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Research 241–270 of 1000+
- Role of skin enzymes in metabolism of topical drugs
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Polycystic ovary syndrome
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Biology of Human Hair: Know Your Hair to Control It
- Steroid-resistant nephrotic syndrome associated with steroid sulfatase deficiency—x-linked recessive ichthyosis: a case report and review of literature
- Induction of dermal fibroblasts into dermal papilla cell-like cells in hydrogel microcapsules for enhanced hair follicle regeneration
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Causal associations between plasma proteins and prostate cancer: a Proteome-Wide Mendelian Randomization
- Integrative Whole-Transcriptome Sequencing Analysis of Skin Tissues with Different Coat Types in Cashmere Goats Across Stages of Hair Follicle Development
- Multiple cell types guided by neurocytes orchestrate horn bud initiation in dairy goats
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Siberian cats help in solving part of the mystery surrounding golden cats
- Several variants on chromosome 10 are associated with coarse hair diameter in Dazu black goats (<i>Capra hircus</i>)
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- Chronic overlapping pain conditions and nociplastic pain
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing