Sfoglia per Autore  

Opzioni
Mostrati risultati da 21 a 26 di 26
Titolo Data di pubblicazione Autori File
Loss-of-function mutations in PTPRJ cause a new form of inherited thrombocytopenia 1-gen-2019 Faleschini, MichelaSavoia, Anna +
Mitochondrial defect in Warsaw syndrome cells genomic integrity and mitochondrial metabolism defects in Warsaw syndrome cells: A comparison with Fanconi anemia 1-gen-2021 Bottega R.Faleschini M.Medagli B.Savoia A. +
Things come in threes: A new complex allele and a novel deletion within the CFTR gene complicate an accurate diagnosis of cystic fibrosis 1-gen-2022 Persico I.Feresin A.Faleschini M.Fontana G.Faletra F.La Bianca M.Morgutti M.D'Adamo A. P.Savoia A.Bottega R. +
GNE-related thrombocytopenia: evidence for a mutational hotspot in the ADP/substrate domain of the GNE bifunctional enzyme 1-gen-2022 Bottega R.Persico I.Faleschini M.Valencic E.d'Adamo A. P.Tommasini A.Faletra F.Savoia A. +
Dysregulation of oncogenic factors by GFI1B p32: investigation of a novel GFI1B germline mutation 1-gen-2022 Faleschini, MichelaPapa, NicoleGiangregorio, TaniaSavoia, AnnaBottega, Roberta +
ETV6-related thrombocytopenia: dominant negative effect of mutations as common pathogenic mechanism 1-gen-2022 Faleschini, MichelaAmmeti, DanielePapa, NicoleBottega, RobertaFontana, GiorgiaCapaci, ValeriaZanchetta, Melania ESavoia, Anna +
Mostrati risultati da 21 a 26 di 26
Legenda icone

  •  file ad accesso aperto
  •  file disponibili sulla rete interna
  •  file disponibili agli utenti autorizzati
  •  file disponibili solo agli amministratori
  •  file sotto embargo
  •  nessun file disponibile