|
🐬
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Decoding ALS: from genes to mechanism
J. Taylor,
Robert H. Brown,
D. Cleveland,
D. Cleveland
|
10 |
2016 |
10
🐬
|
|
🐢
|
Molecular biology of amyotrophic lateral sclerosis: insights from genetics
P. Pasinelli,
Robert H. Brown
|
10 |
2006 |
10
🐢
|
|
🐜
|
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
71 auth.
E. Cirulli,
Brittany N. Lasseigne,
S. Petrovski,
P. Sapp,
P. Dion,
C. Leblond,
Julien Couthouis,
Yi-Fan Lu,
Quanli Wang,
Brian J. Krueger,
Z. Ren,
Jonathan E. M. Keebler,
Yujun Han,
S. Levy,
B. Boone,
...
Jack R. Wimbish,
L. Waite,
Angela L. Jones,
J. Carulli,
A. Day-Williams,
J. Staropoli,
W. Xin,
A. Chesi,
Alya R. Raphael,
D. McKenna-Yasek,
J. Cady,
J. M. B. Vianney de Jong,
K. Kenna,
Bradley N. Smith,
S. Topp,
Jack W. Miller,
A. Gkazi,
A. Al-Chalabi,
L. H. van den Berg,
J. Veldink,
V. Silani,
N. Ticozzi,
C. Shaw,
R. Baloh,
S. Appel,
E. Simpson,
C. Lagier-Tourenne,
S. Pulst,
S. Gibson,
J. Trojanowski,
L. Elman,
L. McCluskey,
M. Grossman,
N. Shneider,
W. Chung,
J. Ravits,
J. Glass,
K. Sims,
V. V. Van Deerlin,
T. Maniatis,
Sebastian Hayes,
A. Ordureau,
Sharan Swarup,
J. Landers,
F. Baas,
A. Allen,
R. Bedlack,
J. Harper,
A. Gitler,
G. Rouleau,
Robert H. Brown,
M. Harms,
G. Cooper,
Tim Harris,
R. Myers,
D. Goldstein
|
9 |
2015 |
9
🐜
|
|
🐜
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Evidence of Increased Oxidative Damage in Both Sporadic and Familial Amyotrophic Lateral Sclerosis
9 auth.
R. Ferrante,
S. Browne,
L. Shinobu,
A. Bowling,
M. Baik,
U. Macgarvey,
...
N. Kowall,
Robert H. Brown,
M. Beal
|
9 |
1997 |
9
🐜
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|
🐢
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Wild-type and mutant SOD1 share an aberrant conformation and a common pathogenic pathway in ALS
18 auth.
D. A. Bosco,
G. Morfini,
G. Morfini,
N. M. Karabacak,
Yuyu Song,
Yuyu Song,
F. Gros-Louis,
P. Pasinelli,
H. Goolsby,
B. Fontaine,
...
N. Lemay,
D. McKenna-Yasek,
M. Frosch,
J. Agar,
J. Julien,
S. Brady,
S. Brady,
Robert H. Brown
|
9 |
2010 |
9
🐢
|
|
🐜
|
ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis
16 auth.
M. Greenway,
P. Andersen,
C. Russ,
S. Ennis,
S. Cashman,
C. Donaghy,
V. Patterson,
R. Swingler,
D. Kieran,
J. Prehn,
...
K. Morrison,
A. Green,
K. Acharya,
Robert H. Brown,
O. Hardiman,
O. Hardiman
|
9 |
2006 |
9
🐜
|
|
🐬
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Superoxide Dismutase Activity, Oxidative Damage, and Mitochondrial Energy Metabolism in Familial and Sporadic Amyotrophic Lateral Sclerosis
A. Bowling,
J. Schulz,
Robert H. Brown,
M. Beal
|
9 |
1993 |
9
🐬
|
|
🦁
|
Amyotrophic Lateral Sclerosis.
Robert H. Brown,
A. Al-Chalabi
|
9 |
2017 |
9
🦁
|
|
🐜
|
dSarm/Sarm1 Is Required for Activation of an Injury-Induced Axon Death Pathway
22 auth.
Jeannette M. Osterloh,
Jing Yang,
T. Rooney,
A. N. Fox,
R. Adalbert,
Eric H. Powell,
Amy E Sheehan,
M. Avery,
R. Hackett,
Mary A. Logan,
...
Jennifer M. MacDonald,
Jennifer S. Ziegenfuss,
S. Milde,
Ying-Ju Hou,
C. Nathan,
A. Ding,
Robert H. Brown,
L. Conforti,
M. Coleman,
M. Tessier-Lavigne,
S. Züchner,
M. Freeman
|
9 |
2012 |
9
🐜
|
|
🐢
|
Increased 3‐nitrotyrosine in both sporadic and familial amyotrophic lateral sclerosis
M. Beal,
R. Ferrante,
S. Browne,
R. T. Matthews,
N. Kowall,
Robert H. Brown
|
9 |
1997 |
9
🐢
|
|
🐜
|
Mutations in the Profilin 1 Gene Cause Familial Amyotrophic Lateral Sclerosis
38 auth.
Chi-Hong Wu,
C. Fallini,
N. Ticozzi,
Pamela J. Keagle,
P. Sapp,
K. Piotrowska,
P. Lowe,
M. Koppers,
D. McKenna-Yasek,
Desiree M. Baron,
J. Kost,
P. Gonzalez-Perez,
A. Fox,
J. Adams,
F. Taroni,
...
C. Tiloca,
A. L. Leclerc,
S. C. Chafe,
D. Mangroo,
M. Moore,
J. Zitzewitz,
Zuoshang Xu,
L. H. van den Berg,
J. Glass,
G. Siciliano,
E. Cirulli,
D. Goldstein,
F. Salachas,
V. Meininger,
W. Rossoll,
A. Ratti,
C. Gellera,
D. A. Bosco,
G. Bassell,
V. Silani,
V. Drory,
Robert H. Brown,
J. Landers
|
9 |
2012 |
9
🐜
|
|
🐜
|
Intrinsic membrane hyperexcitability of amyotrophic lateral sclerosis patient-derived motor neurons.
16 auth.
Brian J. Wainger,
E. Kiskinis,
Cassidy Mellin,
Ole Wiskow,
Steve S. W. Han,
Jackson Sandoe,
Numa P. Perez,
Luis A. Williams,
Seungkyu Lee,
G. Boulting,
...
J. Berry,
Robert H. Brown,
M. Cudkowicz,
B. Bean,
K. Eggan,
C. Woolf
|
9 |
2014 |
9
🐜
|
|
🐜
|
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2
21 auth.
S. Hadano,
C. Hand,
H. Osuga,
Y. Yanagisawa,
A. Otomo,
R. S. Devon,
N. Miyamoto,
J. Showguchi-Miyata,
Yoshinori Okada,
R. Singaraja,
...
D. Figlewicz,
T. Kwiatkowski,
B. Hosler,
T. Sagie,
J. Skaug,
J. Nasir,
Robert H. Brown,
S. Scherer,
G. Rouleau,
M. Hayden,
J. Ikeda
|
9 |
2001 |
9
🐜
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