Sandrine Lenglez
发表
S. Rorive,
I. Salmon,
Sylvain Brohée,
2014,
Nature.
G. Fénelon,
A. Boland,
J. Deleuze,
2021,
Human molecular genetics.
L. Michaux,
P. Saussoy,
J. Demoulin,
2020,
Journal of cellular and molecular medicine.
J. Demoulin,
J. Lennartsson,
F. Houssiau,
2009,
Arthritis and rheumatism.
Sandrine Lenglez,
A. Decottignies,
G. Tilman,
2012,
Cellular signalling.
R. Yi,
C. Dubois,
C. Blanpain,
2017,
Cell stem cell.
Sandrine Lenglez,
A. Loriot,
C. De Smet,
2012,
Epigenetics.
R. Yi,
C. Dubois,
C. Blanpain,
2017
.
C. Blanpain,
B. Simons,
M. Aragona,
2017,
Nature Communications.
D. Hermand,
Sandrine Lenglez,
A. Decottignies,
2010,
Genome research.
Penttinen syndrome‐associated PDGFRB Val665Ala variant causes aberrant constitutive STAT1 signalling
J. Demoulin,
Sandrine Lenglez,
Emilie Guérit,
2022,
Journal of cellular and molecular medicine.
J. Demoulin,
Emeline Bollaert,
A. Essaghir,
2021,
International journal of molecular sciences.