Suchergebnisse - "Carella, Massimo"

PubPharm (354)

1

APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants

enthalten in: bioRxiv.org | 2024

von Bianco, S. | Parca, L. | Petrizzelli, F. | +12

2

Human leukocyte antigen variants associate with BNT162b2 mRNA vaccine response

enthalten in: Communications medicine | 2024

von Esposito, M. | Minnai, F. | Copetti, M. | +22

3

Phenotypic Description of A Patient with ODLURO Syndrome and Functional Characterization of the Pathogenetic Role of A Synonymous Variant c.186G>A in KMT2E Gene

enthalten in: Genes | 2024

von Benvenuto, M. | Cesarini, S. | Severi, G. | +8

4

A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death

enthalten in: Scientific reports | 2024

von Minnai, F. | Biscarini, F. | Esposito, M. | +120

5

Sodium-glucose cotransporter-2 inhibitors : A potential novel treatment for Lafora disease?

enthalten in: Pharmacological research | 2024

von Imbrici, P. | d'Orsi, G. | Carella, M. | +4

6

Phase I clinical trial of intracerebroventricular transplantation of allogeneic neural stem cells in people with progressive multiple sclerosis

enthalten in: Cell stem cell | 2023

von Leone, M. | Gelati, M. | Profico, D. | +41

7

Identification of a Novel FOXP1 Variant in a Patient with Hypotonia, Intellectual Disability, and Severe Speech Impairment

enthalten in: Genes | 2023

von Benvenuto, M. | Palumbo, P. | Di Muro, E. | +5

8

APOGEE 2 : multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants

enthalten in: Nature communications | 2023

von Bianco, S. | Parca, L. | Petrizzelli, F. | +12

9

Ultra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorder

enthalten in: Respiratory research | 2023

von Bergantini, L. | Baldassarri, M. | d'Alessandro, M. | +108

10

A t(4;13)(q21;q14) translocation in B-cell chronic lymphocytic leukemia causing concomitant homozygous DLEU2/miR15a/miR16-1 and heterozygous ARHGAP24 deletions

enthalten in: Cancer genetics | 2023

von Tolomeo, D. | Agostini, A. | Solimando, A. | +8

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