Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

English (EN)·Polski (PL)·Ukraiński (UK)
Przejdź do strony domowej biblioteki Uniwersytet Ekonomiczny we Wrocławiu Link otwiera się w nowym oknie Logo biblioteki Prolib Integro - strona głównaUniwersytet Ekonomiczny we Wrocławiu

Wyszukujesz frazę ""Horie M"" wg kryterium: Autor

  Lista filtrów
Wyrównaj
    Wyświetlanie 1-16 z 16
    Tytuł:
    Telethonin variants found in Brugada syndrome, J-wave pattern ECG, and ARVC reduce peak Na v 1.5 currents in HEK-293 cells.
    Autorzy:
    Turker I; Department of Medicine, Krannert Institute of Cardiology, Indiana University School of Medicine, Indianapolis, Indiana.
    Makiyama T; Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.
    Ueyama T; Department of Cardiology, Yamaguchi University School of Medical Science, Yamaguchi, Japan.
    Shimizu A; Department of Cardiology, Yamaguchi University School of Medical Science, Yamaguchi, Japan.
    Yamakawa M; Department of Pediatrics, Kobe City Medical Center General Hospital, Kobe, Japan.
    Chen PS; Department of Medicine, Krannert Institute of Cardiology, Indiana University School of Medicine, Indianapolis, Indiana.
    Vatta M; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana.
    Horie M; Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Science, Shiga, Japan.
    Ai T; Department of Medicine, Krannert Institute of Cardiology, Indiana University School of Medicine, Indianapolis, Indiana.; Department of Clinical Laboratory Medicine, Juntendo University School of Medicine, Tokyo, Japan.
    Pokaż więcej
    Źródło:
    Pacing and clinical electrophysiology : PACE [Pacing Clin Electrophysiol] 2020 Aug; Vol. 43 (8), pp. 838-846. Date of Electronic Publication: 2020 Jul 07.
    Typ publikacji:
    Journal Article
    MeSH Terms:
    Arrhythmogenic Right Ventricular Dysplasia/*genetics
    Brugada Syndrome/*genetics
    Connectin/*genetics
    NAV1.5 Voltage-Gated Sodium Channel/*genetics
    Adolescent ; Adult ; Aged ; Arrhythmogenic Right Ventricular Dysplasia/physiopathology ; Brugada Syndrome/physiopathology ; Electrocardiography ; HEK293 Cells ; Humans ; Male ; Middle Aged ; Patch-Clamp Techniques
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    A Novel SCN5A Mutation Associated with Drug Induced Brugada Type ECG.
    Autorzy:
    Turker I; Krannert Institute of Cardiology, Indiana University, Indianapolis, IN, United States of America.
    Makiyama T; Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.
    Vatta M; Department of Cardiovascular Genetics, Indiana University, Indianapolis, IN, United States of America.
    Itoh H; Cardiovascular and Respiratory Medicine, Shiga Univ. School of Medicine, Otsu, Japan.
    Ueyama T; Cardiology, Yamaguchi University School of Medicine, Yamaguchi, Japan.
    Shimizu A; Cardiology, Yamaguchi University School of Medicine, Yamaguchi, Japan.
    Ai T; Krannert Institute of Cardiology, Indiana University, Indianapolis, IN, United States of America.; Molecular Pathogenesis, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
    Horie M; Cardiovascular and Respiratory Medicine, Shiga Univ. School of Medicine, Otsu, Japan.
    Pokaż więcej
    Źródło:
    PloS one [PLoS One] 2016 Aug 25; Vol. 11 (8), pp. e0161872. Date of Electronic Publication: 2016 Aug 25 (Print Publication: 2016).
    Typ publikacji:
    Case Reports; Journal Article
    MeSH Terms:
    Mutation, Missense*
    Anti-Arrhythmia Agents/*adverse effects
    Brugada Syndrome/*genetics
    NAV1.5 Voltage-Gated Sodium Channel/*genetics
    Aged ; Atrial Fibrillation/drug therapy ; Atrial Fibrillation/physiopathology ; Atrial Flutter/drug therapy ; Atrial Flutter/physiopathology ; Base Sequence ; Brugada Syndrome/chemically induced ; Brugada Syndrome/physiopathology ; DNA Mutational Analysis ; Electrocardiography ; HEK293 Cells ; Humans ; Lidocaine/adverse effects ; Lidocaine/analogs & derivatives ; Male
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    Gain-of-function KCNH2 mutations in patients with Brugada syndrome.
    Autorzy:
    Wang QI; Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Science, Otsu, Japan.
    Ohno S; Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Science, Otsu, Japan.
