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- Insertional mutation of the hairless locus on mouse Chromosome 14
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Hox demarcates regional regeneration of adult hair follicle stem cells
- A Small Deletion Hotspot in the Type II Keratin Gene<i>mK6irs1/Krt2-6g</i>on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (<i>Ca</i>) Mutation
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Copy number variation regions in Nellore cattle: Evidences of environment adaptation
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Several variants on chromosome 10 are associated with coarse hair diameter in Dazu black goats (<i>Capra hircus</i>)
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- Genome Report: chromosome-scale genome assembly of the African spiny mouse (<i>Acomys cahirinus</i>)
- Sex-limited chromosomes and non-reproductive traits
- Loss of the Y Chromosome: A Review of Molecular Mechanisms, Age Inference, and Implications for Men’s Health
- Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition
- Disease causing homozygous variants in the human hairless gene
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- British Society for Dermatopathology
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- Sperm aneuploidy in infertile male patients: a systematic review of the literature
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Combinatorial expression of cell cycle regulators is more suitable for immortalization than oncogenic methods in dermal papilla cells
- Biological Function of Long Non-coding RNA (LncRNA) Xist
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes