|
🐜
|
TIM-4 is the ligand for TIM-1, and the TIM-1–TIM-4 interaction regulates T cell proliferation
12 auth.
J. H. Meyers,
S. Chakravarti,
D. Schlesinger,
Z. Illés,
H. Waldner,
S. Umetsu,
...
J. Kenny,
X. Zheng,
D. Umetsu,
R. DeKruyff,
T. Strom,
V. Kuchroo
|
8 |
2005 |
8
🐜
|
|
🐜
|
Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia.
11 auth.
P. Valdmanis,
I. Meijer,
Annie Reynolds,
Adrienne Lei,
P. Macleod,
D. Schlesinger,
...
M. Zatz,
E. Reid,
P. Dion,
P. Drapeau,
G. Rouleau
|
7 |
2007 |
7
🐜
|
|
🐜
|
A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G).
19 auth.
N. Vieira,
M. Naslavsky,
L. Licinio,
F. Kok,
D. Schlesinger,
M. Vainzof,
N. Sanchez,
J. Kitajima,
L. Gal,
N. Cavaçana,
...
P. R. Serafini,
S. Chuartzman,
Cristina Vasquez,
A. Mimbacas,
V. Nigro,
R. Pavanello,
M. Schuldiner,
L. Kunkel,
M. Zatz
|
6 |
2014 |
6
🐜
|
|
🐜
|
Screening of ARHSP‐TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion
55 auth.
P. Denora,
D. Schlesinger,
C. Casali,
F. Kok,
A. Tessa,
A. Boukhris,
H. Azzedine,
M. Dotti,
C. Bruno,
J. Truchetto,
R. Biancheri,
E. Fédirko,
M. Di Rocco,
C. Bueno,
A. Malandrini,
...
R. Battini,
E. Sickl,
M. D. de Leva,
O. Boespflug-Tanguy,
G. Silvestri,
A. Simonati,
E. Said,
A. Ferbert,
C. Criscuolo,
K. Heinimann,
A. Modoni,
P. Weber,
S. Palmeri,
M. Plášilová,
F. Pauri,
D. Cassandrini,
C. Battisti,
A. Pini,
M. Tosetti,
E. Hauser,
M. Masciullo,
R. Fabio,
F. Piccolo,
E. Denis,
G. Cioni,
R. Massa,
E. Giustina,
O. Calabrese,
M. Melone,
G. De Michele,
A. Federico,
E. Bertini,
A. Durr,
K. Brockmann,
M. S. van der Knaap,
M. Zatz,
A. Filla,
A. Brice,
G. Stevanin,
F. Santorelli
|
6 |
2009 |
6
🐜
|
|
🐜
|
IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population
14 auth.
L. Brito,
Camila Fernandes Silva Bassi,
C. Masotti,
Carolina Malcher,
K. Rocha,
D. Schlesinger,
D. Bueno,
L. A. Cruz,
Ligia K. Barbara,
D. Bertola,
...
D. Meyer,
D. Franco,
N. Alonso,
M. Passos-Bueno
|
5 |
2012 |
5
🐜
|
|
🐜
|
Detection of germline variants in Brazilian breast cancer patients using multigene panel testing
13 auth.
R. Guindalini,
Danilo V. Viana,
J. Kitajima,
Vinícius Marques Rocha,
R. M. López,
Yonglan Zheng,
E. Freitas,
F. Monteiro,
A. Valim,
D. Schlesinger,
...
F. Kok,
O. Olopade,
M. A. Folgueira
|
5 |
2022 |
5
🐜
|
|
🐜
|
Region 8q24 is a susceptibility locus for nonsyndromic oral clefting in Brazil.
16 auth.
L. Brito,
L. Paranaíba,
Camila Fernandes Silva Bassi,
C. Masotti,
Carolina Malcher,
D. Schlesinger,
K. Rocha,
L. A. Cruz,
Ligia K. Barbara,
N. Alonso,
...
D. Franco,
Elizabete Bagordakis,
H. Martelli,
D. Meyer,
R. Coletta,
M. Passos-Bueno
|
5 |
2012 |
5
🐜
|
|
🐬
|
Autosomal recessive ataxias: 20 types, and counting.
E. Embiruçu,
M. Martyn,
D. Schlesinger,
F. Kok
|
5 |
2009 |
5
🐬
|
|
🐜
|
Experimental autoimmune encephalomyelitis can be prevented and cured by infection with Trypanosoma cruzi.
9 auth.
C. Tadokoro,
A. Vallochi,
L. S. Rios,
G. Martins,
D. Schlesinger,
T. Mosca,
...
V. Kuchroo,
L. Rizzo,
I. Abrahamsohn
|
5 |
2004 |
5
🐜
|
