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Research 61–90 of 1000+
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Histologic and Cell Kinetic Studies of Hair Loss and Subsequent Recovery Process of Human Scalp Hair Follicles Grafted onto Severe Combined Immunodeficient Mice
- Characterization of the epidermal-dermal junction in hiPSC-derived skin organoids
- Treatment and prevention of chemotherapy-induced alopecia with PTH-CBD, a collagen-targeted parathyroid hormone analog, in a non-depilated mouse model
- The Transient Role for Calcium and Vitamin D during the Developmental Hair Follicle Cycle
- Osseous Metaplasia and Mature Bone Formation With Extramedullary Hematopoiesis in Trichilemmal Cyst
- Mesenchymal Stem Cells for the Treatment of Skin Diseases
- A Comprehensive Literature Review of JAK Inhibitors in Treatment of Alopecia Areata
- Why Do Not All Chemotherapy Patients Lose Their Hair? Answering an Intriguing Question
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Effect of N-acetylcysteine on hair follicle changes in mouse model of cyclophosphamide-induced alopecia: histological and biochemical study
- AIRE Deficiency Leads to the Development of Alopecia Areata‒Like Lesions in Mice
- The dental needs of children with Epidermolysis Bullosa and service delivery: a scoping review
- Platelet-rich plasma, the ultimate secret for youthful skin elixir and hair growth triggering
- Evaluation of Clinical and Oral Findings in Patients with Epidermolysis bullosa
- 1457 CellutomeTM epidermal harvesting system and in vivo reflectance confocal microscopy as a novel wound healing assessment protocol
- Mechanisms of Impaired Skeletal Muscle Regeneration and Therapeutic Approaches in Aging and Chronic Disease
- POSTĘP W DIAGNOZIE I LECZENIU STWARDNIENIA ROZSIANEGO
- PŁYNY- NIE ZA DUŻO, NIE ZA MAŁO, LECZ W SAM RAZ
- Skin problems in the long‐distance runner 2500 years after the Battle of Marathon
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Recently Identified Forms of Epidermolysis Bullosa
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Generalized atrophic benign epidermolysis bullosa.
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Mediterranean Basin Erica Species: Traditional Uses, Phytochemistry and Pharmacological Properties
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis