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Research 31–60 of 1000+
- Disorders of Sex Development
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Genome-Wide Associations with Body and Fleece Weight in United States Sheep
- The Majority of Multipotent Epidermal Stem Cells Do Not Protect Their Genome by Asymmetrical Chromosome Segregation
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Susceptibility variants for male-pattern baldness on chromosome 20p11
- Androgen receptors and their biology
- Human Derived Immortalized Dermal Papilla Cells With a Constant Expression of Testosterone Receptor
- Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Lanceolate hair-J (lahJ): a mouse model for human hair disorders [In Process Citation]
- Phenotypic, transcriptomic, and genomic analyses reveal the spatiotemporal patterns and associated genes of coarse hair density in goats
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Lanceolate hair-J (<i>lah<sup>J</sup> </i> ): A mouse model for human hair disorders
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- New familial association between ocular coloboma and loose anagen syndrome
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Male-pattern baldness susceptibility locus at 20p11
- Polycystic ovary syndrome (PCOS) trilogy: a translational and clinical review
- Eruptive syringomas in Down’s syndrome
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Papular atrichia
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Increased copy number of the TERT and TERC telomerase subunit genes in cancer cells
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- A 10 Mb duplication in chromosome band 5q31.3–5q33.1 associated with late-onset lipodystrophy, ichthyosis, epilepsy and glomerulonephritis
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.