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Research 121–150 of 1000+
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Hair Loss in Children
- Clinical Management in Psychodermatology
- The Spectrum of Skin Disease Among Indian Children
- Christmas article: Case of uncombable hair syndrome discovered after publication of article in Ugeskrift for Læger
- Alopecia Areata: Current Review
- Use of chemotherapy during human pregnancy
- Transforming growth factor-β in stem cells and tissue homeostasis
- ATP-dependent chromatin remodeling during mammalian development
- Feather arrays are patterned by interacting signalling and cell density waves
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Darier Sign: A Historical Note
- Células-tronco foliculares e aspectos histopatológicos cutâneos tardios após prolongada remoção de pêlos a laser
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Congenital atrichia associated with nevus flammeus: A rare association
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- A Case Report of Cronkhite-Canada Syndrome Complicated by Membranous Nephropathy
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Sostdc1 defines the size and number of skin appendage placodes
- [The Netherton syndrome with alopecia and prolinuria].
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Epidermal patterning and induction of different hair types during mouse embryonic development
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Type I Keratin 17 Protein Is Phosphorylated on Serine 44 by p90 Ribosomal Protein S6 Kinase 1 (RSK1) in a Growth- and Stress-dependent Fashion
- Loss of Msx2 Function Down-Regulates the FoxE3 Expression and Results in Anterior Segment Dysgenesis Resembling Peters Anomaly
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice