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1دورية أكاديمية
المؤلفون: Chuanling Yin, Fanpeng Zeng, Puyi Huang, Zhengqi Shi, Qianyi Yang, Zhenduo Pei, Xin Wang, Longhui Chai, Shipei Zhang, Shilong Yang, Wenqi Dong, Xiancui Lu, Yunfei Wang
المصدر: Toxins; Volume 15; Issue 1; Pages: 70
مصطلحات موضوعية: tree frogs, skin secretion, paxilline, KCNK18, defensive strategy
جغرافية الموضوع: agris
وصف الملف: application/pdf
العلاقة: Animal Venoms; https://dx.doi.org/10.3390/toxins15010070Test
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2دورية أكاديمية
المؤلفون: Markel, Katherine Alexis, Curtis, David
المصدر: Annals of Human Genetics (2022) (In press).
مصطلحات موضوعية: KCNK18, TRESK, exome, genetic variant, migraine
وصف الملف: text
العلاقة: https://discovery.ucl.ac.uk/id/eprint/10155291/1/Curtis_Annals%20of%20Human%20Genetics%20-%202022%20.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10155291Test/
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3دورية أكاديمية
المؤلفون: Pavinato L., Nematian-Ardestani E., Zonta A., De Rubeis S., Buxbaum J., Mancini C., Bruselles A., Tartaglia M., Pessia M., Tucker S. J., D'adamo M. C., Brusco A.
المساهمون: Pavinato L., Nematian-Ardestani E., Zonta A., De Rubeis S., Buxbaum J., Mancini C., Bruselles A., Tartaglia M., Pessia M., Tucker S.J., D'adamo M.C., Brusco A.
مصطلحات موضوعية: Autism spectrum disorder, Intellectual disability, K2P, KCNK18, Potassium channel, TRESK, Calcineurin, Ion Channel Gating, Ionomycin, Mutation, Neurodevelopmental Disorder, Xenopus laevis
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34199759; info:eu-repo/semantics/altIdentifier/wos/WOS:000660148300001; volume:22; issue:11; firstpage:1; lastpage:13; numberofpages:13; journal:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES; http://hdl.handle.net/2318/1808623Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85107284344; https://www.mdpi.com/1422-0067/22/11/6064Test
الإتاحة: https://doi.org/10.3390/ijms22116064Test
http://hdl.handle.net/2318/1808623Test
https://www.mdpi.com/1422-0067/22/11/6064Test -
4دورية أكاديمية
المؤلفون: Lisa Pavinato, Ehsan Nematian-Ardestani, Andrea Zonta, Silvia De Rubeis, Joseph Buxbaum, Cecilia Mancini, Alessandro Bruselles, Marco Tartaglia, Mauro Pessia, Stephen J. Tucker, Maria Cristina D’Adamo, Alfredo Brusco
المصدر: International Journal of Molecular Sciences; Volume 22; Issue 11; Pages: 6064
مصطلحات موضوعية: KCNK18, TRESK, K2P, intellectual disability, potassium channel, autism spectrum disorder, ASD
جغرافية الموضوع: agris
وصف الملف: application/pdf
العلاقة: Biochemistry; https://dx.doi.org/10.3390/ijms22116064Test
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5دورية أكاديمية
المؤلفون: Albury, Cassie, Stuart, Shani, Haupt, Larisa, Griffiths, Lyn
المصدر: Molecular Genetics and Genomics
مصطلحات موضوعية: HEPH, Hephaestin, Ion channelopathies, KCNK18, Migraine
وصف الملف: application/pdf
العلاقة: https://eprints.qut.edu.au/106007/1/Albury_2017_MGG.pdfTest; Albury, Cassie, Stuart, Shani, Haupt, Larisa, & Griffiths, Lyn (2017) Ion channelopathies and migraine pathogenesis. Molecular Genetics and Genomics, 292(4), pp. 729-739.; https://eprints.qut.edu.au/106007Test/; Faculty of Health; Institute of Health and Biomedical Innovation
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المؤلفون: Maria Cristina D'Adamo, Cecilia Mancini, Lisa Pavinato, Stephen J. Tucker, Alessandro Bruselles, Alfredo Brusco, Mauro Pessia, Marco Tartaglia, Ehsan Nematian-Ardestani, Joseph D. Buxbaum, Silvia De Rubeis, Andrea Zonta
المصدر: International Journal of Molecular Sciences, Vol 22, Iss 6064, p 6064 (2021)
International Journal of Molecular Sciences
Volume 22
Issue 11مصطلحات موضوعية: TRESK, Aura, QH301-705.5, Regulatory site, autism spectrum disorder, Biology, medicine.disease_cause, ASD, Catalysis, Article, Inorganic Chemistry, Xenopus laevis, KCNK18, Intellectual disability, medicine, Missense mutation, Physical and Theoretical Chemistry, Biology (General), Molecular Biology, Gene, QD1-999, Spectroscopy, Genetics, Mutation, K2P, Calcineurin, Ionomycin, Organic Chemistry, General Medicine, medicine.disease, Potassium channel, Computer Science Applications, Autism spectrum disorder, Ion Channel Gating, Neurodevelopmental Disorders, Chemistry, intellectual disability, potassium channel
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2246cf8e188bb53682c65b1eaaed511bTest
https://ora.ox.ac.uk/objects/uuid:41e86133-61c1-492c-b03d-c4431c54a6a1Test -
7دورية أكاديمية
المؤلفون: Imbrici P., Nematian-Ardestani E., Hasan S., Pessia M., Tucker S. J., D'Adamo M. C.
المساهمون: Imbrici, P., Nematian-Ardestani, E., Hasan, S., Pessia, M., Tucker, S. J., D'Adamo, M. C.
مصطلحات موضوعية: Calcineurin-dependent regulation, KCNK18 gene missense mutation, TRESK K2P, Two-electrode-voltage-clamp, Xenopus oocytes
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32394190; info:eu-repo/semantics/altIdentifier/wos/WOS:000531762600002; volume:472; issue:7; firstpage:923; lastpage:930; numberofpages:8; journal:PFLÜGERS ARCHIV; http://hdl.handle.net/11586/311506Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85084444812
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8دورية أكاديمية
المؤلفون: Rainero, Innocenzo, Rubino, Elisa, Paemeleire, Koen, Gai, Annalisa, Vacca, Alessandro, De Martino, Paola, Gentile, Salvatore, Sarchielli, Paola, Pinessi, Lorenzo
المصدر: JOURNAL OF HEADACHE AND PAIN ; ISSN: 1129-2369
مصطلحات موضوعية: Biology and Life Sciences, Genes, Primary headaches, MHTFR, KCNK18, HCRTR1, HCRTR2, FAMILIAL HEMIPLEGIC MIGRAINE, OREXIN RECEPTOR ANTAGONIST, GENOME-WIDE ASSOCIATION, MTHFR C677T GENOTYPE, CLUSTER HEADACHE, K+ CHANNEL, G1246A POLYMORPHISM, METHYLENETETRAHYDROFOLATE REDUCTASE, HYPOCRETIN-RECEPTOR-2 GENE, VITAMIN SUPPLEMENTATION
وصف الملف: application/pdf
العلاقة: https://biblio.ugent.be/publication/4108111Test; http://hdl.handle.net/1854/LU-4108111Test; http://dx.doi.org/10.1186/1129-2377-14-61Test; https://biblio.ugent.be/publication/4108111/file/4108112Test
الإتاحة: https://doi.org/10.1186/1129-2377-14-61Test
https://biblio.ugent.be/publication/4108111Test
http://hdl.handle.net/1854/LU-4108111Test
https://biblio.ugent.be/publication/4108111/file/4108112Test -
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المؤلفون: Sheikh Arslan Sehgal, Mubashir Hassan, Sajid Rashid
المصدر: Drug Design, Development and Therapy
مصطلحات موضوعية: Drug, Models, Molecular, TRESK, Potassium Channels, Pharmacoinformatics, media_common.quotation_subject, Migraine Disorders, Pharmaceutical Science, Computational biology, Pharmacology, Molecular Docking Simulation, LigandScout, Structure-Activity Relationship, Drug Discovery, Humans, migraine, media_common, Original Research, Virtual screening, Drug Design, Development and Therapy, KCNK18, Chemistry, Computational Biology, bioinformatics, Druglikeness, virtual screening, Docking (molecular), modeling and docking, pharmacoinformatics, Drug Design, Mutagenesis, Site-Directed, Pharmacophore
وصف الملف: text/html
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7915dd3d86bd041d083703bf537e1b47Test
http://europepmc.org/articles/PMC4038526Test -
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المؤلفون: Michalina Kosiorek, Anna Kamińska, Cezary Żekanowski, Izabela Domitrz
المصدر: Human Genomics
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Potassium Channels, Migraine Disorders, Migraine with Aura, Mutation, Missense, Aura migraine, SNP, Biology, Bioinformatics, medicine.disease_cause, Polymorphism, Single Nucleotide, 03 medical and health sciences, Exon, 0302 clinical medicine, Splice variants, Polymorphism (computer science), ATP1A2, Drug Discovery, Genetics, medicine, Humans, Missense mutation, SCN1A, Molecular Biology, Familial hemiplegic migraine, Mutation, KCNK18, Exons, Middle Aged, Genetic background, medicine.disease, Migraine with aura, Neoplasm Proteins, Pedigree, Repressor Proteins, 030104 developmental biology, Migraine, Missense mutations, Molecular Medicine, Female, Calcium Channels, Sodium-Potassium-Exchanging ATPase, medicine.symptom, Primary Research, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6324f8dba2722b0de2c5cb6dde99a89Test
https://doi.org/10.1186/s40246-015-0057-8Test