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A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

Next-generation sequencing greatly improves understanding and treatment of genetic hair disorders.

The study concludes that regulating apoptosis could lead to new treatments for various skin and hair conditions.

This rare genetic disorder causes permanent hair loss and skin bumps from birth.

Stem cells from whiskers can be transplanted to stimulate hair growth.

Spermidine may improve skin health and hair growth by enhancing cell function.

Six genetic conditions are often linked to complete scalp hair loss in children.

Certain short peptides can increase root hair growth in tobacco plants.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Liposomes with certain properties can effectively deliver drugs deep into hair follicles.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

A mutant FERONIA gene affects root hair growth at high temperatures.

Sunscreens with higher SPF and UVA filters offer the best protection against skin aging from UVA rays.

Hair follicles play a crucial role in regulating skin barrier function.

Male mice with FGF5 mutations grow longer hair than females.

Hedgehog signaling in certain cells is crucial for hair growth during wound healing.

Vitamin C deficiency changes gene expression, affecting skin and hair health.

A specific DNA duplication in Polish chickens affects feather shape by altering gene expression.

Dkk genes evolved faster in birds and reptiles, affecting hair development functions.

Scalp melanoma, a deadly skin cancer, is often found late due to its hard-to-see location, especially in older men. Early detection, possible treatments, and the role of hairdressers in spotting it early are discussed. More research is needed to improve detection and treatment.

Ovalbumin–aluminum sensitization causes increased pain sensitivity and nerve changes in mice.

Specific gene variants affect wool traits in Chinese Tan sheep.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Vitamin D receptor is crucial for hair health and may help treat hair loss.

Removing senescent cells can improve hair growth and regeneration.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

Boron deficiency in maize affects leaf boron levels and nutrient uptake differently depending on root hair presence and soil type.

CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.