Zobrazeno 1 - 10
of 60
pro vyhledávání: '"ion channel genes"'
Publikováno v:
Heliyon, Vol 10, Iss 7, Pp e27301- (2024)
Background: Less than 10% of people who have pancreatic ductal adenocarcinoma (PDAC) will survive the malignancy for five years. The ion channel genes-related biomarker and predictive model were needed for exploitation. Methods: Differentially expres
Externí odkaz:
https://doaj.org/article/360c362af9764d1c8e7bfa12bcbaa9eb
Autor:
Milena Ślęczkowska, Kaalindi Misra, Silvia Santoro, Monique M. Gerrits, Janneke G. J. Hoeijmakers
Publikováno v:
Biomedicines, Vol 11, Iss 10, p 2680 (2023)
Neuropathic pain (NP) is a typical symptom of peripheral nerve disorders, including painful neuropathy. The biological mechanisms that control ion channels are important for many cell activities and are also therapeutic targets. Disruption of the cel
Externí odkaz:
https://doaj.org/article/1fc93650b37148679eea92ac8e45e0ee
Autor:
Rong Luo, Chenqing Zheng, Hao Yang, Xuepin Chen, Panpan Jiang, Xiushan Wu, Zhenglin Yang, Xia Shen, Xiaoping Li
Publikováno v:
Clinical and Translational Medicine, Vol 10, Iss 1, Pp 238-257 (2020)
Abstract Background Atrioventricular nodal reentry tachycardia (AVNRT) is the most common manifestation of paroxysmal supraventricular tachycardia (PSVT). Increasing data have indicated familial clustering and participation of genetic factors in AVNR
Externí odkaz:
https://doaj.org/article/8cafa6a0f0964e3781186123239a3333
Akademický článek
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Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
The clinical heterogeneity of autism spectrum disorder (ASD) is closely associated with the diversity of genes related to ASD pathogenesis. With their low effect size, it has been hard to define the role of common variants of genes in ASD phenotype.
Externí odkaz:
https://doaj.org/article/f41d7b1bb13842788a8d80805fc22c08
Autor:
Heidi G. Sutherland, Neven Maksemous, Cassie L. Albury, Omar Ibrahim, Robert A. Smith, Rod A. Lea, Larisa M. Haupt, Bronwyn Jenkins, Benjamin Tsang, Lyn R. Griffiths
Publikováno v:
Cells, Vol 9, Iss 11, p 2368 (2020)
Hemiplegic migraine (HM) is a rare migraine disorder with aura subtype including temporary weakness and visual, sensory, and/or speech symptoms. To date, three main genes—CACNA1A, ATP1A2, and SCN1A—have been found to cause HM. These encode ion ch
Externí odkaz:
https://doaj.org/article/25e3376889694022a9810496bcdda98f
Autor:
Xia Shen, Panpan Jiang, Chenqing Zheng, Xuepin Chen, Zhenglin Yang, Xiaoping Li, Hao Yang, Rong Luo, Xiushan Wu
Publikováno v:
Clinical and Translational Medicine, Vol 10, Iss 1, Pp 238-257 (2020)
Clinical and Translational Medicine
Luo, R, Zheng, C, Yang, H, Chen, X, Jiang, P, Wu, X, Yang, Z, Shen, X & Li, X 2020, ' Identification of potential candidate genes and pathways in atrioventricular nodal reentry tachycardia by whole-exome sequencing ', Clinical and Translational Medicine, vol. 10, no. 1, pp. 238-257 . https://doi.org/10.1002/ctm2.25
Clinical and Translational Medicine
Luo, R, Zheng, C, Yang, H, Chen, X, Jiang, P, Wu, X, Yang, Z, Shen, X & Li, X 2020, ' Identification of potential candidate genes and pathways in atrioventricular nodal reentry tachycardia by whole-exome sequencing ', Clinical and Translational Medicine, vol. 10, no. 1, pp. 238-257 . https://doi.org/10.1002/ctm2.25
BACKGROUND: Atrioventricular nodal reentry tachycardia (AVNRT) is the most common manifestation of paroxysmal supraventricular tachycardia (PSVT). Increasing data have indicated familial clustering and participation of genetic factors in AVNRT, and n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6eae75a113f1ff666e10cf51d6a75425
https://doi.org/10.1002/ctm2.25
https://doi.org/10.1002/ctm2.25
Autor:
Neven Maksemous, Omar Ibrahim, Rod A. Lea, Cassie L. Albury, Larisa M. Haupt, Bronwyn Jenkins, Benjamin Tsang, Heidi G. Sutherland, Lyn R. Griffiths, Robert A. Smith
Publikováno v:
Cells
Cells, Vol 9, Iss 2368, p 2368 (2020)
Volume 9
Issue 11
Cells, Vol 9, Iss 2368, p 2368 (2020)
Volume 9
Issue 11
Hemiplegic migraine (HM) is a rare migraine disorder with aura subtype including temporary weakness and visual, sensory, and/or speech symptoms. To date, three main genes&mdash
CACNA1A, ATP1A2, and SCN1A&mdash
have been found to cause HM. T
CACNA1A, ATP1A2, and SCN1A&mdash
have been found to cause HM. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f7547e8fa8927ea6b4390606fbe31f0
https://pubmed.ncbi.nlm.nih.gov/33126486
https://pubmed.ncbi.nlm.nih.gov/33126486
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 12 (2021)
Frontiers in Genetics, Vol 12 (2021)
The clinical heterogeneity of autism spectrum disorder (ASD) is closely associated with the diversity of genes related to ASD pathogenesis. With their low effect size, it has been hard to define the role of common variants of genes in ASD phenotype.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc03fc4337364bf0573274d8398a8276
https://pubmed.ncbi.nlm.nih.gov/34712263
https://pubmed.ncbi.nlm.nih.gov/34712263
Akademický článek
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