    Ding WG; Division of Physiology, Shiga University of Medical Science, Otsu, Japan.
    Fukuyama M; Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Science, Otsu, Japan.
    Miyamoto A; Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Science, Otsu, Japan.
    Itoh H; Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Science, Otsu, Japan.
    Makiyama T; Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.
    Wu J; Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Science, Otsu, Japan.
    Bai J; Division of Physiology, Shiga University of Medical Science, Otsu, Japan.
    Hasegawa K; Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Science, Otsu, Japan.
    Shinohara T; Department of Cardiology and Clinical Examination, Oita University Faculty of Medicine, Yufu, Japan.
    Takahashi N; Department of Cardiology and Clinical Examination, Oita University Faculty of Medicine, Yufu, Japan.
    Shimizu A; Faculty of Health Sciences, Yamaguchi Graduate School of Medicine, Ube, Japan.
    Matsuura H; Division of Physiology, Shiga University of Medical Science, Otsu, Japan.
    Horie M; Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Science, Otsu, Japan.
    Pokaż więcej
    Źródło:
    Journal of cardiovascular electrophysiology [J Cardiovasc Electrophysiol] 2014 May; Vol. 25 (5), pp. 522-530. Date of Electronic Publication: 2014 Jan 30.
    Typ publikacji:
    Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Mutation*
    Brugada Syndrome/*genetics
    Ether-A-Go-Go Potassium Channels/*genetics
    Action Potentials ; Adult ; Animals ; Brugada Syndrome/diagnosis ; Brugada Syndrome/metabolism ; Brugada Syndrome/physiopathology ; Brugada Syndrome/therapy ; CHO Cells ; Calcium Channels, L-Type/genetics ; Cricetulus ; DNA Mutational Analysis ; ERG1 Potassium Channel ; Electrocardiography ; Ether-A-Go-Go Potassium Channels/metabolism ; Genetic Predisposition to Disease ; Genetic Testing/methods ; Humans ; Kinetics ; Male ; Middle Aged ; NAV1.5 Voltage-Gated Sodium Channel/genetics ; Patch-Clamp Techniques ; Phenotype ; Prognosis ; Transfection
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
    Autorzy:
    Bezzina CR; Department of Clinical and Experimental Cardiology, Heart Failure Research Center, Academic Medical Center, Amsterdam, The Netherlands. />Barc J
    Mizusawa Y
    Remme CA
    Gourraud JB
    Simonet F
    Verkerk AO
    Schwartz PJ
    Crotti L
    Dagradi F
    Guicheney P
    Fressart V
    Leenhardt A
    Antzelevitch C
    Bartkowiak S
    Borggrefe M
    Schimpf R
    Schulze-Bahr E
    Zumhagen S
    Behr ER
    Bastiaenen R
    Tfelt-Hansen J
    Olesen MS
    Kääb S
    Beckmann BM
    Weeke P
    Watanabe H
    Endo N
    Minamino T
    Horie M
    Ohno S
    Hasegawa K
    Makita N
    Nogami A
    Shimizu W
    Aiba T
    Froguel P
    Balkau B
    Lantieri O
    Torchio M
    Wiese C
    Weber D
    Wolswinkel R
    Coronel R
    Boukens BJ
    Bézieau S
    Charpentier E
    Chatel S
    Despres A
    Gros F
    Kyndt F
    Lecointe S
    Lindenbaum P
    Portero V
    Violleau J
    Gessler M
    Tan HL
    Roden DM
    Christoffels VM
    Le Marec H
    Wilde AA
    Probst V
    Schott JJ
    Dina C
    Redon R
    Pokaż więcej
    Źródło:
    Nature genetics [Nat Genet] 2013 Sep; Vol. 45 (9), pp. 1044-9. Date of Electronic Publication: 2013 Jul 21.
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Genetic Variation*
    Basic Helix-Loop-Helix Transcription Factors/*genetics
    Brugada Syndrome/*complications
    Brugada Syndrome/*genetics
    Death, Sudden, Cardiac/*etiology
    NAV1.5 Voltage-Gated Sodium Channel/*genetics
    NAV1.8 Voltage-Gated Sodium Channel/*genetics
    Repressor Proteins/*genetics
    Alleles ; Animals ; Case-Control Studies ; Chromosomes, Human, Pair 3 ; Chromosomes, Human, Pair 6 ; Female ; Genetic Predisposition to Disease ; Genome-Wide Association Study ; Humans ; Male ; Mice ; Mice, Knockout ; Odds Ratio ; Polymorphism, Single Nucleotide ; Sodium Channels/genetics ; Sodium Channels/metabolism
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
      Wyświetlanie 1-16 z 16

      Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies