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Scientists found new and known long non-coding RNAs in mouse hair follicle stem cells that may be important for stem cell function and could be targets for cancer treatment.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

The Ysc84/SH3yl1 protein family is important for cell movement and the process of taking in materials by interacting with actin and cell membranes.

BBS7 is crucial for maintaining healthy gums by regulating important signaling pathways.

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

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

Lateral plate mesoderm helps create skin and amnion-like tissues for studying development and therapies.

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

7DHC and BM15766 damage hair follicle structure and reduce key gene expression.

Lamins are vital for cell survival, organ development, and preventing premature aging.

The osteopontin gene is active in a specific part of rat hair follicles during a certain hair growth phase and might affect hair cycle and diseases.

RORA boosts autophagy in hair follicle stem cells, potentially aiding hair growth.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Id2 gene helps keep hair follicle stem cells inactive.

Early involution in Hirosaki hairless rats' mammary glands is linked to a unique modification of STAT5A.

REV7 is crucial for genome stability and cancer treatment, making it a potential target for therapy.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

Defective nuclear transport may cause gene expression changes in Progeria.

SOX9 is essential for the development of various organs and hair follicles.

4-O-Methylhonokiol helps protect skin cells from growth-stopping effects of a protein by regulating growth-related pathways.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

RORA plays a key role in controlling seasonal hair molting by affecting hair follicle cell activity.

A specific DNA duplication in Polish chickens affects feather shape by altering gene expression.

BMP-2 activates the Dlx3 gene in mouse skin cells, important for hair and skin development.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

Several genes, including Hox-7A, Stra6, and Lim-1, are involved in normal palate formation.