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Research 481–510 of 1000+
- The Rho GTPase exchange factor Vav2 promotes extensive age-dependent rewiring of the hair follicle stem cell transcriptome
- Identification of immune microenvironment changes, immune-related pathways and genes in male androgenetic alopecia
- Meeting Report: 68th Montagna Symposium on the Biology of Skin “Decoding Complex Skin Diseases: Integrating Genetics, Genomics, and Disease Biology”
- Transcriptome Profiling of Pilosebaceous Units in Male Androgenetic Alopecia Reveals Altered Junctional Networks
- Exosomal Micro RNAs Derived from Dermal Papilla Cells Mediate Hair Follicle Stem Cell Proliferation and Differentiation
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Prevention of Male Late-Onset Hypogonadism by Natural Polyphenolic Antioxidants
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- GWASs Identify Genetic Loci Associated with Human Scalp Hair Whorl Direction
- Molecular Evolution and Protein Structure Variation of Dkk Family
- Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies
- Diseases of the Canine Prostate Gland
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Atypical presentation of Acrodermatitis enteropathica in a child: later onset with life-threatening severe extensive dermatitis and septic shock
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- The role of hsa‐miR‐193a‐5p as an important factor for control of inositol in alopecia areata
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- Fibrotic enzymes modulate wound‐induced skin tumorigenesis
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway