Myosin VIIa as a common component of cilia and microvilli.

No abstract is available for this paper.

• Publication year

  1998

• Venue

  Cell Motility and the Cytoskeleton

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1002/(SICI)1097-0169(1998)40:3<261::AID-CM5>3.0.CO;2-GPMID 9678669
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells.

  1998cited by this paper
• Myosin VIIa, the product of the Usher 1B syndrome gene, is concentrated in the connecting cilia of photoreceptor cells.

  1997cited by this paper
• Unconventional Myosins in Inner-Ear Sensory Epithelia

  1997influential reference
• Effects of shaker-1 mutations on myosin-VIIa protein and mRNA expression.

  1997influential reference
• Expression of myosin VIIA during mouse embryogenesis

  1997cited by this paper
• Mutation analysis of the mouse myosin VIIA deafness gene.

  1997cited by this paper
• Olfactory loss in Usher syndrome: another sensory deficit?

  1996influential reference
• Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells.

  1996cited by this paper
• Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia.

  1996cited by this paper
• Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B.

  1995influential reference
• The kinocilium of auditory hair cells and evidence for its morphogenetic role during the regeneration of stereocilia and cuticular plates

  1995cited by this paper
• A type VII myosin encoded by the mouse deafness gene shaker-1

  1995cited by this paper
• Defective myosin VIIA gene responsible for Usher syndrome type IB

  1995cited by this paper
• Selective Proteolysis of Arrestin by Calpain

  1995cited by this paper
• Centrin in the photoreceptor cells of mammalian retinae.

  1995cited by this paper
• Bronchial asthma in a patient with Usher syndrome: case report.

  1994cited by this paper
• Multiple unconventional myosin domains of the intestinal brush border cytoskeleton.

  1994cited by this paper
• Acetylated alpha-tubulin in the connecting cilium of developing rat photoreceptors.

  1993cited by this paper
• Usher syndrome type I associated with bronchiectasis and immotile nasal cilia in two brothers.

  1993cited by this paper
• Ultrastructure of connecting cilia in different forms of retinitis pigmentosa.

  1992cited by this paper
• Maturation of kinocilia in amphibian hair cells: growth and shortening related to kinociliary bulb formation.

  1992cited by this paper
• Ectoplasmic (“Junctional”) Specializations in Mammalian Sertoli Cells: Influence on Spermatogenic Cells a

  1991cited by this paper
• The Photoreceptor Connecting Cilium A Model for the Transition Zone

  1990cited by this paper
• Actin filament polarity at the site of rod outer segment disk morphogenesis.

  1989cited by this paper
• Organization of actin filaments and immunocolocalization of alpha‐actinin in the connecting cilium of rat photoreceptors

  1989cited by this paper
• Distribution of acetylated α‐tubulin in retina and in in vitro—assembled microtubules

  1988cited by this paper
• Two monoclonal antibodies to actin: one muscle selective and one generally reactive.

  1988cited by this paper
• Distribution of acetylated alpha-tubulin in retina and in vitro-assembled microtubules.

  1988cited by this paper
• Cytoskeletal-membrane interactions: a stable interaction between cell surface glycoconjugates and doublet microtubules of the photoreceptor connecting cilium

  1987influential reference
• The distribution of F-actin in cells isolated from vertebrate retinas.

  1987cited by this paper
• Posttranslational modification and microtubule stability

  1987cited by this paper
• Abnormal sperm and photoreceptor axonemes in Usher's syndrome.

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• Sertoli cell junctions: morphological and functional correlates.

  1985cited by this paper
• Organization, chemistry, and assembly of the cytoskeletal apparatus of the intestinal brush border.

  1985cited by this paper
• Ciliated and microvillous structures of rat olfactory and nasal respiratory epithelia

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• Mechanism and control of animal fertilization

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• Histochemical demonstration of heavy metals

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• Association of guanylate cyclase with the axoneme of retinal rods.

  1980influential reference
• The organization of actin filaments in the stereocilia of cochlear hair cells

  1980cited by this paper
• Increased incidence of abnormal nasal cilia in patients with retinitis pigmentosa

  1979cited by this paper
• An actin-like protein is a component of axonemes from Chlamydomonas flagella.

