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Spontaneous mutations of the Zpld1 gene in mice cause semicircular canal dysfunction but do not impair gravity receptor or hearing functions.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-48835-5
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- Article
Genetic variation in thyroid folliculogenesis influences susceptibility to hypothyroidism-induced hearing impairment.
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- Mammalian Genome, 2019, v. 30, n. 1/2, p. 5, doi. 10.1007/s00335-019-09792-6
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- Article
Deletion of a Long-Range Dlx5 Enhancer Disrupts Inner Ear Development in Mice.
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- Genetics, 2018, v. 208, n. 3, p. 1165, doi. 10.1534/genetics.117.300447
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- Article
ELMOD1 Stimulates ARF6-GTP Hydrolysis to Stabilize Apical Structures in Developing Vestibular Hair Cells.
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- Journal of Neuroscience, 2018, v. 38, n. 4, p. 843, doi. 10.1523/JNEUROSCI.2658-17.2017
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- Article
Hearing loss without overt metabolic acidosis in ATP6V1B1 deficient MRL mice, a new genetic model for non-syndromic deafness with enlarged vestibular aqueducts.
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- Human Molecular Genetics, 2017, v. 26, n. 19, p. 3722, doi. 10.1093/hmg/ddx257
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- Article
Effects of Cdh23 single nucleotide substitutions on age-related hearing loss in C57BL/6 and 129S1/Sv mice and comparisons with congenic strains.
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- Scientific Reports, 2017, p. 44450, doi. 10.1038/srep44450
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- Article
Ectopic Mineralization and Conductive Hearing Loss in Enpp1<sup>asj</sup> Mutant Mice, a New Model for Otitis Media and Tympanosclerosis.
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- PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0168159
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- Article
Application of Mouse Models to Research in Hearing and Balance.
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- 2016
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- journal article
A Lack of Immune System Genes Causes Loss in High Frequency Hearing but Does Not Disrupt Cochlear Synapse Maturation in Mice.
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- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0094549
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- Article
CLIC5 stabilizes membrane-actin filament linkages at the base of hair cell stereocilia in a molecular complex with radixin, taperin, and myosin VI.
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- Cytoskeleton, 2014, v. 71, n. 1, p. 61, doi. 10.1002/cm.21159
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- Article
β-Actin and Fascin-2 Cooperate to Maintain Stereocilia Length.
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- Journal of Neuroscience, 2013, v. 33, n. 19, p. 8114, doi. 10.1523/JNEUROSCI.0238-13.2013
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- Article
Retrotransposon Insertion in the T-cell Acute Lymphocytic Leukemia 1 (Tal1) Gene Is Associated with Severe Renal Disease and Patchy Alopecia in Hairpatches (Hpt) Mice.
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- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0053426
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- Article
Mutations of the Mouse ELMO Domain Containing 1 Gene (Elmod1) Link Small GTPase Signaling to Actin Cytoskeleton Dynamics in Hair Cell Stereocilia.
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- PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0036074
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- Article
The R109H Variant of Fascin-2, a Developmentally Regulated Actin Crosslinker in Hair-Cell Stereocilia, Underlies Early-Onset Hearing Loss of DBA/2J Mice.
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- Journal of Neuroscience, 2010, v. 30, n. 29, p. 9683, doi. 10.1523/JNEUROSCI.1541-10.2010
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- Article
The podosomal-adaptor protein SH3PXD2B is essential for normal postnatal development.
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- Mammalian Genome, 2009, v. 20, n. 8, p. 462, doi. 10.1007/s00335-009-9210-9
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- Article
Targeted knockout and lacZ reporter expression of the mouse Tmhs deafness gene and characterization of the hscy-2J mutation.
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- Mammalian Genome, 2007, v. 18, n. 9, p. 646, doi. 10.1007/s00335-007-9049-x
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- Article
Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid mice.
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- Mammalian Genome, 2007, v. 18, n. 8, p. 596, doi. 10.1007/s00335-007-9038-0
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- Article
The Chloride Intracellular Channel Protein CLIC5 Is Expressed at High Levels in Hair Cell Stereocilia and Is Essential for Normal Inner Ear Function.
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- Journal of Neuroscience, 2006, v. 26, n. 40, p. 10188, doi. 10.1523/JNEUROSCI.2166-06.2006
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- Publication type:
- Article
A quantitative survey of gravity receptor function in mutant mouse strains.
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- 2005
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- Publication type:
- journal article
Applications of tool support for risk-informed requirements reasoning.
