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The study concluded that hair growth in mice is regulated by a stable interaction between skin cell types, and disrupting this can cause hair loss.

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

Hair follicles help substances penetrate the skin faster and more effectively.

Selective breeding caused the unique curly hair in Mangalitza pigs.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

Cornu cervi pantotrichum pharmacopuncture solution helps mice grow hair by increasing hair follicle cell growth and a growth factor important for hair development.

Faulty inflammasome activation may lead to autoimmune skin diseases and could be a target for new treatments.

FGF18 treatment during hair's resting phase can protect against hair loss from radiation.

Diagnosing alopecia areata is challenging and requires careful examination and various tests to distinguish it from other hair loss types.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Adding soybean oil to Nonomuraea dietziae increases production of a beneficial compound by improving metabolism and enzyme systems.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

Wnt-10b is important for keeping mouse skin cells healthy for hair growth.

The research found that certain microRNAs are important for human hair growth and health.

DHT reduces a cell's ability to promote hair growth, while 3D culture without DHT improves it.

The endocannabinoid system affects oil production and inflammation in skin cells.

Zinc deficiency disrupts hair growth and cycle, but zinc supplements can fix this.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

The research found that people's hair proteins vary, especially by ethnicity and body part, which could help identify individuals in forensic science.

The research found that people's hair proteins vary by individual and body part, with some differences between ethnic groups, which could help in forensics.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

sPLA2-X is crucial for normal hair growth and follicle health.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Human hair proteins vary by individual, body site, and ethnicity, useful for forensics.

LPA3 signaling in the uterus is crucial for placental formation and fetal development.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.