Search

everythinglearnresearchcommunity

for

Search:↓

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

Both Platelet-Rich Plasma and Minoxidil foam increase hair count in women with hair loss, but Minoxidil is more effective. However, women were more satisfied with Platelet-Rich Plasma treatment.

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

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

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

Scientists found new genetic areas that affect how rice root hairs grow and develop.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Hair loss caused by longer latent hair cycle and sudden miniaturization, not gradual follicle size reduction.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

OsPRX83 helps rice survive stress by improving stress response and antioxidant activity.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive stomach cancer.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive forestomach cancer.

A rare genetic disease causes rickets and often hair loss in young children, which can improve with specific treatments.

Certain gene mutations can weaken the skin barrier and, when combined with environmental factors, lead to eczema and severe itching.

Genetically repaired stem cells may treat certain genetic diseases, Th17 cells are key in fighting systemic fungal infections, hair loss in AGA is due to progenitor cell loss, and α-synuclein transfer might contribute to Parkinson's disease progression.

Red blood cell folate levels are reliable indicators of long-term folate status in alopecia areata patients.

Hair loss caused by longer latent hair cycle and sudden miniaturization, not gradual follicle size reduction.

Understanding where cancer cells come from helps create better prevention and treatment methods.

Vitamin A affects hair loss and immune response in alopecia areata.

The document concludes that both internal stem cell factors and external influences like the environment and hormones affect hair loss and aging, with potential treatments focusing on these areas.

The document suggests using standardized methods to track and measure hair loss in alopecia areata, including patient self-assessment and a 50% improvement in specific scores as a treatment goal.

Androgens may influence T cells, contributing to higher autoimmune liver disease risk in women.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

Thiopurines help treat IBD but require genetic testing to avoid side effects.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

New treatments for male hair loss show promise but need more research for safety and effectiveness.

Hair loss in women can be slowed with treatment, but more research needed for better solutions.

Unconventional lymphocytes are important for quick immune responses and healing of skin and mucosal barriers.