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Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

Rare adrenal cancers that secrete androgens or estrogens have a poor prognosis and are treated primarily with surgery.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

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

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

DNA can predict physical traits like eye and hair color accurately, especially in Europeans, but predicting other traits and in diverse populations needs more research.

The meeting highlighted important advances in stem cell research and its potential for creating new medical treatments.

OsUEV1B protein is essential for controlling phosphate levels in rice.

Some people have a genetic variation that makes them less effective at breaking down drugs.

Ripretinib is effective and safe for treating advanced GIST in Chinese patients, particularly for non-gastric GISTs.

Activating β-catenin increases melanocytes and decreases Schwann cells.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

New hair regrowth model proposed, imiquimod found to kill skin cancer cells, T-cadherin loss linked to invasive skin cancer, no clear gene link to skin cancer after transplant, and study on children's hair loss shows male dominance and genetic ties.

Hair follicles are essential for skin health, aiding in hair growth, wound healing, and immune function.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

Androgenetic alopecia, or hair loss, is caused by genetic factors and hormones, with different mechanisms in men and women, and can be linked to insulin resistance and polycystic ovary syndrome.

Scientists found a specific group of itch-sensing nerve cells in mice important for feeling itch but not for sensing heat or touch.

Androgenetic alopecia is mainly caused by genetic factors and increased androgen activity, leading to hair follicle miniaturization.

BMP4 gene is crucial for hair follicle development in Liaoning cashmere goats.

Wild strawberry waste extract can be a sustainable cosmetic ingredient for treating acne and hair loss.

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

Cedrol may be an effective treatment for colorectal cancer.

Scientists successfully edited a goat's genes to grow more and longer cashmere hair.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

KRT80 may worsen cancer by increasing growth and spread, but its full effects on treatment and outcomes need more research.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

Key genes and RNAs related to hair growth in sheep were identified, aiding future breeding improvements.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.