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Mostrando 101 - 120 Resultados de 1,763 Para Buscar '"Usher"', tiempo de consulta: 0.16s Limitar resultados
  1. 101
    por Sugita, Junichi, Fujiu, Katsuhito
    Publicado 2019
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    Emerging Function of Cardiac Macrophages Ushers in a New Era for the Electrophysiology of the Heart
  2. 102
    por Touchett, Hilary
    Publicado 2021
    “…One silver lining of COVID-19 has been the ushering in of ‘the golden age of telehealth’. However, this unplanned rapid conversion to telehealth left many providers and clinics unprepared to address systemic barriers that adversely affect older adults, particularly those with disabilities. …”
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    Ushering in the Silver Age of Telehealth: Addressing Telehealth Disparities for Older Adults With Disabilities
  3. 103
    “…Usher syndrome (USH) is an autosomal recessively inherited disease characterized by sensorineural hearing loss (SNHL) and retinitis pigmentosa (RP) with or without vestibular dysfunction. …”
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    Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variants
  4. 104
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    CRISPR/Cas systems usher in a new era of disease treatment and diagnosis
  5. 105
    “…Human Usher syndrome (USH) is the most common form of hereditary combined deaf-blindness. …”
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    The Usher syndrome 1C protein harmonin regulates canonical Wnt signaling
  6. 106
    por Demontis, Fabio, Dahmann, Christian
    Publicado 2009
    “…BACKGROUND: The Usher syndrome (USH) is the most frequent deaf-blindness hereditary disease in humans. …”
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    Characterization of the Drosophila Ortholog of the Human Usher Syndrome Type 1G Protein Sans
  7. 107
    “…PURPOSE: It has been demonstrated that mutations in deafness, autosomal recessive 31 (DFNB31), the gene encoding whirlin, is responsible for nonsyndromic hearing loss (NSHL; DFNB31) and Usher syndrome type II (USH2D). We screened DFNB31 in a large cohort of patients with different clinical subtypes of Usher syndrome (USH) to determine the prevalence of DFNB31 mutations among USH patients. …”
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    Sequence variants of the DFNB31 gene among Usher syndrome patients of diverse origin
  8. 108
    por Suchert, Steffen
    Publicado 2010
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    A "Family Project" to fight Usher, a rare disease leading to deaf-blindness
  9. 109
    “…Yersinia pestis genome sequencing projects have revealed six intact uncharacterized chaperone/usher systems with the potential to play roles in plague pathogenesis. …”
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    Contributions of chaperone/usher systems to cell binding, biofilm formation and Yersinia pestis virulence
  10. 110
    “…Mutations in the PCDH15 gene are responsible for Usher syndrome type I (USH1F) and non-syndromic hearing loss (DFNB23). …”
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    Mutation screening of the PCDH15 gene in Spanish patients with Usher syndrome type I
  11. 111
    “…The mechanisms underlying retinal dystrophy in Usher syndrome type I (USH1) remain unknown because mutant mice lacking any of the USH1 proteins—myosin VIIa, harmonin, cadherin-23, protocadherin-15, sans—do not display retinal degeneration. …”
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    Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice
  12. 112
    “…BACKGROUND: Mutations in the gene for Usher syndrome 2A (USH2A) are causative for non-syndromic retinitis pigmentosa and Usher syndrome, a condition that is the most common cause of combined deaf-blindness. …”
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    The mitotic spindle protein SPAG5/Astrin connects to the Usher protein network postmitotically
  13. 113
    “…Usher syndrome is an autosomal recessive disorder manifesting hearing loss, retinitis pigmentosa and vestibular dysfunction, and having three clinical subtypes. …”
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    Massively Parallel DNA Sequencing Facilitates Diagnosis of Patients with Usher Syndrome Type 1
  14. 114
    “…Usher syndrome is an autosomal recessive disorder that causes hearing loss, Retinitis Pigmentosa (RP) and vestibular dysfunction. …”
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    Domain analyses of Usher syndrome causing Clarin-1 and GPR98 protein models
  15. 115
    “…Chaperone/usher (CU) assembly pathway is used by a wide range of Enterobacteriaceae to assemble adhesive surface structures called pili or fimbriae that play a role in bacteria-host cell interactions. …”
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    In Silico Analysis of Usher Encoding Genes in Klebsiella pneumoniae and Characterization of Their Role in Adhesion and Colonization
  16. 116
    “…To portray Usher Syndrome type 2, analyzing choroidal thickness and comparing data reported in published literature on RP and healthy subjects. …”
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    Choroidal Thickness Analysis in Patients with Usher Syndrome Type 2 Using EDI OCT
  17. 117
    “…Usher syndrome is a group of autosomal recessive diseases characterized by congenital deafness and retinitis pigmentosa. …”
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    The Time Course of Deafness and Retinal Degeneration in a Kunming Mouse Model for Usher Syndrome
  18. 118
    “…Usher syndrome type 1 (USH1) is the most severe of the three USH subtypes due to its profound hearing loss, absent vestibular response and retinitis pigmentosa appearing at a prepubescent age. …”
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    Frequency of Usher syndrome type 1 in deaf children by massively parallel DNA sequencing
  19. 119
    “…Among the 25 different ETEC adhesins, 22 are known as “colonization factors” (CFs), of which 17 are assembled by the chaperone-usher (CU) mechanism. Currently, there is no preventive therapy against ETEC, and CFs have been proposed as components for vaccine development. …”
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    Chaperone-Usher Pili Loci of Colonization Factor-Negative Human Enterotoxigenic Escherichia coli
  20. 120
    “…OBJECTIVES: Usher syndrome is the leading cause of hereditary deaf‐blindness. …”
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    Hearing aid fitting for visual and hearing impaired patients with Usher syndrome type IIa
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