|
🐜
|
Localization of I2-Imidazoline Binding Sites on Monoamine Oxidases (*)
8 auth.
F. Tesson,
I. Limon-Boulez,
P. Urban,
M. Puype,
Jol Vandekerckhove,
I. Coupry,
...
D. Pompon,
A. Parini
|
7 |
1995 |
7
🐜
|
|
🐜
|
Thrombocytopenia resulting from mutations in filamin A can be expressed as an isolated syndrome.
20 auth.
P. Nurden,
N. Debili,
I. Coupry,
M. Bryckaert,
Ibtissam Youlyouz‐Marfak,
G. Solé,
Anne-Cécile Pons,
E. Berrou,
F. Adam,
A. Kauskot,
...
J. Lamazière,
P. Rameau,
P. Fergelot,
C. Rooryck,
D. Cailley,
B. Arveiler,
D. Lacombe,
W. Vainchenker,
A. Nurden,
C. Goizet
|
7 |
2011 |
7
🐜
|
|
🐜
|
COL4A1 mutation in Axenfeld–Rieger anomaly with leukoencephalopathy and stroke
13 auth.
I. Sibon,
I. Coupry,
P. Menegon,
J. Bouchet,
P. Gorry,
I. Burgelin,
P. Calvas,
I. Orignac,
V. Dousset,
D. Lacombe,
...
J. Orgogozo,
B. Arveiler,
C. Goizet
|
7 |
2007 |
7
🐜
|
|
🦁
|
Molecular analysis of the CBP gene in 60 patients with Rubinstein-Taybi syndrome
10 auth.
I. Coupry,
C. Roudaut,
M. Stef,
M. Delrue,
M. Marche,
I. Burgelin,
...
L. Taine,
C. Cruaud,
D. Lacombe,
B. Arveiler
|
6 |
2002 |
6
🦁
|
|
🦁
|
Evidence for imidazoline binding sites in basolateral membranes from rabbit kidney.
I. Coupry,
R. Podevin,
J. Dausse,
A. Parini
|
6 |
1987 |
6
🦁
|
|
🐬
|
Characterization of an imidazoline/guanidinium receptive site distinct from the alpha 2-adrenergic receptor.
A. Parini,
I. Coupry,
R. Graham,
I. Uzielli,
D. Atlas,
S. Lanier
|
6 |
1989 |
6
🐬
|
|
🦁
|
Imidazoline-guanidinium receptive site in renal proximal tubule: asymmetric distribution, regulation by cations and interaction with an endogenous clonidine displacing substance.
I. Coupry,
D. Atlas,
Podevin Ra,
I. Uzielli,
A. Parini
|
6 |
1990 |
6
🦁
|
|
🐜
|
REEP1 mutations in SPG31: Frequency, mutational spectrum, and potential association with mitochondrial morpho‐functional dysfunction
29 auth.
C. Goizet,
C. Depienne,
G. Bénard,
A. Boukhris,
E. Mundwiller,
G. Solé,
I. Coupry,
J. Pilliod,
M. Martin‐Négrier,
E. Fédirko,
S. Forlani,
C. Cazeneuve,
D. Hannequin,
P. Charles,
I. Feki,
...
J. Pinel,
A. Ouvrard-Hernandez,
S. Lyonnet,
E. Ollagnon‐Roman,
J. Yaouanq,
A. Toutain,
C. Dussert,
B. Fontaine,
E. Leguern,
D. Lacombe,
A. Durr,
R. Rossignol,
A. Brice,
G. Stevanin
|
6 |
2011 |
6
🐜
|
|
🐜
|
A mutation in the 3'-UTR of the HDAC6 gene abolishing the post-transcriptional regulation mediated by hsa-miR-433 is linked to a new form of dominant X-linked chondrodysplasia.
14 auth.
D. Simon,
Benoît Laloo,
M. Barillot,
T. Barnetche,
Camille Blanchard,
C. Rooryck,
M. Marche,
I. Burgelin,
I. Coupry,
N. Chassaing,
...
B. Gilbert-Dussardier,
D. Lacombe,
C. Grosset,
B. Arveiler
|
6 |
2010 |
6
🐜
|
|
🦁
|
Ophthalmological features associated with COL4A1 mutations.
I. Coupry,
I. Sibon,
B. Mortemousque,
F. Rouanet,
M. Miné,
C. Goizet
|
6 |
2010 |
6
🦁
|
