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2-DG reduces seizures by enhancing brain inhibition through specific receptor activation.

sPLA2-IIA increases growth in hair follicle stem cells and cancer cells, suggesting it could be targeted for hair growth and cancer treatment.

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

The KRTAP gene family helps understand hair evolution and hair disorders.

Hair proteins in preschool children and their mothers could indicate developmental changes and health status.

DKK-1 gene linked to hair loss in AGA and AA patients; more research needed for potential therapy.

EGFR helps control how hair grows and forms without needing p53 protein.

Keratins 6, 16, and 17 increase in damaged or diseased skin and may help diagnose skin issues.

Certain defective glucocorticoid receptor mutants move faster inside cell nuclei and work less effectively.

Family members have similar hair protein patterns, which could be useful for genetic studies.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

Keratinocyte growth factor promotes hair growth and reduces hair loss from chemotherapy.

Granzyme B is important in autoimmune skin diseases and could be a new treatment target.

Higher DKK-1 levels found in hair loss patients; L-ascorbic acid 2-phosphate, L-threonate, and ginsenoside F2 may help promote hair growth.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

The scraggly mutation causes hair loss and skin defects in mice.

PI3Kδ inhibition may effectively treat cutaneous chronic graft-versus-host disease.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

Human hair contains many proteins, with some being highly abundant and modified.

Phospholipase A2 enzymes play key roles in skin health and disease.

LHX2, with other markers, can identify hair placodes in rats.

Stress keratins are expressed less in diseased skin and are linked to differentiation, inflammation, and immunity.

Collagen peptides may boost skin and hair-related gene expression.

A protein called sFRP4 can slow down hair regrowth.