Search

everythinglearnresearchcommunity

for

Search:↓

Certain hairstyles can cause scalp diseases, smoking is linked to hair loss, 5% minoxidil foam is effective for hair loss treatment, and various factors influence wound healing and hair growth.

The hypothesis suggests that PCOS may start early in life due to genetic and environmental factors, influencing future reproductive and metabolic problems.

The document concludes that understanding hair follicle biology can lead to better hair loss treatments.

Alopecia areata is likely an autoimmune disease with unclear triggers, involving various immune cells and molecules, and currently has no cure.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Researchers created human hair follicles using a new method that could help treat hair loss.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Hair color production is closely linked to the active growth phase of hair in mice and may also influence hair growth itself.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Genes and hormones cause hair loss, with four genes contributing equally.

People with atopic dermatitis are more likely to develop other skin conditions due to shared genetics and immune pathways.

GmMAX3b gene in soybeans boosts nodulation and affects hormone levels.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Female pattern hair loss involves hormonal factors, genetics, and may be linked to low ferritin levels.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

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

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

Autophagy is crucial for normal sebaceous gland function and sebum composition.

Finasteride has a higher risk of reproductive side effects than minoxidil.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

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

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Both gene and non-gene areas of DNA evolved to make some mammals hairless.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

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

Cannabinoid receptor-1 signaling is essential for the survival and growth of human hair follicle stem cells.