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Research 991–1000 of 1000+
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Genome-wide Maps of Histone Modifications Unwind In Vivo Chromatin States of the Hair Follicle Lineage
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Melatonin: A Cutaneous Perspective on its Production, Metabolism, and Functions
- A Nonredundant Human Protein Chip for Antibody Screening and Serum Profiling
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Regulated Proenkephalin Expression in Human Skin and Cultured Skin Cells
- Peptidylarginine Deiminase Isoforms Are Differentially Expressed in the Anagen Hair Follicles and Other Human Skin Appendages
- Requirement of zinc transporter ZIP10 for epidermal development: Implication of the ZIP10–p63 axis in epithelial homeostasis