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- Computer Systems Science & Engineering, 2005, v. 20, n. 1, p. 5
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- Publication type:
- Article
Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans.
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- Human Molecular Genetics, 2005, v. 14, n. 1, p. 103, doi. 10.1093/hmg/ddi010
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- Article
New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice.
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- Mammalian Genome, 2004, v. 15, n. 3, p. 151, doi. 10.1007/s00335-003-2310-z
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- Article
Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene.
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- Human Molecular Genetics, 2003, v. 12, n. 23, p. 3075, doi. 10.1093/hmg/ddg332
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- Article
A Missense Mutation in the Mouse Col2a1 Gene Causes Spondyloepiphyseal Dysplasia Congenita, Hearing Loss, and Retinoschisis.
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- Journal of Bone & Mineral Research, 2003, v. 18, n. 9, p. 1612, doi. 10.1359/jbmr.2003.18.9.1612
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- Article
Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss.
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- Nature Genetics, 2003, v. 35, n. 1, p. 21, doi. 10.1038/ng1226
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- Article
Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6.
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- Human Molecular Genetics, 2002, v. 11, n. 16, p. 1887, doi. 10.1093/hmg/11.16.1887
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- Article
Microtubule-associated protein 1A is a modifier of tubby hearing (moth1).
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- Nature Genetics, 2002, v. 30, n. 4, p. 401, doi. 10.1038/ng838
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- Article
A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice.
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- Nature Genetics, 2001, v. 27, n. 2, p. 191, doi. 10.1038/84831
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- Article
Grey intense: a new mouse mutation affecting pigmentation.
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- Mammalian Genome, 2000, v. 11, n. 12, p. 1139, doi. 10.1007/s003350010165
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- Article
Neuromuscular ataxia: a new spontaneous mutation in the mouse.
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- Mammalian Genome, 2000, v. 11, n. 10, p. 820, doi. 10.1007/s003350010167
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- Article
Genetic modification of hearing in tubby mice: evidence for the existence of a major gene (moth1) which protects tubby mice from hearing loss.
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- Human Molecular Genetics, 1999, v. 8, n. 9, p. 1761, doi. 10.1093/hmg/8.9.1761
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- Article
A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant.
- Published in:
- Nature Genetics, 1999, v. 23, n. 1, p. 104, doi. 10.1038/12709
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- Article
Inner ear and kidney anomalies caused by IAP insertion in an intron of the gene in a mouse model of BOR syndrome.
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- Human Molecular Genetics, 1999, v. 8, n. 4, p. 645, doi. 10.1093/hmg/8.4.645
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- Article
A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactyly.
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- Human Molecular Genetics, 1998, v. 7, n. 6, p. 1033, doi. 10.1093/hmg/7.6.1033
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- Article
James E. Wright, Jr.
- Published in:
- Journal of Heredity, 1998, v. 89, n. 3, p. 285
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- Article
Maid: a maternally transcribed novel gene encoding a potential negative regulator of bHLH proteins in the mouse egg and zygote.
- Published in:
- Developmental Dynamics, 1997, v. 209, n. 2, p. 217, doi. 10.1002/(SICI)1097-0177(199706)209:2<217::AID-AJA7>3.0.CO;2-L
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- Article
Developmentally Regulated Mouse Gene NK10 Encodes a Zinc Finger Repressor Protein with Differential DNA-Binding Domains.
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- DNA & Cell Biology, 1995, v. 14, n. 11, p. 971, doi. 10.1089/dna.1995.14.971
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- Article
Cloning and Functional Characterization of a Family of Receptors for the Melanotropic Peptides.
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- Annals of the New York Academy of Sciences, 1993, v. 680, n. 1, p. 342, doi. 10.1111/j.1749-6632.1993.tb19694.x
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- Article
Linkage associations in hybridized Salvelinus genomes.
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- Journal of Heredity, 1984, v. 75, n. 4, p. 253
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- Article
A Comparison of Black Dialect-Speaking Children and Standard English-Speaking Children and Their Ability to Hear Final Consonant Stops.
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- TESOL Quarterly, 1974, v. 8, n. 4, p. 375, doi. 10.2307/3585469
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- Article
WHEN SHOULD STANDARD ENGLISH BE TAUGHT TO SPEAKERS OF NONSTANDARD NEGRO DIALECT?
- Published in:
- Language Learning, 1970, v. 20, n. 1, p. 19, doi. 10.1111/j.1467-1770.1970.tb00042.x
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- Publication type:
- Article