Author Search Results

1

Unraveling the mysteries of pre-mRNA splicing in the retina via stem cell technology by Collin, Rob W. J.

Published 2016

Get full text Get full text Get full text
Text

Save to List

Saved in:
2

Preface of Special Issue "Molecular Therapies for Inherited Retinal Diseases" by Collin, Rob W.J., Garanto, Alejandro

Published 2020

Get full text Get full text Get full text
Text

Save to List

Saved in:
3

Species-Dependent Splice Recognition of a Cryptic Exon Resulting from a Recurrent Intronic CEP290 Mutation that Causes Congenital Blindness by Garanto, Alejandro, Duijkers, Lonneke, Collin, Rob W. J.

Published 2015

Get full text Get full text Get full text
Text

Save to List

Saved in:
4

Molecular Therapies for Inherited Retinal Diseases—Current Standing, Opportunities and Challenges by Vázquez-Domínguez, Irene, Garanto, Alejandro, Collin, Rob W. J.

Published 2019

Get full text Get full text Get full text
Text

Save to List

Saved in:
5

Antisense Oligonucleotide Screening to Optimize the Rescue of the Splicing Defect Caused by the Recurrent Deep-Intronic ABCA4 Variant c.4539+2001G>A in Stargardt Disease by Garanto, Alejandro, Duijkers, Lonneke, Tomkiewicz, Tomasz Z., Collin, Rob W. J.

Published 2019

Get full text Get full text Get full text
Text

Save to List

Saved in:
6

Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations by Cremers, Frans P.M., Lee, Winston, Collin, Rob W.J., Allikmets, Rando

Published 2020

Get full text Get full text Get full text
Text

Save to List

Saved in:
7

Correction: P-cadherin mutations are associated with high basal Wnt activity and stemness in canine mammary tumor cell lines by Timmermans-Sprang, Elpetra, Collin, Rob W.J., Henkes, Arjen, Philipsen, Meike, Mol, Jan A.

Published 2020

Get full text Get full text Get full text
Text

Save to List

Saved in:
8

Genomic Approaches For the Discovery of Genes Mutated in Inherited Retinal Degeneration by Siemiatkowska, Anna M., Collin, Rob W.J., den Hollander, Anneke I., Cremers, Frans P.M.

Published 2014

Get full text Get full text Get full text
Text

Save to List

Saved in:
9

Detection and quantification of a KIF11 mosaicism in a subject presenting familial exudative vitreoretinopathy with microcephaly by Karjosukarso, Dyah W., Cremers, Frans P. M., van Nouhuys, C. Erik, Collin, Rob W. J.

Published 2018

Get full text Get full text Get full text
Text

Save to List

Saved in:
10

Antisense Oligonucleotide-Based Rescue of Aberrant Splicing Defects Caused by 15 Pathogenic Variants in ABCA4 by Tomkiewicz, Tomasz Z., Suárez-Herrera, Nuria, Cremers, Frans P. M., Collin, Rob W. J., Garanto, Alejandro

Published 2021

Get full text Get full text Get full text
Text

Save to List

Saved in:
11

Variants in Nebulin (NEB) Are Linked to the Development of Familial Primary Angle Closure Glaucoma in Basset Hounds by Ahram, Dina F., Grozdanic, Sinisa D., Kecova, Helga, Henkes, Arjen, Collin, Rob W. J., Kuehn, Markus H.

Published 2015

Get full text Get full text Get full text
Text

Save to List

Saved in:
12

A look into retinal organoids: methods, analytical techniques, and applications by Afanasyeva, Tess A. V., Corral-Serrano, Julio C., Garanto, Alejandro, Roepman, Ronald, Cheetham, Michael E., Collin, Rob W. J.

Published 2021

Get full text Get full text Get full text
Text

Save to List

Saved in:
13

Unexpected CEP290 mRNA Splicing in a Humanized Knock-In Mouse Model for Leber Congenital Amaurosis by Garanto, Alejandro, van Beersum, Sylvia E. C., Peters, Theo A., Roepman, Ronald, Cremers, Frans P. M., Collin, Rob W. J.

