|
๐
|
Doublecortin Is a Developmentally Regulated, Microtubule-Associated Protein Expressed in Migrating and Differentiating Neurons
14 auth.
F. Francis,
A. Koulakoff,
D. Boucher,
P. Chafey,
B. Schaar,
M. Vinet,
G. Friocourt,
Nathalie McDonnell,
O. Reiner,
A. Kahn,
...
S. Mcconnell,
Y. BerwaldโNetter,
P. Denoulet,
J. Chelly
|
9 |
1999 |
9
๐
|
|
๐
|
A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome
14 auth.
V. Portes,
J. Pinard,
P. Billuart,
M. Vinet,
A. Koulakoff,
A. Carrieฬ,
A. Gelot,
Elisabeth Dupuis,
J. Motte,
Y. BerwaldโNetter,
...
M. Catala,
A. Kahn,
C. Beldjord,
J. Chelly
|
9 |
1998 |
9
๐
|
|
๐
|
Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation
17 auth.
P. Billuart,
T. Bienvenu,
N. Ronce,
V. Portes,
M. Vinet,
R. Zemni,
H. R. Crollius,
A. Carrieฬ,
F. Fauchereau,
M. Cherry,
...
S. Briault,
B. Hamel,
J. Fryns,
C. Beldjord,
A. Kahn,
C. Moraine,
J. Chelly
|
8 |
1998 |
8
๐
|
|
๐
|
A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation
22 auth.
A. Carrieฬ,
Lin Jun,
T. Bienvenu,
M. Vinet,
N. Mcdonell,
P. Couvert,
R. Zemni,
A. Cardona,
G. Buggenhout,
S. Frints,
...
B. Hamel,
C. Moraine,
H. Ropers,
T. Strom,
G. Howell,
A. Whittaker,
M. Ross,
A. Kahn,
J. Fryns,
C. Beldjord,
P. Marynen,
J. Chelly
|
8 |
1999 |
8
๐
|
|
๐
|
MECP2 mutations account for most cases of typical forms of Rett syndrome.
12 auth.
T. Bienvenu,
A. Carrieฬ,
N. Roux,
M. Vinet,
P. Jonveaux,
P. Couvert,
...
L. Villard,
A. Arzimanoglou,
C. Beldjord,
M. Fonteฬs,
M. Tardieu,
J. Chelly
|
8 |
2000 |
8
๐
|
|
๐
|
ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation.
23 auth.
T. Bienvenu,
K. Poirier,
G. Friocourt,
N. Bahi,
Delphine Beaumont,
F. Fauchereau,
Lamia Ben Jeema,
R. Zemni,
M. Vinet,
F. Francis,
...
P. Couvert,
M. Gomot,
C. Moraine,
H. van Bokhoven,
V. Kalscheuer,
S. Frints,
J. Gecz,
Kanae Ohzaki,
H. Chaabouni,
J. Fryns,
V. Desportes,
C. Beldjord,
J. Chelly
|
8 |
2002 |
8
๐
|
|
๐
|
A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation
26 auth.
R. Zemni,
T. Bienvenu,
M. Vinet,
A. Sefiani,
A. Carrieฬ,
P. Billuart,
N. Mcdonell,
P. Couvert,
F. Francis,
P. Chafey,
F. Fauchereau,
G. Friocourt,
V. Portes,
A. Cardona,
S. Frints,
...
A. Meindl,
O. Brandau,
N. Ronce,
C. Moraine,
H. Bokhoven,
H. Ropers,
R. Sudbrak,
A. Kahn,
J. Fryns,
C. Beldjord,
J. Chelly
|
7 |
2000 |
7
๐
|
|
๐
|
The RhoGAP activity of OPHN1, a new F-actin-binding protein, is negatively controlled by its amino-terminal domain
9 auth.
F. Fauchereau,
U. Herbrand,
P. Chafey,
Alexander Eberth,
A. Koulakoff,
M. Vinet,
...
M. Ahmadian,
J. Chelly,
P. Billuart
|
6 |
2003 |
6
๐
|
|
๐
|
Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12.
18 auth.
Kemal Azlbi,
Luclen Bachner,
Jacques S.Beckmann,
Kllchlro Matsumura,
Elhadl Hamouda,
Mallka Chaouch,
Athmane Chaouch,
Rachlda Alt-Ouarab,
Alaln Vlgnal,
J. Welssenbach,
...
M. Vinet,
F. Leturcq,
Huguette Collln,
Fernando M.S.Tomรฉ,
A. Reghis,
M. Fardeau,
Kevin P.Campbell,
Jean-Claude Kaplan
|
6 |
1993 |
6
๐
|
|
๐
|
Non-specific X-linked semidominant mental retardation by mutations in a Rab GDP-dissociation inhibitor.
17 auth.
Thierry Bienvenu,
Vincent des Portes,
Anne Saint,
Martin,
N. Mcdonell,
P. Billuart,
Alain Carriรฉ,
M. Vinet,
P. Couvert,
Daniela Toniolo,
...
H. Ropers,
C. Moraine,
H. van Bokhoven,
J. Fryns,
Axel Kahn,
C. Beldjord,
Jamel Chelly
|
6 |
1998 |
6
๐
|
|
๐
|
Doublecortin Interacts with ฮผ Subunits of Clathrin Adaptor Complexes in the Developing Nervous System
9 auth.
G. Friocourt,
P. Chafey,
P. Billuart,
A. Koulakoff,
M. Vinet,
B. Schaar,
...
S. Mcconnell,
F. Francis,
J. Chelly
|
5 |
2001 |
5
๐
|
