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Items: 1 to 20 of 63

1.

RPGR-Associated Dystrophies: Clinical, Genetic, and Histopathological Features.

Nguyen XT, Talib M, van Schooneveld MJ, Brinks J, Ten Brink J, Florijn RJ, Wijnholds J, Verdijk RM, Bergen AA, Boon CJF.

Int J Mol Sci. 2020 Jan 28;21(3). pii: E835. doi: 10.3390/ijms21030835.

2.

Microglial Cell Dysfunction in CRB1-Associated Retinopathies.

Alves CH, Wijnholds J.

Adv Exp Med Biol. 2019;1185:159-163. doi: 10.1007/978-3-030-27378-1_26. Review.

PMID:
31884605
3.

Retinogenesis of the Human Fetal Retina: An Apical Polarity Perspective.

Quinn PMJ, Wijnholds J.

Genes (Basel). 2019 Nov 29;10(12). pii: E987. doi: 10.3390/genes10120987. Review.

4.

CRB2 Loss in Rod Photoreceptors Is Associated with Progressive Loss of Retinal Contrast Sensitivity.

Alves CH, Boon N, Mulder AA, Koster AJ, Jost CR, Wijnholds J.

Int J Mol Sci. 2019 Aug 21;20(17). pii: E4069. doi: 10.3390/ijms20174069.

5.

Human iPSC-Derived Retinas Recapitulate the Fetal CRB1 CRB2 Complex Formation and Demonstrate that Photoreceptors and Müller Glia Are Targets of AAV5.

Quinn PM, Buck TM, Mulder AA, Ohonin C, Alves CH, Vos RM, Bialecka M, van Herwaarden T, van Dijk EHC, Talib M, Freund C, Mikkers HMM, Hoeben RC, Goumans MJ, Boon CJF, Koster AJ, Chuva de Sousa Lopes SM, Jost CR, Wijnholds J.

Stem Cell Reports. 2019 May 14;12(5):906-919. doi: 10.1016/j.stemcr.2019.03.002. Epub 2019 Apr 4.

6.

"Basal Cell Migration" in Regeneration of the Corneal Wound-Bed.

Wijnholds J.

Stem Cell Reports. 2019 Jan 8;12(1):3-5. doi: 10.1016/j.stemcr.2018.12.009.

7.

Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype.

Quinn PM, Mulder AA, Henrique Alves C, Desrosiers M, de Vries SI, Klooster J, Dalkara D, Koster AJ, Jost CR, Wijnholds J.

Hum Mol Genet. 2019 Jan 1;28(1):105-123. doi: 10.1093/hmg/ddy337.

PMID:
30239717
8.

The Spectrum of Structural and Functional Abnormalities in Female Carriers of Pathogenic Variants in the RPGR Gene.

Talib M, van Schooneveld MJ, Van Cauwenbergh C, Wijnholds J, Ten Brink JB, Florijn RJ, Schalij-Delfos NE, Dagnelie G, van Genderen MM, De Baere E, Meester-Smoor MA, De Zaeytijd J, Cremers FPM, van den Born LI, Thiadens AA, Hoyng CB, Klaver CC, Leroy BP, Bergen AA, Boon CJF.

Invest Ophthalmol Vis Sci. 2018 Aug 1;59(10):4123-4133. doi: 10.1167/iovs.17-23453.

PMID:
30105367
9.

CRB2 in immature photoreceptors determines the superior-inferior symmetry of the developing retina to maintain retinal structure and function.

Quinn PM, Alves CH, Klooster J, Wijnholds J.

Hum Mol Genet. 2018 Sep 15;27(18):3137-3153. doi: 10.1093/hmg/ddy194.

PMID:
29893966
10.

CLINICAL AND GENETIC CHARACTERISTICS OF MALE PATIENTS WITH RPGR-ASSOCIATED RETINAL DYSTROPHIES: A Long-Term Follow-up Study.

Talib M, van Schooneveld MJ, Thiadens AA, Fiocco M, Wijnholds J, Florijn RJ, Schalij-Delfos NE, van Genderen MM, Putter H, Cremers FPM, Dagnelie G, Ten Brink JB, Klaver CCW, van den Born LI, Hoyng CB, Bergen AA, Boon CJF.

