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Research 31–60 of 72
- STUDY OF CUTANEOUS MANIFESTATIONS IN THYROID DISORDERS
- The human keratins: biology and pathology
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Keratins and skin disease
- A new type of pachyonychia congenita.
- Skin Cyst: A Pathological Dead-End With a New Twist of Morphogenetic Potentials in Organoid Cultures
- Pathologic Quiz Case: An 84-Year-Old Woman With a Skin Cyst Containing Ziehl-Neelsen–Positive Structures
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Resident’s Bag
- A descriptive study of alopecia patterns and their relation to thyroid dysfunction
- Painful thickened skin on the soles of the feet
- The investigation of insulin resistance and metabolic syndrome in male patients with early-onset androgenetic alopecia
- Dermoscopy of cutaneous adnexal tumours: a systematic review of the literature
- Folliculosebaceous Cystic Hamartoma with Spindle Cell Lipomatous and Neural Components
- Hair Matrix Cyst
- Calcified Epidermal Cyst on the Neck
- Defining pseudofolliculitis barbae in 2001: A review of the literature and current trends
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- The molecular basis of human keratin disorders
- The Two Functional Keratin 6 Genes of Mouse Are Differentially Regulated and Evolved Independently from Their Human Orthologs
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Type I Keratin 17 Protein Is Phosphorylated on Serine 44 by p90 Ribosomal Protein S6 Kinase 1 (RSK1) in a Growth- and Stress-dependent Fashion
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Sebaceous immunobiology - skin homeostasis, pathophysiology, coordination of innate immunity and inflammatory response and disease associations
- Hidradenitis Suppurativa and Comorbid Disorder Biomarkers, Druggable Genes, New Drugs and Drug Repurposing—A Molecular Meta-Analysis
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82