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Research 901–930 of 1000+
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Bachmann–Bupp syndrome and treatment
- Clinical case of alopecia totalis in pediatric practice
- Comparative Analysis of mRNA and miRNA Expression between Dermal Papilla Cells and Hair Matrix Cells of Hair Follicles in Yak
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- 865 Single-cell protein activity inference analysis of full-thickness skin uncovers novel pathways and a rare Arg1+ macrophage population in AA
- DataSheet1_Single-Cell Transcriptomics Reveals the Molecular Anatomy of Sheep Hair Follicle Heterogeneity and Wool Curvature.zip
- Re-discovery of Trichophyton bullosum in North Africa as a cause of severe dermatophytosis in donkeys
- Author response: Dynamics of nevus development implicate cell cooperation in the growth arrest of transformed melanocytes
- Meeting Report: 68th Montagna Symposium on the Biology of Skin “Decoding Complex Skin Diseases: Integrating Genetics, Genomics, and Disease Biology”
- The Case | Bilateral kidney tumors and lung cysts
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Metabolic disease with autoimmune phenomena: 2 cases of SLE-like disease in young children diagnosed with lysinuric protein intolerance
- Genetic analysis of the role of androgen metabolism in the pathogenesis of prostate cancer
- Bifidobacterium Is Enriched in Gut Microbiome of Kashmiri Women with Polycystic Ovary Syndrome
- Decoding Gut Microbiome Dysbiosis as a Non-Invasive Diagnostic Biomarker for Alopecia Areata
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- The Follicular Skin Microbiome in Patients With Hidradenitis Suppurativa and Healthy Controls
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- The Skin Microbiome: Current Landscape and Future Opportunities
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Recent advances in Forensic DNA Phenotyping of appearance, ancestry and age
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?