Retina. 2019 Jun;39(6):1186-1199. doi: 10.1097/IAE.0000000000002125.

PMID:
29528978
11.

AAV Serotype Testing on Cultured Human Donor Retinal Explants.

Buck TM, Pellissier LP, Vos RM, van Dijk EHC, Boon CJF, Wijnholds J.

Methods Mol Biol. 2018;1715:275-288. doi: 10.1007/978-1-4939-7522-8_20.

PMID:
29188521
12.

Production of iPS-Derived Human Retinal Organoids for Use in Transgene Expression Assays.

Quinn PM, Buck TM, Ohonin C, Mikkers HMM, Wijnholds J.

Methods Mol Biol. 2018;1715:261-273. doi: 10.1007/978-1-4939-7522-8_19.

PMID:
29188520
13.

AAV Gene Augmentation Therapy for CRB1-Associated Retinitis Pigmentosa.

Alves CH, Wijnholds J.

Methods Mol Biol. 2018;1715:135-151. doi: 10.1007/978-1-4939-7522-8_10.

PMID:
29188511
14.

Genetic and Molecular Approaches to Study Neuronal Migration in the Developing Cerebral Cortex.

Dudok JJ, Leonards PEG, Wijnholds J.

Brain Sci. 2017 May 5;7(5). pii: E53. doi: 10.3390/brainsci7050053. Review.

15.

The CRB1 Complex: Following the Trail of Crumbs to a Feasible Gene Therapy Strategy.

Quinn PM, Pellissier LP, Wijnholds J.

Front Neurosci. 2017 Apr 5;11:175. doi: 10.3389/fnins.2017.00175. eCollection 2017. Review.

16.

Genotypic and Phenotypic Characteristics of CRB1-Associated Retinal Dystrophies: A Long-Term Follow-up Study.

Talib M, van Schooneveld MJ, van Genderen MM, Wijnholds J, Florijn RJ, Ten Brink JB, Schalij-Delfos NE, Dagnelie G, Cremers FPM, Wolterbeek R, Fiocco M, Thiadens AA, Hoyng CB, Klaver CC, Bergen AA, Boon CJF.

Ophthalmology. 2017 Jun;124(6):884-895. doi: 10.1016/j.ophtha.2017.01.047. Epub 2017 Mar 21.

PMID:
28341475
17.

Crumbs2 promotes cell ingression during the epithelial-to-mesenchymal transition at gastrulation.

Ramkumar N, Omelchenko T, Silva-Gagliardi NF, McGlade CJ, Wijnholds J, Anderson KV.

Nat Cell Biol. 2016 Dec;18(12):1281-1291. doi: 10.1038/ncb3442. Epub 2016 Nov 21.

18.

Crumbs 2 prevents cortical abnormalities in mouse dorsal telencephalon.

Dudok JJ, Murtaza M, Henrique Alves C, Rashbass P, Wijnholds J.

Neurosci Res. 2016 Jul;108:12-23. doi: 10.1016/j.neures.2016.01.001. Epub 2016 Jan 21.

19.

Protein O-Glucosyltransferase 1 (POGLUT1) Promotes Mouse Gastrulation through Modification of the Apical Polarity Protein CRUMBS2.

Ramkumar N, Harvey BM, Lee JD, Alcorn HL, Silva-Gagliardi NF, McGlade CJ, Bestor TH, Wijnholds J, Haltiwanger RS, Anderson KV.

PLoS Genet. 2015 Oct 23;11(10):e1005551. doi: 10.1371/journal.pgen.1005551. eCollection 2015 Oct.

20.

A new CRB1 rat mutation links Müller glial cells to retinal telangiectasia.

Zhao M, Andrieu-Soler C, Kowalczuk L, Paz Cortés M, Berdugo M, Dernigoghossian M, Halili F, Jeanny JC, Goldenberg B, Savoldelli M, El Sanharawi M, Naud MC, van Ijcken W, Pescini-Gobert R, Martinet D, Maass A, Wijnholds J, Crisanti P, Rivolta C, Behar-Cohen F.

J Neurosci. 2015 Apr 15;35(15):6093-106. doi: 10.1523/JNEUROSCI.3412-14.2015.

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