|
🐜
|
Slipped-CAG DNA binding small molecule induces trinucleotide repeat contractions in vivo
32 auth.
M. Nakamori,
G. Panigrahi,
Stella Lanni,
Terence Gall-Duncan,
H. Hayakawa,
Hana Tanaka,
Jennifer Luo,
Takahiro Otabe,
Jinxing Li,
Akihiro Sakata,
Marie-christine Caron,
Niraj R. Joshi,
Tanya Prasolava,
K. Chiang,
J. Masson,
...
M. Wold,
Xiaoxiao Wang,
Marietta Y. W. T. Lee,
J. Huddleston,
Katherine M. Munson,
S. Davidson,
M. Layeghifard,
Lisa-Monique Edward,
R. Gallon,
M. Santibanez-Koref,
A. Murata,
M. Takahashi,
E. Eichler,
A. Shlien,
K. Nakatani,
H. Mochizuki,
C. E. Pearson
|
6 |
2020 |
6
🐜
|
|
🐜
|
CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy
22 auth.
L. Barbé,
Stella Lanni,
Arturo López-Castel,
S. Franck,
C. Spits,
K. Keymolen,
S. Seneca,
S. Tomé,
Ioana Miron,
Julie Létourneau,
...
Minggao Liang,
S. Choufani,
R. Weksberg,
M. Wilson,
Z. Sedlacek,
C. Gagnon,
Z. Mušová,
D. Chitayat,
P. Shannon,
J. Mathieu,
K. Sermon,
C. E. Pearson
|
6 |
2017 |
6
🐜
|
|
🦁
|
Molecular genetics of congenital myotonic dystrophy
Stella Lanni,
C. E. Pearson
|
5 |
2019 |
5
🦁
|
|
🦁
|
Role of CTCF Protein in Regulating FMR1 Locus Transcription
10 auth.
Stella Lanni,
Martina Goracci,
Loredana Borrelli,
G. Mancano,
P. Chiurazzi,
U. Moscato,
...
F. Ferrè,
M. Helmer-Citterich,
E. Tabolacci,
G. Neri
|
5 |
2013 |
5
🦁
|
|
🐜
|
FAN1, a DNA Repair Nuclease, as a Modifier of Repeat Expansion Disorders
9 auth.
A. L. Deshmukh,
Antonio Porro,
Mohiuddin Mohiuddin,
Stella Lanni,
G. Panigrahi,
Marie-christine Caron,
...
J. Masson,
A. Sartori,
C. E. Pearson
|
5 |
2021 |
5
🐜
|
|
🐜
|
Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cells
8 auth.
E. Tabolacci,
G. Mancano,
Stella Lanni,
Federica Palumbo,
Martina Goracci,
F. Ferrè,
...
M. Helmer-Citterich,
G. Neri
|
4 |
2016 |
4
🐜
|
|
🐜
|
Functional Repair Assay for the Diagnosis of Constitutional Mismatch Repair Deficiency From Non-Neoplastic Tissue.
54 auth.
Andrew Y. Shuen,
Stella Lanni,
G. Panigrahi,
M. Edwards,
Lisa Yu,
B. Campbell,
Ariane Mandel,
Cindy H. Zhang,
N. Zhukova,
Musa Alharbi,
M. Bernstein,
D. Bowers,
S. Carroll,
K. Cole,
S. Constantini,
...
B. Crooks,
R. Dvir,
R. Farah,
N. Hijiya,
B. George,
T. Laetsch,
Valérie Larouche,
S. Lindhorst,
Rebecca C. Luiten,
Vanan Magimairajan,
G. Mason,
W. Mason,
O. Mordechai,
N. Mushtaq,
G. Nicholas,
M. Oren,
Laura Palma,
L. A. Pedroza,
J. Ramdas,
David Samuel,
K. Wolfe Schneider,
Andrea Seeley,
K. Semotiuk,
Ashraf Shamvil,
D. Sumerauer,
H. Toledano,
Patrick Tomboc,
M. Wierman,
An Van Damme,
Yi-Yen Lee,
M. Zápotocký,
E. Bouffet,
C. Durno,
M. Aronson,
S. Gallinger,
W. Foulkes,
D. Malkin,
U. Tabori,
C. E. Pearson
|
4 |
2019 |
4
🐜
|
|
🐜
|
Altered mitochondrial function in cells carrying a premutation or unmethylated full mutation of the FMR1 gene
20 auth.
Veronica Nobile,
Federica Palumbo,
Stella Lanni,
Valentina Ghisio,
A. Vitali,
M. Castagnola,
V. Marzano,
G. Maulucci,
Claudio De Angelis,
M. De Spirito,
...
L. Pacini,
L. D’Andrea,
R. Ragno,
G. Stazi,
S. Valente,
A. Mai,
P. Chiurazzi,
M. Genuardi,
G. Neri,
E. Tabolacci
|
4 |
2020 |
4
🐜
|
