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Research 451–480 of 1000+
- Advancements in hydrogel-based design and applications of hair follicle organoids
- Hoxc13 polyglycine repeat gain-of-function drives mammalian integument evolution by altering targeted genes and interactions
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- From basic biology to engineered therapies: the keratinocyte stem cell playbook
- Hair shaft disorders
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- A rare case of chronic genian fistula with oral mucosal hair follicle inclusion: case report and review of the literature
- Synergizing biomaterials and cellular molecular pathways: a new frontier in hair follicle generation
- An Uncontrolled Innovative Test of Cryo-Chilled Carbon Dioxide as A Novel Amplification of a Nano-Botanical Multi-Acting Therapy in Advanced Stage Androgenetic Alopecia (Aga)
- Hair Shaft Fracture in a Young Athlete: A Rare Case Report of Acquired Trichorrhexis Nodosa
- Evaluating the Role of Thyroid Stimulating Hormone and Ferritin Levels with Hair Loss among Patients with COVID-19: Case-Control Study
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Hair shaft disorders: a rare case series
- Alopecia Areata: Current Review
- Inherited Epidermolysis Bullosa: A Clinical Case
- WNT10B (wingless-type MMTV integration site family)
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Hair Loss in Children
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- Autoimmune polyendocrine syndrome type 1 a case report from Bangladesh
- Alopecia Areata and Medical Modulation of the Intrinsic Property of Melanin to Transform Light Into Chemical Energy Through the Water Dissociation
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Clinical Management in Psychodermatology
- PHILADELPHIA DERMATOLOGICAL SOCIETY
- Generation of an integration-free human induced pluripotent stem cell line MUSIi010-A from occipital scalp fibroblasts of a male patient with androgenetic alopecia
- LITERATURE REVIEW