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Research 361–390 of 1000+
- Molecular Regulatory Mechanisms in Chicken Feather Follicle Morphogenesis
- Hair for brain trade-off, a metabolic bypass for encephalization
- Inheritance-Specific Dysregulation of Th1- and Th17-Associated Cytokines in Alopecia Areata
- Novel Insights into TSC22D Family Genes in Metabolic Diseases and Cancer
- Microneedle-Mediated Transdermal Drug Delivery for the Treatment of Multiple Skin Diseases
- Immune and Non-immune Interactions in the Pathogenesis of Androgenetic Alopecia
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Ptosis in childhood
- Lymphotoxin-β regulates periderm differentiation during embryonic skin development
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- The Rotterdam Study: objectives and design update
- Deciphering the Complex Immunopathogenesis of Alopecia Areata
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Understanding the Intricate Pathophysiology of Psoriasis and Related Skin Disorders
- Phylloid terminal hair nevus: A unique clinical entity
- Polycystic Ovarian Syndrome - What is New
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Alopecias
- Clinical Snippets
- Identification of novel glucocorticoid receptor-regulated genes involved in epidermal homeostasis and hair follicle differentiation
- A review of hyperandrogenism state in polycystic ovarian syndrome
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Sequence Data and Chromosomal Localization of Human Type I and Type II Hair Keratin Genes
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Do Changes in Chromosomes Cause Aging?
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- A cluster of 21 keratin-associated protein genes within introns of another gene on human chromosome 21q22.3
- Becker's nevus associated with chromosomal mosaicism and congenital adrenal hyperplasia
- Characterization and Chromosomal Localization of Human Hair-Specific Keratin Genes and Comparative Expression During the Hair Growth Cycle