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Researchers found new hair and nail genes, how hair reacts to UV, differences in white and pigmented hair growth, nerve changes in alopecia, treatments for baldness and alopecia, a toenail condition linked to a genetic disorder, and that nail fungus is more common in people with psoriasis.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

Genetic differences between young and old Tan sheep explain why their fleece changes from curly to straight as they age.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

Sun exposure and genetics increase skin cancer risk from precancerous lesions.

The transition from growth to regression in Cashmere goat hair follicles involves changes in expression of genes related to keratin and cell differentiation.

Lack of cystatin M/E causes thin hair and dry skin.

A mutation in the KRT75 gene causes frizzle feathers in chickens.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Nociplastic pain is a complex, heritable trait with genetic links to chronic and neuropathic pain.

Norfolk Terriers have a genetic skin defect causing scaling and blisters due to a keratin issue.

New genetic variants linked to albinism were found in Pakistani families.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Phosphorylation controls TFEB's location in the cell, affecting cell metabolism and stress response.

New treatments targeting specific genes show promise for treating keratin disorders.

The conclusion is that genetic differences affect how the cochlea heals after hair cell loss, which may challenge the creation of hearing loss treatments.

The study mapped genetic variations in sheep, linking them to traits like milk production and growth.

FOXN1 gene variants cause low T cells and immune issues from birth.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Myhre syndrome symptoms worsen over time, with specific genetic variants affecting severity.

Trichilemmal carcinoma shares genetic changes with other skin cancers, suggesting similar causes and potential treatments.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

The study found that genetic differences related to hair growth and other traits help cashmere goats adapt to high-altitude environments.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

Pangolins have lost some skin-related genes, but kept others, leading to their unique scales and skin features.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.