يعرض 1 - 10 نتائج من 25 نتيجة بحث عن '"Sonia Hasan"', وقت الاستعلام: 1.91s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Locus Coeruleus Neurons’ Firing Pattern Is Regulated by ERG Voltage-Gated K+ Channels

    المؤلفون: Sonia Hasan, Francis Delicata, Leonardo Guasti, Claudia Duranti, Fatemah Mousalem Haidar, Annarosa Arcangeli, Paola Imbrici, Mauro Pessia, Mario Valentino, Maria Cristina D’Adamo

    المصدر: International Journal of Molecular Sciences, Vol 23, Iss 23, p 15334 (2022)

    مصطلحات موضوعية: locus coeruleus neurons, noradrenergic system, ERG K+ channels, ether-à-go-go–related gene, WAY-123,398, class III anti-arrhythmic drug, Biology (General), QH301-705.5, Chemistry, QD1-999

    وصف الملف: electronic resource

    Relation: https://www.mdpi.com/1422-0067/23/23/15334; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067

    URL الوصول: https://doaj.org/article/d9a82f5a759a45f7bb6ee16b3bb42346

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  2. 2
    دورية أكاديمية
    Kcnj16 (Kir5.1) Gene Ablation Causes Subfertility and Increases the Prevalence of Morphologically Abnormal Spermatozoa

    المؤلفون: Giulia Poli, Sonia Hasan, Silvia Belia, Marta Cenciarini, Stephen J. Tucker, Paola Imbrici, Safa Shehab, Mauro Pessia, Stefano Brancorsini, Maria Cristina D'Adamo

    المصدر: International Journal of Molecular Sciences, Vol 22, Iss 11, p 5972 (2021)

    مصطلحات موضوعية: Kir4.1, KCNJ10, Kir4.2, KCNJ15, KCNJ16, Kir5.1, Biology (General), QH301-705.5, Chemistry, QD1-999

    وصف الملف: electronic resource

    Relation: https://www.mdpi.com/1422-0067/22/11/5972; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067

    URL الوصول: https://doaj.org/article/983f01a228eb404c89663173f059f272

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  3. 3
    دورية أكاديمية
    A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia

    المؤلفون: Sonia Hasan, Cecilia Bove, Gabriella Silvestri, Elide Mantuano, Anna Modoni, Liana Veneziano, Lara Macchioni, Therese Hunter, Gary Hunter, Mauro Pessia, Maria Cristina D’Adamo

    المصدر: Scientific Reports, Vol 7, Iss 1, Pp 1-13 (2017)

    مصطلحات موضوعية: Medicine, Science

    وصف الملف: electronic resource

    Relation: https://doaj.org/toc/2045-2322

    URL الوصول: https://doaj.org/article/02ddbd2c1d7742bb819b694818c46801

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  4. 4
    دورية أكاديمية
    Commentary: A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia

    المؤلفون: Sonia Hasan, Therese Hunter, Gary Hunter, Mauro Pessia, Maria Cristina D'Adamo

    المصدر: Frontiers in Cellular Neuroscience, Vol 12 (2018)

    مصطلحات موضوعية: KV1.1, channelopathy, potassium channels, voltage-gated, hydrophobic gating, shaker-related, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

    وصف الملف: electronic resource

    Relation: https://www.frontiersin.org/article/10.3389/fncel.2018.00174/full; https://doaj.org/toc/1662-5102

    URL الوصول: https://doaj.org/article/0477f51432574a33b6785852def359a2

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  5. 5
    دورية أكاديمية
    A Calsequestrin-1 Mutation Associated with a Skeletal Muscle Disease Alters Sarcoplasmic Ca2+ Release.

    المؤلفون: Maria Cristina D'Adamo, Luigi Sforna, Sergio Visentin, Alessandro Grottesi, Llenio Servettini, Luca Guglielmi, Lara Macchioni, Simona Saredi, Maurizio Curcio, Chiara De Nuccio, Sonia Hasan, Lanfranco Corazzi, Fabio Franciolini, Marina Mora, Luigi Catacuzzeno, Mauro Pessia

    المصدر: PLoS ONE, Vol 11, Iss 5, p e0155516 (2016)

    مصطلحات موضوعية: Medicine, Science

    وصف الملف: electronic resource

    Relation: http://europepmc.org/articles/PMC4873205?pdf=render; https://doaj.org/toc/1932-6203

    URL الوصول: https://doaj.org/article/623e7a096e0b4a789396a7b416a2851c

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  6. 6
    Electromechanical coupling of the Kv1.1 voltage-gated K+ channel is fine-tuned by the simplest amino acid residue in the S4-S5 linker

    المؤلفون: Maria Cristina D'Adamo, Lorena Coretti, Fabio Massimo Botti, Harry W.M. Steinbusch, Paola Imbrici, Gary J. Hunter, Sonia Hasan, Alfredo Megaro, Therese Hunter, Marta Cenciarini, Mauro Pessia

    المساهمون: Hasan, Sonia, Megaro, Alfredo, Cenciarini, Marta, Coretti, Lorena, Botti, Fabio Massimo, Imbrici, Paola, Steinbusch, Harry W M, Hunter, Therese, Hunter, Gary, Pessia, Mauro, D'Adamo, Maria Cristina, Faculteit FHML Centraal, RS: MHeNs - R3 - Neuroscience

    المصدر: Pflugers Archiv-European Journal of Physiology, 472(7), 899-909. Springer Verlag

