Results
|
38061.
|
|
|
38062.
|
|
|
38063.
|
|
|
38064.
|
|
|
38065.
|
|
|
38066.
|
|
|
38067.
|
|
|
38068.
|
Mutations in ACTL6B, coding for a subunit of the neuron-specific chromatin remodeling complex nBAF, cause early onset severe developmental and epileptic encephalopathy with brain hypomyelination and cerebellar atrophy. [electronic resource] by
- Fichera, Marco
- Failla, Pinella
- Saccuzzo, Lucia
- Miceli, Martina
- Salvo, Eliana
- Castiglia, Lucia
- Galesi, Ornella
- Grillo, Lucia
- Calì, Francesco
- Greco, Donatella
- Amato, Carmelo
- Romano, Corrado
- Elia, Maurizio
Producer: 20190219
In:
Human genetics vol. 138
Availability: No items available.
|
|
38069.
|
|
|
38070.
|
|
|
38071.
|
|
|
38072.
|
|
|
38073.
|
|
|
38074.
|
|
|
38075.
|
|
|
38076.
|
|
|
38077.
|
|
|
38078.
|
NK cells specifically TCR-dressed to kill cancer cells. [electronic resource] by
- Mensali, Nadia
- Dillard, Pierre
- Hebeisen, Michael
- Lorenz, Susanne
- Theodossiou, Theodossis
- Myhre, Marit Renée
- Fåne, Anne
- Gaudernack, Gustav
- Kvalheim, Gunnar
- Myklebust, June Helen
- Inderberg, Else Marit
- Wälchli, Sébastien
Producer: 20190625
In:
EBioMedicine vol. 40
Availability: No items available.
|
|
38079.
|
|
|
38080.
|
|