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Research 271–300 of 1000+
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Keratinocytes and Associates With the Intermediate Filament Protein Cytokeratin 17
- Bone marrow-derived vasculogenesis leads to scarless regeneration in deep wounds with periosteal defects
- Symposium Proceedings of the 4th Intercontinental Meeting of Hair Research Societies: “The World of Hair 2004”
- Adipose-derived stem cells applied in skin diseases, wound healing and skin defects: a review
- Keratin 17 modulates hair follicle cycling in a TN<i>Fα</i>-dependent fashion
- ARHGEF3 Regulates Hair Follicle Morphogenesis
- Biotinidase deficiency characterized by skin and hair findings
- Signaling pathways in hair aging
- 376 Tsc2 disruption in mesenchymal progenitors regulates hair follicles and TGF beta signaling
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Trichorrhexis Invaginata and Netherton’s Syndrome
- Masquerading of trichotillomania in a family with monilethrix
- A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?
- Inducible deletion of epidermal <i>Dicer</i> and <i>Drosha</i> reveals multiple functions for miRNAs in postnatal skin
- Inducible expression of gasdermin A3 in the epidermis causes epidermal hyperplasia and skin inflammation
- Tricorrexis nudosa localizada por aplicación compulsiva de minoxidil
- Epidermal differentiation: The role of proteases and their inhibitors
- Adverse Effects and Safety of 5-alpha Reductase Inhibitors (Finasteride, Dutasteride): A Systematic Review.
- Alopezien und Hypotrichosen im Kindesalter
- Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report
- Alopecia Areata with Renal Dysgenesis
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Monilethrix – Case report of a rare disease
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Claves diagnósticas en displasias pilosas II
- 092 Novel biallelic RIPK4 mutations cause ectodermal dysplasia with cutaneous syndactyly
- Proliferative and Non-Proliferative Lesions of the Rat and Mouse Integument