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	1.	Unraveling the mysteries of pre-mRNA splicing in the retina via stem cell technology. [electronic resource] by Collin, Rob W J Publication details: Stem cell investigation 2016 In: Stem cell investigation vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Preface of Special Issue "Molecular Therapies for Inherited Retinal Diseases". [electronic resource] by Collin, Rob W J Garanto, Alejandro Producer: 20201201 In: Genes vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Applications of antisense oligonucleotides for the treatment of inherited retinal diseases. [electronic resource] by Collin, Rob W J Garanto, Alejandro Producer: 20170418 In: Current opinion in ophthalmology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Design and In Vitro Use of Antisense Oligonucleotides to Correct Pre-mRNA Splicing Defects in Inherited Retinal Dystrophies. [electronic resource] by Garanto, Alejandro Collin, Rob W J Producer: 20180702 In: Methods in molecular biology (Clifton, N.J.) vol. 1715 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	The coding sequence of amyloid-beta precursor protein APP contains a neural-specific promoter element. [electronic resource] by Collin, Rob W J Martens, Gerard J M Producer: 20060825 In: Brain research vol. 1087 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Species-dependent splice recognition of a cryptic exon resulting from a recurrent intronic CEP290 mutation that causes congenital blindness. [electronic resource] by Garanto, Alejandro Duijkers, Lonneke Collin, Rob W J Producer: 20151117 In: International journal of molecular sciences vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	The amyloid-beta precursor-like protein APLP2 and its relative APP are differentially regulated during neuroendocrine cell activation. [electronic resource] by Collin, Rob W J Martens, Gerard J M Producer: 20060105 In: Molecular and cellular neurosciences vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Promises and challenges of genetic therapy for blindness. [electronic resource] by Cremers, Frans P M Collin, Rob W J Producer: 20091123 In: Lancet (London, England) vol. 374 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Molecular Therapies for Inherited Retinal Diseases-Current Standing, Opportunities and Challenges. [electronic resource] by Vázquez-Domínguez, Irene Garanto, Alejandro Collin, Rob W J Producer: 20200210 In: Genes vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Antisense Oligonucleotide Screening to Optimize the Rescue of the Splicing Defect Caused by the Recurrent Deep-Intronic [electronic resource] by Garanto, Alejandro Duijkers, Lonneke Tomkiewicz, Tomasz Z Collin, Rob W J Producer: 20191225 In: Genes vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Antisense Oligonucleotide Therapy for Inherited Retinal Dystrophies. [electronic resource] by Gerard, Xavier Garanto, Alejandro Rozet, Jean-Michel Collin, Rob W J Producer: 20160418 In: Advances in experimental medicine and biology vol. 854 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations. [electronic resource] by Cremers, Frans P M Lee, Winston Collin, Rob W J Allikmets, Rando Producer: 20210531 In: Progress in retinal and eye research vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Biosynthesis and differential processing of two pools of amyloid-beta precursor protein in a physiologically inducible neuroendocrine cell. [electronic resource] by Collin, Rob W J van den Hurk, Wilhelmina H Martens, Gerard J M Producer: 20050927 In: Journal of neurochemistry vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Correction: P-cadherin mutations are associated with high basal Wnt activity and stemness in canine mammary tumor cell lines. [electronic resource] by Timmermans-Sprang, Elpetra Collin, Rob W J Henkes, Arjen Philipsen, Meike Mol, Jan A Publication details: Oncotarget Feb 2020 In: Oncotarget vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Identification and analysis of inherited retinal disease genes. [electronic resource] by Neveling, Kornelia den Hollander, Anneke I Cremers, Frans P M Collin, Rob W J Producer: 20130417 In: Methods in molecular biology (Clifton, N.J.) vol. 935 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Genomic approaches for the discovery of genes mutated in inherited retinal degeneration. [electronic resource] by Siemiatkowska, Anna M Collin, Rob W J den Hollander, Anneke I Cremers, Frans P M Producer: 20150417 In: Cold Spring Harbor perspectives in medicine vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Detection and quantification of a KIF11 mosaicism in a subject presenting familial exudative vitreoretinopathy with microcephaly. [electronic resource] by Karjosukarso, Dyah W Cremers, Frans P M van Nouhuys, C Erik Collin, Rob W J Producer: 20190328 In: European journal of human genetics : EJHG vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Identification and expression of the first nonmammalian amyloid-beta precursor-like protein APLP2 in the amphibian Xenopus laevis. [electronic resource] by Collin, Rob W J van Strien, Denise Leunissen, Jack A M Martens, Gerard J M Producer: 20040713 In: European journal of biochemistry vol. 271 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	The power of homozygosity mapping: discovery of new genetic defects in patients with retinal dystrophy. [electronic resource] by Littink, Karin W den Hollander, Anneke I Cremers, Frans P M Collin, Rob W J Producer: 20120413 In: Advances in experimental medicine and biology vol. 723 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	EYS mutation update: In silico assessment of 271 reported and 26 novel variants in patients with retinitis pigmentosa. [electronic resource] by Messchaert, Muriël Haer-Wigman, Lonneke Khan, Muhammad I Cremers, Frans P M Collin, Rob W J Producer: 20190107 In: Human mutation vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 114 results.