UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 1.183

Sortiert nach

032 DNA based prenatal diagnosis of recessive dystrophic epidermolysis bullosa: first successful application in a Japanese family

Journal of dermatological science, 1995-07, Vol.10 (1), p.68-68

1995

Link zum Volltext

Verfügbarkeit prüfen

044 Metatranscriptomics reveals association of α-, β-, and γ-HPVs with typical epidermodysplasia verruciformis in a large cohort of patients with CIB1, TMC6, or TMC8 mutations

Journal of investigative dermatology, 2022-12, Vol.142 (12), p.S188-S188

2022

Link zum Volltext

Verfügbarkeit prüfen

053 Novel mutations in the LAMB3 gene in two Japanese families with Herlitz junctional epidermolysis bullosa and their application for prenatal diagnosis

Journal of dermatological science, 1997-08, Vol.15 (2), p.111-111

1997

Link zum Volltext

Verfügbarkeit prüfen

054 Variable expression of plectin epitopes in patients with epidermolysis bullosa simplex associated with muscular dystrophy (EBS/MD)

Journal of dermatological science, 1997-08, Vol.15 (2), p.111-111

1997

Link zum Volltext

Verfügbarkeit prüfen

055 Whole-transcriptome Sequencing-Based Profiling of the Cutaneous Virome in Patients with Secondary Immunodeficiency

Journal of investigative dermatology, 2022-12, Vol.142 (12), p.S190-S190

2022

Link zum Volltext

Verfügbarkeit prüfen

064 Quantitative RT-PCR study for the effect of TGF-β1 on the 230kDa bullous pemphigoid antigen (BPAG1) gene expression in human keratinocytes

Journal of dermatological science, 1996-06, Vol.12 (2), p.192-192

1996

Link zum Volltext

Verfügbarkeit prüfen

067 cDNA cloning of the mouse homologue of the linear IgA disease antigen gene

Journal of dermatological science, 1996-06, Vol.12 (2), p.193-193

1996

Link zum Volltext

Verfügbarkeit prüfen

068 Characteristic immunohistochemical and ultrastructural features of Kindler's syndrome distinguishing it from dystrophic epidermolysis bullosa

Journal of dermatological science, 1996-06, Vol.12 (2), p.193-193

1996

Link zum Volltext

Verfügbarkeit prüfen

098 Differential molecular mechanism for down-regulation of the 230kDa bullous pemphigoid antigen (bpag1) gene expression by interferon-gamma (IFN-γ) and transforming growth factor beta (TGF-β)

Journal of dermatological science, 1995-07, Vol.10 (1), p.79-79

1995

Link zum Volltext

Verfügbarkeit prüfen

1103 SCLERODERMA-LIKE SYNDROME AND THE NON-ENZYMATIC GLUCOSYLATION OF COLLAGEN IN CHILDREN WITH POORLY CONTROLLED INSULIN DEPENDENT DIABETES (IDDM)

Pediatric research, 1981-04, Vol.15, p.626-626

1981

Link zum Volltext

Verfügbarkeit prüfen

141 Potential consequences of the interaction of squamous cell carcinoma cells with EDA fibronectin in recessive dystrophic epidermolysis bullosa

Journal of investigative dermatology, 2018-05, Vol.138 (5), p.S24-S24

2018

Link zum Volltext

Verfügbarkeit prüfen

157 Efficacy and mechanism of amlexanox for potential treatment of recessive dystrophic epidermolysis bullosa

Journal of investigative dermatology, 2016-09, Vol.136 (9), p.S187-S187

2016

Link zum Volltext

Verfügbarkeit prüfen

159 PASH syndrome is not a genetically distinct entity but belongs to the spectrum of autoinflammatory skin phenotypes

Journal of investigative dermatology, 2016-09, Vol.136 (9), p.S188-S188

2016

Link zum Volltext

Verfügbarkeit prüfen

160 A novel rapid, and sensitive method for evaluating compounds offering protection against cutaneous photodamage

Journal of dermatological science, 1996-06, Vol.12 (2), p.208-208

1996

Link zum Volltext

Verfügbarkeit prüfen

160 Demonstration of the critical role of the liver in systemic PPi homeostasis using a novel Abcc6 knockout rat model of PXE

Journal of investigative dermatology, 2016-09, Vol.136 (9), p.S188-S188

2016

Link zum Volltext

Verfügbarkeit prüfen

164 ENPP1 variants in patients with GACI and PXE: Genotype/phenotype overlap of heritable disorders with ectopic mineralization

Journal of investigative dermatology, 2021-05, Vol.141 (5), p.S29

2021

Link zum Volltext

Verfügbarkeit prüfen

166 Functional characterization of missense variants in ABCC6, the gene responsible for pseudoxanthoma elasticum

Journal of investigative dermatology, 2021-05, Vol.141 (5), p.S29

2021

Link zum Volltext

Verfügbarkeit prüfen

167 INZ-701 prevents ectopic mineralization in an Abcc6 mouse model of pseudoxanthoma elasticum

Journal of investigative dermatology, 2021-05, Vol.141 (5), p.S30

2021

Link zum Volltext

Verfügbarkeit prüfen

172 Inherited STK4/MST1 deficiency in two unrelated families with atypical epidermodysplasia verruciformis

Journal of investigative dermatology, 2021-05, Vol.141 (5), p.S30

2021

Link zum Volltext

Verfügbarkeit prüfen

174 Knock-down of SDR9C7 impairs epidermal barrier function

Journal of investigative dermatology, 2021-05, Vol.141 (5), p.S31

2021

Link zum Volltext

Verfügbarkeit prüfen

176 A distinct cutaneous blistering phenotype with multi-system manifestations caused by a mutation in CD151, the 20th causative gene in epidermolysis bullosa

