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PubPharm (33)
1
A maternal-effect Padi6 variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos
enthalten in:
Genes & development
| 2024
von
Giaccari, C.
|
Cecere, F.
|
Argenziano, L.
| +13
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2
Exploring ligand interactions with human phosphomannomutases using recombinant bacterial thermal shift assay and biochemical validation
enthalten in:
Biochimie
| 2024
von
Monticelli, M.
|
Hay Mele, B.
|
Wright, D.
| +3
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3
Drug Repurposing and Lysosomal Storage Disorders : A Trick to Treat
enthalten in:
Genes
| 2024
von
Hay Mele, B.
|
Rossetti, F.
|
Cubellis, M.
| +2
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4
Oxidoreductases and metal cofactors in the functioning of the earth
enthalten in:
Essays in biochemistry
| 2023
von
Hay Mele, B.
|
Monticelli, M.
|
Leone, S.
| +10
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5
Computational Strategies in Nutrigenetics: Constructing a Reference Dataset of Nutrition-Associated Genetic Polymorphisms
enthalten in:
bioRxiv.org
| 2023
von
De Filippis, G.
|
Monticelli, M.
|
Pollice, A.
| +3
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6
Female Sex Determination Factors in Ceratitis capitata : Molecular and Structural Basis of TRA and TRA2 Recognition
enthalten in:
Insects
| 2023
von
Perrotta, M.
|
Lucibelli, F.
|
Mazzucchiello, S.
| +8
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7
Co-Occurrence of Beckwith-Wiedemann Syndrome and Early-Onset Colorectal Cancer
enthalten in:
Cancers
| 2023
von
Cecere, F.
|
Pignata, L.
|
Hay Mele, B.
| +11
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8
Computational modeling of cambium activity provides a regulatory framework for simulating radial plant growth
enthalten in:
eLife
| 2023
von
Lebovka, I.
|
Hay Mele, B.
|
Liu, X.
| +6
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9
Characterization of Linezolid-Analogue L3-Resistance Mutation in Staphylococcus aureus
enthalten in:
Microorganisms
| 2023
von
Zanfardino, A.
|
Di Napoli, M.
|
Migliore, F.
| +5
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10
Enzyme Replacement Therapy for FABRY Disease : Possible Strategies to Improve Its Efficacy
enthalten in:
International journal of molecular sciences
| 2023
von
Iacobucci, I.
|
Hay Mele, B.
|
Cozzolino, F.
| +5
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BMC bioinformatics
6
International journal of molecular sciences
4
Clinical epigenetics
2
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2
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2
Orphanet journal of rare diseases
1
Biochimie
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Thema
20
Journal Article
6
Fabry disease
6
Genomic imprinting
5
Beckwith–Wiedemann syndrome
5
DNA methylation
5
EC 3.2.1.22
5
Research Support, Non-U.S. Gov't
5
alpha-Galactosidase
5
drug repositioning
4
Infertility
4
Maternal-effect variants
4
Multi-locus imprinting disturbance
4
Pseudohypoparathyroidism
4
Recurrent pregnancy loss
4
Subcortical maternal complex
3
Bioinformatics
3
Clinical informatics
3
Computer-based learning
3
Graduate education
3
Marine biotechnology
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Erscheinungszeitraum
25
2020-
8
2010-2019
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32
Englisch
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