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Research 931–960 of 1000+
- Marie‐Unna Hereditary Hypotrichosis or Autosomal Recessive Hereditary Hypotrichosis with Woolly Hair: The Diagnostic Dilemma of Labeling Cases with Hypotrichosis
- Nanocomposite patches for transdermal drug delivery: A review
- 18F-FDG PET Uptake in the Scalp After Platelet-Rich Plasma Therapy
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- Gender-Affirming Hormonal Treatment in Transgender People Assigned Female at Birth (AFAB)
- Determining the Quality of Life of People with Alopecia areata and Associated Factors in Tertiary Hospitals in Capital City of Malaysia
- Prevalence and Patterns of Dermatological Diseases in Lesbian, Gay, Bisexual, Transgender, and Queer Population: A Cross-Sectional Survey
- Inovasi pewarna rambut alami: Formulasi gel berbahan dasar ekstrak umbi bawang dayak (Eleutherine bulbosa (mill.)Urb.) dan uji sifat fisiknya
- Anxiety, depression and low self-esteem among people with alopecia
- COVID-19 Clinical Outcomes and Nationality: Results from a Nationwide Registry in Kuwait
- Phosphodiesterase (PDE) Inhibitors for the Treatment of Inflammatory Skin Conditions
- Genome size determination of <i>Eclipta alba</i> and <i>Aloe barbadensis </i>
- Letters to the Editors: Re: Rare Complication of Forehead Taping
- Acidic and basic hair/nail ("hard") keratins: their colocalization in upper cortical and cuticle cells of the human hair follicle and their relationship to "soft" keratins.
- Structure and biochemistry of mammalian hard keratin
- The complement of native α-keratin polypeptides of hair-forming cells: A subset of eight polypeptides that differ from epithelial cytokeratins
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Hair Color, Molt, and Testis Size in Male, Short-Tailed Weasels Treated with Melatonin
- Chapter 2 The Human Keratin Genes and Their Differential Expression
- A Nonredundant Human Protein Chip for Antibody Screening and Serum Profiling
- The role of vitamin D receptor mutations in the development of alopecia
- Multicentric parallel phase II trial of the polo-like kinase 1 inhibitor BI 2536 in patients with advanced head and neck cancer, breast cancer, ovarian cancer, soft tissue sarcoma and melanoma. The first protocol of the European Organization for Research and Treatment of Cancer (EORTC) Network Of Core Institutes (NOCI)
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Beauty is skin deep: the fascinating biology of the epidermis and its appendages.
- The skin landscape in diabetes mellitus. Focus on dermocosmetic management
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Phytochemical Profile and Biological Activities of Ethylacetate Extract of Peanut (Arachis hypogaea L.) Stems: In-Vitro and In-Silico Studies with Bibliometric Analysis
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis