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Mice without the p21 gene can fully regenerate injured ears due to reduced Sdf1 increase and leukocyte recruitment, suggesting new ways to induce tissue regeneration in mammals.

Upadacitinib may effectively treat twenty-nail dystrophy without causing pain.

CDP is crucial for lung and hair follicle cell development.

pCLCA2 protein may help maintain skin structure and function.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

A certain gene variation can affect protein production and is linked to male pattern baldness.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

KRT72 gene helps form hair.

Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.

The study found nine new hair protein genes in human hair follicles.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

A new gene mutation causes a rare type of hair loss.

CaV1.2 helps activate hair follicle stem cells without calcium flux.

PAK4 is crucial in cancer progression, brain development, and could be a therapeutic target, especially through the PAK4-CREB axis.

PP2Acα is essential for proper hair and skin development.

A genetic marker linked to a type of hair loss was found in most patients studied.

α-parvin is necessary for skin and hair growth and for the correct orientation of skin cells.

A new gene mutation linked to a skin condition was found in a Spanish family.

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

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

Nexin 1 may help control hair growth.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

Only one K16 gene on chromosome 17 makes a functional keratin protein.

Twist1 is crucial for UVB-induced skin cancer development.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Hair stem cells produce a protein called COL17A1 that plays a key role in their development and is linked to hair thinning and baldness.