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Research 31–60 of 1000+
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Development of squamous cell carcinoma from erythroplasia of Queyrat following photodynamic therapy
- Alopecia and Its homoeopathic treatment
- Two females with hair loss
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Genome-wide association study of skin complex diseases
- Peripheral blood gene expression in alopecia areata reveals molecular pathways distinguishing heritability, disease and severity
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Genetic Hair Disorders: A Review
- An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15
- Congenital atrichia associated with situs inversus and mesocardia
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- WNT Signaling in Disease
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Current Genetics in Hair Diseases
- Focused Review on Metal Nanoparticles in Hair Regeneration and Alopecia: Insights into Mechanisms, Assessment Techniques, Toxicity, Regulatory and Intellectual Property Perspectives
- Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- A group of type I keratin genes on human chromosome 17: characterization and expression.
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Characterization of a Cluster of Human High/Ultrahigh Sulfur Keratin-associated Protein Genes Embedded in the Type I Keratin Gene Domain on Chromosome 17q12-21
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- The Majority of Multipotent Epidermal Stem Cells Do Not Protect Their Genome by Asymmetrical Chromosome Segregation