Search

everythinglearnresearchcommunity

for

Search:↓

The protein EZH2 blocks microRNA-22, increasing STK40 protein, which helps hair follicle stem cells change and grow hair.

A genetic variant linked to hair thinning in Japanese women was found.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Nonmelanoma skin cancers have higher levels of certain osteopontin variants than normal skin.

Mutations in the HOXC13 gene cause hair and nail development issues.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

A new therapy for a skin blistering condition has not been developed yet.

TSPO might help treat anxiety and depression.

The TRPV3 gene mutation affects hair growth by keeping mice in the growth phase longer, which could help treat hair loss.

A new change in the WNT10A gene caused a condition leading to short hair growth in a Chinese family.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Some thymic peptides can increase human hair growth, while others may inhibit it.

Certain plasma proteins and genes are linked to obstructive sleep apnea, suggesting potential new treatments.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

FOXN1 gene variants cause low T cells and immune issues from birth.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Increasing TSPO in the brain reduces anxiety and depression.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

TLR2 is crucial for hair growth and regeneration, and boosting it can help prevent hair loss.

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

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

TLR2, a component in hair follicle stem cells, is crucial for healthy hair growth and regeneration, and its decrease can lead to hair loss.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.