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Research 601–630 of 1000+
- Steroidogenic Isoenzymes in Human Hair and Their Potential Role in Androgenetic Alopecia
- Normal and Aging Hair Biology and Structure ‘Aging and Hair'
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Tenascin-C expressing touch dome keratinocytes exhibit characteristics of all epidermal lineages
- LncRNAs regulate the cyclic growth and development of hair follicles in Dorper sheep
- Health Messages
- Main Plenary Sessions: Summaries of Papers
- Gender aspects in skin diseases
- Defining stem cell dynamics and migration during wound healing in mouse skin epidermis
- Obesity and polycystic ovary syndrome
- Idiopathic Hirsutism*
- Are fingernails a key to unlocking the puzzle of mammalian limb regeneration?
- Follicular Unit Extraction: Minimally Invasive Surgery for Hair Transplantation
- The essential oils of Chamaecyparis obtusa promote hair growth through the induction of vascular endothelial growth factor gene
- A Case of Kerion Celsi Caused by Microsporum gypseum (Arthroderma gypseum ) in a Child
- Tp63-expressing adult epithelial stem cells cross lineages boundaries revealing latent hairy skin competence
- <i>AXR3</i>and<i>SHY2</i>interact to regulate root hair development
- Morpho‐regulation in diverse chicken feather formation: Integrating branching modules and sex hormone‐dependent morpho‐regulatory modules
- Ottawa, Ontario, Canada, February 13–16, 2013
- Transcriptomic crossroads: Decoding genes and pathways that connect alopecia areata with chronic inflammatory skin disorders
- Identification of genes influencing formation of the Type III Brush Hair in Yangtze River Delta white goats by differential display of mRNA
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- The up‐regulation of 14‐3‐3 proteins in Smad4 deficient epidermis and hair follicles at catagen
- Comprehensive transcriptome profiling between balding and non-balding scalp of Female pattern hair loss in Asian
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Development of Heritable Melanoma in Transgenic Mice
- Keratins and skin disease
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex