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Researchers identified genes linked to coat color, body size, cashmere production, and high altitude adaptation in goats.

The TGF-β family helps control how cells change and move, affecting skin, hair, and organ development.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

The study found that alopecia areata is strongly linked to autoimmune diseases and may indicate a genetic predisposition to such conditions.

The vitamin D receptor can act without its usual activating molecule, affecting hair growth and skin cancer, but its full range of actions is not well understood.

Women with PCOS are at high risk of glucose metabolism issues and heart diseases, especially if overweight, highlighting the need for early intervention.

Early stage bald spots are linked to skin inflammation and damage to the upper part of the hair follicle.

No genetic link between prostaglandins and hair loss found.

Growing human skin cells in a 3D environment can stimulate new hair growth.

Certain gene variations may protect against skin issues and oxidative stress in women with PCOS.

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

Long-term use of finasteride and dutasteride can cause serious health issues like diabetes and liver problems.

Different scalp and hair disorders are more common in certain ethnic groups, with the most common being androgenetic alopecia, which is treated with medications like minoxidil and finasteride.

New research is helping develop better treatments for alopecia areata.

Personalized treatment with inhibitors, minoxidil, and laser therapy helps hair loss.

The health of the gut may be important in developing new ways to prevent, diagnose, and treat alopecia areata.

Hdac1 and Hdac2 help maintain and protect the cells that control hair growth.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

A new gene mutation causes insulin resistance in a girl and her mother.

Children, especially teenagers, can get severe SARS-CoV infection with symptoms similar to adults, but they typically recover well with supportive care.

TrichoScan is reliable for counting and measuring hair density but may not accurately assess hair types in women with hair loss.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

Biotin and acetazolamide improved hair and nail growth, mental function, and reduced headaches in a child with autism.

PRP and HF-MSCs treatment improves hair growth, thickness, and density in androgenetic alopecia.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Ingenol mebutate gel changes gene expression related to skin development and immune response in actinic keratosis.

Using human fat tissue derived stem cells in micrografts can safely and effectively increase hair density in people with hair loss.

Men generally have more severe COVID-19 cases and higher death rates than women due to biological differences.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Different parts of the body's fat tissue have unique cell types and characteristics, which could help treat chronic wounds.