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Research 181–210 of 1000+
- Establishment of keratinocyte cell lines from human hair follicles
- Hair loss
- Diseases of Periocular Hair
- Study on the mechanism of cadmium chloride pollution accelerating skin tissue metabolism disorder, aging and inhibiting hair regeneration
- Retinoids in scarless skin regeneration: from molecular mechanisms to therapeutic strategies
- Disorders of the skin appendages
- Westwood Carolina Conference on Clinical Dermatology
- Oral cyclosporin does not arrest progression of androgenetic alopecia
- Retinoid-mediated stimulation of steroid sulfatase activity in myeloid leukemic cell lines requires RARα and RXR and involves the phosphoinositide 3-kinase and ERK-MAP kinase pathways
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- Structural and Molecular Hair Abnormalities in Trichothiodystrophy
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Dramatic Clinical Improvement With Biotin Mega‐Dose Therapy in a Neonate With Holocarboxylase Synthetase Deficiency
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- [Acitretine].
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Keratins and skin disease
- New clinico‐genetic classification of trichothiodystrophy
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Nilotinib-Induced Keratosis Pilaris
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Microscopic polyangiitis secondary to Mycobacterium abscessus in a patient with bronchiectasis: a case report
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Differential expression of KRT83 regulated by the transcript factor CAP1 in Chinese Tan sheep