    مصطلحات موضوعية: 0301 basic medicine, PROTEINS, Physiology, Clinical Biochemistry, Gating, Kv, Xenopus laevis, 03 medical and health sciences, Residue (chemistry), 0302 clinical medicine, Physiology (medical), Side chain, kv1, Episodic ataxia type 1, chemistry.chemical_classification, model, Voltage-gated ion channel, MUTATIONS, Chemistry, 1S4-S5 linker, Kv1.1, S4-S5 linker, SENSOR, Episodic ataxia type 1, KCNA1, Kv, Kv1, 1S4-S5 linker, Xenopus laevis, Amino acid, 030104 developmental biology, KCNA1, EXCITABILITY, Glycine, Helix, Biophysics, Linker, 030217 neurology & neurosurgery

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb92f74a225f2e9daf47d860941645e6
    https://doi.org/10.1007/s00424-020-02414-0

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  7. 7
    Altered functional properties of a missense variant in the TRESK K+ channel (KCNK18) associated with migraine and intellectual disability

    المؤلفون: Maria Cristina D'Adamo, Ehsan Nematian-Ardestani, Paola Imbrici, Stephen J. Tucker, Sonia Hasan, Mauro Pessia

    المصدر: Pflügers Archiv - European Journal of Physiology. 472:923-930

    مصطلحات موضوعية: 0301 basic medicine, Genetics, Mutation, Physiology, Aura, Clinical Biochemistry, Mutant, Xenopus, Biology, biology.organism_classification, medicine.disease_cause, Potassium channel, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, Physiology (medical), medicine, Missense mutation, KCNJ5 Gene, 030217 neurology & neurosurgery, Ion channel

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::273beee3a879970c2dc870016bfe7d0e
    https://doi.org/10.1007/s00424-020-02382-5

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  8. 8
    Kcnj16 (Kir5.1) gene ablation causes subfertility and increases the prevalence of morphologically abnormal spermatozoa

    المؤلفون: Maria Cristina D'Adamo, Silvia Belia, Marta Cenciarini, Stefano Brancorsini, Paola Imbrici, Stephen J. Tucker, Safa Shehab, Sonia Hasan, Giulia Poli, Mauro Pessia

    المصدر: International Journal of Molecular Sciences
    Volume 22
    Issue 11
    International Journal of Molecular Sciences, Vol 22, Iss 5972, p 5972 (2021)

    مصطلحات موضوعية: 0301 basic medicine, Kir4.2, Kir5.1, Kir4.1, QH301-705.5, KCNJ15, Motility, Biology, KCNJ10, testis, Catalysis, Article, flagellar morphology, male fertility, Inorganic Chemistry, Andrology, 03 medical and health sciences, 0302 clinical medicine, Human fertilization, spermatozoa, KCNJ16, medicine, Extracellular, sperm motility, Biology (General), Physical and Theoretical Chemistry, QD1-999, Molecular Biology, Spectroscopy, Sperm motility, 030219 obstetrics & reproductive medicine, Organic Chemistry, General Medicine, Oocyte, Epididymis, Sperm, Computer Science Applications, Chemistry, 030104 developmental biology, medicine.anatomical_structure, biology.protein, epididymis, potassium channel

    وصف الملف: application/pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7e2fa7181b7cc6da4da7169bfc187e4
    https://doi.org/10.3390/ijms22115972

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  9. 9
    Electromechanical coupling of the Kv1.1 voltage-gated K

    المؤلفون: Sonia, Hasan, Alfredo, Megaro, Marta, Cenciarini, Lorena, Coretti, Fabio Massimo, Botti, Paola, Imbrici, Harry W M, Steinbusch, Therese, Hunter, Gary, Hunter, Mauro, Pessia, Maria Cristina, D'Adamo

    المصدر: Pflugers Archiv : European journal of physiology. 472(7)

    مصطلحات موضوعية: Xenopus laevis, Animals, Ataxia, Amino Acid Sequence, Amino Acids, Kv1.1 Potassium Channel, Ion Channel Gating

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::48fdfed36d08cf6dd3d8466679f3276b
    https://pubmed.ncbi.nlm.nih.gov/32577860

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  10. 10
    KCNA4deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability

    المؤلفون: Banan Al-Younes, Brian F. Meyer, Maria Cristina D'Adamo, Rawan Almass, Jawaher Al-Zahrani, Dilek Colak, Faten B. Almutairi, Osama M. Mustafa, Rosan Kenana, Namik Kaya, Maysoon Alsagob, Dorota Monies, Fatema Almutairi, Mauro Pessia, Alya Qari, Faisal S. BinHumaid, Mohammed Al-Owain, Mazhor Al-Dosary, Sonia Hasan, Maria Muccioli, Albandary Al-Bakheet, Timothy F. Plageman, Ewa A. Naim

    المصدر: Journal of Medical Genetics. 53:786-792

    مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Retina, Potassium Channel, Linkage, Central nervous system, Wild type, Striatum, Biology, medicine.disease, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, Endocrinology, medicine.anatomical_structure, Internal medicine, Intellectual disability, Genetics, Genetics (clinical), medicine, Missense mutation, Attention deficit hyperactivity disorder, 030217 neurology & neurosurgery, Exome sequencing

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52673f1f979cf787f250e2d1cbf989a7
    https://doi.org/10.1136/jmedgenet-2015-103637

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