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A woman's hair loss worsened after starting hepatitis C treatment due to immune changes in her hair follicles.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Certain proteins and their receptors are more active during the growth phase of human hair and could be targeted to treat hair disorders.

Lipase H is important for hair follicle function and shaping hair fibers.

Overexpression of sPLA2-IIA in mouse skin reduces hair stem cells and increases cell differentiation through JNK/c-Jun pathway activation.

K6hf is found in specific parts of hair follicles, nails, and tongue, and is linked to hair growth and structure.

Type II keratin genes are crucial for hair follicle differentiation and have a conserved structure and expression pattern.

Overexpressing 14-3-3σ in mice skin reduces cell growth and hair density.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

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.

Finasteride increases CD8+ T cells in BPH tissues.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

Tgm2 helps stabilize dying cells and aids fibroblast attachment to the extracellular matrix.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

Foxp1 helps control hair stem cell growth and response to stress during hair growth cycles.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

CRAC channels are crucial for the development and function of specialized immune cells, preventing severe inflammation and autoimmune diseases.

ASLNC168501 can help treat hair loss by restoring hair follicle stem cell function.

Targeting THY1 can improve skin repair and healing.

The hHa7 gene is regulated by androgens in certain body hair, not scalp hair.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

ASLNC168501 may help treat hair loss by boosting hair follicle stem cell activity.

Specific immune cells cause alopecia areata and blocking certain proteins can prevent it.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

BTNL2 helps protect hair follicles from immune attacks, which could aid in treating alopecia areata.

A specific gene mutation causes congenital hair loss.