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Structural recovery of the retina in a retinoschisin-deficient mouse after gene replacement therapy by solid lipid nanoparticles

Biomaterials, 2016-06, Vol.90, p.40-49

2016

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Cloning and characterization of the murine Vmd2 RFP-TM gene family

Cytogenetic and genome research, 2004-01, Vol.105 (1), p.107-114

2004

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The role of caspases in photoreceptor cell death of the retinoschisin-deficient mouse

Cytogenetic and genome research, 2006-01, Vol.115 (1), p.35-44

2006

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Solid lipid nanoparticle-based vectors intended for the treatment of X-linked juvenile retinoschisis by gene therapy: In vivo approaches in Rs1h-deficient mouse model

Journal of controlled release, 2015-11, Vol.217, p.273-283

2015

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The role of Properdin in the development and progression of age-related macular degeneration

Molecular immunology, 2013-12, Vol.56 (3), p.291-291

2013

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Altersabhängige Makuladegeneration

Medizinische Genetik, 2007-09, Vol.19 (3), p.369-377

2007

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Comparative mapping of human claudin-1 (CLDN1) in great apes

Cytogenetic and genome research, 2005-01, Vol.108 (1-3), p.229-233

2005

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Identifying differentially expressed genes in the mammalian retina and the retinal pigment epithelium by suppression subtractive hybridization

Cytogenetic and genome research, 2004-01, Vol.106 (1), p.74-81

2004

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Differential diagnosis of primary failure of eruption (PFE) with and without evidence of pathogenic mutations in the PTHR1 gene

Journal of orofacial orthopedics, 2014-05, Vol.75 (3), p.226-239

2014

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EST mining of the UniGene dataset to identify retina-specific genes

Cytogenetic and genome research, 2000-01, Vol.91 (1-4), p.267-277

2000

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Wie groß sind die kleinen genetischen Risiken?

Medizinische Genetik, 2011-09, Vol.23 (3), p.377-384

2011

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Identification of an oncostatin M receptor mutation associated with familial primary cutaneous amyloidosis

British journal of dermatology (1951), 2009-10, Vol.161 (4), p.944-947

2009

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Altersabhängige Makuladegeneration: Neue Einblicke in Genetik und Pathogenese einer komplexen Erkrankung

Medizinische Genetik, 2007-09, Vol.19 (3), p.369-377

2007

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Wie groß sind die kleinen genetischen Risiken?

Medizinische Genetik, 2011-11, Vol.23 (3), p.377-384

2011

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Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk

American journal of ophthalmology, 2006, Vol.141 (1), p.237-237

2006

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PTEN mutations do not cause nuclear β-catenin accumulation in endometrial carcinomas

Human pathology, 2004-10, Vol.35 (10), p.1260-1265

2004

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PTEN mutations do not cause nuclear [beta]-catenin accumulation in endometrial carcinomas

Human pathology, 2004-10, Vol.35 (10), p.1260

2004

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cDNA cloning and genomic structure of a novel gene (C11orf9) localized to chromosome 11q12-->q13.1 which encodes a highly conserved, potential membrane-associated protein

Cytogenetic and genome research, 2000-01, Vol.88 (3-4), p.211-216

2000

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Recent advances in the molecular genetics of hereditary retinal dystrophies with primary involvement of the macula

Acta anatomica, 1998-01, Vol.162 (2-3), p.65-74

Weber, B H

1998

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Isolation of a Drosophila T-box gene closely related to human TBX1

Gene, 1998-06, Vol.212 (2), p.237-248

1998

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Genomic organization and chromosomal localization of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene: a candidate for 6q-linked retinopathies

Cytogenetic and genome research, 1998, Vol.81 (1), p.12-17

1998

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Genetic analysis of candidate genes modifying the age-at-onset in Huntington's Disease: results of a large European association study

Aktuelle Neurologie, 2005, Vol.32 (S 4)

2005

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EFEMP1 is not associated with sporadic early onset drusen

Ophthalmic genetics, 2001, Vol.22 (1), p.27-34

2001

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Best's Vitelliform Dystrophy (VMD2) Maps between D11S903 and PYGM: No Evidence for Locus Heterogeneity

Genomics (San Diego, Calif.), 1994-03, Vol.20 (2), p.267-274

1994

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Structural recovery of the retina in a retinoschisin-deficient mouse after gene replacement therapy by solid lipid nanoparticles

Cloning and characterization of the murine Vmd2 RFP-TM gene family

The role of caspases in photoreceptor cell death of the retinoschisin-deficient mouse

Solid lipid nanoparticle-based vectors intended for the treatment of X-linked juvenile retinoschisis by gene therapy: In vivo approaches in Rs1h-deficient mouse model

The role of Properdin in the development and progression of age-related macular degeneration

Altersabhängige Makuladegeneration

Comparative mapping of human claudin-1 (CLDN1) in great apes

Identifying differentially expressed genes in the mammalian retina and the retinal pigment epithelium by suppression subtractive hybridization

Differential diagnosis of primary failure of eruption (PFE) with and without evidence of pathogenic mutations in the PTHR1 gene

EST mining of the UniGene dataset to identify retina-specific genes

Wie groß sind die kleinen genetischen Risiken?

Identification of an oncostatin M receptor mutation associated with familial primary cutaneous amyloidosis

Altersabhängige Makuladegeneration: Neue Einblicke in Genetik und Pathogenese einer komplexen Erkrankung

Wie groß sind die kleinen genetischen Risiken?

Retina

Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk

PTEN mutations do not cause nuclear β-catenin accumulation in endometrial carcinomas

PTEN mutations do not cause nuclear [beta]-catenin accumulation in endometrial carcinomas

cDNA cloning and genomic structure of a novel gene (C11orf9) localized to chromosome 11q12-->q13.1 which encodes a highly conserved, potential membrane-associated protein

Recent advances in the molecular genetics of hereditary retinal dystrophies with primary involvement of the macula

Isolation of a Drosophila T-box gene closely related to human TBX1

Genomic organization and chromosomal localization of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene: a candidate for 6q-linked retinopathies

Genetic analysis of candidate genes modifying the age-at-onset in Huntington's Disease: results of a large European association study

EFEMP1 is not associated with sporadic early onset drusen

Best's Vitelliform Dystrophy (VMD2) Maps between D11S903 and PYGM: No Evidence for Locus Heterogeneity

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