UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Prevalence, pathophysiology and management of itch in epidermolysis bullosa

British journal of dermatology (1951), 2021-05, Vol.184 (5), p.816-825

2021

Volltextzugriff (PDF)

Fibroblast cell therapy enhances initial healing in recessive dystrophic epidermolysis bullosa wounds: results of a randomized, vehicle-controlled trial

British journal of dermatology (1951), 2013-11, Vol.169 (5), p.1025-1033

2013

Volltextzugriff (PDF)

The role of fibroblasts in tissue engineering and regeneration

British journal of dermatology (1951), 2007-06, Vol.156 (6), p.1149-1155

2007

Volltextzugriff (PDF)

Immune tolerance of allogeneic haematopoietic cell transplantation supports donor epidermal grafting of recessive dystrophic epidermolysis bullosa chronic wounds

British journal of dermatology (1951), 2021-06, Vol.184 (6), p.1161-1169

2021

Volltextzugriff (PDF)

Revertant mosaic fibroblasts in recessive dystrophic epidermolysis bullosa

British journal of dermatology (1951), 2019-12, Vol.181 (6), p.1247-1253

2019

Volltextzugriff (PDF)

PM exposure variations due to different time activity profile simulations within a single dwelling

Building and environment, 2017-05, Vol.116, p.55-63

2017

Volltextzugriff (PDF)

The role of kindlins in cell biology and relevance to human disease

The international journal of biochemistry & cell biology, 2010-05, Vol.42 (5), p.595-603

2010

Volltextzugriff (PDF)

Kindler syndrome: a focal adhesion genodermatosis

British journal of dermatology (1951), 2009-02, Vol.160 (2), p.233-242

2009

Volltextzugriff (PDF)

Whole-exome sequencing diagnosis of two autosomal recessive disorders in one family

British journal of dermatology (1951), 2015-05, Vol.172 (5), p.1407-1411

2015

Volltextzugriff (PDF)

Matrix metalloproteinase-7 activates heparin-binding epidermal growth factor-like growth factor in cutaneous squamous cell carcinoma

British journal of dermatology (1951), 2010-10, Vol.163 (4), p.726-735

2010

Volltextzugriff (PDF)

Founder mutation in dystonin-e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait

British journal of dermatology (1951), 2015-02, Vol.172 (2), p.527-531

2015

Volltextzugriff (PDF)

Skin differences based on age and chronicity of ultraviolet exposure: results from a gene expression profiling study

British journal of dermatology (1951), 2012-06, Vol.166 (s2), p.9-15

2012

Volltextzugriff (PDF)

Stem cell therapies for recessive dystrophic epidermolysis bullosa

British journal of dermatology (1951), 2010-12, Vol.163 (6), p.1149-1156

2010

Volltextzugriff (PDF)

Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis

British journal of dermatology (1951), 2015-11, Vol.173 (5), p.1291-1294

2015

Volltextzugriff (PDF)

299 High efficiency and safe base editor correction of recurrent COL7A1 mutations underlying dominant dystrophic epidermolysis bullosa

Journal of investigative dermatology, 2022-12, Vol.142 (12), p.S231-S231

2022

Volltextzugriff (PDF)

Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility

British journal of dermatology (1951), 2020-10, Vol.183 (4), p.614-627

2020

Volltextzugriff (PDF)

823 Methotrexate improves pruritus in patients with recessive dystrophic epidermolysis bullosa

Journal of investigative dermatology, 2023-05, Vol.143 (5), p.S141-S141

2023

Volltextzugriff (PDF)

A novel mutation in the VDR gene in hereditary vitamin D-resistant rickets

British journal of dermatology (1951), 2008-01, Vol.158 (1), p.168-171

2008

Volltextzugriff (PDF)

Development and successful clinical application of preimplantation genetic haplotyping for Herlitz junctional epidermolysis bullosa

British journal of dermatology (1951), 2010-06, Vol.162 (6), p.1330-1336

2010

Volltextzugriff (PDF)

206 KLICK syndrome is a hyperproliferative inflammatory skin disorder

Journal of investigative dermatology, 2022-12, Vol.142 (12), p.S215-S215

2022

Volltextzugriff (PDF)

283 Optimising specificity and applicability of base editing for COL7A1 mutations in recessive dystrophic epidermolysis bullosa

Journal of investigative dermatology, 2022-12, Vol.142 (12), p.S229-S229

2022

Volltextzugriff (PDF)

Mutations in genes encoding desmosomal proteins: spectrum of cutaneous and extracutaneous abnormalities

British journal of dermatology (1951), 2021-04, Vol.184 (4), p.596-605

2021

Volltextzugriff (PDF)

Acantholytic ectodermal dysplasia: clinicopathological study of a new desmosomal disorder

British journal of dermatology (1951), 2009-04, Vol.160 (4), p.868-874

2009

Volltextzugriff (PDF)

Heterozygous Mutation in the SAM Domain of p63 Underlies Rapp-Hodgkin Ectodermal Dysplasia

Journal of dental research, 2003-06, Vol.82 (6), p.433-437

2003

Volltextzugriff (PDF)

LB1779 Optimization of RDEB patient-derived induced pluripotent stem cell (iPSC) differentiation into keratinocytes and fibroblasts

Journal of investigative dermatology, 2023-09, Vol.143 (9), p.B32

2023

Volltextzugriff (PDF)

1 – 25 von 321

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(288)
Mit Volltextzugriff
(312)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Prevalence, pathophysiology and management of itch in epidermolysis bullosa

Fibroblast cell therapy enhances initial healing in recessive dystrophic epidermolysis bullosa wounds: results of a randomized, vehicle-controlled trial

The role of fibroblasts in tissue engineering and regeneration

Immune tolerance of allogeneic haematopoietic cell transplantation supports donor epidermal grafting of recessive dystrophic epidermolysis bullosa chronic wounds

Revertant mosaic fibroblasts in recessive dystrophic epidermolysis bullosa

PM exposure variations due to different time activity profile simulations within a single dwelling

The role of kindlins in cell biology and relevance to human disease

Kindler syndrome: a focal adhesion genodermatosis

Whole-exome sequencing diagnosis of two autosomal recessive disorders in one family

Matrix metalloproteinase-7 activates heparin-binding epidermal growth factor-like growth factor in cutaneous squamous cell carcinoma

Founder mutation in dystonin-e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait

Skin differences based on age and chronicity of ultraviolet exposure: results from a gene expression profiling study

Stem cell therapies for recessive dystrophic epidermolysis bullosa

Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis

299 High efficiency and safe base editor correction of recurrent COL7A1 mutations underlying dominant dystrophic epidermolysis bullosa

Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility

823 Methotrexate improves pruritus in patients with recessive dystrophic epidermolysis bullosa

A novel mutation in the VDR gene in hereditary vitamin D-resistant rickets

Development and successful clinical application of preimplantation genetic haplotyping for Herlitz junctional epidermolysis bullosa

206 KLICK syndrome is a hyperproliferative inflammatory skin disorder

283 Optimising specificity and applicability of base editing for COL7A1 mutations in recessive dystrophic epidermolysis bullosa

Mutations in genes encoding desmosomal proteins: spectrum of cutaneous and extracutaneous abnormalities

Acantholytic ectodermal dysplasia: clinicopathological study of a new desmosomal disorder

Heterozygous Mutation in the SAM Domain of p63 Underlies Rapp-Hodgkin Ectodermal Dysplasia

LB1779 Optimization of RDEB patient-derived induced pluripotent stem cell (iPSC) differentiation into keratinocytes and fibroblasts

Suchergebnisse filtern