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Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

The 2004 hair research meeting presented new findings on hair cell differentiation, genetic factors in hair loss, hair pigmentation, and potential targeted therapies.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

Keratosis pilaris is a common skin condition where hair follicles get clogged with keratin, mostly on the arms and thighs.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

Hair and nails are similar keratin structures with different shapes and growth, affected by the same diseases and environmental factors.

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

Chicken feather gene mutation helps understand human hair disorders.

Human hair proteins, especially keratins, can protect cells from oxidative stress in lab settings.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

Hairless mammals evolved quickly in both gene and non-gene areas related to skin and hair.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

Keratosis pilaris is a common skin condition causing a bumpy texture, sometimes linked to other diseases, with various treatments available.

A girl with a rare skin condition improved after one month of treatment with acitretin.

AP collagen peptides improve hair elasticity and gloss.

The study found that a key immune pathway protecting hair follicles is reduced in a mouse model of scarring hair loss.

Boswellia may improve skin inflammation symptoms and positively influence hair growth in mice.

Hair fiber research combines multiple sciences to improve hair care products.

A spayed dog with vaginal bone structures causing infection was successfully treated by removing the bones and administering medication.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

Scientists created a long-lasting stem cell line from human hair that can turn into different skin and hair cell types.

The study found that genetic differences related to hair growth and other traits help cashmere goats adapt to high-altitude environments.

Telogen is an active phase with important biological processes, not a resting phase.

The research identified key proteins and genes that may influence wool bending in goats.