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A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

DNA methylation controls lncRNA2919, which negatively affects hair growth.

The study found stem cells in minor salivary glands that can differentiate and are involved in tumor formation when exposed to tobacco.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

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

GLI2 activates GLI1, promoting skin tumor growth and hair development.

Certain gene combinations improve cashmere quality and production in Liaoning goats.

Turning off the Lhx2 gene in mouse embryos leads to slower wound healing and scars.

A genetic variant in goats is linked to cashmere growth.

The gene GJA1 is important for regulating coarse hair density in goats.

AtCSLD3 and GhCSLD3 genes enhance root growth and cell elongation in plants.

Blocking a certain signal in the gp130 receptor can improve tissue healing and lessen osteoarthritis symptoms.

RNase L hinders hair growth by altering immune signals.

Progranulin overexpression leads to shorter, thinner hair and increased cell death in mouse hair follicles.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

The protein SLC1A3 is important for activating skin stem cells and is necessary for normal hair and skin growth in mice.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

GLPLS is a rare skin condition with specific hair loss and skin symptoms.

Hair loss gene found on chromosome 3q26.

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

The Itpr3 gene causes a specific hair pattern in mice.

Sry may regulate fatty acid metabolism and shows different expression levels in rat tissues.

Certain long non-coding RNAs are important for controlling hair growth cycles in sheep.