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A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Thyrotropin-releasing hormone may help control skin and hair growth and could aid in treating related disorders.

Keratin 33A is a key protein in goat winter coats, especially in high-producing breeds.

Applying the anti-cancer drug Bortezomib to skin can promote hair growth and increase hair proteins through the GATA-3 factor.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

Keratin 17 is crucial for early hair strength and cell survival.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

Keratin is crucial for keeping skin cells healthy and its changes can lead to diseases and affect cell behavior.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Human hair contains diverse proteins, including keratins and histones, which could help assess hair health and aging.

The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Keratin 75 might be important in oral cancer progression.

m-Aminophenol in hair dye can cause skin cell toxicity and stress responses.

Keratins help protect cells, aid in cancer diagnosis, and influence cancer behavior and treatment.

Keratin 17 is crucial for normal hair growth by regulating hair cycle transitions with TNFα.

Keratin expression reflects cell organization and differentiation, not causes it.

TNF alpha in skin cells causes weight loss, hair and fat issues, and skin inflammation in mice.

Keratin 15 is not a reliable sole marker for identifying epidermal stem cells because it's found in various cell types.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

The nude gene causes skin cell overgrowth and improper development, leading to hair and urinary issues.

The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.

Keratin 79 marks a new group of cells that are key for creating and repairing the hair follicle's structure.

Different hair protein amounts change the strength of keratin/chitosan gels, useful for making predictable tissue engineering materials.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

Different combinations of human hair keratins affect how hair fibers form.

Keratin injections can promote hair growth by affecting hair-forming cells and tissue development.

Understanding how keratin structures in hair are arranged and interact is key for creating methods to extract and purify them.

Seasonal changes affect gene activity linked to hair growth in Angora goats, influencing mohair quality.