|
🐜
|
A peptide inhibitor of c-Jun N-terminal kinase protects against excitotoxicity and cerebral ischemia
8 auth.
T. Borsello,
P. Clarke,
L. Hirt,
A. Vercelli,
M. Repici,
D. Schorderet,
...
J. Bogousslavsky,
C. Bonny
|
9 |
2003 |
9
🐜
|
|
🐢
|
Cell-Permeable Peptide Inhibitors of JNK: Novel Blockers of β-Cell Death
C. Bonny,
A. Oberson,
S. Negri,
C. Sauser,
D. Schorderet
|
9 |
2001 |
9
🐢
|
|
🐢
|
Kerato-epithelin mutations in four 5q31-linked corneal dystrophies
7 auth.
F. Munier,
E. Korvatska,
A. Djemaï,
D. Paslier,
L. Zografos,
G. Pescia,
...
D. Schorderet
|
8 |
1997 |
8
🐢
|
|
🐜
|
Mutations of keratinocyte transglutaminase in lamellar ichthyosis
10 auth.
M. Huber,
I. Rettler,
K. Bernasconi,
E. Frenk,
S. Lavrijsen,
M. Ponec,
...
A. Bon,
Stefan Lautenschlager,
D. Schorderet,
D. Hohl
|
8 |
1995 |
8
🐜
|
|
🐢
|
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy
16 auth.
E. Stone,
A. Lotery,
F. Munier,
E. Héon,
B. Piguet,
R. Guymer,
K. Vandenburgh,
P. Cousin,
D. Nishimura,
R. Swiderski,
...
G. Silvestri,
D. Mackey,
G. Hageman,
A. Bird,
V. Sheffield,
D. Schorderet
|
8 |
1999 |
8
🐢
|
|
🐜
|
Estimation of the Mutation Frequencies in Charcot-Marie-Tooth Disease Type 1 and Hereditary Neuropathy with Liability to Pressure Palsies: A European Collaborative Study
54 auth.
E. Nelis,
C. Broeckhoven,
P. Jonghe,
A. Löfgren,
A. Vandenberghe,
P. Latour,
É. Guern,
A. Brice,
M. Mostacciuolo,
F. Schiavon,
F. Palau,
S. Bort,
M. Upadhyaya,
M. Rocchi,
N. Archidiacono,
...
P. Mandich,
E. Bellone,
K. Silander,
M. Savontaus,
R. Navon,
H. Goldberg-Stern,
X. Estivill,
V. Volpini,
W. Friedl,
K. Zerres,
J. Tyson,
S. Malcolm,
B. Holmberg,
G. Holmgren,
E. Mariman,
A. Gabreëls-Festen,
C. Yapijakis,
D. Vassilopoulos,
C. Clark,
N. Haites,
P. Hilbert,
L. Maldergem,
B. Rautenstrauss,
H. Grehl,
R. Mountford,
K. Mann,
T. Bettecken,
J. Burgunder,
C. Hanemann,
H. Müller,
J. Hertz,
D. Schorderet,
T. Küntzer,
C. Wolf,
E. Kunert,
F. Muntoni,
P. Emmerick-Bock,
U. Orth,
A. Gal
|
8 |
1996 |
8
🐜
|
|
🐜
|
Zebrafish: Housing and husbandry recommendations
7 auth.
P. Aleström,
L. D’Angelo,
P. Midtlyng,
D. Schorderet,
S. Schulte-Merker,
F. Sohm,
...
Susan Warner
|
8 |
2019 |
8
🐜
|
|
🐜
|
Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy.
18 auth.
S. Biswas,
Francis L. Munier,
J. Yardley,
N. Hart‐Holden,
R. Perveen,
P. Cousin,
J. Sutphin,
Bruce Noble,
M. Batterbury,
C. Kielty,
...
A. Hackett,
R. Bonshek,
A. Ridgway,
David McLeod,
V. Sheffield,
E. Stone,
D. Schorderet,
G. Black
|
8 |
2001 |
8
🐜
|
|
🐜
|
Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2.
21 auth.
Anren Li,
Xiaodong Jiao,
F. Munier,
D. Schorderet,
Wenliang Yao,
F. Iwata,
F. Iwata,
M. Hayakawa,
A. Kanai,
M. Chen,
...
R. Lewis,
J. Heckenlively,
R. Weleber,
E. Traboulsi,
Qingjiong Zhang,
Qingjiong Zhang,
Xueshan Xiao,
Xueshan Xiao,
M. Kaiser-Kupfer,
Y. Sergeev,
J. Hejtmancik
|
8 |
2004 |
8
🐜
|
|
🐜
|
Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice.
33 auth.
Zhenglin Yang,
Yali Chen,
C. Lillo,
J. Chien,
Zhengya Yu,
M. Michaelides,
M. Klein,
K. Howes,
Yang Li,
Y. Kaminoh,
H. Chen,
Chao Zhao,
Yuhong Chen,
Y. Al-sheikh,
Goutam Karan,
...
D. Corbeil,
P. Escher,
S. Kamaya,
Chunmei Li,
Samantha Johnson,
J. Frederick,
Yu Zhao,
Changguan Wang,
D. J. Cameron,
W. Huttner,
D. Schorderet,
F. Munier,
A. Moore,
D. Birch,
W. Baehr,
D. Hunt,
David S. Williams,
Kang Zhang
|
8 |
2008 |
8
🐜
|
|
🐢
|
Cell-permeable peptide inhibitors of JNK: novel blockers of beta-cell death.
C. Bonny,
A. Oberson,
S. Negri,
C. Sauser,
D. Schorderet
|
7 |
2001 |
7
🐢
|
|
🐜
|
The γ-Crystallins and Human Cataracts: A Puzzle Made Clearer
7 auth.
E. Héon,
M. Priston,
D. Schorderet,
G. Billingsley,
P. Girard,
N. Lubsen,
...
F. Munier
|
7 |
1999 |
7
🐜
|
