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Research 271–300 of 1000+
- Progeroide Syndrome
- 601 Hair growth properties of Cinchona succirubra Extract, Leontopodium alpinum Extract and Manganese PCA in human hair follicle dermal papilla cells
- 600 Evaluation of anti-hairloss shampoo through in vitro activity in human hair follicule dermal papilla cells and sensorial study
- Wnt Signaling in Skin Development, Homeostasis, and Disease
- Congenital hypotrichosis due to short anagen
- p53‐dependent transcriptional regulation of EDA2R and its involvement in chemotherapy‐induced hair loss
- Secondary cicatricial and other permanent alopecias
- Hair follicles and their role in skin health
- Molecular Genetics of Alopecias
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Hair loss and its management in children
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- A Review on Herbal Drugs Used For Hair Growth Promotion
- The rising burden of alopecia: A review on aetiology, prevalence and role of homoeopathy
- Alopecia and Its homoeopathic treatment
- Abnormal fingerprints and immigration delay disease
- Case of Cronkhite Canada Syndrome - A Non-Inherited Gastrointestinal Polyposis Syndrome
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Symmetrical alopecia in the dog
- Wnt signaling: the good and the bad
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Mesenchymal–epithelial interactions during hair follicle morphogenesis and cycling
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Alopecia Areata: A tissue specific autoimmune disease of the hair follicle
- Skin and hair: models for exploring organ regeneration
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- Hair Loss in Children
- ALOPECIA AREATA-A CLINICAL ANALYSIS
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation