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Research 211–240 of 1000+
- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered
- Targeting the Wnt pathways for therapies
- 1315 An Integrated model of alopecia areata biomarkers highlights both Th1/Th2 upregulation, with stronger correlations between Th2 activation and disease severity
- Disorders of the skin appendages
- Australasian Society for Dermatology Research Meeting, May 2007
- Clinical Approach to the Patient With Alopecia
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Dermatopathology and molecular genetics
- Cicatricial alopecia
- Australasian Society for Dermatology Research Meeting, May 2006
- Uncombable hair improved by biotin
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Hair fragility (trichorrhexis nodosa) in alopecic Pomeranian dogs
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Epidermal patterning and induction of different hair types during mouse embryonic development
- Recent Progress in the Understanding of the Effect of Sympathetic Nerves on Hair Follicle Growth
- A Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy
- Ectodermal Dysplasia: Variable Expressions
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Amino Acid Content of Damaged Human Hair
- Molecular Mechanisms Regulating Hair Follicle Development
- Involvement of the Edar Signaling in the Control of Hair Follicle Involution (Catagen)
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Hair & Cutaneous Development
- MicroRNA-214 controls skin and hair follicle development by modulating the activity of the Wnt pathway
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles