Search

everythinglearnresearchcommunity

for

Search:↓

Blocking a key energy pathway in human hair follicles can trigger stress responses that stop cell growth.

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

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Deleting MED1 in skin cells causes hair loss and skin changes.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

A man with Acrodermatitis continua did not get better with etanercept treatment, and his condition worsened, suggesting treatment effectiveness may vary by genetics and race.

Too much AKR1C3 enzyme causes resistance to finasteride by increasing testosterone.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

Higher expression of the keratin-associated protein 8.1 gene in Liaoning cashmere goats is linked to finer cashmere fibers.

Keratin 15 expression in skin cells is regulated by two mechanisms involving PKC/AP-1 and FOXM1.

CAR is a useful marker for assessing alopecia areata severity.

EGM2 and SOX2 help form beige adipocytes by maintaining ASC immaturity and activating brown adipocytes.

A certain gene variation can affect protein production and is linked to male pattern baldness.

Increasing isoleucine intake improved skin and health issues in an infant with maple syrup urine disease.

MPA increases cancer spread by boosting Eph A2 activity.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

The protein CTCF is essential for skin development, maintaining hair follicles, and preventing inflammation.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

Androgens increase muscle mass by promoting myoblast growth through ornithine decarboxylase.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

CYP11A1 is crucial for skin health and disease by producing important steroids.

CCCA involves immune response and metabolism issues, suggesting new treatment options.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.