Search

everythinglearnresearchcommunity

for

Search:↓

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Certain genetic variations in the FST gene are linked to better wool quality in Chinese Merino sheep.

Chicken feather gene mutation helps understand human hair disorders.

The research found specific genes and proteins that affect how fast chickens' feathers grow, which is not solely determined by traditional inheritance patterns.

The article concludes that the wool follicle is a valuable model for studying tissue interactions and has potential for genetic improvements in wool production.

Some African American women's central scalp hair loss is linked to genetics and past fungal scalp infections, with more research needed on other causes.

Skin and hair can regenerate after injury due to changes in gene activity, with potential links to how cancer spreads. Future research should focus on how new hair follicles form and the processes that trigger their creation.

Facial dark spots can be caused by the sun, genetics, makeup, or medicine, and are diagnosed by patient history and skin tests.

Researchers found genes that control hair color and growth change before the visible coat color changes in snowshoe hares.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Antiandrogen therapy helps treat genetic hair loss.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Injecting CHIR-99021 into goose embryos improves feather growth by changing gene activity and energy processes.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Scientists developed tools to observe hair regeneration in real time and assess skin health, using glowing mice and light-controlled genes.

Genes controlling hair growth and immune response are disrupted in male pattern baldness.

Obesity is linked to various skin problems and may increase the risk of skin cancer.

Hair ages due to genetics and environmental factors, leading to graying and thinning, with treatments available for some conditions.

Women's hair generally gets thinner and less dense starting in their mid-thirties, with hair loss becoming more common as they age due to both genetics and environment.

Runx1 controls fat-related genes important for normal and cancer cell growth, affecting skin and hair cell behavior.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

No link found between new male baldness genes and female hair loss.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Beard hair transplantation is generally satisfying, requires 250-800 grafts, uses FUE to avoid scars, needs careful planning, has some risks, and hair regrowth starts after 4-6 months.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

Melatonin increased the activity of a hair growth gene in Cashmere goats.

Teriflunomide is effective and generally safe for treating relapsing multiple sclerosis, reducing relapse rates and disability progression.

The document concludes that oral finasteride and topical minoxidil are effective for genetic hair loss, while other treatments for different types of hair loss show promise but need more research.