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Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

The Hippo signaling pathway helps control organ size during regeneration by regulating gene expression.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

Blocking certain proteins in mouse skin can reduce and shrink skin tumors.

Researchers found new genes involved in hair growth, which could help develop new hair treatments.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

The TIP1 gene is crucial for normal plant cell growth in Arabidopsis.

ROR2 is crucial for hair follicle stem cell maintenance and self-renewal.

Too much Sonic Hedgehog protein stops hair growth in embryos.

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

The hr gene is linked to hair loss in Valle del Belice sheep.

Different PIN proteins affect plant root hair growth by changing how auxin is transported.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Ovol2 is important for proper skin healing and hair growth.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

WNT10B affects hair growth by altering gene activity in hair cells.

Blocking BACE1 and BACE2 enzymes causes hair color loss in mice.

GLABRA 2 controls ethylene production to help root hair growth during nutrient deficiency.

Tet1/2/3 enzymes affect hair follicle cell development by influencing BMP signaling.

Hairless protein and putrescine regulate each other, affecting hair growth and skin balance.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.