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Research 931–960 of 1000+
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Visualising Androgen Receptor Activity in Male and Female Mice
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- A missense mutation in the type II hair keratin hHb3 is associated with monilethrix
- Alopecia: evaluation and treatment
- Stress and the Hair Growth Cycle: Cortisol-Induced Hair Growth Disruption.
- Efficient In Vivo Targeting of Epidermal Stem Cells by Early Gestational Intraamniotic Injection of Lentiviral Vector Driven by the Keratin 5 Promoter
- Current Advanced Therapies Based on Human Mesenchymal Stem Cells for Skin Diseases
- Chemotherapy‐induced alopecia management: Clinical experience and practical advice
- Perifollicular erythema as a trichoscopy sign of progression in frontal fibrosing alopecia
- Genetic hair and nail disorders
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Vitamin A toxicity: When one a day doesn't keep the doctor away
- Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literature
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- [Trichothiodystrophy: a morphological and biochemical study].
- Prevention and Treatment of Chemotherapy-Induced Alopecia
- The dermatoscope in the hair clinic: Trichoscopy of scarring and nonscarring alopecia
- Treatment for chemotherapy‐induced alopecia in mice using parathyroid hormone agonists and antagonists linked to a collagen binding domain
- Gomez–Lopez-Hernandez Syndrome: Two New Cases and Review of the Literature
- Pathogenesis in pili torti: morphological study
- Bone vs. fat: Embryonic origin of progenitors determines response to androgen in adipocytes and osteoblasts
- Systematic analyses of murine masculinization processes based on genital sex differentiation parameters
- What Color Is the Skin of a Mouse?
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Cronkhite-Canada Syndrome (CCS)—A Rare Case Report
- Study of the efficacy of carboxytherapy in alopecia
- Brazilian Experience of the Treatment of Alopecia Universalis with the Novel Antirheumatic Therapy Tofacitinib: A Case Series
- Alopecia universalis during treatment with leflunomide and adalimumab - Case report