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Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

Hoxc genes control hair growth through Wnt signaling.

A unique gene mutation was found in a family with monilethrix.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

MEX3A is crucial for maintaining intestinal stem cells in mice.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

miR-129-5p affects hair growth by targeting the HOXC13 gene.

The HCR gene contributes to psoriasis risk.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

A specific gene mutation causes congenital hair loss.

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

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Type XIX Collagen is present in specific skin and hair cells during development.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

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

The LMNA mutation affects skin structure even in asymptomatic carriers.

Vaccines and targeting TrxR variants can help prevent cancer and reduce metastasis.

Dermal EZH2 controls skin cell development and hair growth in mice.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

A specific gene mutation causes long hair in Angora rabbits.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.