|
🐜
|
Subgroup-specific prognostic implications of TP53 mutation in medulloblastoma.
61 auth.
N. Zhukova,
V. Ramaswamy,
M. Remke,
E. Pfaff,
D. Shih,
D. Martin,
P. Castelo-Branco,
B. Baskin,
P. Ray,
E. Bouffet,
A. V. von Bueren,
David T. W. Jones,
P. Northcott,
M. Kool,
D. Sturm,
...
Trevor J Pugh,
S. Pomeroy,
Yoon-Jae Cho,
T. Pietsch,
M. Gessi,
S. Rutkowski,
L. Bognár,
Á. Klekner,
B. Cho,
Seung-Ki Kim,
K. Wang,
C. Eberhart,
M. Fèvre-Montange,
M. Fouladi,
P. French,
M. Kros,
W. Grajkowska,
N. Gupta,
W. Weiss,
P. Hauser,
N. Jabado,
A. Jouvet,
Shin Jung,
T. Kumabe,
B. Lach,
J. Leonard,
J. Rubin,
L. Liau,
L. Massimi,
I. Pollack,
Young Shin Ra,
Erwin G. Van Meir,
K. Zitterbart,
U. Schüller,
Rebecca M Hill,
J. Lindsey,
E. Schwalbe,
S. Bailey,
D. Ellison,
C. Hawkins,
D. Malkin,
S. Clifford,
A. Korshunov,
S. Pfister,
Michael D. Taylor,
U. Tabori
|
8 |
2013 |
8
🐜
|
|
🐬
|
Structural Basis for Autoinhibition of the EphB2 Receptor Tyrosine Kinase by the Unphosphorylated Juxtamembrane Region
L. Wybenga-Groot,
B. Baskin,
S. Ong,
Jiefei Tong,
T. Pawson,
F. Sicheri
|
8 |
2001 |
8
🐬
|
|
🐜
|
PreBIND and Textomy – mining the biomedical literature for protein-protein interactions using a support vector machine
12 auth.
I. Donaldson,
Joel D. Martin,
Berry de Bruijn,
Cheryl Wolting,
V. Lay,
Brigitte Tuekam,
...
Shudong Zhang,
B. Baskin,
Gary D Bader,
K. Michalickova,
T. Pawson,
C. Hogue
|
8 |
2003 |
8
🐜
|
|
🐜
|
Expression of Bruton's agammaglobulinemia tyrosine kinase gene, BTK, is selectively down-regulated in T lymphocytes and plasma cells.
10 auth.
C. I. Smith,
B. Baskin,
P. Humire-Greiff,
J. Zhou,
P. G. Olsson,
H. Maniar,
...
P. Kjellén,
John D Lambris,
Birger Christensson,
Lennart Hammarström
|
8 |
1994 |
8
🐜
|
|
🐜
|
TP53 alterations determine clinical subgroups and survival of patients with choroid plexus tumors.
16 auth.
U. Tabori,
A. Shlien,
B. Baskin,
S. Levitt,
P. Ray,
N. Alon,
C. Hawkins,
E. Bouffet,
M. Pienkowska,
L. Lafay-Cousin,
...
Alexa Gozali,
N. Zhukova,
L. Shane,
I. González,
J. Finlay,
D. Malkin
|
7 |
2010 |
7
🐜
|
|
🐜
|
Recurrent focal copy-number changes and loss of heterozygosity implicate two noncoding RNAs and one tumor suppressor gene at chromosome 3q13.31 in osteosarcoma.
8 auth.
Ivan Pasic,
A. Shlien,
Adam D. Durbin,
D. Stavropoulos,
B. Baskin,
P. Ray,
...
A. Novokmet,
D. Malkin
|
7 |
2010 |
7
🐜
|
|
🐜
|
Functional Dysregulation of CDC42 Causes Diverse Developmental Phenotypes.
48 auth.
S. Martinelli,
Oliver H. F. Krumbach,
F. Pantaleoni,
Simona Coppola,
Ehsan Amin,
L. Pannone,
K. Nouri,
L. Fariña,
R. Dvorsky,
F. Lepri,
Marcel Buchholzer,
Raphael Konopatzki,
L. Walsh,
K. Payne,
M. Pierpont,
...
