A. Beqqali

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In vitro overexpression of CHAPa and CHAPb in mouse cardiomyocytes and skeletal muscle cells interferes with Z-disc integrity and decreases fetal gene expression

J. Monshouwer-Kloots, R. Passier, C. Mummery, 2013 .

Z-disc protein CHAPb induces cardiomyopathy and diastolic dysfunction

R. Passier, C. Mummery, P. Steendijk, 2013 .

Cytoskeletal heart-enriched actin-associated protein (CHAP) is expressed in striated and smooth muscle cells in chick and mouse during embryonic and adult stages.

J. Monshouwer-Kloots, R. Passier, C. Mummery, 2011, The International journal of developmental biology.

A targeted metabolomics assay for cardiac metabolism and demonstration using a mouse model of dilated cardiomyopathy

Eloisa Arbustini, Julian L. Griffin, Yigal M. Pinto, 2016, Metabolomics.

The MEF2 transcriptional target DMPK induces loss of sarcomere structure and cardiomyopathy

I. van der Made, Y. Pinto, M. M. G. van den Hoogenhof, 2018, Cardiovascular research.

Cardiac circRNAs arise mainly from constitutive exons rather than alternatively spliced exons

Yolan J. Reckman, I. van der Made, Y. Pinto, 2018, RNA.

Z-disc protein CHAPb induces cardiomyopathy and contractile dysfunction in the postnatal heart

J. Monshouwer-Kloots, R. Passier, C. Mummery, 2017, PloS one.

CHAP is a newly identified Z-disc protein essential for heart and skeletal muscle function

J. Monshouwer-Kloots, R. Passier, C. Mummery, 2010, Journal of Cell Science.

The RNA-binding protein Rbm38 is dispensable during pressure overload-induced cardiac remodeling in mice

I. van der Made, Y. Pinto, E. Creemers, 2017, PloS one.

CAZIP, a novel protein expressed in the developing heart and nervous system

J. Monshouwer-Kloots, R. Passier, B. Roelen, 2009, Developmental dynamics : an official publication of the American Association of Anatomists.

Human embryonic stem cell-derived endothelial cell product injection attenuates cardiac remodeling in myocardial infarction

M. Brittan, A. Spiroski, M. Lalwani, 2022, Frontiers in Cardiovascular Medicine.

Mapping the developing human cardiac endothelium at single-cell resolution identifies MECOM as a regulator of arteriovenous gene expression

C. Ponting, M. Brittan, N. Henderson, 2022, Cardiovascular research.

Long Non-Coding RNA Malat-1 Is Dispensable during Pressure Overload-Induced Cardiac Remodeling and Failure in Mice

B. Schroen, S. Heymans, K. Prasanth, 2016, PloS one.

Genome‐Wide Transcriptional Profiling of Human Embryonic Stem Cells Differentiating to Cardiomyocytes

Robert Passier, Christine Mummery, R. Passier, 2006 .

Insights into alternative splicing of sarcomeric genes in the heart.

E. Creemers, A. Beqqali, M. V. D. van den Hoogenhof, 2015, Journal of molecular and cellular cardiology.

RBM20 Mutations Induce an Arrhythmogenic Dilated Cardiomyopathy Related to Disturbed Calcium Handling

I. van der Made, Y. Pinto, E. Creemers, 2018, Circulation.

RBM20 Regulates Circular RNA Production From the Titin Gene.

Yolan J. Reckman, I. van der Made, Y. Pinto, 2016, Circulation research.

Sarcosin (Krp1) in skeletal muscle differentiation: gene expression profiling and knockdown experiments.

R. Passier, B. Roelen, H. V. van Tol, 2012, The International journal of developmental biology.

Heterozygous loss of Rbm24 in the adult mouse heart increases sarcomere slack length but does not affect function

I. van der Made, Y. Pinto, E. Creemers, 2020, Scientific Reports.

Human stem cells as a model for cardiac differentiation and disease

R. Passier, C. Mummery, W. V. Eldik, 2009, Cellular and Molecular Life Sciences.

The clinical outcome of LMNA missense mutations can be associated with the amount of mutated protein in the nuclear envelope

Y. Pinto, P. Bross, J. Mogensen, 2018, European journal of heart failure.

e role of CHAP during heart development: in vivo and in vitro knockdown in mouse and chick

R. Passier, C. Mummery, S. Loughna, 2013 .

Alternative splicing in cardiomyopathy

A. Beqqali, 2018, Biophysical Reviews.

Editorial: RNA Biology in Cardiovascular Disease

H. el Azzouzi, A. Beqqali, M. V. D. van den Hoogenhof, 2021, Frontiers in Genetics.

5 A Mutation in the Glutamate-rich Region of RBM 20 Causes Dilated Cardiomyopathy through Missplicing of Titin and Impaired Frank-Starling Mechanism

J. Mogensen, N. Hubner, J. Haas, 2017 .

A mutation in the glutamate-rich region of RNA-binding motif protein 20 causes dilated cardiomyopathy through missplicing of titin and impaired Frank-Starling mechanism.

Y. Pinto, E. Creemers, J. Mogensen, 2016, Cardiovascular research.

The LMNA mutation p.Arg321Ter associated with dilated cardiomyopathy leads to reduced expression and a skewed ratio of lamin A and lamin C proteins.

Y. Pinto, P. Bross, J. Mogensen, 2013, Experimental cell research.

The paper of the month : Identification of Novel Mutations in RBM 20 in Patients with Dilated Cardiomyopathy

N. Norton, Duanxiang Li, M. Hofmeyer, 2010 .

TECRL, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT

Brian J. Stevenson, J. Rioux, Z. Kutalik, 2016, EMBO molecular medicine.

Genome‐Wide Transcriptional Profiling of Human Embryonic Stem Cells Differentiating to Cardiomyocytes

Robert Passier, Christine Mummery, R. Passier, 2006, Stem cells.

Human AdV-20-42-42, a Promising Novel Adenoviral Vector for Gene Therapy and Vaccine Product Development

M. Havenga, A. Lemckert, H. M. van der Schaar, 2021, bioRxiv.

Extracellular Vesicle miRNAs in the Promotion of Cardiac Neovascularisation

M. Brittan, L. D. de Windt, P. A. da Costa Martins, 2020, Frontiers in Physiology.

A targeted metabolomics assay for cardiac metabolism and demonstration using a mouse model of dilated cardiomyopathy

Y. Pinto, E. Arbustini, P. Elliott, 2016, Metabolomics.

Chapter 4 A splice site mutation in TECRL is associated with inherited lethal arrhythmias in humans

Brian J. Stevenson, R. Passier, C. Mummery, 2016 .

Heterozygous loss of Rbm24 in the adult mouse heart increases sarcomere slack length but does not affect function

Y. Pinto, E. Creemers, J. Velden, 2020, Scientific Reports.