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Research 181–210 of 1000+
- Transforming growth factor-β in stem cells and tissue homeostasis
- Teriflunomide in multiple sclerosis: an update
- New ethanol and propylene glycol free gel formulations containing a minoxidil-methyl-β-cyclodextrin complex as promising tools for alopecia treatment
- Indian Gooseberry (<i>Emblica officinalis</i>Gaertn.)
- The skin findings of pregnant women and our treatment choices. A Turkish experience: a 5-year survey.
- A comparative analysis of three explanatory models of mental disorder and a preferred focus of explanation
- Clinical Approach to the Patient With Alopecia
- Successful induction of oral tolerance in Netherton syndrome
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Alopecia areata update
- Lipedematous Alopecia: Clinical, Histopathological, and Trichoscopic Findings of a Single Case and Review of the Literature
- Frontal Fibrosing Alopecia
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- Quality of life in children with scalp hair loss: a Clinico-epidemiological study
- Uncombable hair in a case of Zellweger syndrome – A new association
- Hair fragility (trichorrhexis nodosa) in alopecic Pomeranian dogs
- Netherton Syndrome With Trichorrhexis Invaginata “Bamboo Hair” Under Dermoscopy: Case Images
- Recent Progress in the Understanding of the Effect of Sympathetic Nerves on Hair Follicle Growth
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- The shampoo pH can affect the hair: Myth or Reality?
- Epidermal patterning and induction of different hair types during mouse embryonic development
- Beyond the Epidermal-Melanin-Unit: The Human Scalp Anagen Hair Bulb Is Home to Multiple Melanocyte Subpopulations of Variable Melanogenic Capacity
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss
- Current Genetics in Hair Diseases
- Platelet-rich Plasma Injection and Lipofilling-assisted Hair Transplantation on Residual Scalp Alopecia Post Aplasia Cutis Congenita Verticis (ACCV)
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Hair, Wool, Quill, Nail, Claw, Hoof, and Horn
- Keratin Expression Provides Novel Insight into the Morphogenesis and Function of the Companion Layer in Hair Follicles