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Research 31–60 of 44
- Defining the Cellular Environment in the Organ of Corti following Extensive Hair Cell Loss: A Basis for Future Sensory Cell Replacement in the Cochlea
- 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
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Molecular pathology of skin adnexal tumours
- Regenerative potential of CD200- subpopulations of hair follicle bulge
- Gap junctions in Turing-type periodic feather pattern formation
- Stem cell dynamics, migration and plasticity during wound healing
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Sox21 Regulates Anapc10 Expression and Determines the Fate of Ectodermal Organ
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Multi-omics analysis unveils the role of cancer-associated fibroblasts in cutaneous squamous cell carcinoma
- eLife assessment: Decoding the complexity of delayed wound healing following Enterococcus faecalis infection
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- 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
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- 9. Immunology and Genetics
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Congenital hair loss disorders: Rare, but not too rare
- Molecular Genetics of Human Hair Diseases
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Genetic hair and nail disorders
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Genetic Hair Disorders: A Review