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Research 271–300 of 1000+
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Trichothiodystrophy: Current Concepts
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- A Comprehensive Review of Management of Patients with Infertility having Polycystic Ovarian Syndrome
- To study on nutritional status in suffering from polycystic ovary syndrome (PCOS)
- A missense mutation in Lama3 causes androgen alopecia
- Oral Presentations
- Hair Follicle Pigmentation
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Trichoscopy and Trichogram
- The Evaluation and Management of Hirsutism
- Investigating the effect of herbal component-based natural hair oil using the Indigenous source of Bangladesh
- Hair and Nail Manifestations of Systemic Disease
- Emerging interactions between skin stem cells and their niches
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- ICP5249 Promotes Hair Growth by Activating the AMPK-Autophagy Signaling Pathway
- Oral Retinoids in Dermatology
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Recent Advances in the Pathogenesis of Autoimmune Hair Loss Disease Alopecia Areata
- Epidemiology and burden of alopecia areata: a systematic review
- Transforming growth factor-β in stem cells and tissue homeostasis
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Alopecia Areata: Pathogenesis, Diagnosis, and Therapies
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Novel potential therapeutic targets of alopecia areata