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: a new player in myeloid cell differentiation.
Haematologica 07, 2019 | Pubmed ID: 30630974
4q-D4Z4 chromatin architecture regulates the transcription of muscle atrophic genes in facioscapulohumeral muscular dystrophy.
Genome research Jun, 2019 | Pubmed ID: 31097473
3D COMBO chrRNA-DNA-ImmunoFISH.
Methods in molecular biology (Clifton, N.J.) , 2021 | Pubmed ID: 32820410
Targeting HDAC8 to ameliorate skeletal muscle differentiation in Duchenne muscular dystrophy.
Pharmacological research Aug, 2021 | Pubmed ID: 34214631
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion.
Nature genetics Feb, 2022 | Pubmed ID: 35039641
Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes.
Human genetics Jun, 2024 | Pubmed ID: 38874808
Istituto Nazionale di Genetica Molecolare "Romeo ed Enrica Invernizzi", INGM
Istituto Nazionale di Genetica Molecolare "Romeo ed Enrica Invernizzi" (INGM)
Federica Marasca1,
Alice Cortesi1,
Lara Manganaro1,
Beatrice Bodega1
1, Istituto Nazionale di Genetica Molecolare "Romeo ed Enrica Invernizzi", INGM
Valeria Di Gioia1,2,
Jan Zamporlini1,3,
Rebecca Vadalà1,3,
Elena Parmigiani4,
Beatrice Bodega1,3,
Federica Marasca1
1, Istituto Nazionale di Genetica Molecolare "Romeo ed Enrica Invernizzi" (INGM),
2, SEMM, European School of Molecular Medicine,
3Department of Biosciences, University of Milan,
4, T-One Therapeutics Srl
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