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Research 31–60 of 1000+
- A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?
- Novel TMEM173 Mutation and the Role of Disease Modifying Alleles
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Characterization of novel TMEM173 mutation with additive IFIH1 risk allele
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Pinkie, the First Viable Germline Hypomorph Allele of Retinoid X Receptor Alpha, Reveals an Important Role for RXRa in Th2 Development.
- Functional Characterization of<i>fer-ts</i>, a Temperature-Sensitive FERONIA Mutant Allele That Alters Root Hair Growth
- A Prospective Study of the Prevalence of Nonclassical Congenital Adrenal Hyperplasia among Women Presenting with Hyperandrogenic Symptoms and Signs
- Autoimmunity: Alopecia Areata
- Mice humanised for the EGF receptor display hypomorphic phenotypes in skin, bone and heart
- Male-pattern baldness susceptibility locus at 20p11
- Disruption of FGF5 in Cashmere Goats Using CRISPR/Cas9 Results in More Secondary Hair Follicles and Longer Fibers
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Evaluation of DNA Variants Associated with Androgenetic Alopecia and Their Potential to Predict Male Pattern Baldness
- The association between Interleukin (IL)-4 gene intron 3 VNTR polymorphism and alopecia areata (AA) in Turkish population
- Androgen receptor gene polymorphisms and risk for androgenetic alopecia: a meta-analysis
- The spectrum of hair loss in patients with mycosis fungoides and Sézary syndrome
- Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Genetic Fate Mapping Using Site-Specific Recombinases
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- Genetically separable determinants of hair keratin gene expression
- Size Polymorphisms in the Human Ultrahigh Sulfur Hair Keratin-Associated Protein 4, KAP4, Gene Family
- Insertional mutation of the hairless locus on mouse Chromosome 14
- The genetics of alopecia areata
- Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population
- Genetic association of complement component 2 polymorphism with systemic lupus erythematosus
- Androgenetic alopecia and polymorphism of the androgen receptor gene (SNP rs6152) in patients with benign prostate hyperplasia or prostate cancer