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Fibroblast Growth Factor-9 helps repair heart damage after a heart attack by creating new blood vessels, especially in diabetics.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

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

Increased TEMRA cells can predict treatment outcomes in rapidly progressive alopecia areata.

Alopecia areata patients have lower SOX9 and CD34 levels, affecting hair growth.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

The STRIPAK complex is crucial for skin cell organization and creating a functional skin barrier.

NDRG1 protein helps infantile hemangioma, a common infant tumor, to grow, and its mismanagement by FOXO1 protein plays a big role in causing the tumor.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.

Two siblings have a rare hair condition caused by a new genetic variant.

Neuropilin 2 may be a biomarker for melanoma and affects melanocyte behavior.

Ritlecitinib shows promise in improving hair regrowth in adolescents with alopecia areata.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

A specific gene mutation causes complete hair loss without other health issues.

Rex rabbit fur is best harvested at 120 days for optimal hair density and quality.

Higher expression of the keratin-associated protein 8.1 gene in Liaoning cashmere goats is linked to finer cashmere fibers.

LncRNA MSTRG.14227.1 hinders hair follicle development in cashmere goats, affecting cashmere quality.

Removing the Crif1 gene in mouse skin disrupts skin balance and hair growth.

Inhibiting retinoic acid activates WNT signaling, potentially aiding hair disorder and skin cancer treatments.

The KRTAP15-1 gene affects cashmere fiber thickness in goats.

FOXN1 duplication can cause excessive hair growth.

BBS7 is crucial for maintaining healthy periodontal ligaments by supporting Shh signaling.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

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