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Prostate cancer cells can make their own androgens to activate the androgen receptor, and treatments like abiraterone may increase this ability, suggesting new therapies should target the entire steroid-making pathway.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Mutations in the KRT85 gene cause hair and nail problems.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

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

ROR2 is essential for hair follicle stem cell renewal and maintenance.

Human hair follicles have their own thyroid hormone system.

A specific gene change in APCDD1 increases the risk of hair loss.

The enzyme 5α-reductase type 1 is important for blood vessel development and fertility in the uterus.

CCL5 is important for the hair growth potential of human dermal papilla cells.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

Certain enzymes react strongly with some hormones in rat skin during hair growth, mainly in sebaceous glands and hair sheaths.

Human scalp hair follicles can produce and respond to several hormones, affecting hair growth and pigmentation.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Activating Kras in mouse skin causes excess skin and hair loss.

Human keratinocytes do not naturally respond to androgens.

Finasteride effectively inhibits the enzyme steroid 5 alpha-reductase II.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

Dermal fibroblasts have adjustable roles in wound healing, with specific cells promoting regeneration or scar formation.

Calorie restriction changes the elemental and isotopic makeup of mouse hair and bone.

The CAP1 gene helps control ammonium levels and is necessary for the proper growth of root hairs in Arabidopsis.

B6.Cg-Tyr c−2J Hr hr /J mice have a stronger delayed sunburn reaction and are good for UV research.

Blocking the CCR5 receptor may be a new way to treat hair loss from alopecia areata.

A rare tumor caused unusual hormone production leading to Cushing syndrome.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

DORN1 receptor affects eATP-induced stomatal changes but not eADP in Arabidopsis thaliana.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Corin helps control salt and sweat release in sweat glands.

Prdm1 is necessary for early whisker development in mice but not for other hair, and its absence changes nerve and brain patterns related to whiskers.

Caloric restriction improves skin and fur structure but can cause muscle loss and movement issues.