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Rice husk and bran extracts from the Bue Bang 3 CMU variety can potentially treat hair loss due to their antioxidant, anti-inflammatory, and anti-androgenic properties.

Biotin supplements significantly improved a young girl's uncombable hair.

Dexamethasone reduces inflammation and delays skin cell changes caused by TPA.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

IL-17 inhibitors for psoriasis may cause unexpected hair loss.

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WNT7A gene expression is higher in early stages of androgenetic alopecia, showing the role of WNT pathway, apoptosis, and inflammation in the disorder.

CK7 and CK20 help identify and classify tumors for accurate cancer diagnosis.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

Vesicles made of behenyltrimethylammonium chloride and stearic acid can triple the skin absorption of hinokitiol, which may help with hair growth.

The technique helps measure how hair styling ingredients affect hair's stiffness and flexibility.

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A cluster of sulfur-rich hair protein genes was found on chromosome 17.

The E2 protein affects gene activity in hair follicles of mice.

Tmem50b and 2610305D13Rik genes play key roles in early mouse embryo development.

Mutations in the KRT85 gene cause hair and nail problems.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

SPT6 prevents excessive skin inflammation by blocking a feedback loop.

The compound (NH4)2Mn0.17Cu0.83Cl4.2H₂O has a specific structure, shows weak magnetism at low temperatures, and undergoes phase changes at high temperatures.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

SARM-induced changes in the androgen receptor are specific to each ligand and affect stability and protein interactions.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.