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A gene variant increases the risk of a type of hair loss by affecting hair protein production.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

The Gsdma3 gene is essential for normal hair development in mice.

CCL5 is important for the hair growth potential of human dermal papilla cells.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

MED23 and GNAQ genes are crucial for chicken feather color.

Androgen receptors help prostate cancer cells grow and resist drugs.

New genes linked to male pattern baldness were found on chromosome 20p11.

Certain miRNAs might be involved in a hair loss condition called frontal fibrosing alopecia and could possibly help in its diagnosis.

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Increasing PDCD4 protein may help prevent or treat some skin cancers.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

A specific RNA helps increase the growth of skin cells in Liaoning cashmere goats by working with a protein to boost a growth-related gene.

Collagen XVII is crucial for preventing hair and pigmentation loss by maintaining melanocyte stem cells.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

A rabbit gene important for hair development was identified and detailed.

Patients with Systemic Sclerosis have much higher levels of GDF-15, which could help predict organ involvement and guide treatment.

The study found that certain mutations in the vitamin D receptor can cause rickets and potentially affect hair growth.

Genetic factors, especially PADI3 gene variants, contribute to CCCA in women of African descent.

Certain genes and pathways are crucial for high-quality brush hair in Yangtze River Delta White Goats.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

Hair loss and aging are caused by the breakdown of a key protein in hair stem cells.

CircAGK affects cell death in hair cells by controlling the miR-3180-5p/BAX pathway, which can lead to hair loss.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

Aging in one type of stem cell can cause aging-like changes in various organs.

Deleting Crif1 in mouse skin disrupts skin balance and hair growth.

DKK2 and SOSTDC1 together are necessary for the normal timing of the first regression phase in the hair growth cycle.