J. Verbeeck

发表

Telomere length homeostasis and telomere position effect on a linear human artificial chromosome are dictated by the genetic background

P. Marynen, T. Voet, L. Schoonjans, 2012, Nucleic acids research.

The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability

J. Rosenfeld, P. Marynen, K. Devriendt, 2013, Human Genetics.

Copy-number gains of HUWE1 due to replication- and recombination-based rearrangements.

P. Marynen, T. Bose, M. Roselló, 2012, American journal of human genetics.

Novel PORCN mutations in focal dermal hypoplasia

P. Marynen, K. Devriendt, H. Van Esch, 2009, Clinical genetics.

The ribosomal RPL10 R98S mutation drives IRES-dependent BCL-2 translation in T-ALL

J. Meijerink, D. Cassiman, J. Cools, 2018, Leukemia.

Increased Dosage of RAB39B Affects Neuronal Development and Could Explain the Cognitive Impairment in Male Patients with Distal Xq28 Copy Number Gains

K. Õunap, H. Esch, M. Raynaud, 2014, Human mutation.

The T-cell leukemia associated ribosomal RPL10 R98S mutation enhances JAK-STAT signaling

J. Meijerink, J. Dinman, J. Cools, 2017, Leukemia.

Dosage-dependent severity of the phenotype in patients with mental retardation due to a recurrent copy-number gain at Xq28 mediated by an unusual recombination.

P. Marynen, H. Van Esch, C. Spaich, 2009, American journal of human genetics.

The ribosomal protein gene RPL5 is a haploinsufficient tumor suppressor in multiple cancer types

Laura Fancello, Kim De Keersmaecker, K. D. Keersmaecker, 2017, Oncotarget.

De novo MECP2 duplications in two females with intellectual disability and unfavorable complete skewed X-inactivation

S. Seneca, P. Marynen, E. Baere, 2014, Human Genetics.

Generation and Characterization of an Nxf7 Knockout Mouse to Study NXF5 Deficiency in a Patient with Intellectual Disability

R. D'Hooge, P. Marynen, A. Roebroek, 2013, PloS one.

A novel fragile X syndrome mutation reveals a conserved role for the carboxy-terminus in FMRP localization and function

Bassem A. Hassan, B. Hassan, K. Devriendt, 2015, EMBO molecular medicine.

The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability

J. Rosenfeld, P. Marynen, K. Devriendt, 2013, Human Genetics.

Translatome analysis reveals altered serine and glycine metabolism in T-cell acute lymphoblastic leukemia cells

R. Agami, M. Fiers, D. Cassiman, 2019, Nature Communications.

Low frequency mutations in ribosomal proteins RPL10 and RPL5 in multiple myeloma

Arlen W. Johnson, P. Sonneveld, L. Michaux, 2017, Haematologica.

Transcription factor NKX2–1 drives serine and glycine synthesis addiction in cancer

D. Lambrechts, J. Cools, A. Uyttebroeck, 2023, British Journal of Cancer.

Early Frameshift Mutation in PIGA Identified in a Large XLID Family Without Neonatal Lethality

V. Kalscheuer, H. Esch, Linzhao Cheng, 2014, Human mutation.

Exploitation of the ribosomal protein L10 R98S mutation to enhance recombinant protein production in mammalian cells

L. Montanaro, Tiziana Girardi, K. De Keersmaecker, 2022, Engineering in life sciences.

The ribosomal RPL10 R98S mutation drives IRES-dependent BCL-2 translation in T-ALL

J. Meijerink, D. Cassiman, J. Cools, 2018, Leukemia.