S. Meulemans

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Deletion of C2orf34, PREPL and SLC3A1 causes atypical hypotonia–cystinuria syndrome

G. Matthijs, J. Creemers, A. Cano, 2008, Journal of Medical Genetics.

Deletion of PREPL, a gene encoding a putative serine oligopeptidase, in patients with hypotonia-cystinuria syndrome.

F. de Zegher, G. Matthijs, F. Eyskens, 2006, American journal of human genetics.

Role of furin in granular acidification in the endocrine pancreas: Identification of the V-ATPase subunit Ac45 as a candidate substrate

A. Roebroek, W. V. D. Van de Ven, R. Quintens, 2008, Proceedings of the National Academy of Sciences.

Internalization of Proprotein Convertase PC7 from Plasma Membrane Is Mediated by a Novel Motif*

J. Creemers, J. Declercq, E. Plets, 2012, The Journal of Biological Chemistry.

Endosome to trans-Golgi network transport of Proprotein Convertase 7 is mediated by a cluster of basic amino acids and palmitoylated cysteines.

W. Annaert, R. Sannerud, J. Creemers, 2017, European journal of cell biology.

PREPL deficiency with or without cystinuria causes a novel myasthenic syndrome

A. Engel, J. Creemers, D. Selcen, 2014, Neurology.

Neuroendocrine-specific Expression of the Human Prohormone Convertase 1 Gene

W. V. D. Van de Ven, T. Ayoubi, E. Jansen, 1995, The Journal of Biological Chemistry.

Production of recombinant proteins in Chinese Hamster Ovary cells overexpressing the subtilisin-like proprotein converting enzyme furin

A. Roebroek, T. Ayoubi, W. V. D. Ven, 2004, Molecular Biology Reports.

Cell Type-specific Protein-DNA Interactions at the cAMP Response Elements of the Prohormone Convertase 1 Promoter

W. V. D. Van de Ven, T. Ayoubi, E. Jansen, 1997, The Journal of Biological Chemistry.

Differential Effects of Furin Deficiency on Insulin Receptor Processing and Glucose Control in Liver and Pancreatic β Cells of Mice

J. Creemers, B. Ramos-Molina, S. Meulemans, 2021, International journal of molecular sciences.

Two novel deletions in hypotonia-cystinuria syndrome.

H. Van Esch, J. Jaeken, J. Creemers, 2012, Molecular genetics and metabolism.

PREPL deficiency: delineation of the phenotype and development of a functional blood assay

N. Voermans, E. Kamsteeg, D. Lederer, 2017, Genetics in Medicine.

PREPL: a putative novel oligopeptidase propelled into the limelight

G. Matthijs, J. Jaeken, R. Derua, 2006, Biological chemistry.

Regulation of human prohormone convertase 2 promoter activity by the transcription factor EGR-1.

W. V. D. Van de Ven, E. Jansen, T. Ayoubi, 1997, The Biochemical journal.

Deletion of C2orf34, PREPL and SLC3A1 causes atypical hypotonia–cystinuria syndrome

G. Matthijs, J. Creemers, A. Cano, 2009, BMJ Case Reports.

Global distribution of the most prevalent deletions causing hypotonia–cystinuria syndrome

Raoul Rooman, G. Matthijs, M. Zaffanello, 2007, European Journal of Human Genetics.

Loss of hypothalamic Furin affects POMC to proACTH cleavage and feeding behavior in high-fat diet-fed mice

J. Creemers, B. Ramos-Molina, Leanne Walker, 2022, Molecular metabolism.

Liver-Specific Inactivation of the Proprotein Convertase FURIN Leads to Increased Hepatocellular Carcinoma Growth

A. Prat, N. Seidah, J. Creemers, 2015, BioMed research international.

Nuclear Localization of the Autism Candidate Gene Neurobeachin and Functional Interaction with the NOTCH1 Intracellular Domain Indicate a Role in Regulating Transcription

J. Creemers, J. Declercq, P. Stijnen, 2016, PloS one.

Chromosomal Microdeletions and Genes' Functions: A Cluster of Chromosomal Microdeletions and the Deleted Genes' Functions

K. Martens, S. Meulemans, D. Tilstra, 2007 .

Metabolic and Behavioural Phenotypes in Nestin-Cre Mice Are Caused by Hypothalamic Expression of Human Growth Hormone

L. Serneels, F. Schuit, J. Creemers, 2015, PloS one.

Regulation of HMGIC expression: an architectural transcription factor involved in growth control and development

T. Ayoubi, W. V. D. Ven, E. Jansen, 1999, Oncogene.

The NNP-1 gene (D21S2056E), which encodes a novel nuclear protein, maps in close proximity to the cystatin B gene within the EPM1 and APECED critical region on 21q22.3.

W. V. D. Van de Ven, E. Jansen, S. Meulemans, 1997, Genomics.

SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesicles.

Jurgen Del-Favero, Kathleen Freson, Peter De Rijk, 2010, Human molecular genetics.

The Focal Adhesion and Nuclear Targeting Capacity of the LIM-containing Lipoma-preferred Partner (LPP) Protein*

W. V. D. Van de Ven, Marleen M. R. Petit, Sandra M. P. Meulemans, 2003, The Journal of Biological Chemistry.

The proprotein convertase furin is a pro-oncogenic driver in KRAS and BRAF driven colorectal cancer

S. Tejpar, Lieven Thorrez, J. Creemers, 2020, Oncogene.

Xiaorong Zhu, D. Steiner, C. Lawrence, 2006, Endocrinology.

The tumor suppressor Scrib interacts with the zyxin-related protein LPP, which shuttles between cell adhesion sites and the nucleus

W. V. D. Van de Ven, T. Ayoubi, Marleen MR Petit, 2005, BMC Cell Biology.

The Dwarf Phenotype in GH240B Mice, Haploinsufficient for the Autism Candidate Gene Neurobeachin, Is Caused by Ectopic Expression of Recombinant Human Growth Hormone

J. Creemers, H. Vankelecom, P. Stijnen, 2014, PloS one.

Heterozygous Mutations Causing Partial Prohormone Convertase 1 Deficiency Contribute to Human Obesity

P. Elliott, M. Jarvelin, F. Horber, 2012, Diabetes.

Generation and characterization of non-competitive furin-inhibiting nanobodies.

S. Muyldermans, I. Lindberg, W. V. D. Van de Ven, 2012, The Biochemical journal.

The tumor suppressor Scrib interacts with the zyxin-related protein LPP, which shuttles between cell adhesion sites and the nucleus.

W. V. D. Van de Ven, T. Ayoubi, E. Jansen, 2005, BMC cell biology.

Generation and characterization of non-competitive furin-inhibiting nanobodies.

S. Muyldermans, I. Lindberg, W. V. D. Van de Ven, 2012, The Biochemical journal.

PREPL deficiency with or without cystinuria causes a novel myasthenic syndrome

A. Engel, J. Creemers, D. Selcen, 2014, Neurology.