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The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

Marsupial hair structure and keratin distribution are similar to placental mammals.

Hair growth-related cells need the enzyme SCD1 to help maintain the area that supports hair growth.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Melanocyte-associated antigens may play a key role in alopecia areata and could be targets for new treatments.

Cathepsin L is essential for normal hair growth and development.

SK2 channels help control sensory signals in rat muscle spindles and hair follicles.

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

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Cells that move well may improve hair loss treatments by entering hair follicles.

The C-terminal tail of AHF/trichohyalin is essential for organizing keratin filaments in keratinocytes.

Mice without the Sept4/ARTS gene heal wounds better due to more stem cells that don't die easily.

A specific gene mutation causes sparse, brittle hair in a family.

CHI3L1 and CXCL5 proteins help promote hair growth.

SCUBE3 is a potential target for cancer and alopecia treatment but is challenging to target due to its varied roles.

A protein called COMP is part of the connective tissue in normal human hair follicles and may be important for hair health.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Ceramide Synthase 4 is crucial for maintaining hair follicle stem cells and preventing hair loss.

Two specific genes are more active during hair growth in mice.

A litter of cats had a hair condition similar to a mouse mutation, leading to hair loss and abnormal hair and skin.

Skin stem cells in hair follicles are important for touch sensation.

Muscarinic acetylcholine receptors in skin cells help regulate and promote hair growth.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.