  1979cited by this paper
• Organization of an actin filament-membrane complex. Filament polarity and membrane attachment in the microvilli of intestinal epithelial cells

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• The sensory cilium of retinal rods is analogous to the transitional zone of motile cilia

  1975cited by this paper
• PERIODATE-LYSINE-PARAFORMALDEHYDE FIXATIVE A NEW FIXATIVE FOR IMMUNOELECTRON MICROSCOPY

  1974cited by this paper
• Hairs of the cochlear sensory cells and their attachment to the tectorial membrane.

  1966cited by this paper
• The development of the organ of Corti in the mouse.

  1965cited by this paper
• THE RELATIONSHIP BETWEEN THE FINE STRUCTURE AND DIRECTION OF BEAT IN GILL CILIA OF A LAMELLIBRANCH MOLLUSC

  1961cited by this paper

• Familial vs sporadic normal pressure hydrocephalus: a comparative study

  2025cites this paper
• In-depth analysis of obesity-associated changes in adipose tissue-derived mesenchymal stromal/stem cells and primary cilia function

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• Morphological phenotyping of the aging cochlea in inbred C57BL/6N and outbred CD1 mouse strains

  2024cites this paper
• A role for mutations in AK9 and other genes affecting ependymal cells in idiopathic normal pressure hydrocephalus

  2023cites this paper
• Functions of actin‐binding proteins in cilia structure remodeling and signaling

  2023cites this paper
• LUZP1: A new player in the actin-microtubule cross-talk.

  2022cites this paper
• A binding protein regulates myosin-7a dimerization and actin bundle assembly

  2021cites this paper
• Decreased activity of piriform cortex and orbitofrontal hyperactivation in Usher Syndrome, a human disorder of ciliary dysfunction

  2021cites this paper
• Usher syndrome: clinical features, molecular genetics and advancing therapeutics

  2020cites this paper
• Mutations in Drosophila crinkled/Myosin VIIA disrupt denticle morphogenesis.

  2020cites this paper
• Actin binding proteins, actin cytoskeleton and spermatogenesis - Lesson from toxicant models.

  2020cites this paper
• Cochlear Implantation From the Perspective of Genetic Background

  2020cites this paper
• Myosin VIIa Supports Spermatid/Organelle Transport and Cell Adhesion During Spermatogenesis in the Rat Testis

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• SANS (USH1G) Molecularly Links the Human Usher Syndrome Protein Network to the Intraflagellar Transport Module by Direct Binding to IFT-B Proteins

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• Genetics of Usher Syndrome: New Insights From a Meta-analysis.

  2019cites this paper
• Chemosensory and Mechanosensory Functions of Olfactory Cilia

  2018cites this paper
• Unconventional myosin VIIA promotes melanoma progression

  2018cites this paper
• Cilium structure, assembly, and disassembly regulated by the cytoskeleton

  2018cites this paper
• Role of Polarity Proteins in the Generation and Organization of Apical Surface Protrusions.

  2018cites this paper
• Investigating the pathophysiology of KCNJ13 and USH2A retinopathies using zebrafish models

  2018cites this paper
• The shaker-1 mouse myosin VIIa deafness mutation results in a severely reduced rate of the ATP hydrolysis step

  2017cites this paper
• Genetic screening revealed usher syndrome in a paediatric Chinese patient

  2017cites this paper
• An Actin Network Dispatches Ciliary GPCRs into Extracellular Vesicles to Modulate Signaling.

  2017cites this paper
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  2016cites this paper
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  2016cites this paper
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  2016cites this paper
• Impact of the Usher syndrome on olfaction.

  2016cites this paper
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  2015cites this paper
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  2015cites this paper
• Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities.

  2015cites this paper
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  2015influential citation
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  2014cites this paper
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  2014influential citation
• myosin 7aa(-/-) mutant zebrafish show mild photoreceptor degeneration and reduced electroretinographic responses.

  2014cites this paper
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  2013cites this paper
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  2011cites this paper
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  2011cites this paper
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• Identification of a Novel Mutation in the Myosin VIIA Motor Domain in a Family with Autosomal Dominant Hearing Loss (DFNA11)

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