Published 2013

Get full text Get full text Get full text
Text

Save to List

Saved in:
14

The Molecular Basis of Retinal Dystrophies in Pakistan by Khan, Muhammad Imran, Azam, Maleeha, Ajmal, Muhammad, Collin, Rob W. J., den Hollander, Anneke I., Cremers, Frans P. M., Qamar, Raheel

Published 2014

Get full text Get full text Get full text
Text

Save to List

Saved in:
15

C2orf71a/pcare1 is important for photoreceptor outer segment morphogenesis and visual function in zebrafish by Corral-Serrano, Julio C., Messchaert, Muriël, Dona, Margo, Peters, Theo A., Kamminga, Leonie M., van Wijk, Erwin, Collin, Rob W. J.

Published 2018

Get full text Get full text Get full text
Text

Save to List

Saved in:
16

Expression of Wild-Type Rp1 Protein in Rp1 Knock-in Mice Rescues the Retinal Degeneration Phenotype by Liu, Qin, Collin, Rob W. J., Cremers, Frans P. M., den Hollander, Anneke I., van den Born, L. Ingeborgh, Pierce, Eric A.

Published 2012

Get full text Get full text Get full text
Text

Save to List

Saved in:
17

Zebrafish as a Model to Evaluate a CRISPR/Cas9-Based Exon Excision Approach as a Future Treatment Option for EYS-Associated Retinitis Pigmentosa by Schellens, Renske, de Vrieze, Erik, Graave, Pam, Broekman, Sanne, Nagel-Wolfrum, Kerstin, Peters, Theo, Kremer, Hannie, Collin, Rob W. J., van Wijk, Erwin

Published 2021

Get full text Get full text Get full text
Text

Save to List

Saved in:
18

A novel crumbs homolog 1 mutation in a family with retinitis pigmentosa, nanophthalmos, and optic disc drusen by Paun, Codrut C., Pijl, Benjamin J., Siemiatkowska, Anna M., Collin, Rob W.J., Cremers, Frans P.M., Hoyng, Carel B., den Hollander, Anneke I.

Published 2012

Get full text Get full text
Text

Save to List

Saved in:
19

Eyes shut homolog is important for the maintenance of photoreceptor morphology and visual function in zebrafish by Messchaert, Muriël, Dona, Margo, Broekman, Sanne, Peters, Theo A., Corral-Serrano, Julio C., Slijkerman, Ralph W. N., van Wijk, Erwin, Collin, Rob W. J.

Published 2018

Get full text Get full text Get full text
Text

Save to List

Saved in:
20

In vitro and in vivo rescue of aberrant splicing in CEP290-associated LCA by antisense oligonucleotide delivery by Garanto, Alejandro, Chung, Daniel C., Duijkers, Lonneke, Corral-Serrano, Julio C., Messchaert, Muriël, Xiao, Ru, Bennett, Jean, Vandenberghe, Luk H., Collin, Rob W.J.

Published 2016

Get full text Get full text Get full text
Text

Save to List

Saved in:

Search Results - Collin, Rob W J

Unraveling the mysteries of pre-mRNA splicing in the retina via stem cell technology by Collin, Rob W. J.

Preface of Special Issue "Molecular Therapies for Inherited Retinal Diseases" by Collin, Rob W.J., Garanto, Alejandro

Species-Dependent Splice Recognition of a Cryptic Exon Resulting from a Recurrent Intronic CEP290 Mutation that Causes Congenital Blindness by Garanto, Alejandro, Duijkers, Lonneke, Collin, Rob W. J.

Molecular Therapies for Inherited Retinal Diseases—Current Standing, Opportunities and Challenges by Vázquez-Domínguez, Irene, Garanto, Alejandro, Collin, Rob W. J.

Antisense Oligonucleotide Screening to Optimize the Rescue of the Splicing Defect Caused by the Recurrent Deep-Intronic ABCA4 Variant c.4539+2001G>A in Stargardt Disease by Garanto, Alejandro, Duijkers, Lonneke, Tomkiewicz, Tomasz Z., Collin, Rob W. J.

Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations by Cremers, Frans P.M., Lee, Winston, Collin, Rob W.J., Allikmets, Rando

Correction: P-cadherin mutations are associated with high basal Wnt activity and stemness in canine mammary tumor cell lines by Timmermans-Sprang, Elpetra, Collin, Rob W.J., Henkes, Arjen, Philipsen, Meike, Mol, Jan A.

Genomic Approaches For the Discovery of Genes Mutated in Inherited Retinal Degeneration by Siemiatkowska, Anna M., Collin, Rob W.J., den Hollander, Anneke I., Cremers, Frans P.M.

Detection and quantification of a KIF11 mosaicism in a subject presenting familial exudative vitreoretinopathy with microcephaly by Karjosukarso, Dyah W., Cremers, Frans P. M., van Nouhuys, C. Erik, Collin, Rob W. J.

Antisense Oligonucleotide-Based Rescue of Aberrant Splicing Defects Caused by 15 Pathogenic Variants in ABCA4 by Tomkiewicz, Tomasz Z., Suárez-Herrera, Nuria, Cremers, Frans P. M., Collin, Rob W. J., Garanto, Alejandro

Variants in Nebulin (NEB) Are Linked to the Development of Familial Primary Angle Closure Glaucoma in Basset Hounds by Ahram, Dina F., Grozdanic, Sinisa D., Kecova, Helga, Henkes, Arjen, Collin, Rob W. J., Kuehn, Markus H.

A look into retinal organoids: methods, analytical techniques, and applications by Afanasyeva, Tess A. V., Corral-Serrano, Julio C., Garanto, Alejandro, Roepman, Ronald, Cheetham, Michael E., Collin, Rob W. J.

Unexpected CEP290 mRNA Splicing in a Humanized Knock-In Mouse Model for Leber Congenital Amaurosis by Garanto, Alejandro, van Beersum, Sylvia E. C., Peters, Theo A., Roepman, Ronald, Cremers, Frans P. M., Collin, Rob W. J.

The Molecular Basis of Retinal Dystrophies in Pakistan by Khan, Muhammad Imran, Azam, Maleeha, Ajmal, Muhammad, Collin, Rob W. J., den Hollander, Anneke I., Cremers, Frans P. M., Qamar, Raheel

C2orf71a/pcare1 is important for photoreceptor outer segment morphogenesis and visual function in zebrafish by Corral-Serrano, Julio C., Messchaert, Muriël, Dona, Margo, Peters, Theo A., Kamminga, Leonie M., van Wijk, Erwin, Collin, Rob W. J.

Expression of Wild-Type Rp1 Protein in Rp1 Knock-in Mice Rescues the Retinal Degeneration Phenotype by Liu, Qin, Collin, Rob W. J., Cremers, Frans P. M., den Hollander, Anneke I., van den Born, L. Ingeborgh, Pierce, Eric A.

A novel crumbs homolog 1 mutation in a family with retinitis pigmentosa, nanophthalmos, and optic disc drusen by Paun, Codrut C., Pijl, Benjamin J., Siemiatkowska, Anna M., Collin, Rob W.J., Cremers, Frans P.M., Hoyng, Carel B., den Hollander, Anneke I.

Eyes shut homolog is important for the maintenance of photoreceptor morphology and visual function in zebrafish by Messchaert, Muriël, Dona, Margo, Broekman, Sanne, Peters, Theo A., Corral-Serrano, Julio C., Slijkerman, Ralph W. N., van Wijk, Erwin, Collin, Rob W. J.

In vitro and in vivo rescue of aberrant splicing in CEP290-associated LCA by antisense oligonucleotide delivery by Garanto, Alejandro, Chung, Daniel C., Duijkers, Lonneke, Corral-Serrano, Julio C., Messchaert, Muriël, Xiao, Ru, Bennett, Jean, Vandenberghe, Luk H., Collin, Rob W.J.

Search Tools: