UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 70

Sortiert nach

Localization of a Gene for Duane Retraction Syndrome to Chromosome 2q31

American journal of human genetics, 1999-12, Vol.65 (6), p.1639-1646

1999

Link zum Volltext

Verfügbarkeit prüfen

Gene therapy for proliferative ocular diseases

Expert opinion on biological therapy, 2004-07, Vol.4 (7), p.1053-1058

2004

Link zum Volltext

Verfügbarkeit prüfen

Efficient and sustained transgene expression in human corneal cells mediated by a lentiviral vector

Gene therapy, 2000-02, Vol.7 (3), p.196-200

2000

Link zum Volltext

Verfügbarkeit prüfen

Rhesus monkeys and humans share common susceptibility genes for age-related macular disease

Human molecular genetics, 2008-09, Vol.17 (17), p.2673-2680

2008

Link zum Volltext

Verfügbarkeit prüfen

Activation of the Mitochondrial Apoptotic Pathway in a Rat Model of Central Retinal Artery Occlusion

Investigative ophthalmology & visual science, 2005-06, Vol.46 (6), p.2133-2139

2005

Link zum Volltext

Verfügbarkeit prüfen

Heterozygous loss of Six5 in mice is sufficient to cause ocular cataracts

Nature genetics, 2000-05, Vol.25 (1), p.110-114

2000

Link zum Volltext

Verfügbarkeit prüfen

Spectrum and Frequency of FZD4 Mutations in Familial Exudative Vitreoretinopathy

Investigative ophthalmology & visual science, 2004-07, Vol.45 (7), p.2083-2090

2004

Link zum Volltext

Verfügbarkeit prüfen

Corneal Transduction to Inhibit Angiogenesis and Graft Failure

Investigative ophthalmology & visual science, 2003-05, Vol.44 (5), p.1837-1842

2003

Link zum Volltext

Verfügbarkeit prüfen

A novel mutation in the Norrie disease gene

Journal of AAPOS, 2000-04, Vol.4 (2), p.125-126

2000

Link zum Volltext

Verfügbarkeit prüfen

Isolation and characterization of the human homeobox gene HOX D1

Molecular biology reports, 2000, Vol.27 (4), p.195-201

2000

Link zum Volltext

Verfügbarkeit prüfen

Evaluation of a novel short polyadenylation signal as an alternative to the SV40 polyadenylation signal

Plasmid, 2006-07, Vol.56 (1), p.62-67

2006

Link zum Volltext

Verfügbarkeit prüfen

An unusual clinical phenotype of avellino corneal dystrophy associated with an Arg124His βiG-H3 mutation in an African-American woman

American journal of ophthalmology, 2004-04, Vol.137 (4), p.765-767

2004

Link zum Volltext

Verfügbarkeit prüfen

An unusual clinical phenotype of Avellino corneal dystrophy associated with an Arg124His βig H3 mutation in an African-American woman

American journal of ophthalmology, 2004-04, Vol.137 (4), p.765-767

2004

Link zum Volltext

Verfügbarkeit prüfen

Localization of the gene encoding human phosphatidylinositol transfer protein (PITPN) to 17p13.3: a gene showing homology to the Drosophila retinal degeneration B gene (rdgB)

Cytogenetics and cell genetics, 1994, Vol.67 (3), p.205

1994

Link zum Volltext

Verfügbarkeit prüfen

DNA-based diagnosis of the von Hippel–Lindau syndrome

American journal of ophthalmology, 2000-02, Vol.129 (2), p.258-260

2000

Link zum Volltext

Verfügbarkeit prüfen

Exclusion of candidate genetic loci for Duane retraction syndrome

American journal of ophthalmology, 1999-03, Vol.127 (3), p.358-360

1999

Link zum Volltext

Verfügbarkeit prüfen

Sequence and Evolution of the Blue Cone Pigment Gene in Old and New World Primates

Genomics (San Diego, Calif.), 1995-06, Vol.27 (3), p.535-538

1995

Link zum Volltext

Verfügbarkeit prüfen

Efficient and sustained trans gene expression in human corneal cells mediated by a lentiviral vector

Gene therapy, 2000, Vol.7 (3), p.196-200

2000

Link zum Volltext

Verfügbarkeit prüfen

Localisation of the human blue cone pigment gene to chromosome band 7q31.3-32

Human genetics, 1994, Vol.93 (1), p.79-80

1994

Link zum Volltext

Verfügbarkeit prüfen

Electronegative electroretinogram in mucolipidosis IV

Archives of ophthalmology (1960), 2002-01, Vol.120 (1), p.45

2002

Link zum Volltext

Verfügbarkeit prüfen

Clinical phenotype associated with the arg141 his mutation in the X-linked retinoschisis gene

