UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 1.302

Sortiert nach

Ex vivo gene modification therapy for genetic skin diseases—recent advances in gene modification technologies and delivery

Experimental dermatology, 2021-07, Vol.30 (7), p.887-896

2021

Volltextzugriff (PDF)

Persistent kallikrein 5 activation induces atopic dermatitis-like skin architecture independent of PAR2 activity

Journal of allergy and clinical immunology, 2017-11, Vol.140 (5), p.1310-1322.e5

2017

Volltextzugriff (PDF)

Tissue Kallikrein Inhibitors Based on the Sunflower Trypsin Inhibitor Scaffold - A Potential Therapeutic Intervention for Skin Diseases

PloS one, 2016-11, Vol.11 (11), p.e0166268-e0166268

2016

Volltextzugriff (PDF)

Inflammatory Skin and Bowel Disease Linked to ADAM17 Deletion

The New England journal of medicine, 2011-10, Vol.365 (16), p.1502-1508

2011

Volltextzugriff (PDF)

Generation and Clinical Application of Gene-Modified Autologous Epidermal Sheets in Netherton Syndrome: Lessons Learned from a Phase 1 Trial

Human gene therapy, 2019-09, Vol.30 (9), p.1067

2019

Volltextzugriff (PDF)

A mechanistic target of rapamycin complex 1/2 (mTORC1)/V-Akt murine thymoma viral oncogene homolog 1 (AKT1)/cathepsin H axis controls filaggrin expression and processing in skin, a novel mechanism for skin barrier disruption in patients with atopic dermatitis

Journal of allergy and clinical immunology, 2017-04, Vol.139 (4), p.1228-1241

2017

Volltextzugriff (PDF)

Short-Term Treatment with Rho-Associated Kinase Inhibitor Preserves Keratinocyte Stem Cell Characteristics In Vitro

Cells (Basel, Switzerland), 2023-01, Vol.12 (3), p.346

2023

Volltextzugriff (PDF)

Case Report: ISG15 deficiency caused by novel variants in two families and effective treatment with Janus kinase inhibition

Frontiers in immunology, 2023-12, Vol.14, p.1287258-1287258

2023

Volltextzugriff (PDF)

Cytosine Deaminase Base Editing to Restore COL7A1 in Dystrophic Epidermolysis Bullosa Human: Murine Skin Model

JID innovations, 2023-05, Vol.3 (3), p.100191-100191, Article 100191

2023

Volltextzugriff (PDF)

Efficient CRISPR-Cas9-Mediated Gene Ablation in Human Keratinocytes to Recapitulate Genodermatoses: Modeling of Netherton Syndrome

Molecular therapy. Methods & clinical development, 2020-09, Vol.18, p.280-290

2020

Volltextzugriff (PDF)

Selection of reference genes for RT-qPCR analysis of Phenacoccus solenopsis (Hemiptera: Pseudococcidae) sex-dimorphic development

Journal of Integrative Agriculture, 2019-04, Vol.18 (4), p.854-864

2019

Volltextzugriff (PDF)

New Role for LEKTI in Skin Barrier Formation: Label-Free Quantitative Proteomic Identification of Caspase 14 as a Novel Target for the Protease Inhibitor LEKTI

Journal of proteome research, 2010-08, Vol.9 (8), p.4289-4294

2010

Volltextzugriff (PDF)

Human Mesenchymal Stromal Cells Engineered to Express Collagen VII Can Restore Anchoring Fibrils in Recessive Dystrophic Epidermolysis Bullosa Skin Graft Chimeras

Journal of investigative dermatology, 2020-01, Vol.140 (1), p.121-131.e6

2020

Volltextzugriff (PDF)

Allele-Specific Small Interfering RNA Corrects Aberrant Cellular Phenotype in Keratitis-Ichthyosis-Deafness Syndrome Keratinocytes

Journal of investigative dermatology, 2020-05, Vol.140 (5), p.1035-1044.e7

2020

Volltextzugriff (PDF)

Sunflower trypsin inhibitor (SFTI-1) analogues of synthetic and biological origin via N→S acyl transfer: potential inhibitors of human Kallikrein-5 (KLK5)

Tetrahedron, 2014-10, Vol.70 (42), p.7675-7680

2014

Volltextzugriff (PDF)

Molecular Genetic Dissection of Inflammatory Linear Verrucous Epidermal Naevus Leads to Successful Targeted Therapy

Journal of investigative dermatology, 2021-12, Vol.141 (12), p.2979-2983.e1

2021

Volltextzugriff (PDF)

Feeding by Whiteflies Suppresses Downstream Jasmonic Acid Signaling by Eliciting Salicylic Acid Signaling

Journal of chemical ecology, 2013-05, Vol.39 (5), p.612-619

2013

Volltextzugriff (PDF)

Connexin Mutations in Skin Disease and Hearing Loss

American journal of human genetics, 2001-03, Vol.68 (3), p.559-568

2001

Volltextzugriff (PDF)

Absence of γ-Chain in Keratinocytes Alters Chemokine Secretion, Resulting in Reduced Immune Cell Recruitment

Journal of investigative dermatology, 2017-10, Vol.137 (10), p.2120-2130

2017

Volltextzugriff (PDF)

Phase I study protocol for ex vivo lentiviral gene therapy for the inherited skin disease, Netherton syndrome

Human gene therapy. Clinical development, 2013-12, Vol.24 (4), p.182

2013

Volltextzugriff (PDF)

