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A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

A gene called Taqpep affects cat coat patterns like stripes and blotches.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

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

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

A specific genetic variation affects wool quality in sheep.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

The LEF-1 gene in cashmere goats was successfully cloned and analyzed, showing potential for improving cashmere production.

Nexin 1 helps control hair growth in young rats.

A specific gene mutation causes a severe skin disorder in a family.

Spermidine may help reduce hair loss and deserves further testing as a treatment.

A gene mutation in mice causes permanent hair loss and skin issues.

The gene Endothelin 3 makes mice's fur darker by increasing pigment cells and pigment levels.

Hedgehog signaling is essential for normal sebaceous gland development and affects keratin 6a expression.

The Itpr3 gene causes a specific hair pattern in mice.

N1-acetylspermidine promotes hair follicle stem cell self-renewal.

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

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

SPT6 prevents excessive skin inflammation by blocking a feedback loop.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

PBX1 reduces aging and cell death in stem cells by boosting SIRT1 and lowering PARP1.

TRPS1 is crucial for bone, kidney, and hair follicle development.

Fadrozole and finasteride change gene expression related to sex hormones and thyroid hormones in frog larvae development.

Nestin identifies specific progenitor cells in hair follicles that can become outer root sheath cells.

Heparanase is essential for hair follicle health and inner root sheath differentiation.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.