...

    Abstract Nuclear receptors (NRs) form a large family of ligand-dependent transcription factors that control the expression of a multitude of genes involved in diverse, vital biological processes [...].
    Mesh-Begriff(e) Humans ; Inflammation/genetics ; Inflammation/metabolism ; Lipid Metabolism ; Peroxisome Proliferator-Activated Receptors/metabolism ; Receptors, Cytoplasmic and Nuclear/genetics ; Receptors, Cytoplasmic and Nuclear/metabolism ; Transcription Factors/metabolism
    Chemische Substanzen Peroxisome Proliferator-Activated Receptors ; Receptors, Cytoplasmic and Nuclear ; Transcription Factors
    Sprache Englisch
    Erscheinungsdatum 2022-04-30
    Erscheinungsland Switzerland
    Dokumenttyp Editorial
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms23095025
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Artikel ; Online: In search of the "metabolic footprint" in cardiovascular disease.

    Vázquez Carrera, Manuel

    Clinica e investigacion en arteriosclerosis : publicacion oficial de la Sociedad Espanola de Arteriosclerosis

    2018  Band 30, Heft 1, Seite(n) 28–29

    Titelübersetzung A la búsqueda de la «huella metabólica» en la enfermedad cardiovascular.
    Mesh-Begriff(e) Cardiovascular Diseases/metabolism ; Cardiovascular Diseases/physiopathology ; Humans ; Lipid Metabolism/physiology ; Metabolomics/methods
    Sprache Spanisch
    Erscheinungsdatum 2018-02-10
    Erscheinungsland Spain
    Dokumenttyp Editorial
    ISSN 1578-1879
    ISSN (online) 1578-1879
    DOI 10.1016/j.arteri.2018.01.001
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  7. Artikel ; Online: GADD45A: With or without you.

    Palomer, Xavier / Salvador, Jesús M / Griñán-Ferré, Christian / Barroso, Emma / Pallàs, Mercè / Vázquez-Carrera, Manuel

    Medicinal research reviews

    2024  

    Abstract: The growth arrest and DNA damage inducible (GADD)45 family includes three small and ubiquitously distributed proteins (GADD45A, GADD45B, and GADD45G) that regulate numerous cellular processes associated with stress signaling and injury response. Here, we ...

    Abstract The growth arrest and DNA damage inducible (GADD)45 family includes three small and ubiquitously distributed proteins (GADD45A, GADD45B, and GADD45G) that regulate numerous cellular processes associated with stress signaling and injury response. Here, we provide a comprehensive review of the current literature investigating GADD45A, the first discovered member of the family. We first depict how its levels are regulated by a myriad of genotoxic and non-genotoxic stressors, and through the combined action of intricate transcriptional, posttranscriptional, and even, posttranslational mechanisms. GADD45A is a recognized tumor suppressor and, for this reason, we next summarize its role in cancer, as well as the different mechanisms by which it regulates cell cycle, DNA repair, and apoptosis. Beyond these most well-known actions, GADD45A may also influence catabolic and anabolic pathways in the liver, adipose tissue and skeletal muscle, among others. Not surprisingly, GADD45A may trigger AMP-activated protein kinase activity, a master regulator of metabolism, and is known to act as a transcriptional coregulator of numerous nuclear receptors. GADD45A has also been reported to display a cytoprotective role by regulating inflammation, fibrosis and oxidative stress in several organs and tissues, and is regarded an important contributor for the development of heart failure. Overall data point to that GADD45A may play an important role in metabolic, neurodegenerative and cardiovascular diseases, and also autoimmune-related disorders. Thus, the potential mechanisms by which dysregulation of GADD45A activity may contribute to the progression of these diseases are also reviewed below.
    Sprache Englisch
    Erscheinungsdatum 2024-01-24
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Review
    ZDB-ID 603210-2
    ISSN 1098-1128 ; 0198-6325
    ISSN (online) 1098-1128
    ISSN 0198-6325
    DOI 10.1002/med.22015
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  8. Artikel ; Online: HSP90 inhibitors as a future therapeutic strategy in diabetes-driven atherosclerosis.

    Vázquez-Carrera, Manuel

    Clinica e investigacion en arteriosclerosis : publicacion oficial de la Sociedad Espanola de Arteriosclerosis

    2017  Band 29, Heft 2, Seite(n) 67–68

    Titelübersetzung Inhibidores de HSP90 como futura estrategia terapéutica en la aterosclerosis asociada a diabetes.
    Mesh-Begriff(e) Animals ; Atherosclerosis/etiology ; Atherosclerosis/prevention & control ; Diabetes Complications/prevention & control ; Diabetes Mellitus/physiopathology ; HSP90 Heat-Shock Proteins/antagonists & inhibitors ; Humans
    Chemische Substanzen HSP90 Heat-Shock Proteins
    Sprache Spanisch
    Erscheinungsdatum 2017-03-07
    Erscheinungsland Spain
    Dokumenttyp Editorial
    ISSN 1578-1879
    ISSN (online) 1578-1879
    DOI 10.1016/j.arteri.2017.02.001
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel ; Online: Striking a gut-liver balance for the antidiabetic effects of metformin.

    Barroso, Emma / Montori-Grau, Marta / Wahli, Walter / Palomer, Xavier / Vázquez-Carrera, Manuel

    Trends in pharmacological sciences

    2023  Band 44, Heft 7, Seite(n) 457–473

    Abstract: Metformin is the most prescribed drug for the treatment of type 2 diabetes mellitus (T2DM), but its mechanism of action has not yet been completely elucidated. Classically, the liver has been considered the major site of action of metformin. However, ... ...

    Abstract Metformin is the most prescribed drug for the treatment of type 2 diabetes mellitus (T2DM), but its mechanism of action has not yet been completely elucidated. Classically, the liver has been considered the major site of action of metformin. However, over the past few years, advances have unveiled the gut as an additional important target of metformin, which contributes to its glucose-lowering effect through new mechanisms of action. A better understanding of the mechanistic details of metformin action in the gut and the liver and its relevance in patients remains the challenge of present and future research and may impact drug development for the treatment of T2DM. Here, we offer a critical analysis of the current status of metformin-driven multiorgan glucose-lowering effects.
    Mesh-Begriff(e) Humans ; Hypoglycemic Agents/pharmacology ; Hypoglycemic Agents/therapeutic use ; Metformin/pharmacology ; Metformin/therapeutic use ; Diabetes Mellitus, Type 2/drug therapy ; Liver ; Glucose
    Chemische Substanzen Hypoglycemic Agents ; Metformin (9100L32L2N) ; Glucose (IY9XDZ35W2)
    Sprache Englisch
    Erscheinungsdatum 2023-05-13
    Erscheinungsland England
    Dokumenttyp Journal Article ; Review
    ZDB-ID 282846-7
    ISSN 1873-3735 ; 0165-6147
    ISSN (online) 1873-3735
    ISSN 0165-6147
    DOI 10.1016/j.tips.2023.04.004
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel ; Online: Unraveling the Effects of PPARβ/δ on Insulin Resistance and Cardiovascular Disease.

    Vázquez-Carrera, Manuel

    Trends in endocrinology and metabolism: TEM

    2016  Band 27, Heft 5, Seite(n) 319–334

    Abstract: Insulin resistance precedes dyslipidemia and type 2 diabetes mellitus (T2DM) development. Preclinical evidence suggests that peroxisome proliferator-activated receptor (PPAR) β/δ activators may prevent and treat obesity-induced insulin resistance and ... ...

    Abstract Insulin resistance precedes dyslipidemia and type 2 diabetes mellitus (T2DM) development. Preclinical evidence suggests that peroxisome proliferator-activated receptor (PPAR) β/δ activators may prevent and treat obesity-induced insulin resistance and T2DM, while clinical trials highlight their potential utility in dyslipidemia. This review summarizes recent mechanistic insights into the antidiabetic effects of PPARβ/δ activators, including their anti-inflammatory actions, their ability to inhibit endoplasmic reticulum (ER) stress and hepatic lipogenesis, and to improve atherogenesis and insulin sensitivity, as well as their capacity to activate pathways that are also stimulated by exercise. Findings from clinical trials are also examined. Dissecting the effects of PPARβ/δ ligands on insulin sensitivity and atherogenesis may provide a basis for the development of therapies for the prevention and treatment of T2DM and cardiovascular disease (CVD).
    Sprache Englisch
    Erscheinungsdatum 2016-05
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Review
    ZDB-ID 1042384-9
    ISSN 1879-3061 ; 1043-2760
    ISSN (online) 1879-3061
    ISSN 1043-2760
    DOI 10.1016/j.tem.2016.02.008
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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