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Connexins and lens biology

16 ta ish

  1. Oxygen-glucose deprivation induces ATP release via maxi-anion channels in astrocytes

    Hongtao Liu, Ravshan Z. Sabirov, Yasunobu Okada

    MaqolaOchiq kirishNeuroscience and Neuropharmacology ResearchPurinergic Signalling200713 iqtibos
    ABI

  2. Maxi-anion channel as a candidate pathway for osmosensitive ATP release from mouse astrocytes in primary culture

    Hongtao Liu, Abduqodir Toychiev, Nobuyuki Takahashi +2

    MaqolaConnexins and lens biologyCell Research200812 iqtibos
    ABI

  3. Maxi-anion channel and pannexin 1 hemichannel constitute separate pathways for swelling-induced ATP release in murine L929 fibrosarcoma cells

    Md. Rafiqul Islam, Hiromi Uramoto, Toshiaki Okada +2

    MaqolaOchiq kirishConnexins and lens biologyAmerican Journal of Physiology-Cell Physiology20128 iqtibos
    ABI

  4. Understanding Osaka mutation polymorphic Aβ fibril response to static and oscillating electric fields: insights from computational modeling

    Mukhriddin Makhkamov, Artyom Y. Baev, Erkin Kurganov +1

    MaqolaOchiq kirishAlzheimer's disease research and treatmentsScientific Reports20242 iqtibos
    ABI

  5. Reparative and antioxidant therapy of chemical eye burns

    Ф. А. Бахритдинова, Б. А. Оралов, S. Sh. Mirrakhimova +2

    MaqolaOchiq kirishCorneal Surgery and TreatmentsRussian Ophthalmological Journal20211 iqtibos
    ABI

  6. Clinical efficacy of individual intraocular lens calculation in children with congenital cataract at risk of abnormal refraction

    Л. С. Хамраева, N. Kh. Latipova, D. U. Narzullaeva

    MaqolaOchiq kirishOphthalmology and Visual Impairment StudiesRussian Ophthalmological Journal20231 iqtibos
    ABI

  7. Membranotropic Effects of Antibodies to S100 Protein in Ultralow Doses

    В. В. Андрианов, Х. Л. Гайнутдинов, Т. Х. Гайнутдинова +3

    MaqolaS100 Proteins and AnnexinsBulletin of Experimental Biology and Medicine20030 iqtibos
    ABI

  8. Differential Effects of Propofol and Sevoflurane on Ischemia-induced Ventricular Arrhythmias and Phosphorylated Connexin 43 Protein in Rats

    Naoyuki Hirata, Noriaki Kanaya, Noriko Kamada +2

    MaqolaOchiq kirishCardiac Ischemia and ReperfusionAnesthesiology20080 iqtibos
    ABI

  9. The Interaction of Sio <sub>2</sub> Nanoparticles with The Neuronal Cell Membrane: Activation of Ionic Channels and Calcium Influx

    Carla Distasi, Marianna Dionisi, Federico Alessandro Ruffinatti +8

    MaqolaOchiq kirishConnexins and lens biologyNanomedicine20190 iqtibos
    ABI

  10. Aspects of Correction of Ametropiya in Children Congenital Cataracts

    Narzullayeva Dildora Uktamovna

    MaqolaOchiq kirishConnexins and lens biologyTrends in Ophthalmology Open Access Journal20190 iqtibos
    ABI

  11. Clinical Evaluation of Connexin-26 Gene Mutation in the Development of Hearing Loss in the Kazakh Population

    Ayat Assemov, С. К. Кудайбергенова, Gulzakhira Djarkinbekova +3

    MaqolaOchiq kirishHearing, Cochlea, Tinnitus, GeneticsElectronic Journal of General Medicine20220 iqtibos
    ABI

  12. Influence of Early Apical Release on Outcomes in Endoscopic Enucleation of the Prostate: Results From a Multicenter Series of 4392 Patients

    Vineet Gauhar, Ee Jean Lim, Khi Yung Fong +17

    MaqolaOchiq kirishUrinary Bladder and Prostate ResearchUrology20240 iqtibos
    ABI

  13. Progression Of Cataract In Patients Following Kidney Transplantation Under Immunosuppressive Therapy

    A. S. Yusupov, Umida Mavlaynova

    MaqolaOchiq kirishIntraocular Surgery and Lenses20260 iqtibos
    ABI

  14. Progression Of Cataract In Patients Following Kidney Transplantation Under Immunosuppressive Therapy

    A. S. Yusupov, Umida Mavlaynova

    MaqolaOchiq kirishIntraocular Surgery and Lenses20260 iqtibos
    ABI

  15. MUTATIONAL SPECTRUM OF THE GJB2 GENE AS THE LEADING GENETIC CAUSE OF NON-SYNDROMIC SENSORINEURAL HEARING LOSS IN CHILDREN

    Madrimova A.G

    MaqolaHearing, Cochlea, Tinnitus, GeneticsZenodo (CERN European Organization for Nuclear Research)20260 iqtibos
    ABI

  16. MUTATIONAL SPECTRUM OF THE GJB2 GENE AS THE LEADING GENETIC CAUSE OF NON-SYNDROMIC SENSORINEURAL HEARING LOSS IN CHILDREN

    Madrimova A.G

    MaqolaOchiq kirishHearing, Cochlea, Tinnitus, GeneticsZenodo (CERN European Organization for Nuclear Research)20260 iqtibos
    ABI