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Hearing Loss is an Early Consequence of Npc1 Gene Deletion in the Mouse Model of Niemann-Pick Disease, Type C.
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- JARO - Journal of the Association for Research in Otolaryngology, 2014, v. 15, n. 4, p. 529, doi. 10.1007/s10162-014-0459-7
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- Article
Multiple Quantitative Trait Loci Modify Cochlear Hair Cell Degeneration in the Beethoven (Tmc1<sup>Bth</sup>) Mouse Model of Progressive Hearing Loss DFNAS6.
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- Genetics, 2006, v. 173, n. 4, p. 2111, doi. 10.1534/genetics.106.057372
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- Article
Tmc2 expression partially restores auditory function in a mouse model of DFNB7/B11 deafness caused by loss of Tmc1 function.
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- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-29709-8
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- Article
Synthesis of Turkey Pit-1 mRNA Variants by Alternative Splicing and Transcription Initiation.
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- DNA & Cell Biology, 1998, v. 17, n. 1, p. 93, doi. 10.1089/dna.1998.17.93
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- Article
Systemic Fluorescent Gentamicin Enters Neonatal Mouse Hair Cells Predominantly Through Sensory Mechanoelectrical Transduction Channels.
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- 2020
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- Publication type:
- journal article
Esophageal xanthoma: presence of M2 macrophages suggests association with late inflammatory and reparative processes.
- Published in:
- Open Medicine, 2017, v. 12, n. 1, p. 335, doi. 10.1515/med-2017-0048
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- Article
Selective binding and transport of protocadherin 15 isoforms by stereocilia unconventional myosins in a heterologous expression system.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-17757-0
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- Article
Amino acid 572 in TMC1: hot spot or critical functional residue for dominant mutations causing hearing impairment.
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- Journal of Human Genetics, 2009, v. 54, n. 3, p. 188, doi. 10.1038/jhg.2009.1
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- Article
Transmembrane channel-like ( TMC) genes are required for auditory and vestibular mechanosensation.
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- Pflügers Archiv: European Journal of Physiology, 2015, v. 467, n. 1, p. 85, doi. 10.1007/s00424-014-1582-3
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- Article
Multiparametric assessment of the impact of opsin expression and anesthesia on striatal cholinergic neurons and auditory brainstem activity.
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- Journal of Comparative Neurology, 2020, v. 528, n. 5, p. 787, doi. 10.1002/cne.24795
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- Article
Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.
- Published in:
- Nature Genetics, 2002, v. 30, n. 3, p. 257, doi. 10.1038/ng848
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- Article
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
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- Nature Genetics, 2002, v. 30, n. 3, p. 277, doi. 10.1038/ng842
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- Article
Cell Type-Specific Transcriptome Analysis Reveals a Major Role for Zeb1 and miR-200b in Mouse Inner Ear Morphogenesis.
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- PLoS Genetics, 2011, v. 7, n. 9, p. 1, doi. 10.1371/journal.pgen.1002309
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- Article
A Noncoding Point Mutation of Zeb1 Causes Multiple Developmental Malformations and Obesity in Twirler Mice.
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- PLoS Genetics, 2011, v. 7, n. 9, p. 1, doi. 10.1371/journal.pgen.1002307
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- Article
Co-expression of low-risk HPV E6/E7 and EBV LMP-1 leads to precancerous lesions by DNA damage.
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- BMC Cancer, 2021, v. 21, n. 1, p. 1, doi. 10.1186/s12885-021-08397-0
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- Article
Co-expression of low-risk HPV E6/E7 and EBV LMP-1 leads to precancerous lesions by DNA damage.
- Published in:
- 2021
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- Publication type:
- journal article
Designing AAV Vectors for Monitoring the Subtle Calcium Fluctuations of Inferior Olive Network in vivo.
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- Frontiers in Cellular Neuroscience, 2022, v. 16, p. 1, doi. 10.3389/fncel.2022.825056
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- Article
Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genes.
- Published in:
- 2011
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- Publication type:
- journal article
Mouse model of enlarged vestibular aqueducts defines temporal requirement of Slc26a4 expression for hearing acquisition.
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- 2011
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- Publication type:
- journal article
Molecular Signature of Tumors with Monoallelic 13q14 Deletion: a Case Series of Spindle Cell Lipoma and Genetically-Related Tumors Demonstrating a Link Between FOXO1 Status and p38 MAPK Pathway.
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- Pathology & Oncology Research, 2018, v. 24, n. 4, p. 861, doi. 10.1007/s12253-017-0303-6
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- Article