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Research 241–270 of 1000+
- Hair & Cutaneous Development
- Keratin Expression Provides Novel Insight into the Morphogenesis and Function of the Companion Layer in Hair Follicles
- Molecular Genetics of Human Hair Diseases
- Diseases of Hair
- Diseases of Hair
- Beyond the Epidermal-Melanin-Unit: The Human Scalp Anagen Hair Bulb Is Home to Multiple Melanocyte Subpopulations of Variable Melanogenic Capacity
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Hirsutism in the Adolescent Female
- Birth Outcomes of Infants Born to Mothers with Alopecia Areata: A Nationwide Population-based Study in Korea
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Exploring the role of Kantavallabha rasa in Polycystic ovarian syndrome management: A pilot Study
- Hyperplasia of the Subcutaneous Adipose Tissue Is the Primary Histopathologic Abnormality in Lipedematous Scalp
- ANDROGENETIC ALOPECIA
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- New clinico‐genetic classification of trichothiodystrophy
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Triangular temporal alopecia: a rare case in adulthood
- Transient treatment response of platelet-rich plasma injection for temporal triangular alopecia: A case report with dermoscopic examination follow-up
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Exploring Pediatric Dermatology in Skin of Color: Focus on Dermoscopy
- Collodion baby case series: the success of oral retinoic acid
- Minoxidil-induced hypertrichosis in a child with alopecia areata
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience