Y. Krom

发表

PABPN1-Dependent mRNA Processing Induces Muscle Wasting

B. Florea, Y. Raz, V. Raz, 2016, PLoS genetics.

Inhibition of neointima formation by local delivery of estrogen receptor alpha and beta specific agonists.

J. Jukema, P. Quax, K. V. van Dijk, 2007, Cardiovascular research.

Long-term Health and Quality-of-Life Consequences of Mass Screening for Childhood Celiac Disease: A 10-Year Follow-up Study

M. Mearin, J. Schweizer, S. Verloove-vanhorick, 2009, Pediatrics.

Dnmt3b regulates DUX4 expression in a tissue-dependent manner in transgenic D4Z4 mice

B. den Hamer, S. M. van der Maarel, Y. Krom, 2020, Skeletal muscle.

Deep characterization of a common D4Z4 variant identifies biallelic DUX4 expression as a modifier for disease penetrance in FSHD2

J. Goeman, S. Tapscott, B. Engelen, 2017, European Journal of Human Genetics.

Administration of 17- -estradiol to an insulin resistant mouse model acutely improves hepatic insulin sensitivity

R. Frants, L. Havekes, Y. Krom, 2006 .

Intrinsic Epigenetic Regulation of the D4Z4 Macrosatellite Repeat in a Transgenic Mouse Model for FSHD

Zizhen Yao, S. Tapscott, Janet M. Young, 2013, PLoS genetics.

Differential myofiber-type transduction preference of adeno-associated virus serotypes 6 and 9

J. Verhaagen, S. M. van der Maarel, Y. Raz, 2015, Skeletal Muscle.

Apolipoprotein CI causes hypertriglyceridemia independent of the very-low-density lipoprotein receptor and apolipoprotein CIII in mice.

K. V. van Dijk, L. Havekes, Y. Krom, 2006, Biochimica et biophysica acta.

Downregulation of microRNA-29, -23, and -21 in urine of Duchenne Muscular Dystrophy patients

V. Ricotti, F. Muntoni, L. Servais, 2018 .

Efficient in vivo knock-down of estrogen receptor alpha: application of recombinant adenovirus vectors for delivery of short hairpin RNA

K. V. van Dijk, Y. Krom, I. Que, 2006, BMC biotechnology.

Efficient targeting of adenoviral vectors to integrin positive vascular cells utilizing a CAR-cyclic RGD linker protein.

K. V. van Dijk, R. Frants, T. V. van Berkel, 2005, Biochemical and biophysical research communications.

Increased DUX4 expression during muscle differentiation correlates with decreased SMCHD1 protein levels at D4Z4

S. Tapscott, R. Tawil, S. M. van der Maarel, 2015, Epigenetics.

Repression of Hepatic Estrogen Receptor Alpha Does Affect Expression of Lipid-Related Gene but Does Not Affect Lipid Metabolism in Female APOE*3 Leiden Mice

R. Frants, Y. Krom, K. V. Dijk, 2006 .

Occurrence of symptoms in different stages of Duchenne muscular dystrophy and their impact on social participation

E. Cup, M. Willemsen, Y. Krom, 2021, Muscle & nerve.

Compliance to DMD Care Considerations in the Netherlands

J. Verschuuren, Y. Krom, I. D. de Groot, 2021, Journal of neuromuscular diseases.

Novel free-circulating and extracellular vesicle-derived miRNAs dysregulated in Duchenne muscular dystrophy.

V. Ricotti, F. Muntoni, L. Servais, 2020, Epigenomics.

Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2

Daniel G. Miller, S. Tapscott, M. Bamshad, 2012, Nature Genetics.

Dnmt3b regulates DUX4 expression in a tissue-dependent manner in transgenic D4Z4 mice

B. den Hamer, S. M. van der Maarel, Y. Krom, 2020, Skeletal muscle.

Smchd1 haploinsufficiency exacerbates the phenotype of a transgenic FSHD1 mouse model

S. Tapscott, L. Snider, M. Blewitt, 2018, Human molecular genetics.

T Cell Responses to Dystrophin in a Natural History Study of Duchenne Muscular Dystrophy.

V. Ricotti, F. Muntoni, L. Servais, 2022, Human gene therapy.

DUX4 induces a transcriptome more characteristic of a less-differentiated cell state and inhibits myogenesis

B. den Hamer, C. Banerji, S. M. van der Maarel, 2016, Development.

DUX4 induces a transcriptome more characteristic of a less-differentiated cell state and inhibits myogenesis

B. den Hamer, C. Banerji, S. M. van der Maarel, 2016, Journal of Cell Science.

Generation of isogenic D4Z4 contracted and noncontracted immortal muscle cell clones from a mosaic patient: a cellular model for FSHD.

Elisa Negroni, Rabi Tawil, S. Tapscott, 2012, The American journal of pathology.

Downregulation of miRNA-29, -23 and -21 in urine of Duchenne muscular dystrophy patients.

V. Ricotti, F. Muntoni, L. Servais, 2018, Epigenomics.

SMCHD1 has separable roles in chromatin architecture and gene silencing that could be targeted in disease

Matthew E. Ritchie, A. Keniry, Shifeng Xue, 2021, bioRxiv.

Deep characterization of a common D4Z4 variant identifies biallelic DUX4 expression as a modifier for disease penetrance in FSHD2

J. Goeman, S. Tapscott, B. Engelen, 2017, European Journal of Human Genetics.

Decision-Making And Selection Bias in Four Observational Studies on Duchenne and Becker Muscular Dystrophy

H. Kan, C. Straathof, Y. Krom, 2020, Journal of neuromuscular diseases.

Modulation of estrogen signaling in hepatic and vascular tissue

Y. Krom, 2006 .

The Dilemma of Choice for Duchenne Patients Eligible for Exon 51 Skipping The European Experience

Annemieke Aartsma-Rus, H. V. van Duyvenvoorde, V. Straub, 2023, Journal of neuromuscular diseases.

Differential myofiber-type transduction preference of adeno-associated virus serotypes 6 and 9

J. Verhaagen, S. M. van der Maarel, Y. Raz, 2015, Skeletal Muscle.

DUX4 induces a transcriptome more characteristic of a less-differentiated cell state and inhibits myogenesis

C. Banerji, S. M. van der Maarel, Y. Krom, 2016, Journal of Cell Science.