Search details
1.
Retinal Ciliopathies and Potential Gene Therapies: A Focus on Human iPSC-Derived Organoid Models.
Int J Mol Sci
; 25(5)2024 Mar 01.
Article
in English
| MEDLINE | ID: mdl-38474133
2.
Crumbs2 mediates ventricular layer remodelling to form the spinal cord central canal.
PLoS Biol
; 18(3): e3000470, 2020 03.
Article
in English
| MEDLINE | ID: mdl-32150534
3.
Crumbs2 Is an Essential Slit Diaphragm Protein of the Renal Filtration Barrier.
J Am Soc Nephrol
; 32(5): 1053-1070, 2021 05 03.
Article
in English
| MEDLINE | ID: mdl-33687977
4.
Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype.
Hum Mol Genet
; 28(1): 105-123, 2019 01 01.
Article
in English
| MEDLINE | ID: mdl-30239717
5.
CLINICAL CHARACTERISTICS AND NATURAL HISTORY OF RHO-ASSOCIATED RETINITIS PIGMENTOSA: A Long-Term Follow-Up Study.
Retina
; 41(1): 213-223, 2021 Jan 01.
Article
in English
| MEDLINE | ID: mdl-32301896
6.
Defining Phenotype, Tropism, and Retinal Gene Therapy Using Adeno-Associated Viral Vectors (AAVs) in New-Born Brown Norway Rats with a Spontaneous Mutation in Crb1.
Int J Mol Sci
; 22(7)2021 Mar 30.
Article
in English
| MEDLINE | ID: mdl-33808129
7.
CRB2 in immature photoreceptors determines the superior-inferior symmetry of the developing retina to maintain retinal structure and function.
Hum Mol Genet
; 27(18): 3137-3153, 2018 09 15.
Article
in English
| MEDLINE | ID: mdl-29893966
8.
Recombinant Adeno-Associated Viral Vectors (rAAV)-Vector Elements in Ocular Gene Therapy Clinical Trials and Transgene Expression and Bioactivity Assays.
Int J Mol Sci
; 21(12)2020 Jun 12.
Article
in English
| MEDLINE | ID: mdl-32545533
9.
RPGR-Associated Dystrophies: Clinical, Genetic, and Histopathological Features.
Int J Mol Sci
; 21(3)2020 Jan 28.
Article
in English
| MEDLINE | ID: mdl-32012938
10.
CLINICAL AND GENETIC CHARACTERISTICS OF MALE PATIENTS WITH RPGR-ASSOCIATED RETINAL DYSTROPHIES: A Long-Term Follow-up Study.
Retina
; 39(6): 1186-1199, 2019 Jun.
Article
in English
| MEDLINE | ID: mdl-29528978
11.
Microglial Cell Dysfunction in CRB1-Associated Retinopathies.
Adv Exp Med Biol
; 1185: 159-163, 2019.
Article
in English
| MEDLINE | ID: mdl-31884605
12.
CRB2 Loss in Rod Photoreceptors Is Associated with Progressive Loss of Retinal Contrast Sensitivity.
Int J Mol Sci
; 20(17)2019 Aug 21.
Article
in English
| MEDLINE | ID: mdl-31438467
13.
Protein O-Glucosyltransferase 1 (POGLUT1) Promotes Mouse Gastrulation through Modification of the Apical Polarity Protein CRUMBS2.
PLoS Genet
; 11(10): e1005551, 2015 Oct.
Article
in English
| MEDLINE | ID: mdl-26496195
14.
Gene therapy into photoreceptors and Müller glial cells restores retinal structure and function in CRB1 retinitis pigmentosa mouse models.
Hum Mol Genet
; 24(11): 3104-18, 2015 Jun 01.
Article
in English
| MEDLINE | ID: mdl-25701872
15.
Genotypic and Phenotypic Characteristics of CRB1-Associated Retinal Dystrophies: A Long-Term Follow-up Study.
Ophthalmology
; 124(6): 884-895, 2017 06.
Article
in English
| MEDLINE | ID: mdl-28341475
16.
A new CRB1 rat mutation links Müller glial cells to retinal telangiectasia.
J Neurosci
; 35(15): 6093-106, 2015 Apr 15.
Article
in English
| MEDLINE | ID: mdl-25878282
17.
CRB2 acts as a modifying factor of CRB1-related retinal dystrophies in mice.
Hum Mol Genet
; 23(14): 3759-71, 2014 Jul 15.
Article
in English
| MEDLINE | ID: mdl-24565864
18.
Targeted ablation of Crb2 in photoreceptor cells induces retinitis pigmentosa.
Hum Mol Genet
; 23(13): 3384-401, 2014 Jul 01.
Article
in English
| MEDLINE | ID: mdl-24493795
19.
Targeted ablation of CRB1 and CRB2 in retinal progenitor cells mimics Leber congenital amaurosis.
PLoS Genet
; 9(12): e1003976, 2013.
Article
in English
| MEDLINE | ID: mdl-24339791
20.
Loss of CRB2 in the mouse retina mimics human retinitis pigmentosa due to mutations in the CRB1 gene.
Hum Mol Genet
; 22(1): 35-50, 2013 Jan 01.
Article
in English
| MEDLINE | ID: mdl-23001562