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Research 61–90 of 75
- The molecular basis of human keratin disorders
- 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
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- The Two Functional Keratin 6 Genes of Mouse Are Differentially Regulated and Evolved Independently from Their Human Orthologs
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- 1375 Cutaneous adnexal cysts revisited: A novel classification based on morphological and molecular features
- Expression of androgen receptors in skin appendage tumors: An immunohistochemical study
- Acne in children
- Cutaneous Hybrid Cyst in a Sprague-Dawley Rat
- 1371 FGF7-dependent inhibition of human hair growth byan osteopontin-derived peptide: A novel solution for hirsutism and hypertrichosis?
- Pattern of Skin disorders across age groups
- Proliferating Hybrid Follicular Tumor
- Immunohistochemical Study of Calretinin in Normal Skin and Cutaneous Adnexal Proliferations
- Steatocystoma Multiplex
- Steatocystomas: Update on Clinical Manifestations, Diagnosis, and Management
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Hidradenitis Suppurativa and Comorbid Disorder Biomarkers, Druggable Genes, New Drugs and Drug Repurposing—A Molecular Meta-Analysis
- Consensus on the use of oral isotretinoin in dermatology - Brazilian Society of Dermatology
- Beyond acne: Current aspects of sebaceous gland biology and function
- Acne
- Sebaceous immunobiology - skin homeostasis, pathophysiology, coordination of innate immunity and inflammatory response and disease associations
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Off-label uses of retinoids in dermatology
- Infections, Infestations and Neoplasms of the Scalp
- Acne Vulgaris
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
- Clinical and Histologic Features of 64 Cases of Steatocystoma Multiplex