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A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Sgk3 is essential for normal hair follicle growth and maintenance.

LncRNA RP11-818024.3 helps hair growth and recovery in hair loss by boosting cell survival and reducing cell death.

A3 antibody helps identify key cells in rat hair follicle development.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

The POMP gene is active in various goat tissues and affects hair growth, with certain treatments influencing its expression.

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

Increased LC3 gene expression may be linked to premature graying of hair.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

Sgk3 kinase is essential for normal hair growth in mice.

The treatment effectively promotes hair regrowth in androgenetic alopecia without causing skin irritation.

Four keratin genes are crucial for hair growth in Xinji fine wool sheep.

A new gene, JMJD1C, may affect testosterone levels in men.

The research suggests that SFRP2 and PTGDS proteins might be indicators of female pattern hair loss and could contribute to hair loss.

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

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

CTCF protein is essential for skin and hair follicle development in mice.

The EDAR gene greatly affects hair thickness in Asian populations.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

PDF2 senses specific lipids and regulates root growth and gene expression in Arabidopsis.

ATP6AP1‐CDG can cause hearing loss, hair loss, and protein issues, even in female carriers.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.