Archives of ophthalmology (1960), 2000-01, Vol.118 (1), p.127

2000

Link zum Volltext

Verfügbarkeit prüfen

Designed and tailor-made double hydrophilic block copolymer-graphene nanoplatelet hybrids for reinforcing epoxy thermosets

Scientific reports, 2024-04, Vol.14 (1), p.8812-8812, Article 8812

2024

Link zum Volltext

Verfügbarkeit prüfen

Role of Polyethylene Glycol as a Catalyst and a Filler in Epoxy Systems

Topics in catalysis, 2024-01, Vol.67 (1-4), p.218-231

2024

Link zum Volltext

Verfügbarkeit prüfen

Graphene oxide as multi-functional initiator and effective molecular reinforcement in PVP/epoxy composites

Journal of molecular structure, 2021-04, Vol.1230, p.129873, Article 129873

2021

Link zum Volltext

Verfügbarkeit prüfen

Modelling of the Rheological Behaviour of Epoxy-Polyethylene Glycol-1000 Blends

Topics in catalysis, 2022-12, Vol.65 (19-20), p.1733-1744

2022

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 70

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(62)
Mit Volltextzugriff
(65)

Publikationsform

Artikel
(66)
Buchkapitel
(4)

Sprache

Englisch
(70)
Japanisch
(6)

Erscheinungsjahr

n.n

Thema

Science & Technology
(54)
Life Sciences & Biomedicine
(36)
Humans
(26)
Biological And Medical Sciences
(14)
Physical Sciences
(13)
Female
(11)
Ophthalmology
(11)
Animals
(10)
Biochemistry & Molecular Biology
(10)
Male
(10)
Chemistry
(9)
Materials Science
(9)
Technology
(9)
Genetics & Heredity
(8)
Medical Sciences
(8)
Fundamental And Applied Biological Sciences. Psychology
(7)
Adult
(6)
Electrospinning
(6)
Fracture Toughness
(6)
Metabolism
(6)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Localization of a Gene for Duane Retraction Syndrome to Chromosome 2q31

Gene therapy for proliferative ocular diseases

Efficient and sustained transgene expression in human corneal cells mediated by a lentiviral vector

Rhesus monkeys and humans share common susceptibility genes for age-related macular disease

Activation of the Mitochondrial Apoptotic Pathway in a Rat Model of Central Retinal Artery Occlusion

Heterozygous loss of Six5 in mice is sufficient to cause ocular cataracts

Spectrum and Frequency of FZD4 Mutations in Familial Exudative Vitreoretinopathy

Corneal Transduction to Inhibit Angiogenesis and Graft Failure

A novel mutation in the Norrie disease gene

Isolation and characterization of the human homeobox gene HOX D1

Evaluation of a novel short polyadenylation signal as an alternative to the SV40 polyadenylation signal

An unusual clinical phenotype of avellino corneal dystrophy associated with an Arg124His βiG-H3 mutation in an African-American woman

An unusual clinical phenotype of Avellino corneal dystrophy associated with an Arg124His βig H3 mutation in an African-American woman

Localization of the gene encoding human phosphatidylinositol transfer protein (PITPN) to 17p13.3: a gene showing homology to the Drosophila retinal degeneration B gene (rdgB)

DNA-based diagnosis of the von Hippel–Lindau syndrome

Exclusion of candidate genetic loci for Duane retraction syndrome

Sequence and Evolution of the Blue Cone Pigment Gene in Old and New World Primates

Efficient and sustained trans gene expression in human corneal cells mediated by a lentiviral vector

Localisation of the human blue cone pigment gene to chromosome band 7q31.3-32

Electronegative electroretinogram in mucolipidosis IV

Clinical phenotype associated with the arg141 his mutation in the X-linked retinoschisis gene

Designed and tailor-made double hydrophilic block copolymer-graphene nanoplatelet hybrids for reinforcing epoxy thermosets

Role of Polyethylene Glycol as a Catalyst and a Filler in Epoxy Systems

Graphene oxide as multi-functional initiator and effective molecular reinforcement in PVP/epoxy composites

Modelling of the Rheological Behaviour of Epoxy-Polyethylene Glycol-1000 Blends

Suchergebnisse filtern