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OpenAlex konusu

Connexins and lens biology

Bu sayfa OpenAlex konu etiketine göre çalışmaları ve o konuda görünen akademisyenleri listeler. YÖKSİS temel alan / yan dal değildir.

OpenAlex 852 eser 15 yazar konusu

Çalışmalar

852 eser

  1. Pericyte contraction induced by oxidative-nitrative stress impairs capillary reflow despite successful opening of an occluded cerebral artery 2009
    YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %1 OpenAlex 99.5%

    Özet henüz yok.

  2. Pericyte contraction induced by oxidative nitrative stress impairs capillary reflow despite successful opening of an occluded cerebral artery 2009
    YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %1 OpenAlex 99.5%

    Özet henüz yok.

  3. Pericyte contraction induced by oxidative nitrative stress impairs capillary reflow despite successful opening of an occluded cerebral artery 2009
    YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %1 OpenAlex 99.5%

    Özet henüz yok.

  4. Pericyte contraction induced by oxidative-nitrative stress impairs capillary reflow despite successful opening of an occluded cerebral artery 2009
    YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %1 OpenAlex 99.5%

    Özet henüz yok.

  5. Gap Junctions Basic Structure and Function 2007
    YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 98.7%

    Özet henüz yok.

  6. Cataract in diabetes mellitus 2019
    YÖKSİS SJR Q3 JCR Q2 OpenAlex üst %10 OpenAlex 98.8%

    Diabetes mellitus (DM) is a chronic systemic disease that has increases in prevalence over time. DM can affect all ocular structures, with cataract being the most common ocular complication. Cataract is the leading cause of blindness worldwide. Due to several mechanisms, there is an increased incidence of cataract for…

  7. Mutations in the Gene Encoding Gap Junction Protein α12 (Connexin 46.6) Cause Pelizaeus-Merzbacher–Like Disease 2004
    OpenAlex üst %10 OpenAlex 97.0%

    Özet henüz yok.

  8. A Comprehensive Mutation Analysis of RP2 and RPGR in a North American Cohort of Families with X-Linked Retinitis Pigmentosa 2002
    OpenAlex üst %10 OpenAlex 93.5%

    Özet henüz yok.

  9. Autosomal recessive nonsyndromic deafness genes a review 2012
    YÖKSİS JCR Q2 OpenAlex üst %10 OpenAlex 97.2%

    More than 50 Percent of prelingual hearing loss is genetic in origin, and of these up to 93 Percent are monogenic autosomal recessive traits. Some forms of genetic deafness can be recognized by their associated syndromic features, but in most cases, hearing loss is the only finding and is referred to as nonsyndromic d…

  10. Autosomal recessive nonsyndromic deafness genes: a review 2012
    YÖKSİS SJR Q1 JCR Q3 OpenAlex üst %10 OpenAlex 97.2%

    More than 50 Percent of prelingual hearing loss is genetic in origin, and of these up to 93 Percent are monogenic autosomal recessive traits. Some forms of genetic deafness can be recognized by their associated syndromic features, but in most cases, hearing loss is the only finding and is referred to as nonsyndromic d…

  11. Differentially altered Ca2 regulation and Ca2 permeability in Cx26 hemichannels formed by the A40V and G45E mutations that cause keratitis ichthyosis deafness syndrome 2010
    YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 95.6%

    Mutations in GJB2, which encodes Cx26, are one of the most common causes of inherited deafness in humans. More than 100 mutations have been identified scattered throughout the Cx26 protein, most of which cause nonsyndromic sensorineural deafness. In a subset of mutations, deafness is accompanied by hyperkeratotic skin…

  12. Lens superoxide dismutase and catalase activities in diabetic cataract 2002
    YÖKSİS SJR Q2 JCR Q2 OpenAlex 61.2%

    Özet henüz yok.

Akademisyenler

15 akademisyen