Search

everythinglearnresearchcommunity

for

Search:↓

sPLA2-IIA increases growth in hair follicle stem cells and cancer cells, suggesting it could be targeted for hair growth and cancer treatment.

Deleting the scd1 gene in mice prevents obesity by disrupting skin lipids and improving heat regulation.

AIMP1 can boost hair growth by increasing stem cell activity.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Blocking CISD1 reduces hearing loss from cisplatin in mice.

LSD1 is essential for healthy skin development and creating the skin's protective barrier.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

SLC3A2 is crucial for hair follicle stem cell function and hair growth.

Mice with the ab gene have abnormal sebaceous gland development, affecting sebum production.

Dsg1 is essential for maintaining a healthy skin barrier in mice.

A new gene mutation causes a rare type of hair loss.

S100A4 and NMIIA promote tumor growth in glioblastoma by enhancing blood vessel functions.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Lack of KSR1 stops certain skin tumors in mice.

GLI1 might protect against the start of skin cancer and is not linked to cancer severity.

Infants with severe KID syndrome may be more prone to serious infections and need close monitoring.

Serine is vital for hair follicle stem cells to balance hair growth and skin repair.

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

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

PIEZO1 helps keep hair follicle stem cells inactive, affecting hair growth.

CCCA in women of African ancestry may be caused by PADI3 gene mutations and intense hair grooming.

The SYP123-VAMP727 complex is important for transporting materials that harden the root hair shank in Arabidopsis.

Mutations in the LIPH gene cause woolly hair in a child.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

SII is a useful and affordable tool to assess and monitor alopecia areata.

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