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The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

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

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Long-term use of difluprednate eye drops in dogs can lead to hair loss and hormone imbalance.

Removing the VDR gene in skin cells reduces their growth and affects hair-related genes.

Some canine hair follicle tumors contain amyloid deposits, with a protein called CK5 involved in their formation.

Actin filaments help root hairs grow faster and longer under low potassium stress.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

The mutation helps mice handle heat better without affecting hair growth.

Understanding hair follicle development can help treat hair loss, skin regeneration, and certain skin cancers.

Activating the Sonic hedgehog gene in mice can start the hair growth phase.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Hormonal interactions, especially involving DHT and estrogen, play a key role in BPH development and treatment.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Dlx3 is essential for hair growth and regeneration.

Androgen receptors are active in many tissues of both male and female mice, not just reproductive organs.

Hydrogen sulfide disrupts protein function and root hair growth in plants by modifying proteins.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Hair follicles in mutant mice self-organize into ordered patterns within a week.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

GmMAX3b gene in soybeans boosts nodulation and affects hormone levels.

Gab1 protein is crucial for hair growth and stem cell renewal, and Mapk signaling helps maintain these processes.

Runx3 helps determine hair shape.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

ICAM-1 helps regulate hair growth cycles and skin remodeling.