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Vitamin A deficiency changes cattle hair structure, while pregnancy may improve it, suggesting hair can indicate cattle health.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.

Sweat gland development involves two unique skin cell programs and a temporary skin environment.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Blocking IL-17 can reduce skin inflammation in a mouse model of pityriasis rubra pilaris.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

CCDC22 and CCDC93 are essential for root and root hair growth in Arabidopsis.

Water and fatty acids affect hair's surface differently based on hair damage, and models can help understand hair-cosmetic interactions.

The conclusion is that certain chemicals from Bacillus subtilis help improve plant root growth through a hormone-related process.

Human hair keratins can be turned into useful 3D biomedical scaffolds through a freeze-thaw process.

Addressing underrepresentation in Parkinson's research is crucial for better treatments and understanding.

The review emphasizes the need to recognize skin conditions that affect hair follicles and sweat glands to avoid misdiagnosis.

Pranlukast and mirabegron may work as new diabetes drugs.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

Mothers have more hair proteins than their children, with age-related differences in protein patterns, and some proteins in hair could indicate early childhood development.

Human hair keratins can self-assemble and support cell growth, useful for biomedical applications.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

L-PGDS has specific binding sites for its functions and could help in drug delivery system design.

The gene Prss53 affects hair shape and bone development in rabbits.

A scalp biopsy revealed systemic amyloidosis in a woman who initially seemed to have a common hair loss condition.

MRI helps distinguish between pituitary adenomas and craniopharyngiomas, guides treatment for pediatric CNS tumors, and assesses rhinocerebral mucormycosis with a high mortality rate in transplanted patients.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Aging causes changes in scalp cells that can negatively affect hair health.

Researchers found a new way to isolate sweat glands from the scalp for study and culture.

GATA6 is important for maintaining and differentiating cells in a key area of human skin.

New drugs targeting the JAK-STAT pathway show promise for treating inflammatory skin diseases.

Trichotillomania is a condition where people repeatedly pull out their hair, which can be triggered by stress and has various physical signs.