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Tet2 and Tet3 enzymes are important for controlling hair growth and shape by affecting gene activity and DNA structure in hair follicles.

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

Tet2 and Tet3 enzymes are essential for controlling hair growth by affecting DNA demethylation and gene expression in mice.

Targeting impaired Nrf2 signaling might help treat hidradenitis suppurativa early on.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

The human skin's outer layer has more variety in cell types and development paths than previously thought.

Human hair follicles can produce stem cells that turn into heart muscle cells.

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

Activating cAMP and ATP improves hair growth and strength.

TRPS1 loss in balding scalp areas contributes to hair loss in androgenic alopecia.

Skin can heal wounds without hair follicle stem cells, but it takes a bit longer.

TGase 3 helps build hair structure by forming strong bonds between proteins.

The research found specific proteins that affect fiber characteristics and hair growth in sheep and goats.

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

Humans, especially vulnerable groups, can catch skin infections from small mammals.

Heating hair proteins changes their structure and may improve their blood clotting ability.

Runx1 helps control the KAP5 gene in human hair follicles.

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

High wool density in Rex rabbits is linked to specific gene activity affecting hair follicle development.

Avoid high-tension styles and use professional treatments to reduce hair damage and health risks.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Hair protein analysis might help identify a person's ethnicity, sex, and age in forensics.

A British Bulldog had a unique viral plaque caused by Canine papillomavirus 18, different from typical tumors.

Different sebaceous gland diseases can be treated with medications, hormone therapy, or surgical methods.

White-tailed deer can get a hair loss condition that might make them more vulnerable to environmental threats.

The man has a genetic skin condition called pachyonychia congenita.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

New imaging technology can show up to 40 different markers in hair loss tissue, helping to understand hair disease better.