Search

everythinglearnresearchcommunity

for

Search:↓

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

The study found that in Latin America, ancestry varies by location, influences physical traits, and affects how people perceive their own heritage.

Fingerprints form uniquely before birth due to specific genetic pathways and local signals.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

Modern hair transplants use small grafts for a natural look and drugs to prevent further loss, with high patient satisfaction.

Barn owls with smaller black spots have higher testosterone levels, which might be due to genetic effects on hormone regulation rather than hormone effects on coloration.

Sardinians were historically short due to a mix of genetics and factors like disease and poor nutrition, but recent height increases suggest better living conditions had a bigger impact.

Researchers identified genes and proteins that may influence wool thickness in sheep.

The machine learning model accurately predicts Systemic Lupus Erythematosus in Omani patients.

Selective breeding can enhance immunity in dairy cattle.

The document concludes that understanding hair loss patterns and careful surgical techniques are key for successful hair transplantation in oral and maxillofacial surgery.

Hair transplantation is beneficial if the right patients are chosen and the procedure is done carefully.

Some drugs can cause rare but potentially deadly skin reactions, and early treatment and avoiding the drug again are key.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Epidermal stem cells are diverse and vary in activity, playing key roles in skin maintenance and repair.

Male pattern baldness involves genetics, hormones, and needs better treatments.

Fat cells in the skin help start healing and form important repair cells after injury.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Minoxidil increases hair weight and count temporarily in men with hair loss.

Correct skin biopsy techniques are crucial to avoid misdiagnosis of skin diseases.

Women with PCOS may take longer to get pregnant but can have a normal family size, and should manage their overall health to reduce long-term health risks.

Genetics and hormones play a role in male and female hair loss, but more research is needed to fully understand it.

Hormones and genetics affect hair growth and patterns, with some changes reversible and others not.

Surgical methods like suction blister grafting and split-thickness skin grafting are highly successful for vitiligo repigmentation, but choosing the right patients is crucial for success.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.