Detalhe da pesquisa
1.
Mutation-Independent Allele-Specific Editing by CRISPR-Cas9, a Novel Approach to Treat Autosomal Dominant Disease.
Mol Ther
; 28(8): 1846-1857, 2020 08 05.
Artigo
Inglês
| MEDLINE | ID: mdl-32416058
2.
Genetic prescreening of a candidate for laser refractive surgery identifies risk for inadequate tissue response: a case report.
J Med Case Rep
; 16(1): 207, 2022 May 16.
Artigo
Inglês
| MEDLINE | ID: mdl-35578349
3.
Gene Editing for Corneal Stromal Regeneration.
Methods Mol Biol
; 2145: 59-75, 2020.
Artigo
Inglês
| MEDLINE | ID: mdl-32542601
4.
Biochemical mechanisms of aggregation in TGFBI-linked corneal dystrophies.
Prog Retin Eye Res
; 77: 100843, 2020 07.
Artigo
Inglês
| MEDLINE | ID: mdl-32004730
5.
Towards personalised allele-specific CRISPR gene editing to treat autosomal dominant disorders.
Sci Rep
; 7(1): 16174, 2017 11 23.
Artigo
Inglês
| MEDLINE | ID: mdl-29170458
6.
Trauma-induced exacerbation of epithelial-stromal TGFBI lattice corneal dystrophy.
Can J Ophthalmol
; 54(1): e47-e49, 2019 02.
Artigo
Inglês
| MEDLINE | ID: mdl-30851800
7.
Late-onset lattice corneal dystrophy associated TGFBI p.H626R mutation in members of a Canadian family.
Can J Ophthalmol
; 54(6): e308-e311, 2019 12.
Artigo
Inglês
| MEDLINE | ID: mdl-31836123