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Research 541–570 of 1000+
- Toxic and Metabolic Disorders of the Nervous System
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Dermatologic Signs in Patients with Eating Disorders
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Role of janus kinase inhibitors in the treatment of alopecia areata
- Keratins 6, 16, and 17 in Health and Disease: A Summary of Recent Findings
- Alopecia and Associated Toxic Agents: A Systematic Review
- p53 Is a Direct Transcriptional Repressor of Keratin 17: Lessons from a Rat Model of Radiation Dermatitis
- Evolution of Trichocyte Keratins
- A “hair‐raising” history of alopecia areata
- Skin manifestations associated with systemic diseases – Part I
- Medical aesthetics – Current trends and a review of its applications
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages
- Cutaneous toxicities of new targeted cancer therapies: must know for diagnosis, management, and patient-proxy empowerment
- Hair Keratin
- A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Planar cell polarity effector gene Intu regulates cell fate-specific differentiation of keratinocytes through the primary cilia
- Transcriptome analysis reveals the genetic basis underlying the development of skin appendages and immunity in hedgehog (Atelerix albiventris)
- Hair fragility (trichorrhexis nodosa) in alopecic Pomeranian dogs