Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Younes El Fersioui"'
Autor:
Yvan Arsenijevic, Ning Chang, Olivier Mercey, Younes El Fersioui, Hanna Koskiniemi-Kuendig, Caroline Joubert, Alexis-Pierre Bemelmans, Carlo Rivolta, Eyal Banin, Dror Sharon, Paul Guichard, Virginie Hamel, Corinne Kostic
Publikováno v:
EMBO Molecular Medicine, Vol 16, Iss 4, Pp 805-822 (2024)
Abstract For 15 years, gene therapy has been viewed as a beacon of hope for inherited retinal diseases. Many preclinical investigations have centered around vectors with maximal gene expression capabilities, yet despite efficient gene transfer, minim
Externí odkaz:
https://doaj.org/article/2bace1c6d9974dd18283e0facc8d9d6c
Publikováno v:
PLoS ONE, Vol 16, Iss 1, p e0245239 (2021)
H6 family homeobox 1 (HMX1) regulates multiple aspects of craniofacial development as it is widely expressed in the eye, peripheral ganglia and branchial arches. Mutations in HMX1 are linked to an ocular defect termed Oculo-auricular syndrome of Scho
Externí odkaz:
https://doaj.org/article/79b113966279455ea85dc416e0d25ce9
Publikováno v:
Cells, Vol 11, Iss 7, p 1088 (2022)
H6 family homeobox 1 (HMX1) regulates multiple aspects of craniofacial development, and mutations in HMX1 are linked to an ocular defect termed oculoauricular syndrome of Schorderet–Munier–Franceschetti (OAS) (MIM #612109). Recently, additional a
Externí odkaz:
https://doaj.org/article/5e3a5185f0a34d9e892297b02ecc9eb3
Publikováno v:
Cells; Volume 11; Issue 7; Pages: 1088
H6 family homeobox 1 (HMX1) regulates multiple aspects of craniofacial development, and mutations in HMX1 are linked to an ocular defect termed oculoauricular syndrome of Schorderet–Munier–Franceschetti (OAS) (MIM #612109). Recently, additional a
Publikováno v:
PLoS ONE, Vol 16, Iss 1, p e0245239 (2021)
PLoS ONE
PLoS ONE
H6 family homeobox 1 (HMX1) regulates multiple aspects of craniofacial development as it is widely expressed in the eye, peripheral ganglia and branchial arches. Mutations in HMX1 are linked to an ocular defect termed Oculo-auricular syndrome of Scho