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Regulation of matrix metalloproteinase-9 protein expression by 1α, 25-(OH)<sub>2</sub>D<sub>3</sub> during osteoclast differentiation.
- Published in:
- Journal of Veterinary Science, 2014, v. 15, n. 1, p. 133, doi. 10.4142/jvs.2014.15.1.133
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- Article
Inhibitory effects of osteoprotegerin on osteoclast formation and function under serum-free conditions.
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- Journal of Veterinary Science, 2014, v. 15, n. 2, p. 405, doi. 10.4142/jvs.2013.14.4.405
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- Article
Inhibitory effects of osteoprotegerin on osteoclast formation and function under serum-free conditions.
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- Journal of Veterinary Science, 2013, v. 14, n. 4, p. 405, doi. 10.4142/jvs.2013.14.4.405
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- Article
Oxygen Saturation in Closed-Globe Blunt Ocular Trauma.
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- BioMed Research International, 2016, v. 2016, p. 1, doi. 10.1155/2016/8232468
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- Article
New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing.
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- Neural Plasticity, 2019, p. 1, doi. 10.1155/2019/7143458
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- Article
Dispersed DNA variants underlie hearing loss in South Florida's minority population.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00556-7
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- Article
Tumor-Associated Macrophages in Vestibular Schwannoma and Relationship to Hearing.
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- OTO Open: The Official Open Access Journal of the American Academy of Otolaryngology Head & Neck Surgery Foundation, 2021, v. 5, n. 4, p. 1, doi. 10.1177/2473974X211059111
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- Article
Alpha-Lipoic Acid Attenuates Cadmium- and Lead-Induced Neurotoxicity by Inhibiting Both Endoplasmic-Reticulum Stress and Activation of Fas/FasL and Mitochondrial Apoptotic Pathways in Rat Cerebral Cortex.
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- Neurotoxicity Research, 2021, v. 39, n. 4, p. 1103, doi. 10.1007/s12640-021-00348-8
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- Article
PDZD7-MYO7A complex identified in enriched stereocilia membranes.
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- eLife, 2016, p. 1, doi. 10.7554/eLife.18312
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- Article
Elucidation of repeat motifs R1‐ and R2‐related TRIOBP variants in autosomal recessive nonsyndromic hearing loss DFNB28 among indigenous South African individuals.
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- Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 10, p. 1, doi. 10.1002/mgg3.2015
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- Article
Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type II.
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- Journal of Human Genetics, 2009, v. 54, n. 12, p. 732, doi. 10.1038/jhg.2009.107
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- Article
The genetic bases for non-syndromic hearing loss among Chinese.
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- Journal of Human Genetics, 2009, v. 54, n. 3, p. 131, doi. 10.1038/jhg.2009.4
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- Article
Refinement of the DFNA41 locus and candidate genes analysis.
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- Journal of Human Genetics, 2005, v. 50, n. 10, p. 516, doi. 10.1007/s10038-005-0286-0
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- Article
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C.
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- Nature Genetics, 2000, v. 26, n. 1, p. 51, doi. 10.1038/79171
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- Article
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene.
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- Nature Genetics, 2000, v. 26, n. 1, p. 56, doi. 10.1038/79178
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- Article
Audioprofiles and antioxidant enzyme genotypes in presbycusis.
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- Laryngoscope, 2012, v. 122, n. 11, p. 2539, doi. 10.1002/lary.23577
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- Article
Clinical comparison of hearing-impaired patients with DFNB1 against heterozygote carriers of connexin 26 mutations.
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- Laryngoscope, 2011, v. 121, n. 4, p. 811, doi. 10.1002/lary.21422
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- Article
Whole-Exome Sequencing to Decipher the Genetic Heterogeneity of Hearing Loss in a Chinese Family with Deaf by Deaf Mating.
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- PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0109178
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- Article
<i>In Vitro</i> Interaction of <i>Pseudomonas aeruginosa</i> with Human Middle Ear Epithelial Cells.
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- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0091885
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- Article
Cadmium-Induced Apoptosis in Primary Rat Cerebral Cortical Neurons Culture Is Mediated by a Calcium Signaling Pathway
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- PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0064330
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- Article
<italic>ELMOD3</italic>, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss.
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- Human Genetics, 2018, v. 137, n. 4, p. 329, doi. 10.1007/s00439-018-1885-0
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- Article
Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31.
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- Human Genetics, 2009, v. 125, n. 1, p. 53, doi. 10.1007/s00439-008-0602-9
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- Article
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population.
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- Human Genetics, 2005, v. 116, n. 4, p. 292, doi. 10.1007/s00439-004-1227-2
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- Article
Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east Asians.
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- Human Genetics, 2003, v. 114, n. 1, p. 44, doi. 10.1007/s00439-003-1018-1
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- Article
Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness.
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- Human Genetics, 2002, v. 111, n. 1, p. 26, doi. 10.1007/s00439-002-0736-0
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- Article
Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians.
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- Human Genetics, 2001, v. 108, n. 5, p. 385, doi. 10.1007/s004390100507
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- Article
Identification of a genetic variant underlying familial cases of recurrent benign paroxysmal positional vertigo.
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- PLoS ONE, 2021, v. 16, n. 5, p. 1, doi. 10.1371/journal.pone.0251386
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- Article
Early Wnt Signaling Activation Promotes Inner Ear Differentiation via Cell Caudalization in Mouse Stem Cell-Derived Organoids.
