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- Australian Hair and Wool Research Society Cutaneous Biology and Endocrinology Workshop
- 0867 The role of schwann cell - macrophage interactions in keloid pathogenesis
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- Abordagens psicológicas e novas terapêuticas perante as escolhas do paciente portador da Síndrome de Morris
- Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome
- Celsr1 and Celsr2 exhibit distinct adhesive interactions and contributions to planar cell polarity
- Anagen Hair Follicles Transplanted into Mature Human Scars Remodel Fibrotic Tissue
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Effects of the prenatal and postnatal nurturing environment on the phenotype and gut microbiota of mice with polycystic ovary syndrome induced by prenatal androgen exposure: a cross-fostering study
- Association of insulin resistance with polycystic ovary syndrome phenotypes and patients’ characteristics: a cross-sectional study in Iran
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- 3D spheroid culture synchronizes heterogeneous MSCs into an immunomodulatory phenotype with enhanced anti-inflammatory effects
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- The PCOS Phenotypes in Unselected Populations (P-PUP) study: participant clinical features and data harmonization on analysis of individual participant data
- Influence of Atopic Dermatitis on the Dermoscopic Phenotype of Positive Patch Test Reactions: A Prospective Comparative Study
- 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
- Evaluation of Retinal Changes in Women with Different Phenotypes of Polycystic Ovary Syndrome
- CRISPR/Cas9-mediated Disruption of Fibroblast Growth Factor 5 in Rabbits Results in a Systemic Long Hair Phenotype by Prolonging Anagen
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- In Vitro Assembly and Structure of Trichocyte Keratin Intermediate Filaments