Search

everythinglearnresearchcommunity

for

Search:↓

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

Genetically modified stem cells from human hair follicles can lower blood sugar and increase survival in diabetic mice.

Myotonic Dystrophy may age cells faster, and drugs that target aging could be potential treatments.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

Humans and pets share similar allergy mechanisms, and studying pet allergies can help treat both human and animal allergies.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

Different fields of expertise must work together to better understand hair growth and create effective hair loss treatments.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

Taurine is important for many body functions and its deficiency can cause health problems.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Edar signaling is crucial for proper hair follicle development and function.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Methionine restriction works better than betaine for treating CBS deficiency symptoms in mice.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

High-frequency ultrasound can effectively visualize and assess hair loss.

New treatments and early diagnosis methods for permanent hair loss due to scar tissue are important for managing its psychological effects.

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

Too much androgen can cause hair loss; finasteride may help.

Minoxidil and finasteride effectively treat hair loss.

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

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

Environmental and cosmetic factors, including heat, chemicals, and sun exposure, can cause hair loss and damage.

The document concludes that hair loss is complex, affects many people, has limited treatments, and requires more research on its causes and psychological impact.