Danny Huylebroeck
Danny Huylebroeck
Erasmus University Medical Center and KULeuven
Geverifieerd e-mailadres voor erasmusmc.nl
Geciteerd door
Geciteerd door
The two-handed E box binding zinc finger protein SIP1 downregulates E-cadherin and induces invasion
J Comijn, G Berx, P Vermassen, K Verschueren, L van Grunsven, ...
Molecular cell 7 (6), 1267-1278, 2001
Identification of a potent Xenopus mesoderm-inducing factor as a homologue of activin A
JC Smith, BMJ Price, K Nimmen, D Huylebroeck
Nature 345 (6277), 729-731, 1990
Osteogenic protein-1 binds to activin type II receptors and induces certain activin-like effects.
H Yamashita, P ten Dijke, D Huylebroeck, TK Sampath, M Andries, ...
The Journal of cell biology 130 (1), 217-226, 1995
Presenilin 2 deficiency causes a mild pulmonary phenotype and no changes in amyloid precursor protein processing but enhances the embryonic lethal phenotype of presenilin 1 …
A Herreman, D Hartmann, W Annaert, P Saftig, K Craessaerts, L Serneels, ...
Proceedings of the National Academy of Sciences 96 (21), 11872-11877, 1999
SIP1, a novel zinc finger/homeodomain repressor, interacts with Smad proteins and binds to 5′-CACCT sequences in candidate target genes
K Verschueren, JE Remacle, C Collart, H Kraft, BS Baker, P Tylzanowski, ...
Journal of Biological Chemistry 274 (29), 20489-20498, 1999
In vitro mutagenesis of a full-length cDNA clone of Semliki Forest virus: the small 6,000-molecular-weight membrane protein modulates virus release
P Liljeström, S Lusa, D Huylebroeck, H Garoff
Journal of virology 65 (8), 4107-4113, 1991
Smad5 knockout mice die at mid-gestation due to multiple embryonic and extraembryonic defects
H Chang, D Huylebroeck, K Verschueren, Q Guo, MM Matzuk, A Zwijsen
Development 126 (8), 1631-1642, 1999
Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis
J Hellemans, O Preobrazhenska, A Willaert, P Debeer, P Verdonk, ...
Nature genetics 36 (11), 1213-1218, 2004
Distinct spatial and temporal expression patterns of two type I receptors for bone morphogenetic proteins during mouse embryogenesis
N Dewulf, K Verschueren, O Lonnoy, A Moren, S Grimsby, ...
Endocrinology 136 (6), 2652-2663, 1995
Endocardial cushion and myocardial defects after cardiac myocyte-specific conditional deletion of the bone morphogenetic protein receptor ALK3
V Gaussin, T Van de Putte, Y Mishina, MC Hanks, A Zwijsen, ...
Proceedings of the National Academy of Sciences 99 (5), 2878-2883, 2002
Mice lacking Zfhx1b, the gene that codes for Smad-interacting protein-1, reveal a role for multiple neural crest cell defects in the etiology of Hirschsprung disease–mental …
T Van de Putte, M Maruhashi, A Francis, L Nelles, H Kondoh, ...
The American Journal of Human Genetics 72 (2), 465-470, 2003
Epidermal differentiation does not involve the pro-apoptotic executioner caspases, but is associated with caspase-14 induction and processing
S Lippens, M Kockx, M Knaapen, L Mortier, R Polakowska, A Verheyen, ...
Cell Death & Differentiation 7 (12), 1218-1224, 2000
New mode of DNA binding of multi-zinc finger transcription factors: δEF1 family members bind with two hands to two target sites
JE Remacle, H Kraft, W Lerchner, G Wuytens, C Collart, K Verschueren, ...
The EMBO journal 18 (18), 5073-5084, 1999
Antigenic drift between the haemagglutinin of the Hong Kong influenza strains A/Aichi/2/68 and A/Victoria/3/75
M Verhoeyen, R Fang, WM Jou, R Devos, D Huylebroeck, E Saman, ...
Nature 286 (5775), 771-776, 1980
The mammalian gene function resource: the International Knockout Mouse Consortium
A Bradley, K Anastassiadis, A Ayadi, JF Battey, C Bell, MC Birling, ...
Mammalian genome 23 (9), 580-586, 2012
Complete structure of the hemagglutinin gene from the human influenza A/Victoria/3/75 (H3N2) strain as determined from cloned DNA
WM Jou, M Verhoeyen, R Devos, E Saman, R Fang, D Huylebroeck, ...
Cell 19 (3), 683-696, 1980
Follistatins neutralize activin bioactivity by inhibition of activin binding to its type II receptors
JP de Winter, P ten Dijke, CJM de Vries, TAE van Achterberg, H Sugino, ...
Molecular and cellular endocrinology 116 (1), 105-114, 1996
Overexpression of activin A in the skin of transgenic mice reveals new activities of activin in epidermal morphogenesis, dermal fibrosis and wound repair
B Munz, H Smola, F Engelhardt, K Bleuel, M Brauchle, I Lein, LW Evans, ...
The EMBO journal 18 (19), 5205-5215, 1999
Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome
JKJ Van Houdt, BA Nowakowska, SB Sousa, BDC Van Schaik, ...
Nature genetics 44 (4), 445-449, 2012
Stalk cell phenotype depends on integration of Notch and Smad1/5 signaling cascades
IM Moya, L Umans, E Maas, PNG Pereira, K Beets, A Francis, W Sents, ...
Developmental cell 22 (3), 501-514, 2012
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