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Research 31–60 of 59
- 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
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Genetics of Inherited Ichthyoses and Related Diseases
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Identification of skin-expressed genes possibly associated with wool growth regulation of Aohan fine wool sheep
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- New developments in the molecular treatment of ichthyosis: review of the literature
- The Role of Nrf2 in Hearing Loss
- Evidence on Hidradenitis Suppurativa as an Autoinflammatory Skin Disease
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Hair follicles modulate skin barrier function
- Histological and Gene Expression Analysis of the Effects of Menopause Status and Hormone Therapy on the Vaginal Introitus and Labia Majora
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Developmentally regulated expression of integrin alpha-6 distinguishes neural crest derivatives in the skin
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Low fucosylation defines the glycocalyx of progenitor cells and melanocytes in the human limbal stem cell niche
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Multi-omics analysis unveils the role of cancer-associated fibroblasts in cutaneous squamous cell carcinoma
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Author response: Hair follicle epidermal stem cells define a niche for tactile sensation
- Decision letter: Hair follicle epidermal stem cells define a niche for tactile sensation
- Genetics
- Molecular Genetics of Human Hair Diseases
- Transcriptome Profiling of Pilosebaceous Units in Male Androgenetic Alopecia Reveals Altered Junctional Networks
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient