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Research 691–720 of 1000+
- Why Do Not All Chemotherapy Patients Lose Their Hair? Answering an Intriguing Question
- Pathological Skin Scarring: From Mechanism to Targeted Local Therapy
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Dissecting Cellulitis of the Scalp
- Epidermal differentiation: The role of proteases and their inhibitors
- High Flexible and Broad Antibacterial Nanodressing Induces Complete Skin Repair with Angiogenic and Follicle Regeneration
- Ornithine decarboxylase transgenic mice as a model for human atrichia with papular lesions
- AN UPDATE OF HAIR SHAFT DISORDERS
- A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- DNA phenotyping: current application in forensic science
- Wound repair at a glance
- Inhibition of Bmp signaling affects growth and differentiation in the anagen hair follicle
- Molecular Mechanisms Responsible for Therapeutic Potential of Mesenchymal Stem Cell-Derived Secretome
- Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.
- Basal cell carcinoma — molecular biology and potential new therapies
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
- Endocrine intervention for transsexuals
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- Involvement of the Edar Signaling in the Control of Hair Follicle Involution (Catagen)
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Assessment of the usefulness of dihydrotestosterone in the diagnostics of patients with androgenetic alopecia
- SKIN AND HAIR COSMETIC ISSUES IN WOMEN OF COLOR
- Gene Delivery to the Hair Follicle
- Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Pseudofolliculitis barbae; current treatment options