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

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

The SbbHLH85 protein helps sweet sorghum grow more root hairs but makes the plant more sensitive to salt.

Different light affects cell functions and can help treat skin conditions.

The technique showed that human hair has two main parts, with 68% being rigid and the rest flexible, and water swelling affects its structure.

A compound from Calophyllum inophyllum L. leaf may help treat non-small cell lung cancer.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

PDI helps restore over-bleached hair's strength and structure by attaching special peptides.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

The Ysc84/SH3yl1 protein family is important for cell movement and the process of taking in materials by interacting with actin and cell membranes.

The study concludes that certain domains in Clostridium histolyticum enzymes are structurally unique, bind calcium to become more stable, and play distinct roles in breaking down collagen, with potential applications in medicine and drug delivery.

Keratin-based particles safely improve hair strength, smoothness, and heat protection.

K6hf is a unique protein found only in a specific layer of hair follicles.

A group has developed therapies that show promise for treating cancer and various other conditions.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

Keratin's mechanical properties are influenced by hydrogen bonds and secondary structure, and can be improved with the SPD-2 peptide.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

The research explains how a human enzyme binds and processes its substrate, which could relate to its role in biological functions and hair loss.

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

Scientists improved an enzyme to better produce a hair growth-promoting chemical from an immunosuppressant.

Scientists made antibodies to tell cashmere and wool apart, which could improve how we identify animal fibers.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

The document concludes that there are still unknowns about the effectiveness, risks, and detection of performance-enhancing drugs, and doping remains a challenge.

Changes to the Foxp3 protein affect how well regulatory T cells can control the immune system, which could help treat immune diseases and cancer.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Cystatin M/E strongly inhibits cathepsin V and cathepsin L, important for skin formation.

Polyglutamic acid is a valuable, sustainable ingredient for skincare and haircare products.