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Research 391–420 of 1000+
- Generalised Gingival Fibromatosis and Hypertrichosis: A Rare Case of Syndromic Presentation
- 712 Using scanning electron microscopy to elucidate the role of hair shaft malformation in the pathogenesis of Central Centrifugal Cicatricial Alopecia
- HAIR KERATINIZATION IN HEALTH AND DISEASE
- Androgenetic alopecia
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Case report on premature hair graying treated with Melitane 5% and oral hair supplements
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Post‐finasteride syndrome: real or myth?
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Index
- Female Androgenetic (?) Alopecia
- Caractérisation d’une modification «bigarré» de la couleur du pelage chez le chat domestique
- Book Review Disorders of Hair Growth: Diagnosis and Treatment Second edition. Edited by Elise A. Olsen. 544 pp., illustrated. New York, McGraw-Hill, 2003. $195. 0-07-136494-3
- Epidemiology, diagnosis, and management of polycystic ovary syndrome
- A molecular wound response program associated with regeneration initiation in planarians
- The evaluation and management of hirsutism*1
- Hedgehog signalling in skin development and cancer
- Adult polycystic ovary syndrome begins in childhood
- Structure of human type II 5 alpha-reductase gene.
- Epithelial Skin Biology
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Beauty is skin deep: the fascinating biology of the epidermis and its appendages.
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Identification and sequence analysis of the keratin-associated protein 24‐1 (KAP24-1) gene homologue in sheep
- Differential Expression between Human Dermal Papilla Cells from Balding and Non-Balding Scalps Reveals New Candidate Genes for Androgenetic Alopecia
- A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity.
- Androgen Receptor Mutations and Polymorphisms in African American Prostate Cancer