S. Vergano,
Katherine G. Langley,
Douglas P. Larsen,
K. Farwell,
Sha Tang,
C. Mroske,
I. Gallotta,
Elia Di Schiavi,
M. Della Monica,
L. Lugli,
C. Rossi,
M. Seri,
G. Cocchi,
Lindsay B. Henderson,
B. Baskin,
M. Alders,
R. Mendoza-Londono,
L. Dupuis,
D. Nickerson,
Jessica X. Chong,
N. Meeks,
K. Brown,
Tahnee N Causey,
M. Cho,
S. Demuth,
M. Digilio,
B. Gelb,
M. Bamshad,
M. Zenker,
M. Ahmadian,
R. Hennekam,
M. Tartaglia,
G. Mirzaa
|
7 |
2018 |
7
🐜
|
|
🐜
|
Universal poor survival in children with medulloblastoma harboring somatic TP53 mutations.
9 auth.
U. Tabori,
B. Baskin,
M. Shago,
N. Alon,
Michael D. Taylor,
P. Ray,
...
E. Bouffet,
D. Malkin,
C. Hawkins
|
7 |
2010 |
7
🐜
|
|
🐜
|
Molecular subgroups of atypical teratoid rhabdoid tumours in children: an integrated genomic and clinicopathological analysis.
72 auth.
J. Torchia,
D. Picard,
L. Lafay-Cousin,
C. Hawkins,
Seung-Ki Kim,
Louis Letourneau,
Y. Ra,
K. Ho,
T. Chan,
P. Sin‐Chan,
C. Dunham,
S. Yip,
H. Ng,
Jian-Qiang Lu,
S. Albrecht,
...
J. Pimentel,
J. Chan,
G. Somers,
M. Zielenska,
C. Faria,
L. Roque,
B. Baskin,
D. Birks,
N. Foreman,
D. Strother,
Á. Klekner,
M. Garami,
P. Hauser,
T. Hortobágyi,
L. Bognár,
B. Wilson,
J. Hukin,
A. Carret,
Timothy Van Meter,
Hideo Nakamura,
H. Toledano,
I. Fried,
D. Fults,
T. Wataya,
C. Fryer,
D. Eisenstat,
Katrin Scheineman,
D. Johnston,
J. Michaud,
S. Zelcer,
R. Hammond,
D. Ramsay,
A. Fleming,
R. Lulla,
J. Fangusaro,
N. Sirachainan,
N. Larbcharoensub,
S. Hongeng,
M. A. Barakzai,
A. Montpetit,
D. Stephens,
R. Grundy,
U. Schüller,
T. Nicolaides,
T. Tihan,
J. Phillips,
Michael D. Taylor,
J. Rutka,
P. Dirks,
Gary D Bader,
M. Warmuth-Metz,
S. Rutkowski,
T. Pietsch,
A. Judkins,
N. Jabado,
E. Bouffet,
A. Huang
|
7 |
2015 |
7
🐜
|
|
🐜
|
X‐Linked Agammaglobulinemia and Other Immunoglobulin Deficiencies
8 auth.
C. I. Smith,
K. Islam,
I. Vořechovský,
O. Olerup,
Erik Wallin,
H. Rabbani,
...
B. Baskin,
L. Hammarström
|
6 |
1994 |
6
🐜
|
|
🐜
|
A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures
41 auth.
V. Gennarino,
E. Palmer,
Laura M McDonell,
Li Wang,
Carolyn J. Adamski,
Amanda M Koire,
Lauren See,
Chun-An Chen,
C. Schaaf,
J. Rosenfeld,
J. Panzer,
U. Moog,
Shuang Hao,
A. Bye,
E. Kirk,
...
P. Stankiewicz,
Amy M. Breman,
A. McBride,
T. Kandula,
Holly A. Dubbs,
R. Macintosh,
M. Cardamone,
Ying Zhu,
Kevin Ying,
Kerith-Rae Dias,
M. Cho,
Lindsay B. Henderson,
B. Baskin,
Paula Morris,
Jiang Tao,
M. Cowley,
M. Dinger,
T. Roscioli,
O. Caluseriu,
O. Suchowersky,
R. Sachdev,
O. Lichtarge,
Jianrong Tang,
K. Boycott,
J. Holder,
H. Zoghbi
|
6 |
2018 |
6
🐜
|
