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TPA strongly increases ODC activity in certain skin cells, potentially aiding tumor growth.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

MPZL3 is important for controlling the hair growth cycle in mice and humans.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

Msx2 deficiency in mice leads to bone growth and organ development problems.

CCCA may involve the PD1/PDL1 pathway and increased caspase 3, leading to permanent hair loss.

PROTACs offer a new, precise way to treat cancer by breaking down harmful proteins.

CRH causes hair loss by reducing cell survival in hair follicles.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

Wnt proteins from certain skin cells are crucial for normal hair growth and renewal.

MEF2C is crucial for normal hair cycle progression.

Tmem30b is essential for hearing by maintaining hair cell structure in the ear.

A rare scalp tumor was removed from a 49-year-old woman, with a good outlook if benign but needing careful monitoring if malignant.

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

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

Cells from a skin condition can create new hair follicles and similar growths in mice, and a specific treatment can reduce these effects.

Peficitinib can turn human fibroblasts into cells that help grow hair.

Centrosomes are essential for healthy skin and hair growth, and their role is different from that of cilia.

A new mouse mutation causes skin and hair issues, influenced by another gene.

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

HLD10 can include increased body hair and Mongolian spots.

Foxn1 helps skin cells mature by controlling a specific protein's activity.

Deleting the BRD4 protein in certain skin cells causes hair loss and skin inflammation.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

ALX4 is crucial for normal craniofacial and hair development, with specific roles in different cell types.

Variation in the TCHH gene affects wool curliness in sheep.