Search

everythinglearnresearchcommunity

for

Search:↓

The analysis found that alopecia areata, a hair loss condition, is not very common in Australia, affecting about 0.13% of people, with new cases most often seen in males aged 19 to 34 years.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Thyroid-related genes are active in skin cells and may affect autoimmune conditions.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

COVID-19 can cause over 50 long-term symptoms, with fatigue and headache being the most common.

PAD is common but often missed, needing lifestyle changes and medication for better outcomes.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

No single treatment is clearly effective for central serous chorioretinopathy.

Mycophenolate mofetil may improve lupus nephritis remission more than cyclophosphamide but with uncertain safety.

Different signals work together to change gene activity and guide hair follicle stem cells to become specific cell types.

Minoxidil and Finasteride are effective for male baldness; more research is needed for hair aging treatments.

The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

The engineered yeast strain BLYAS can quickly and sensitively detect androgenic chemicals.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Oral isotretinoin may slightly improve acne but increases the risk of side effects like dry lips and skin; more research is needed to understand its full risks and benefits.

Goats with BSE or scrapie show varying symptoms, and using only clinical signs may not detect all scrapie cases.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

Early recognition and treatment of Peripheral Arterial Disease is crucial to improve survival and health outcomes.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

A protein in plants needs to bind two lipids to help with root hair growth, and this process is similar across different plant species.

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

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

The review concluded that reporting on PRP therapy is often incomplete, leading to uncertainty about its effectiveness.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Scientists successfully made a human growth factor in a plant, which could help with hair growth and bone development.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

Intralesional triamcinolone injections can effectively stop frontal fibrosing alopecia with minimal side effects.

A protein found in safflower seeds can stimulate hair growth and speed up wound healing in mice.