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Research 151–180 of 810
- Histological and molecular restoration of type VII collagen in Recessive dystrophic epidermolysis bullosa mouse skin by topical injection of keratinocyte-like cells differentiated from human adipose-derived mesenchymal stromal cells
- Junctional Epidermolysis Bullosa, Generalized Intermediate Type
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield
- 0873 Modeling junctional epidermolysis bullosa using tissue-engineered skin substitutes
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- The epidermis: rising to the surface
- Transplantation of autologous single hair units heals chronic wounds in autosomal recessive dystrophic epidermolysis bullosa: A proof-of-concept study
- Genetic hair and nail disorders
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Characterization of the epidermal-dermal junction in hiPSC-derived skin organoids
- Whole-genome resequencing to investigate the genetic diversity and the molecular basis underlying key economic traits in indigenous sheep breeds adapted to hypoxic environments
- Industry Updates from the Field of Stem Cell Research and Regenerative Medicine in December 2019
- Life before and beyond blistering: The role of collagen XVII in epidermal physiology
- Author response: Type XVII collagen coordinates proliferation in the interfollicular epidermis
- Decision letter: Type XVII collagen coordinates proliferation in the interfollicular epidermis
- Cell-Type-Specific Chromatin States Differentially Prime Squamous Cell Carcinoma Tumor-Initiating Cells for Epithelial to Mesenchymal Transition
- High-confidence cancer patient stratification through multiomics investigation of DNA repair disorders
- Identification of an osteopontin-derived peptide that binds neuropilin-1 and activates vascular repair responses and angiogenesis
- Spatial Gene Profiling in the Ischemic Heart
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Collagen XVIIα1 in skin and hair aging: Mechanisms, stem cell niche regulation, and translational strategies
- The stiffness of the extracellular matrix is a key factor in tumor progression
- Analysis of the abnormal human hair keratins by two-dimensional polyacrylamide gel electrophoresis
- Evaluation of Clinical and Oral Findings in Patients with Epidermolysis bullosa
- Biomedical engineering approaches for the delivery of JAGGED1 as a potential tissue regenerative therapy
- Nutritional Disorders of the Hair and Their Management
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Ernährungsstörungen des Haares und deren Management
- Ehlers-Danlos syndrome: From bedside to bench