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Research 30 of 45
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Current Genetics in Hair Diseases
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Clouston’s syndrome: a rare case report
- Defining stem cell dynamics and migration during wound healing in mouse skin epidermis
- Stem cell dynamics, migration and plasticity during wound healing
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Congenital hair loss disorders: Rare, but not too rare
- Molecular pathology of skin adnexal tumours
- Gap junctions in Turing-type periodic feather pattern formation
- Transcriptomics analysis reveals molecular alterations underpinning spaceflight dermatology
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Inherited Disorders of the Hair
- Regenerative potential of CD200- subpopulations of hair follicle bulge
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- 9. Immunology and Genetics
- Additional file 12 of Time-course RNA-seq analysis reveals stage-specific and melatonin-triggered gene expression patterns during the hair follicle growth cycle in Capra hircus
- Genetic hair and nail disorders
- An Integrated Transcriptome Atlas of Embryonic Hair Follicle Progenitors, Their Niche, and the Developing Skin
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- m6A Methylation Analysis of Differentially Expressed Genes in Skin Tissues of Coarse and Fine Type Liaoning Cashmere Goats
- Defining the Cellular Environment in the Organ of Corti following Extensive Hair Cell Loss: A Basis for Future Sensory Cell Replacement in the Cochlea
- Genetic Hair Disorders: A Review