Zobrazeno 1 - 10
of 31
pro vyhledávání: '"ATP1A4"'
Autor:
Giangennaro Coppola, Grazia Maria Giovanna Pastorino, Luigi Vetri, Floriana D’Onofrio, Francesca Felicia Operto
Publikováno v:
Brain Sciences, Vol 10, Iss 6, p 372 (2020)
An Italian family with familial hemiplegic migraine (FHM) with the absence of mutations in the known genes associated with this disorder, namely ATP1A2, ATP1A3, CACNA1A, and SCN1A, has recently been reported. Soon afterward, whole exome sequencing al
Externí odkaz:
https://doaj.org/article/75dd7b948f1c4d2f909987a58a69bbcf
Publikováno v:
J Assist Reprod Genet
PURPOSE: The aim of this study is to investigate the mechanisms by which the testis specific Na,K-ATPase ion transport system (Atp1a4) controls sperm morphology and shape. METHODS: Sperm from wild-type (WT) and Atp1a4 knockout (Atp1a4 KO) mice were a
Autor:
Gladis Sánchez, Gustavo Blanco, Shameem Sultana Syeda, Gunda I. Georg, Kwon Ho Hong, Jeffrey McDermott
Publikováno v:
Biology of Reproduction
One of the mechanisms that cells have developed to fulfil their specialized tasks is to express different molecular variants of a particular protein that has unique functional properties. Na,K-ATPase (NKA), the ion transport mechanism that maintains
Publikováno v:
Larsen, K, Henriksen, C, Kristensen, K K, Momeni, J & Farajzadeh, L 2019, ' Molecular cloning and characterization of porcine Na⁺/K⁺-ATPase isoform α4 ', Biochimie, vol. 158, pp. 149-155 . https://doi.org/10.1016/j.biochi.2019.01.003
Na+/K+-ATPase is responsible for maintaining electrochemical gradients of Na+ and K+, which is essential for a variety of cellular functions including neuronal activity. The α-subunit of the Na+/K+-ATPase is composed of four different polypeptides (
Publikováno v:
Cancer Cell International
Cancer Cell International, Vol 20, Iss 1, Pp 1-13 (2020)
Cancer Cell International, Vol 20, Iss 1, Pp 1-13 (2020)
Background Ovarian serous cystadenocarcinoma (OSC) is the most common and lethal gynecological cancer in women worldwide; however, biomarkers to diagnose and predict prognosis of OSC remain limited. Therefore, the present study aimed to investigate w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59ddd5873d0f69bc21787f8309c8128c
https://doi.org/10.21203/rs.3.rs-23702/v2
https://doi.org/10.21203/rs.3.rs-23702/v2
Autor:
Francesca Felicia Operto, Luigi Vetri, Giangennaro Coppola, Floriana D'Onofrio, Grazia Maria Giovanna Pastorino
Publikováno v:
Brain Sciences, Vol 10, Iss 372, p 372 (2020)
Brain Sciences
Brain Sciences
An Italian family with familial hemiplegic migraine (FHM) with the absence of mutations in the known genes associated with this disorder, namely ATP1A2, ATP1A3, CACNA1A, and SCN1A, has recently been reported. Soon afterward, whole exome sequencing al
Autor:
Preeti Verma, Shelesh Kumar Swami, Vijay Lakshmi Sharma, Parvesh Kumari, Monika Sodhi, Ankita Sharma, Ramneek Kaur, Manishi Mukesh
Publikováno v:
Gene Reports. 10:97-108
Na + /K + -ATPase is an integral plasma membrane protein complex which maintains the active transport of Na + and K + ions across the plasma membrane in the animal. The alpha subunit harbours the binding and catalytic site for Na + , K + and ATP hydr
Autor:
Pietro, Palumbo1, Orazio, Palumbo1, Francesca Felicia Operto2, Stefano, Castellana3, Ester Di Muro1, 4, Maria Pia Leone1, Tommaso, Biagini3, Grazia, Pastorino2, Tommaso, Mazza3, Massimo, Carella, Coppola, Giangennaro
Hemiplegic migraine (HM) is a rare form of migraine characterized by severe attacks of unilateral and pulsating headache (associated with photophobia, phonophobia or nausea). To date, mutations in three different genes, ATP1A2, CACNA1A and SCN1A, are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6bc4be9b78e8921edd6e31bdfe8c114
http://hdl.handle.net/11386/4737625
http://hdl.handle.net/11386/4737625
Autor:
Yuan Pan, Modestos A Modestou, Joseph G. Laird, Maxim Sokolov, David M. Yamaguchi, Sheila A. Baker, Hongman Song
Publikováno v:
Traffic. 16:1239-1253
Na(+) /K(+) -ATPase (NKA) participates in setting electrochemical gradients, cardiotonic steroid signaling and cellular adhesion. Distinct isoforms of NKA are found in different tissues and subcellular localization patterns. For example, NKA α1 is w
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