TY  - JOUR
AU  - Sánchez Cruz, Alonso
AU  - Canto Méndez, Andrea
AU  - Lizasoain, Ignacio
AU  - de la Villa, Pedro
AU  - Rosa, Enrique J. de la
AU  - Hernández Sánchez, Catalina
PY  - 2021
DO  - 10.3390/ijms22157815
SN  - 1422-0067
UR  - https://hdl.handle.net/20.500.14352/7056
T2  - International Journal of Molecular Sciences
AB  - Although considered a rare retinal dystrophy, retinitis pigmentosa (RP) is the primary cause of hereditary blindness. Given its diverse genetic etiology (>3000 mutations in >60 genes), there is an urgent need for novel treatments that target common...
LA  - eng
M2  - 7815
PB  - MPDI
KW  - retinitis pigmentosa
KW  - retina
KW  - TLR
KW  - TLR2
KW  - microglia
KW  - innate immunity
KW  - neurodegeneration
KW  - rd10
KW  - P23H
TI  - Tlr2 Gene Deletion Delays Retinal Degeneration in Two Genetically Distinct Mouse Models of Retinitis Pigmentosa
TY  - journal article
VL  - 22
ER  -