Journal of investigative dermatology, 2017-10, Vol.137 (10), p.S223-S223

2017

Link zum Volltext

Verfügbarkeit prüfen

179 Systemic administration of HMGB1 peptide drastically improves survival of the RDEB model mice by mobilizing multipotent stem/progenitor cells from bone marrow

Journal of investigative dermatology, 2017-10, Vol.137 (10), p.S223-S223

2017

Link zum Volltext

Verfügbarkeit prüfen

180-kD bullous pemphigoid antigen/type XVII collagen: Tissue-specific expression and molecular interactions with keratin 18

Journal of cellular biochemistry, 1999-03, Vol.72 (3), p.356-367

1999

Link zum Volltext

Verfügbarkeit prüfen

184 Whole-transcriptome analysis by RNA-Seq for genetic diagnosis of Mendelian skin disorders in the context of consanguinity

Journal of investigative dermatology, 2021-05, Vol.141 (5), p.S32

2021

Link zum Volltext

Verfügbarkeit prüfen

185 GJB2 mutations in patients with ichthyosis follicularis and histopathology of porokeratotic adnexal ostial nevus

Journal of investigative dermatology, 2021-05, Vol.141 (5), p.S33

2021

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 1.183

Suche als RSS-Feed

Aktive Filter

ThemaGenetics

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(1.029)
Mit Volltextzugriff
(1.020)

Publikationsform

2 weitere anzeigen...

Weniger anzeigen...

Sprache

Englisch
(1.176)
Japanisch
(182)
Finnisch
(3)
Französisch
(2)
Deutsch
(2)

Erscheinungsjahr

n.n

Thema

Humans
(669)
Science & Technology
(656)
Life Sciences & Biomedicine
(634)
Biological And Medical Sciences
(380)
Dermatology
(351)
Medical Sciences
(286)
Animals
(220)
Male
(217)
Female
(209)
Adult
(161)
Cells, Cultured
(161)
Molecular Sequence Data
(137)
Collagen - Genetics
(123)
Mutation
(121)
Base Sequence
(118)
Biochemistry & Molecular Biology
(111)
Fundamental And Applied Biological Sciences. Psychology
(99)
Cell Biology
(97)
Middle Aged
(95)
Pedigree
(94)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

032 DNA based prenatal diagnosis of recessive dystrophic epidermolysis bullosa: first successful application in a Japanese family

044 Metatranscriptomics reveals association of α-, β-, and γ-HPVs with typical epidermodysplasia verruciformis in a large cohort of patients with CIB1, TMC6, or TMC8 mutations

053 Novel mutations in the LAMB3 gene in two Japanese families with Herlitz junctional epidermolysis bullosa and their application for prenatal diagnosis

054 Variable expression of plectin epitopes in patients with epidermolysis bullosa simplex associated with muscular dystrophy (EBS/MD)

055 Whole-transcriptome Sequencing-Based Profiling of the Cutaneous Virome in Patients with Secondary Immunodeficiency

064 Quantitative RT-PCR study for the effect of TGF-β1 on the 230kDa bullous pemphigoid antigen (BPAG1) gene expression in human keratinocytes

067 cDNA cloning of the mouse homologue of the linear IgA disease antigen gene

068 Characteristic immunohistochemical and ultrastructural features of Kindler's syndrome distinguishing it from dystrophic epidermolysis bullosa

098 Differential molecular mechanism for down-regulation of the 230kDa bullous pemphigoid antigen (bpag1) gene expression by interferon-gamma (IFN-γ) and transforming growth factor beta (TGF-β)

1103 SCLERODERMA-LIKE SYNDROME AND THE NON-ENZYMATIC GLUCOSYLATION OF COLLAGEN IN CHILDREN WITH POORLY CONTROLLED INSULIN DEPENDENT DIABETES (IDDM)

141 Potential consequences of the interaction of squamous cell carcinoma cells with EDA fibronectin in recessive dystrophic epidermolysis bullosa

157 Efficacy and mechanism of amlexanox for potential treatment of recessive dystrophic epidermolysis bullosa

159 PASH syndrome is not a genetically distinct entity but belongs to the spectrum of autoinflammatory skin phenotypes

160 A novel rapid, and sensitive method for evaluating compounds offering protection against cutaneous photodamage

160 Demonstration of the critical role of the liver in systemic PPi homeostasis using a novel Abcc6 knockout rat model of PXE

164 ENPP1 variants in patients with GACI and PXE: Genotype/phenotype overlap of heritable disorders with ectopic mineralization

166 Functional characterization of missense variants in ABCC6, the gene responsible for pseudoxanthoma elasticum

167 INZ-701 prevents ectopic mineralization in an Abcc6 mouse model of pseudoxanthoma elasticum

172 Inherited STK4/MST1 deficiency in two unrelated families with atypical epidermodysplasia verruciformis

174 Knock-down of SDR9C7 impairs epidermal barrier function

176 A distinct cutaneous blistering phenotype with multi-system manifestations caused by a mutation in CD151, the 20th causative gene in epidermolysis bullosa

179 Systemic administration of HMGB1 peptide drastically improves survival of the RDEB model mice by mobilizing multipotent stem/progenitor cells from bone marrow

180-kD bullous pemphigoid antigen/type XVII collagen: Tissue-specific expression and molecular interactions with keratin 18

184 Whole-transcriptome analysis by RNA-Seq for genetic diagnosis of Mendelian skin disorders in the context of consanguinity

185 GJB2 mutations in patients with ichthyosis follicularis and histopathology of porokeratotic adnexal ostial nevus

Aktive Filter

Suchergebnisse filtern