Found: 24
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The usherin mutation c.2299delG leads to its mislocalization and disrupts interactions with whirlin and VLGR1.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-36431-1
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- Article
Ramipril therapy in integrin α1‐null, autosomal recessive Alport mice triples lifespan: mechanistic clues from RNA‐seq analysis.
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- Journal of Pathology, 2024, v. 262, n. 3, p. 296, doi. 10.1002/path.6231
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- Article
Dual inhibition of the endothelin and angiotensin receptor ameliorates renal and inner ear pathologies in Alport mice.
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- Journal of Pathology, 2023, v. 260, n. 3, p. 353, doi. 10.1002/path.6087
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- Article
Glomerular basement membrane deposition of collagen α1(III) in Alport glomeruli by mesangial filopodia injures podocytes via aberrant signaling through DDR1 and integrin α2β1.
- Published in:
- Journal of Pathology, 2022, v. 258, n. 1, p. 26, doi. 10.1002/path.5969
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- Article
Human alpha1 type IV collagen NC1 domain exhibits distinct antiangiogenic activity mediated by alpha1beta1 integrin.
- Published in:
- 2005
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- Publication type:
- journal article
A Post-Embedding Colloidal Gold Immunocytochemical Approach To The Study Of Matrix Accumulation In Glomerular Basement Membrane.
- Published in:
- Microscopy & Microanalysis, 1999, p. 1336, doi. 10.1017/S1431927600020006
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- Article
Biomechanical strain causes maladaptive gene regulation, contributing to Alport glomerular disease.
- Published in:
- Kidney International, 2009, v. 76, n. 9, p. 968, doi. 10.1038/ki.2009.324
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- Article
Laminin α2-Mediated Focal Adhesion Kinase Activation Triggers Alport Glomerular Pathogenesis.
- Published in:
- PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0099083
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- Article
EIAV-Based Retinal Gene Therapy in the <i>shaker1</i> Mouse Model for Usher Syndrome Type 1B: Development of UshStat.
- Published in:
- PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0094272
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- Article
Light-Induced Translocation of RGS9-1 and Gβ5L in Mouse Rod Photoreceptors.
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- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0058832
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- Article
Role for a Novel Usher Protein Complex in Hair Cell Synaptic Maturation.
- Published in:
- PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0030573
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- Publication type:
- Article
Sodium butyrate-mediated induction of the glycoprotein hormone α-subunit gene: Requirement for continued protein synthesis, identification of a butyrate-responsive element, and inhibition of promoter activation by 2-deoxyglucose.
- Published in:
- Journal of Cellular Biochemistry, 1999, v. 74, n. 2, p. 242, doi. 10.1002/(SICI)1097-4644(19990801)74:2<242::AID-JCB10>3.0.CO;2-9
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- Publication type:
- Article
RNA-seq analysis of gene expression profiles in isolated stria vascularis from wild-type and Alport mice reveals key pathways underling Alport strial pathogenesis.
- Published in:
- PLoS ONE, 2020, v. 15, n. 8, p. 1, doi. 10.1371/journal.pone.0237907
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- Publication type:
- Article
Human α1 type IV collagen NC1 domain exhibits distinct antiangiogenic activity mediated by α1β1 integrin.
- Published in:
- 2020
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- Publication type:
- journal article
Modular retro-vectors for transgenic and therapeutic use.
- Published in:
- Molecular Reproduction & Development, 2000, v. 56, n. S2, p. 309, doi. 10.1002/(SICI)1098-2795(200006)56:2+<309::AID-MRD22>3.0.CO;2-Y
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- Publication type:
- Article
Glomerular pathology in Alport syndrome: a molecular perspective.
- Published in:
- Pediatric Nephrology, 2012, v. 27, n. 6, p. 885, doi. 10.1007/s00467-011-1868-z
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- Publication type:
- Article
Dysregulation of renal MMP-3 and MMP-7 in canine X-linked Alport syndrome.
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- Pediatric Nephrology, 2005, v. 20, n. 6, p. 732, doi. 10.1007/s00467-004-1805-5
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- Article
X-Linked Alport Dogs Demonstrate Mesangial Filopodial Invasion of the Capillary Tuft as an Early Event in Glomerular Damage.
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- PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0168343
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- Article
Stem cell therapy for Alport syndrome: the hope beyond the hype.
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- Nephrology Dialysis Transplantation, 2009, v. 24, n. 3, p. 731
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- Article
Stage-specific action of matrix metalloproteinases influences progressive hereditary kidney disease.
- Published in:
- 2006
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- Publication type:
- journal article
Increased expression of MMP-2, MMP-9 (type IV collagenases/gelatinases), and MT1-MMP in canine X-linked Alport syndrome (XLAS).
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- Kidney International, 2003, v. 63, n. 5, p. 1736, doi. 10.1046/j.1523-1755.2003.00939.x
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- Publication type:
- Article
Monocytes may promote myofibroblast accumulation and apoptosis in Alport renal fibrosis<sup>1</sup>.
- Published in:
- Kidney International, 2003, v. 63, n. 4, p. 1338, doi. 10.1046/j.1523-1755.2003.00871.x
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- Publication type:
- Article
Role for transforming growth factor-β1 in Alport renal disease progression.
- Published in:
- Kidney International, 1999, v. 56, n. 5, p. 1662, doi. 10.1046/j.1523-1755.1999.00744.x
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- Article
Regulated Vesicular Trafficking of Specific PCDH15 and VLGRl Variants in Auditory Hair Cells.
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- Journal of Neuroscience, 2012, v. 32, n. 40, p. 13841, doi. 10.1523/JNEUROSCI.1242-12.2012
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- Publication type:
- Article