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LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.

YAP1 helps fat cell formation by influencing the Hippo pathway.

Shi-Bi-Man activates hair follicle stem cells and promotes hair growth by changing lactic acid metabolism and other cellular processes.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Blocking miR-27a increases sheep hair follicle stem cell growth and decreases cell death, which could help improve wool quality and treat hair loss.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

The Cashmere goat hair keratin gene is crucial for hair structure.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

Removing the Crif1 gene in mouse skin disrupts skin balance and hair growth.

Camellia seed cake extract helps hair grow by affecting cell growth and growth factor levels.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

NXC736 significantly reduced hair loss in mice with alopecia areata.

HAPLN1 can promote hair growth and may help treat hair loss.

SAHA syndrome links oily skin, acne, excess hair, and hair loss in women, similar to PCOS.

Systemic sclerosis skin shows varied gene patterns, suggesting potential for personalized treatment.

A specific gene mutation causes severe skin and nail issues and hair loss.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

Netherton's disease causes multiple hair defects.

The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

Removing Lrig1-positive stem cells in mice causes temporary loss of sebaceous glands.

Alopecia is common in severe cases of autosomal recessive congenital ichthyosis.

Cannabinoid receptor-1 signaling is essential for the survival and growth of human hair follicle stem cells.

LSD1 is crucial for regenerating hair cells in zebrafish.