RNDr. Iveta Valášková, Ph.D.

2023

• 20 let diagnostiky maligní hypertermie v České a Slovenské republice.

  KLINCOVÁ Martina ŠTĚPÁNKOVÁ Dagmar SCHRÖDEROVÁ Ivana KLABUSAYOVÁ Eva OŠŤÁDALOVÁ Edita VALÁŠKOVÁ Iveta FAJKUSOVÁ Lenka ZÍDKOVÁ Jana GAILLYOVÁ Renata ŠTOURAČ Petr

  Article in Periodical

  ANESTEZIOLOGIE A INTENZIVNI MEDICINA, year: 2023, volume: 34, edition: 3, DOI

2021

• Long-QT founder variant T309I-Kv7.1 with dominant negative pattern may predispose delayed afterdepolarizations under β-adrenergic stimulation

  SYNKOVÁ Iva BÉBAROVÁ Markéta ANDRŠOVÁ Irena CHMELIKOVA Larisa ŠVECOVÁ Olga HOSEK Jan PÁSEK Michal VÍT Pavel VALÁŠKOVÁ Iveta GAILLYOVÁ Renata NAVRATIL Rostislav NOVOTNÝ Tomáš

  Article in Periodical

  Nature Scientific Reports, year: 2021, volume: 11, edition: 1, DOI

• Molekulárně-genetická diagnostika hereditární hemoragické teleangiektázie.

  VINOHRADSKÁ Jana VALÁŠKOVÁ Iveta

  Conference abstract

  Year: 2021, type: Conference abstract

2020

• Next generation sequencing in newborn screening for cystic fibrosis

  VINOHRADSKÁ Jana VALÁŠKOVÁ Iveta GAILLYOVÁ Renata

  Conference abstract

  Year: 2020, type: Conference abstract

• Organoids as a personalized medicine tool for ultra-rare mutations in cystic fibrosis: The case of S955P and 1717-2A > G

  SILVA I. A.L . DOUSOVA Tereza RAMALHO S. CENTEIO R. CLARKE L. A. RAILEAN V. BOTELHO H. M. HOLUBOVA Andrea VALÁŠKOVÁ Iveta YEH J. T. HWANG T. C. FARINHA C. M. KUNZELMANN K. AMARAL M. D.

  Article in Periodical

  Biochimica et Biophysica Acta - Molecular Basis of Disease, year: 2020, volume: 1866, edition: 11, DOI

2019

• Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotype

  SZAFRANSKI Przemyslaw LIU Qian KAROLAK Justyna A. SONG Xiaofei DE LEEUW Nicole FAAS Brigitte GERYCHOVÁ Romana JANKŮ Petr JEŽOVÁ Marta VALÁŠKOVÁ Iveta GIBBS Kathleen A. SURREY Lea F. POISSON Virginie BERUBE Denis OLIGNY Luc L. MICHAUD Jacques L. POPEK Edwina STANKIEWICZ Pawel

  Article in Periodical

  Human Genetics, year: 2019, volume: 138, edition: 11-12, DOI

• Dystrophin Deficiency Leads to Genomic Instability in Human Pluripotent Stem Cells via NO Synthase-Induced Oxidative Stress

  JELÍNKOVÁ Šárka KOHUTOVÁ Aneta FOJTÍK Petr KRUTÁ Miriama VILOTIĆ Aleksandra PEŠL Martin VRBSKÝ Jan GAILLYOVÁ Renata VALÁŠKOVÁ Iveta FRÁK Ivan FORTE Giancarlo DVOŘÁK Petr MELI Albano ROTREKL Vladimír MARKOVÁ Lenka JURÁKOVÁ Tereza LACAMPAGNE Alain

  Article in Periodical

  Cells, year: 2019, volume: 8, edition: 1, DOI

• Generation of two Duchenne muscular dystrophy patient-specific induced pluripotent stem cell lines DMD02 and DMD03 (MUNIi001-A and MUNIi003-A)

  JELÍNKOVÁ Šárka MARKOVÁ Lenka PEŠL Martin VALÁŠKOVÁ Iveta MAKATUROVÁ Eva JUŘÍKOVÁ Lenka VONDRÁČEK Petr LACAMPAGNE Alain DVOŘÁK Petr MELI Albano ROTREKL Vladimír

  Article in Periodical

  STEM CELL RESEARCH, year: 2019, volume: 40, edition: OCT 2019, DOI

• Molecular analysis confirmed common ancestor of 10 Czech families with long QT syndrome carrying C926T-KCNQ1 variant

  SYNKOVÁ Iva VALÁŠKOVÁ Iveta GAILLYOVÁ Renata NOVOTNÝ Tomáš BÉBAROVÁ Markéta ANDRŠOVÁ Irena FLORIANOVA A. VÍT Pavel NAVRATIL R.

  Conference abstract

  Year: 2019, type: Conference abstract

• Mutace T309I asociovaná se syndromem dlouhého QT typu 1: akumulace IKs jako mechanismus ochrany srdce proti arytmii

  BÉBAROVÁ Markéta SYNKOVÁ Iva ANDRŠOVÁ Irena BAIAZITOVA Larisa ŠVECOVÁ Olga HOŠEK Jan PÁSEK Michal VÍT Pavel VALÁŠKOVÁ Iveta GAILLYOVÁ Renata NAVRÁTIL Rostislav NOVOTNÝ Tomáš

  Conference abstract

  Year: 2019, type: Conference abstract