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The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

Acne patients have higher mTOR gene expression.

Tofacitinib effectively improved severe skin symptoms in a patient with Hypohidrotic Ectodermal Dysplasia.

TEC kinases may help cause inflammation in vitiligo and could be targeted for treatment.

PXX is an effective and affordable photocatalyst for creating new chemical bonds in organic synthesis.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Sweat gland development involves two unique skin cell programs and a temporary skin environment.

A new type of nerve cell involved in itch perception was discovered.

KRT72 gene helps form hair.

Skin changes in Pseudoxanthoma elasticum patients can indicate the severity of related health issues.

AVT is highly conserved and may have antimicrobial properties.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

Lack of cystatin M/E causes thin hair and dry skin.

The LAMTOR3 gene is involved in cashmere goat hair growth and is affected by certain treatments and other genes.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

Hair follicle stem cells help maintain skin health by moving to and supporting the skin's surface layers.

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

Reducing Tyrosinase prevents mature color pigment cells from forming in mouse hair.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

Endoglin is important for proper hair growth cycles and stem cell activation in hair follicles.

Certain gene variations are found in people with polycystic ovary syndrome.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

A genetic variant in the KRT25 gene causes tightly curled hair.

The enzymes Tet1, Tet2, and Tet3 are important for the development of hair follicles and determining hair shape by controlling hair keratin genes.

Dermal EZH2 controls skin cell growth and differentiation in mice.

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