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The calcineurin/NFAT pathway plays a significant role in the development and growth of a type of skin cancer called cutaneous squamous cell carcinoma.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

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

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

The combined treatment effectively managed severe skin issues in Olmsted syndrome.

The TRPV3 channel structure changes linked to severe itch and hyperkeratosis were identified using cryo-EM.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

Immune cells might contribute to hair loss caused by a specific mutation.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

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

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Activating TRPA1 reduces scarring and promotes tissue regeneration.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

A specific gene mutation causes Olmsted syndrome.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

Disrupting YAP signaling in skin cells leads to scar-free healing directed by specific cell signals.

CBD can either promote or inhibit hair growth depending on the concentration used.

Hair follicles in androgenetic alopecia age faster, especially in the front.

Minoxidil improved hair growth in a child with a rare genetic disorder.

The research identified specific genes that are active in the cells crucial for hair growth.

A 21-year-old male with a rare genetic disorder experienced sudden hair loss and high DHEAS levels, likely due to a condition similar to PCOS, usually seen in women.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Bacteria can help skin regenerate through a process called IL-1β signaling.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

Scientists found key proteins and genes that affect skin and hair health, and identified potential new treatments for hair loss, skin disorders, and wound healing.