Expanding the scope of N → S acyl transfer in native peptide sequences

Organic & biomolecular chemistry, 2015-07, Vol.13 (27), p.7469-7476

2015

Volltextzugriff (PDF)

Lentiviral Engineered Fibroblasts Expressing Codon-Optimized COL7A1 Restore Anchoring Fibrils in RDEB

Journal of investigative dermatology, 2016-01, Vol.136 (1), p.284-292

2016

Volltextzugriff (PDF)

Ex-vivo Gene Therapy Restores LEKTI Activity and Corrects the Architecture of Netherton Syndrome-derived Skin Grafts

Molecular therapy, 2011-02, Vol.19 (2), p.408-416

2011

Volltextzugriff (PDF)

Safety and early efficacy outcomes for lentiviral fibroblast gene therapy in recessive dystrophic epidermolysis bullosa

JCI insight, 2019-06, Vol.4 (11)

2019

Volltextzugriff (PDF)

Inherited duplications of PPP2R3B predispose to nevi and melanoma via a C21orf91-driven proliferative phenotype

Genetics in medicine, 2021-09, Vol.23 (9), p.1636-1647

2021

Volltextzugriff (PDF)

1 – 25 von 1.302

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(1.103)
Mit Volltextzugriff
(1.217)

Publikationsform

2 weitere anzeigen...

Weniger anzeigen...

Sprache

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(892)
Life Sciences & Biomedicine
(516)
Humans
(278)
Physical Sciences
(270)
Technology
(239)
Chemistry
(164)
Animals
(150)
Male
(139)
Female
(130)
Engineering
(125)
Materials Science
(110)
Science & Technology - Other Topics
(101)
Materials Science, Multidisciplinary
(93)
Physics
(88)
Adult
(84)
Middle Aged
(82)
Chemistry, Multidisciplinary
(76)
Mice
(73)
Environmental Sciences & Ecology
(66)
Environmental Sciences
(64)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Ex vivo gene modification therapy for genetic skin diseases—recent advances in gene modification technologies and delivery

Persistent kallikrein 5 activation induces atopic dermatitis-like skin architecture independent of PAR2 activity

Tissue Kallikrein Inhibitors Based on the Sunflower Trypsin Inhibitor Scaffold - A Potential Therapeutic Intervention for Skin Diseases

Inflammatory Skin and Bowel Disease Linked to ADAM17 Deletion

Generation and Clinical Application of Gene-Modified Autologous Epidermal Sheets in Netherton Syndrome: Lessons Learned from a Phase 1 Trial

A mechanistic target of rapamycin complex 1/2 (mTORC1)/V-Akt murine thymoma viral oncogene homolog 1 (AKT1)/cathepsin H axis controls filaggrin expression and processing in skin, a novel mechanism for skin barrier disruption in patients with atopic dermatitis

Short-Term Treatment with Rho-Associated Kinase Inhibitor Preserves Keratinocyte Stem Cell Characteristics In Vitro

Case Report: ISG15 deficiency caused by novel variants in two families and effective treatment with Janus kinase inhibition

Cytosine Deaminase Base Editing to Restore COL7A1 in Dystrophic Epidermolysis Bullosa Human: Murine Skin Model

Efficient CRISPR-Cas9-Mediated Gene Ablation in Human Keratinocytes to Recapitulate Genodermatoses: Modeling of Netherton Syndrome

Selection of reference genes for RT-qPCR analysis of Phenacoccus solenopsis (Hemiptera: Pseudococcidae) sex-dimorphic development

New Role for LEKTI in Skin Barrier Formation: Label-Free Quantitative Proteomic Identification of Caspase 14 as a Novel Target for the Protease Inhibitor LEKTI

Human Mesenchymal Stromal Cells Engineered to Express Collagen VII Can Restore Anchoring Fibrils in Recessive Dystrophic Epidermolysis Bullosa Skin Graft Chimeras

Allele-Specific Small Interfering RNA Corrects Aberrant Cellular Phenotype in Keratitis-Ichthyosis-Deafness Syndrome Keratinocytes

Sunflower trypsin inhibitor (SFTI-1) analogues of synthetic and biological origin via N→S acyl transfer: potential inhibitors of human Kallikrein-5 (KLK5)

Molecular Genetic Dissection of Inflammatory Linear Verrucous Epidermal Naevus Leads to Successful Targeted Therapy

Feeding by Whiteflies Suppresses Downstream Jasmonic Acid Signaling by Eliciting Salicylic Acid Signaling

Connexin Mutations in Skin Disease and Hearing Loss

Absence of γ-Chain in Keratinocytes Alters Chemokine Secretion, Resulting in Reduced Immune Cell Recruitment

Phase I study protocol for ex vivo lentiviral gene therapy for the inherited skin disease, Netherton syndrome

Expanding the scope of N → S acyl transfer in native peptide sequences

Lentiviral Engineered Fibroblasts Expressing Codon-Optimized COL7A1 Restore Anchoring Fibrils in RDEB

Ex-vivo Gene Therapy Restores LEKTI Activity and Corrects the Architecture of Netherton Syndrome-derived Skin Grafts

Safety and early efficacy outcomes for lentiviral fibroblast gene therapy in recessive dystrophic epidermolysis bullosa

Inherited duplications of PPP2R3B predispose to nevi and melanoma via a C21orf91-driven proliferative phenotype

Suchergebnisse filtern