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Research 841–870 of 1000+
- Tissue engineering strategies combining molecular targets against inflammation and fibrosis, and umbilical cord blood stem cells to improve hampered muscle and skin regeneration following cleft repair
- 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
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Genetic Hair Disorders: A Review
- Transcriptomic landscape of early hair follicle and epidermal development
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Fluoride exposure and pubertal development in children living in Mexico City
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Scientific Opinion on the substantiation of health claims related to soy isoflavones and protection of DNA, proteins and lipids from oxidative damage (ID 1286, 4245), maintenance of normal blood LDL cholesterol concentrations (ID 1135, 1704a, 3093a), reduction of vasomotor symptoms associated with menopause (ID 1654, 1704b, 2140, 3093b, 3154, 3590), maintenance of normal skin tonicity (ID 1704a), contribution to normal hair growth (ID 1704a, 4254), “cardiovascular health” (ID 3587), treatment …
- FGF-9 accelerates epithelial invagination for ectodermal organogenesis in real time bioengineered organ manipulation
- Transient agonism of the sonic hedgehog pathway triggers a permanent transition of skin appendage fate in the chicken embryo
- Recent advances in the characterization of hair of mummies from the Chilean Andean coast
- A “hair‐raising” history of alopecia areata
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Bioactive Glasses: Advancing Skin Tissue Repair through Multifunctional Mechanisms and Innovations
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Vitamin D-Dependent Rickets Type II with Alopecia: A Rare Case Report.
- Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature
- Dermoscopy: A rapid bedside tool to assess monilethrix
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Generation of bioengineered feather buds on a reconstructed chick skin from dissociated epithelial and mesenchymal cells
- Pica for Uncooked Basmati Rice in Two Women with Iron Deficiency and a Review of Ryzophagia
- Organizational principles of integumentary organs: Maximizing variations for effective adaptation
- Tp63-expressing adult epithelial stem cells cross lineages boundaries revealing latent hairy skin competence
- Comparative transcriptomic analysis of human mesenchymal stem cells derived from dental pulp and adipose tissues
- Congenital atrichia with papular lesions
- Atrichia with papular lesions
- Transcriptome analyses of reprogrammed feather / scale chimeric explants revealed co-expressed epithelial gene networks during organ specification