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Research 61–90 of 172
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- The Genetics of Human Skin Disease
- Molecular pathology of skin adnexal tumours
- Topical L‐thyroxine: The Cinderella among hormones waiting to dance on the floor of dermatological therapy?
- Hair tourniquet syndrome of toes and fingers in infants
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Inherited Disorders of the Hair
- Acne
- Neuroendocrine Controls of Keratin Expression in Human Skin
- UNCONVENTIONAL PROTEIN SECRETION OF KERATIN 75 BY AMELOBLASTS IN VIVO
- The successful treatment of nephrogenic fibrosing dermopathy (NFD) with mycophenolate mofetil (MMF)
- The prevalence of itch and pain and its characteristics in patients with mild to moderate insufficiency and its relationship to the degree of venous insufficiency
- The use of diphencyprone in dermatology: A retospective audit
- Their year at Parkland Memorial Hospital (2005)
- Hair Tourniquet Syndrome of the Toe: Report of 2 New Cases
- Quality of life in children with scalp hair loss: a Clinico-epidemiological study
- p53 Is a Direct Transcriptional Repressor of Keratin 17: Lessons from a Rat Model of Radiation Dermatitis
- Keratins: the hair shaft's backbone revealed
- Semidominant Inheritance in Epidermolytic Ichthyosis
- 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
- Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- Expression of MK6a dominant-negative and C-terminal mutant transgenes in mice has distinct phenotypic consequences in the epidermis and hair follicle
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- SkIndia Quiz 24: Itchy papules over face
- TONGUE, RED
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report