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Research 61–90 of 585
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- The molecular pathogenesis of Trichilemmal carcinoma
- Comprehensive Genomic Profiling of Cutaneous Adnexal Carcinomas: A Genomic Landscape Study
- A cross-sectional study of clinical, dermoscopic, histopathological, and molecular patterns of scalp melanoma in patients with or without androgenetic alopecia
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Restoration of Spermatogenesis and Male Fertility Using an Androgen Receptor Transgene
- Switching roles: the functional plasticity of adult tissue stem cells
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- <i>Hoxc13</i> mutant mice lack external hair
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Activated Kras Alters Epidermal Homeostasis of Mouse Skin, Resulting in Redundant Skin and Defective Hair Cycling
- Current Genetics in Hair Diseases
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- A kindred with mutant IKAROS and autoimmunity
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- An essential role for <i>Rxrα</i> in the development of Th2 responses
- Outcomes in Clinically Relevant Patient Subgroups From the EMBRACA Study: Talazoparib vs Physician’s Choice Standard-of-Care Chemotherapy
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Recently Identified Forms of Epidermolysis Bullosa
- Short-term Efficacy of Tofacitinib, a JAK Inhibitor, in IFIH1-related Aicardi-Goutières Syndrome
- <i>WNT10A</i> , dermatology and dentistry
- Fatal autoimmunity results from the conditional deletion of Snai2 and Snai3
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders