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Research 331–360 of 1000+
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Bachmann–Bupp syndrome and treatment
- Role of Sulfur Metabolism Gene and High-Sulfur Gene Expression in Wool Growth Regulation in the Cashmere Goat
- [Androgenetic alopecia].
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- Shh maintains dermal papilla identity and hair morphogenesis via a Noggin–Shh regulatory loop
- Case report on premature hair graying treated with Melitane 5% and oral hair supplements
- Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Isolation and Characterization of Mouse High-glycine/Tyrosine Proteins
- 268 Male-pattern baldness and its association with coronary heart disease
- Hirsutism in the Adolescent Female
- Androgenetic alopecia: An update
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Proteome Analysis of Human Hair Shaft
- Idiopathic Hirsutism*
- The role of WNT10B in physiology and disease: A 10-year update
- Androgenetic alopecia, hirsutism and hypertrichosis
- Management of congenital ichthyoses: European guidelines of care, part two
- TỔNG QUAN VỀ SINH HỌC CỦA TÓC, MÔ HÌNH NGHIÊN CỨU VÀ ĐÁNH GIÁ KHẢ NĂNG MỌC LẠI TÓC TRÊN IN-VITRO VÀ IN-VIVO
- Epithelial Skin Biology
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Cutaneous signals of immune system disease
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- A Screen for Key Genes and Pathways Involved in High-Quality Brush Hair in the Yangtze River Delta White Goat