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Research 361–390 of 1000+
- Hair: Its structure and response to cosmetic preparations
- Epidermal patterning and induction of different hair types during mouse embryonic development
- Telogen Effluvium: A Review
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Hair Shaft Abnormalities – Clues to Diagnosis and Treatment
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- Clinicoepidemiological Observational Study of Acquired Alopecias in Females Correlating with Anemia and Thyroid Function
- Keratins: the hair shaft's backbone revealed
- Eyelash Transplantation Using Leg Hair by Follicular Unit Extraction
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Interleukin 6 and STAT3 regulate p63 isoform expression in keratinocytes during regeneration
- High-sulfur protein deficient human hair: clinical aspects and biochemical study of two unreported cases of a variant type of trichothiodystrophy
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- GRowing an Epidermal Tumor
- Trichothiodystrophy: Current Concepts
- Hypotrichosis with juvenile macular dystrophy
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Tricorrexis nudosa localizada por aplicación compulsiva de minoxidil
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- A Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy
- 1313 Fzd2 controls multiple aspects of epidermal development through distinct signaling mechanisms
- Hair That Is Difficult to Manage in a Hispanic Girl
- Introduction to JID Symposium Proceedings 52nd Annual Montagna Symposium on the Biology of Skin “Stem Cells in Skin” Held at Snowmass, Colorado, USA, June 13–17, 2003
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration