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The Extracellular Matrix and Cardiac Pressure Overload: Focus on Novel Treatment Targets.
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- Cells (2073-4409), 2024, v. 13, n. 20, p. 1685, doi. 10.3390/cells13201685
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- Article
Multi-Omics Profiling in Marfan Syndrome: Further Insights into the Molecular Mechanisms Involved in Aortic Disease.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 1, p. 438, doi. 10.3390/ijms23010438
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- Article
In Vivo Renin Activity Imaging in the Kidney of Progeroid Ercc1 Mutant Mice.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 22, p. 12433, doi. 10.3390/ijms222212433
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- Article
Chronic Sildenafil Treatment Improves Vasomotor Function in a Mouse Model of Accelerated Aging.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 13, p. 4667, doi. 10.3390/ijms21134667
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- Article
Vascular Ageing Features Caused by Selective DNA Damage in Smooth Muscle Cell.
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- Oxidative Medicine & Cellular Longevity, 2021, p. 1, doi. 10.1155/2021/2308317
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- Article
Extracellular Matrix Defects in Aneurysmal Fibulin-4 Mice Predispose to Lung Emphysema.
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- PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0106054
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- Article
Increased vascular smooth muscle cell senescence in aneurysmal Fibulin-4 mutant mice.
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- NPJ Aging, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41514-024-00154-4
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- Article
Hybrid Molecular and Functional Micro-CT Imaging Reveals Increased Myocardial Apoptosis Preceding Cardiac Failure in Progeroid Ercc1 Mice.
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- Molecular Imaging & Biology, 2024, v. 26, n. 4, p. 628, doi. 10.1007/s11307-024-01902-4
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- Article
Decreased mitochondrial respiration in aneurysmal aortas of Fibulin-4 mutant mice is linked to PGC1A regulation.
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- Cardiovascular Research, 2018, v. 114, n. 13, p. 1776, doi. 10.1093/cvr/cvy150
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- Article
Accumulation of mitochondrial DNA damage and bioenergetic dysfunction in CSB defective cells.
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- FEBS Journal, 2009, v. 276, n. 10, p. 2811, doi. 10.1111/j.1742-4658.2009.07004.x
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- Article
Functional analysis of cell lines derived from SMAD3-related Loeys-Dietz syndrome patients provides insights into genotype-phenotype relation.
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- Human Molecular Genetics, 2024, v. 33, n. 12, p. 1090, doi. 10.1093/hmg/ddae044
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- Article
Molecular phenotyping and functional assessment of smooth muscle-like cells with pathogenic variants in aneurysm genes ACTA2, MYH11, SMAD3 and FBN1.
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- Human Molecular Genetics, 2021, v. 30, n. 24, p. 2286, doi. 10.1093/hmg/ddab190
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- Article
Molecular phenotyping and functional assessment of smooth muscle-like cells with pathogenic variants in aneurysm genes ACTA2, MYH11, SMAD3 and FBN1.
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- Human Molecular Genetics, 2021, v. 30, n. 23, p. 2286, doi. 10.1093/hmg/ddab190
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- Article
Slc2a10 knock-out mice deficient in ascorbic acid synthesis recapitulate aspects of arterial tortuosity syndrome and display mitochondrial respiration defects.
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- Human Molecular Genetics, 2020, v. 29, n. 9, p. 1476, doi. 10.1093/hmg/ddaa071
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- Article
Tissue-Specific Suppression of Thyroid Hormone Signaling in Various Mouse Models of Aging.
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- PLoS ONE, 2016, v. 11, n. 3, p. 1, doi. 10.1371/journal.pone.0149941
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- Article
Correction: Impaired Genome Maintenance Suppresses the Growth HormoneInsulin-Like Growth Factor 1 Axis in Mice with Cockayne Syndrome.
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- 2008
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- Correction Notice
Impaired Genome Maintenance Suppresses the Growth Hormone--Insulin-Like Growth Factor 1 Axis in Mice with Cockayne Syndrome.
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- PLoS Biology, 2007, v. 5, n. 1, p. 23, doi. 10.1371/journal.pbio.0050002
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- Publication type:
- Article
Transforming Growth Factor-β and the Renin-Angiotensin System in Syndromic Thoracic Aortic Aneurysms: Implications for Treatment.
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- Cardiovascular Drugs & Therapy, 2021, v. 35, n. 6, p. 1233, doi. 10.1007/s10557-020-07116-4
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- Article
Age-related motor neuron degeneration in DNA repair-deficient Ercc1 mice.
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- Acta Neuropathologica, 2010, v. 120, n. 4, p. 461, doi. 10.1007/s00401-010-0715-9
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- Article
Dietary restriction but not angiotensin II type 1 receptor blockade improves DNA damage-related vasodilator dysfunction in rapidly aging Ercc1<sup>Δ/−</sup> mice.
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- Clinical Science, 2017, v. 131, n. 15, p. 1941, doi. 10.1042/CS20170026
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- Article
Cell-Autonomous Progeroid Changes in Conditional Mouse Models for Repair Endonuclease XPG Deficiency.
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- PLoS Genetics, 2014, v. 10, n. 10, p. 1, doi. 10.1371/journal.pgen.1004686
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- Article
Age-Related Neuronal Degeneration: Complementary Roles of Nucleotide Excision Repair and Transcription- Coupled Repair in Preventing Neuropathology.
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- PLoS Genetics, 2011, v. 7, n. 12, p. 1, doi. 10.1371/journal.pgen.1002405
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- Article
Delayed and Accelerated Aging Share Common Longevity Assurance Mechanisms.
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- PLoS Genetics, 2008, v. 4, n. 8, p. 1, doi. 10.1371/journal.pgen.1000161
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- Article
Premature aging in mice activates a systemic metabolic response involving autophagy induction.
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- Human Molecular Genetics, 2008, v. 17, n. 14, p. 2196
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- Article
Model Systems to Study the Mechanism of Vascular Aging.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 20, p. 15379, doi. 10.3390/ijms242015379
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- Article
Ercc1 DNA repair deficiency results in vascular aging characterized by VSMC phenotype switching, ECM remodeling, and an increased stress response.
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- Aging Cell, 2024, v. 23, n. 5, p. 1, doi. 10.1111/acel.14126
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- Article
Soluble guanylate cyclase activator BAY 54–6544 improves vasomotor function and survival in an accelerated ageing mouse model.
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- Aging Cell, 2022, v. 21, n. 9, p. 1, doi. 10.1111/acel.13683
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- Article
Cockayne Syndrome Group B (Csb) and Group A (Csa) Deficiencies Predispose to Hearing Loss and Cochlear Hair Cell Degeneration in Mice.
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- Journal of Neuroscience, 2015, v. 35, n. 10, p. 4280, doi. 10.1523/JNEUROSCI.5063-14.2015
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- Article
Accelerated Age-Related Cognitive Decline and Neurodegeneration, Caused by Deficient DNA Repair.
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- Journal of Neuroscience, 2011, v. 31, n. 35, p. 12543, doi. 10.1523/JNEUROSCI.1589-11.2011
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- Article