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akaturk Akademik ölçüm

OpenAlex konusu

Hearing, Cochlea, Tinnitus, Genetics

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

OpenAlex 3.234 eser 270 yazar konusu

Çalışmalar

3.234 eser

  1. OpenAlex üst %10 OpenAlex 91.7%

    The anatomical and biophysical specializations of octopus cells allow them to detect the coincident firing of groups of auditory nerve fibers and to convey the precise timing of that coincidence to their targets. Octopus cells occupy a sharply defined region of the most caudal and dorsal part of the mammalian ventral…

  2. YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 98.2%

    Özet henüz yok.

  3. YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 98.2%

    Özet henüz yok.

  4. YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 98.2%

    Özet henüz yok.

  5. YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 98.6%

    Identification of the pathogenic mutations underlying autosomal recessive nonsyndromic hearing loss (ARNSHL) is difficult, since causative mutations in 39 different genes have so far been reported. After excluding mutations in the most common ARNSHL gene, GJB2, via Sanger sequencing, we performed whole-exome sequencin…

  6. YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 98.6%

    Identification of the pathogenic mutations underlying autosomal recessive nonsyndromic hearing loss (ARNSHL) is difficult, since causative mutations in 39 different genes have so far been reported. After excluding mutations in the most common ARNSHL gene, GJB2, via Sanger sequencing, we performed whole-exome sequencin…

  7. YÖKSİS SJR Q2 JCR Q3 OpenAlex üst %1 OpenAlex 99.8%

    Özet henüz yok.

  8. 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…

  9. 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…

  10. YÖKSİS SJR Q1 JCR Q2 OpenAlex 88.5%

    OBJECTIVE: To assess the correct incidence of horizontal semicircular canal (H-SCC) benign paroxysmal positional vertigo (BPPV). STUDY DESIGN: Retrospective assessment of patients with BPPV. METHODS: All patients with BPPV were included and the rates of involvement of posterior, horizontal, and anterior SCCs were dete…

  11. OpenAlex üst %10 OpenAlex 98.1%

    1. The inhibitory effects of the GABAA agonist muscimol and the GABAB agonist baclofen on tonically active medial vestibular nucleus (MVN) neurones were recorded in slices of the rat dorsal brainstem in vitro, to determine whether any changes occurred in the functional efficacy of GABAergic inhibition in these cells d…

  12. YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 98.6%

    Özet henüz yok.

Akademisyenler

270 akademisyen