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

Higher FABP4 levels may indicate more severe alopecia areata.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

The HR protein's role as a repressor is essential for controlling hair growth.

S100A6 protein is linked to disease progression, especially in cancers.

Increasing PBX1 reduces aging and cell death in hair follicle stem cells by boosting SIRT1 and lowering PARP1 activity.

A genetic marker linked to a type of hair loss was found in most patients studied.

ASH2L is essential for skin and hair development.

Smad4 is important for healthy hair follicles because it helps produce a protein needed for hair to stick together and grow.

Removing SIX1 in fat cells reduces skin fibrosis.

Modified HDL can better deliver drugs and genes, potentially improving treatments and reducing side effects.

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

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

Increasing miR-149 reduces hair follicle stem cell growth and hair development by affecting certain cell growth pathways.

SASH1 gene mutations are linked to various inherited skin pigmentation disorders.

Researchers found a non-functional sheep keratin gene due to mutations.

Two new proteins, hKAP1.6 and hKAP1.7, are found in the hair follicle cortex.

Hairless protein is key for hair growth, cell differences cause gene expression variation, and the N-end rule pathway senses nitric oxide for protein breakdown.

Naked-mouse hair lacks certain proteins and has less soluble fibril.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

SH-SY5Y cell lysate is effective for diagnosing Satoyoshi syndrome.

Ectodin integrates BMP, SHH, and FGF signals in developing ectodermal organs.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Knockout mice showed anemia and hair loss, suggesting other ways exist for iron absorption.

NXC736 significantly reduced hair loss in mice with alopecia areata.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.