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- Stem Cells, 2023, v. 41, n. 1, p. 26, doi. 10.1093/stmcls/sxac071
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- Article
Analysis of subcellular localization of Myo7a, Pcdh15 and Sans in Ush1c knockout mice.
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- International Journal of Experimental Pathology, 2011, v. 92, n. 1, p. 66, doi. 10.1111/j.1365-2613.2010.00751.x
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- Article
Chronic Rhinosinusitis Disease Disparity in the South Florida Hispanic Population.
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- Laryngoscope, 2021, v. 131, n. 12, p. 2659, doi. 10.1002/lary.29664
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- Article
Progressive Dominant Hearing Loss (Autosomal Dominant Deafness-41) and P2RX2 Gene Mutations: A Phenotype-Genotype Study.
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- 2020
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- Publication type:
- journal article
Recent Perspectives on Gene-Microbe Interactions Determining Predisposition to Otitis Media.
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- Frontiers in Genetics, 2019, v. 10, p. 1, doi. 10.3389/fgene.2019.01230
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- Article
1α,25-Dihydroxyvitamin D3 inhibits the differentiation and bone resorption by osteoclasts generated from Wistar rat bone marrow-derived macrophages.
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- Experimental & Therapeutic Medicine, 2015, v. 10, n. 3, p. 1039, doi. 10.3892/etm.2015.2632
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- Article
Association of PRPS1 Mutations with Disease Phenotypes.
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- Disease Markers, 2015, p. 1, doi. 10.1155/2015/127013
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- Article
The Effects of Autophagy and PI3K/AKT/m-TOR Signaling Pathway on the Cell-Cycle Arrest of Rats Primary Sertoli Cells Induced by Zearalenone.
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- Toxins, 2018, v. 10, n. 10, p. 398, doi. 10.3390/toxins10100398
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- Article
ROS-Mediated Cell Cycle Arrest and Apoptosis Induced by Zearalenone in Mouse Sertoli Cells via ER Stress and the ATP/AMPK Pathway.
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- Toxins, 2018, v. 10, n. 1, p. 24, doi. 10.3390/toxins10010024
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- Publication type:
- Article
Cadmium-induced autophagy is mediated by oxidative signaling in PC-12 cells and is associated with cytoprotection.
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- Molecular Medicine Reports, 2015, v. 12, n. 3, p. 4448, doi. 10.3892/mmr.2015.3907
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- Article
Cadmium-induced autophagy promotes survival of rat cerebral cortical neurons by activating class III phosphoinositide-kinase/beclin-1/B-cell lymphoma 2 signaling pathways.
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- Molecular Medicine Reports, 2015, v. 12, n. 2, p. 2912, doi. 10.3892/mmr.2015.3755
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- Article
Targeted Resequencing of Deafness Genes Reveals a Founder MYO15A Variant in Northeastern Brazil.
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- Annals of Human Genetics, 2016, v. 80, n. 6, p. 327, doi. 10.1111/ahg.12177
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- Article
Research on technological optimization of hemicellulose from corncob by ultrasound-microwave synergistic extraction.
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- Feed Research, 2022, v. 45, n. 9, p. 75, doi. 10.13557/j.cnki.issn1002-2813.2022.09.017
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- Article
A Possible Association Between Hearing Loss and Zika Virus Infections.
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- 2018
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- Publication type:
- journal article
An Update on Phosphodiesterase Mutations Underlying Genetic Etiology of Hearing Loss and Retinitis Pigmentosa.
- Published in:
- Frontiers in Genetics, 2018, p. 1, doi. 10.3389/fgene.2018.00009
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- Publication type:
- Article
Generation and characterization of a P2rx2 V60L mouse model for DFNA41.
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- Human Molecular Genetics, 2021, v. 30, n. 11, p. 985, doi. 10.1093/hmg/ddab077
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- Article
A missense mutation in DCDC2 causeshuman recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation.
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- Human Molecular Genetics, 2015, v. 24, n. 9, p. 2482, doi. 10.1093/hmg/ddv009
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- Publication type:
- Article
A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 9, p. 2482, doi. 10.1093/hmg/ddv009
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- Publication type:
- Article
Transcriptomic Analyses of Inner Ear Sensory Epithelia in Zebrafish.
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- Anatomical Record: Advances in Integrative Anatomy & Evolutionary Biology, 2020, v. 303, n. 3, p. 527, doi. 10.1002/ar.24331
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- Article
Congenital Middle Ear Malformation with Common Deafness Gene Mutation Analysis: A Review of 813 Profound Sensorineural Hearing Loss Child Patients.
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- Anatomical Record: Advances in Integrative Anatomy & Evolutionary Biology, 2020, v. 303, n. 3, p. 594, doi. 10.1002/ar.24330
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- Article
The Generation of Zebrafish Mariner Model Using the CRISPR/Cas9 System.
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- Anatomical Record: Advances in Integrative Anatomy & Evolutionary Biology, 2020, v. 303, n. 3, p. 556, doi. 10.1002/ar.24221
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- Article
Zebrafish Model for Nonsyndromic X‐Linked Sensorineural Deafness, DFNX1.
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- Anatomical Record: Advances in Integrative Anatomy & Evolutionary Biology, 2020, v. 303, n. 3, p. 544, doi. 10.1002/ar.24115
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- Article
Genetics of Hearing and Deafness.
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- Anatomical Record: Advances in Integrative Anatomy & Evolutionary Biology, 2012, v. 295, n. 11, p. 1, doi. 10.1002/ar.22579
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- Publication type:
- Article