Search
for
Sort by
Research 31–60 of 45
- Sox21 Regulates Anapc10 Expression and Determines the Fate of Ectodermal Organ
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Genetic analysis of a novel antioxidant multi-target iron chelator, M30 protecting against chemotherapy-induced alopecia in mice
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- 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
- 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
- Painful thickened skin on the soles of the feet
- Molecular Genetics of Human Hair Diseases
- Transcriptome Profiling of Pilosebaceous Units in Male Androgenetic Alopecia Reveals Altered Junctional Networks
- 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