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Research 31–60 of 43
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Multi-omics analysis unveils the role of cancer-associated fibroblasts in cutaneous squamous cell carcinoma
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Defining stem cell dynamics and migration during wound healing in mouse skin epidermis
- Regenerative potential of CD200- subpopulations of hair follicle bulge
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- An Integrated Transcriptome Atlas of Embryonic Hair Follicle Progenitors, Their Niche, and the Developing Skin
- m6A Methylation Analysis of Differentially Expressed Genes in Skin Tissues of Coarse and Fine Type Liaoning Cashmere Goats
- Genetic analysis of a novel antioxidant multi-target iron chelator, M30 protecting against chemotherapy-induced alopecia in mice
- Integrated Meta-Analysis of Scalp Transcriptomics and Serum Proteomics Defines Alopecia Areata Subtypes and Core Disease Pathways
- Prediction of cell states and key transcription factors of the human cornea through integrated single-cell omics analyses
- eLife assessment: Decoding the complexity of delayed wound healing following Enterococcus faecalis infection
- Transcriptome Profiling of Pilosebaceous Units in Male Androgenetic Alopecia Reveals Altered Junctional Networks
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Current Genetics in Hair Diseases
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Clouston’s syndrome: a rare case report
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- 9. Immunology and Genetics
- Congenital hair loss disorders: Rare, but not too rare
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Painful thickened skin on the soles of the feet