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Revolutionising healing: Gene Editing's breakthrough against sickle cell disease.
Annarita Miccio
Source :
Blood Rev2024 mar 7Pmid / DOI:
38493007 -
Annarita Miccio
Source :
Mol Ther Nucleic Acids2023 déc 12Pmid / DOI:
38034032 -
TUBB4B variants specifically impact ciliary function, causing a ciliopathic spectrum
Jeanne Amiel, Jean-Michel Rozet, Jean-Michel Rozet
Source :
Cold Spring Harbor Laboratory2023 nov 20Pmid / DOI:
https://doi.org/10.1101/2022.10.19.22280748 -
Ségolène Bernheim , Emeline Perthame, Audrey Desgrange, Cindy Michel, Laurent GUILLEMOT, Damien Bonnet, Sigolène Meilhac
Source :
Dev Cell2023 nov 6Pmid / DOI:
37852253 -
TUBB4B variants specifically impact ciliary function, causing a ciliopathic spectrum
Jeanne Amiel, Jean-Michel Rozet, Jean-Michel Rozet
Source :
Cold Spring Harbor Laboratory2023 oct 16Pmid / DOI:
https://doi.org/10.1101/2022.10.19.22280748 -
Jeanne Amiel, Pierre David, Nathalie Boddaert, Jean-Michel Rozet
Source :
Cold Spring Harbor Laboratory2023 oct 13Pmid / DOI:
https://doi.org/10.1101/2023.08.19.23293832 -
Jeanne Amiel, Pierre David, Nathalie Boddaert, Jean-Michel Rozet
Source :
Cold Spring Harbor Laboratory2023 oct 13Pmid / DOI:
10.1101/2023.08.19.23293832 -
Ségolène Bernheim , Emeline Perthame, Audrey Desgrange, Cindy Michel, Laurent GUILLEMOT, Damien Bonnet, Sigolène Meilhac
Source :
Dev Cell2023 oct 13Pmid / DOI:
37852253 -
Jean-Michel Rozet
Source :
Cell Rep2023 aoû 29Pmid / DOI:
37480564 -
Sickle Cell Disease: From Genetics to Curative Approaches.
Giulia Hardouin, Marina Cavazzana, Annarita Miccio
Source :
Annu Rev Genomics Hum Genet2023 aoû 25Pmid / DOI:
37624668 -
Yoann Saillour, Vicente Elorriaga, Elodie Delberghe, Alessandra Pierani, Frédéric Causeret
Source :
Dev Cell2023 aoû 7Pmid / DOI:
37321213 -
Autosomal recessive pathogenic MSTO1 variants in hereditary optic atrophy.
Jean-Michel Rozet
Source :
EMBO Mol Med2023 aoû 7Pmid / DOI:
37431816 -
Yoann Saillour, Vicente Elorriaga, Elodie Delberghe, Alessandra Pierani, Frédéric Causeret
Source :
Dev Cell2023 aoû 7Pmid / DOI:
37321213 -
A wave of deep intronic mutations in X-linked Alport syndrome.
Christelle Arrondel, Hassan Saei, Laurence Heidet, Jessica Kachmar, Philippe Couarch, Olivier Gribouval, Mélanie Parisot, Patrick Nitschké, Corinne Antignac, Guillaume Dorval
Source :
Kidney Int2023 aoû 1Pmid / DOI:
37230224 -
The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies.
Friederike Petzold, Katy Billot, Xiaoyi Chen, Yoann Martin, Maxime Douillet, Cécile Jeanpierre, Olivia Boyer, Aude Servais, Alexandre Benmerah , Laurence Heidet, Nicolas Garcelon, Corinne Antignac, Sophie Saunier, Tania Attié-Bitach, Jean-Michel Rozet, Lydie Burglen, Marlène Rio, Sabine Sarnacki
Source :
Kidney Int2023 aoû 1Pmid / DOI:
37230223