Search Results - "Lentink, Viola"

Regulation of Cardiac Gene Expression by KLF15, a Repressor of Myocardin Activity by Leenders, Joost J., Wijnen, Wino J., Hiller, Monika, van der Made, Ingeborg, Lentink, Viola, van Leeuwen, Rick E.W., Herias, Veronica, Pokharel, Saraswati, Heymans, Stephane, de Windt, Leon J., Høydal, Morten A., Pinto, Yigal M., Creemers, Esther E.

“…Pathological forms of left ventricular hypertrophy (LVH) often progress to heart failure. Specific transcription factors have been identified that activate the…”
Get full text

Long-QT mutation p.K557E-Kv7.1: dominant-negative suppression of IKs, but preserved cAMP-dependent up-regulation by Spätjens, Roel L.H.M.G., Bébarová, Markéta, Seyen, Sandrine R.M., Lentink, Viola, Jongbloed, Roselie J., Arens, Yvonne H.J.M., Heijman, Jordi, Volders, Paul G.A.

Get full text

miR-133 and miR-30 Regulate Connective Tissue Growth Factor: Implications for a Role of MicroRNAs in Myocardial Matrix Remodeling by Duisters, Rudy F, Tijsen, Anke J, Schroen, Blanche, Leenders, Joost J, Lentink, Viola, van der Made, Ingeborg, Herias, Veronica, van Leeuwen, Rick E, Schellings, Mark W, Barenbrug, Paul, Maessen, Jos G, Heymans, Stephane, Pinto, Yigal M, Creemers, Esther E

“…The myocardium of the failing heart undergoes a number of structural alterations, most notably hypertrophy of cardiac myocytes and an increase in extracellular…”
Get full text

Dominant-Negative Control of cAMP-Dependent I Ks Upregulation in Human Long-QT Syndrome Type 1 by Heijman, Jordi, Spätjens, Roel L.H.M.G., Seyen, Sandrine R.M., Lentink, Viola, Kuijpers, Helma J.H., Boulet, Inge R., de Windt, Leon J., David, Miren, Volders, Paul G.A.

“…Rationale: The mutation A341V in the S6 transmembrane segment of KCNQ1 , the α-subunit of the slowly activating delayed-rectifier K + (I Ks ) channel,…”
Get full text

Dominant-Negative Control of cAMP-Dependent IKs Upregulation in Human Long-QT Syndrome Type 1 by Heijman, Jordi, Spätjens, Roel L.H.M.G, Seyen, Sandrine R.M, Lentink, Viola, Kuijpers, Helma J.H, Boulet, Inge R, de Windt, Leon J, David, Miren, Volders, Paul G.A

“…RATIONALE:The mutation A341V in the S6 transmembrane segment of KCNQ1, the α-subunit of the slowly activating delayed-rectifier K (IKs) channel, predisposes to…”
Get full text

Long-QT mutation p.K557E-Kv7.1: dominant-negative suppression of IKs, but preserved cAMP-dependent up-regulation by Spätjens, Roel L H M G, Bébarová, Markéta, Seyen, Sandrine R M, Lentink, Viola, Jongbloed, Roselie J, Arens, Yvonne H J M, Heijman, Jordi, Volders, Paul G A

“…Mutations in KCNQ1, encoding for Kv7.1, the α-subunit of the IKs channel, cause long-QT syndrome type 1, potentially predisposing patients to ventricular…”
Get full text