Alexandra Belayew
Alexandra Belayew
Professor Emeritus, Molecular Biology, University of Mons, Belgium
Підтверджена електронна адреса в
Transcriptional control of the murine albumin/alpha-fetoprotein locus during development
SM Tilghman, A Belayew
Proceedings of the National Academy of Sciences 79 (17), 5254-5257, 1982
Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element
J Gabriels, MC Beckers, H Ding, A De Vriese, S Plaisance, ...
Gene 236 (1), 25-32, 1999
DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1
M Dixit, E Ansseau, A Tassin, S Winokur, R Shi, H Qian, S Sauvage, ...
Proceedings of the National Academy of Sciences 104 (46), 18157-18162, 2007
The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein
V Kowaljow, A Marcowycz, E Ansseau, CB Conde, S Sauvage, C Mattéotti, ...
Neuromuscular Disorders 17 (8), 611-623, 2007
Locus unlinked to alpha-fetoprotein under the control of the murine raf and Rif genes
V Pachnis, A Belayew, SM Tilghman
Proceedings of the National Academy of Sciences 81 (17), 5523-5527, 1984
An isogenetic myoblast expression screen identifies DUX4‐mediated FSHD‐associated molecular pathologies
D Bosnakovski, Z Xu, E Ji Gang, CL Galindo, M Liu, T Simsek, HR Garner, ...
The EMBO journal 27 (20), 2766-2779, 2008
The human genome contains hundreds of genes coding for finger proteins of the Krüppel type
EJ Bellefroid, PJ Lecocq, A Benhida, DA Poncelet, A Belayew, JA Martial
Dna 8 (6), 377-387, 1989
DUX4, a candidate gene for facioscapulohumeral muscular dystrophy, causes p53‐dependent myopathy in vivo
LM Wallace, SE Garwick, W Mei, A Belayew, F Coppee, KJ Ladner, ...
Annals of neurology 69 (3), 540-552, 2011
Isolation and characterization of the human prolactin gene.
AT Truong, C Duez, A Belayew, A Renard, R Pictet, GI Bell, JA Martial
The EMBO journal 3 (2), 429-437, 1984
Genetic analysis of alpha-fetoprotein synthesis in mice.
A Belayew, SM Tilghman
Molecular and Cellular Biology 2 (11), 1427-1435, 1982
The FSHD atrophic myotube phenotype is caused by DUX4 expression
C Vanderplanck, E Ansseau, S Charron, N Stricwant, A Tassin, ...
PloS one 6 (10), e26820, 2011
Functional muscle impairment in facioscapulohumeral muscular dystrophy is correlated with oxidative stress and mitochondrial dysfunction
A Turki, M Hayot, G Carnac, F Pillard, E Passerieux, S Bommart, ...
Free Radical Biology and Medicine 53 (5), 1068-1079, 2012
Regulatory elements controlling pituitary-specific expression of the human prolactin gene.
B Peers, ML Voz, P Monget, M Mathy-Hartert, M Berwaer, A Belayew, ...
Molecular and cellular biology 10 (9), 4690-4700, 1990
DUX 4 expression in FSHD muscle cells: how could such a rare protein cause a myopathy?
A Tassin, D Laoudj‐Chenivesse, C Vanderplanck, M Barro, S Charron, ...
Journal of cellular and molecular medicine 17 (1), 76-89, 2013
DUX4c, an FSHD candidate gene, interferes with myogenic regulators and abolishes myoblast differentiation
D Bosnakovski, S Lamb, T Simsek, Z Xu, A Belayew, R Perlingeiro, ...
Experimental neurology 214 (1), 87-96, 2008
Functional interactions between Sp1 or Sp3 and the helicase-like transcription factor mediate basal expression from the human plasminogen activator inhibitor-1 gene
H Ding, AM Benotmane, G Suske, D Collen, A Belayew
Journal of Biological Chemistry 274 (28), 19573-19580, 1999
Multihormonal regulation of the human prolactin gene expression from 5000 bp of its upstream sequence
M Berwaer, P Monget, B Peers, M Mathy-Hartert, E Bellefroid, JRE Davis, ...
Molecular and cellular endocrinology 80 (1-3), 53-64, 1991
Nonisotopic quantitative analysis of protein–DNA interactions at equilibrium
AM Benotmane, MF Hoylaerts, D Collen, A Belayew
Analytical biochemistry 250 (2), 181-185, 1997
Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?
M Richards, F Coppée, N Thomas, A Belayew, M Upadhyaya
Human genetics 131 (3), 325-340, 2012
Retinoic acid induction of human tissue-type plasminogen activator gene expression via a direct repeat element (DR5) located at− 7 kilobases
F Bulens, I Ibañez-Tallon, P Van Acker, A De Vriese, L Nelles, A Belayew, ...
Journal of Biological Chemistry 270 (13), 7167-7175, 1995
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