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A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

FERONIA and LRX proteins help control cell growth in plants by regulating vacuole expansion.

Keratin mutations cause skin diseases and could lead to new treatments.

The study identified key genes and pathways linked to hair disorders, aiding precision medicine.

BMI1 is essential for preventing hair greying and maintaining hair color.

Overactive Wnt5a disrupts hair follicle orientation in mice.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

Type XVII collagen helps control skin cell growth and could be a target for anti-aging treatments.

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

The Arabidopsis rhd2 mutant is more sensitive to drought because of changes in cell membrane proteins and cell structure.

PAK4 is crucial in cancer progression, brain development, and could be a therapeutic target, especially through the PAK4-CREB axis.

A girl had rickets due to a gene mutation affecting vitamin D response.

KRTAP2-3 could help predict cancer recurrence by identifying specific cancer cells.

Lrig1 and Lgr6 stem cells help maintain hair follicles and influence skin cancer development.

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

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

GLABRA2 gene controls root-hair growth by regulating phospholipid signaling.

FTase and GGTase-I are essential for skin keratinocyte health.

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

Follistatin and LIN28B together improve the ability of inner ear cells in mice to regenerate into hearing cells.

Sdr16c5 and Sdr16c6 genes regulate a key point in lipid production that affects eye and skin gland function.

RNA aptamers can specifically block FGF5-related cell growth, potentially treating related diseases or hair disorders.

DA-9401 helps protect rat testis from finasteride damage.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.

The vitamin D receptor helps control hair growth and may protect against certain skin tumors.

Wnt/β-catenin signaling is crucial for cell fusion in placental development.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.