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Articles published in Proc Natl Acad Sci U S A

Retrieve available abstracts of 13 articles:
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Single Articles


    June 2022
  1. BADEMCI G, Lachgar-Ruiz M, Deokar M, Zafeer MF, et al
    Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice.
    Proc Natl Acad Sci U S A. 2022;119:e2204084119.
    PubMed     Abstract available


  2. BABAHOSSEINI H, Belyantseva IA, Yousaf R, Tona R, et al
    Unbalanced bidirectional radial stiffness gradients within the organ of Corti promoted by TRIOBP.
    Proc Natl Acad Sci U S A. 2022;119:e2115190119.
    PubMed     Abstract available


    May 2022
  3. QUIAT D, Kim SW, Zhang Q, Morton SU, et al
    An ancient founder mutation located between ROBO1 and ROBO2 is responsible for increased microtia risk in Amerindigenous populations.
    Proc Natl Acad Sci U S A. 2022;119:e2203928119.
    PubMed     Abstract available


    March 2022
  4. FU X, Li P, Zhang L, Song Y, et al
    Activation of Rictor/mTORC2 signaling acts as a pivotal strategy to protect against sensorineural hearing loss.
    Proc Natl Acad Sci U S A. 2022;119:e2107357119.
    PubMed     Abstract available


    October 2021
  5. SONG C, Li J, Liu S, Hou H, et al
    An L1 retrotransposon insertion-induced deafness mouse model for studying the development and function of the cochlear stria vascularis.
    Proc Natl Acad Sci U S A. 2021;118.
    PubMed     Abstract available


    September 2021
  6. HAYASHI Y, Chiang H, Tian C, Indzhykulian AA, et al
    Norrie disease protein is essential for cochlear hair cell maturation.
    Proc Natl Acad Sci U S A. 2021;118.
    PubMed     Abstract available


    June 2021
  7. JANG MW, Oh DY, Yi E, Liu X, et al
    A nonsense TMEM43 variant leads to disruption of connexin-linked function and autosomal dominant auditory neuropathy spectrum disorder.
    Proc Natl Acad Sci U S A. 2021;118.
    PubMed     Abstract available


    May 2021
  8. KEPPELER D, Kampshoff CA, Thirumalai A, Duque-Afonso CJ, et al
    Multiscale photonic imaging of the native and implanted cochlea.
    Proc Natl Acad Sci U S A. 2021;118.
    PubMed     Abstract available


    February 2021
  9. ANDEREGG WRL, Abatzoglou JT, Anderegg LDL, Bielory L, et al
    Anthropogenic climate change is worsening North American pollen seasons.
    Proc Natl Acad Sci U S A. 2021;118.
    PubMed     Abstract available


    December 2020
  10. BOUCHER S, Tai FWJ, Delmaghani S, Lelli A, et al
    Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis.
    Proc Natl Acad Sci U S A. 2020;117:31278-31289.
    PubMed     Abstract available


    November 2020
  11. YU X, Zhao Q, Li X, Chen Y, et al
    Deafness mutation D572N of TMC1 destabilizes TMC1 expression by disrupting LHFPL5 binding.
    Proc Natl Acad Sci U S A. 2020;117:29894-29903.
    PubMed     Abstract available


    September 2020
  12. GU S, Knowland D, Matta JA, O'Carroll ML, et al
    Hair cell alpha9alpha10 nicotinic acetylcholine receptor functional expression regulated by ligand binding and deafness gene products.
    Proc Natl Acad Sci U S A. 2020;117:24534-24544.
    PubMed     Abstract available


    August 2020
  13. ABU RAYYAN A, Kamal L, Casadei S, Brownstein Z, et al
    Genomic analysis of inherited hearing loss in the Palestinian population.
    Proc Natl Acad Sci U S A. 2020;117:20070-20076.
    PubMed     Abstract available


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