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Research 31–60 of 1000+
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Congenital hair loss disorders: Rare, but not too rare
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Nucleating agent solves a packaging problem
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Male fertility and skin diseases
- Molecular basis of androgen insensitivity
- Female Adolescent Hair Disorders
- ALOPECIA AREATA IN INFANTS: IS IT UNCOMMON?
- Hair loss in women
- Ectodermal Dysplasia: Variable Expressions
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Central Centrifugal Cicatricial Alopecia in the Adolescent Population: An Overview of Available Literature
- E-Poster
- Follicular and Scarring Disorders in Skin of Color: Presentation and Management
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Prostate volume and its relationship with anthropometric variables among different ethnic groups of South-Kivu, DR Congo
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Genetic Basis of Male Pattern Baldness
- A Study on the Pattern of Genetic Inheritance of Polycystic Ovarian Syndrome
- Characterization of Hair Follicle Antigens Targeted by the Anti-Hair Follicle Immune Response
- Analysis of hidradenitis suppurativa–linked mutations in four genes and the effects of PSEN1-P242LfsX11 on cytokine and chemokine expression in macrophages
- Sanhuang Fukang oil alleviates X-ray-induced skin injury by reducing inflammation and apoptosis: an in vivo study
- A Tale of Two Haplotypes: The EDA2R/AR Intergenic Region is the Most Divergent Genomic Segment between Africans and East Asians in the Human Genome
- 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.