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Overexpressing the glucocorticoid receptor in mice leads to abnormal skin development and reduced inflammation.

A low dose of rapamycin increases inner ear hair cell creation by boosting SOX2+ cell numbers.

Removing certain hair follicle stem cells worsens skin reactions to allergens.

Dexamethasone affects hair growth by altering levels of proteins that either promote or inhibit hair follicle growth.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

WNT10A gene mutations cause short anagen hair syndrome.

The enzymes Aldh1a2 and Aldh1a3 are involved in making retinoic acid in hair follicles and have different roles in hair growth.

Key genes and RNA networks regulate hair growth and follicle density in Rex rabbits.

The gene URB is more active in human hair growth cells and responds to a hair-related hormone.

A protein called sFRP4 can slow down hair regrowth.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

SASH1 gene mutations are linked to various inherited skin pigmentation disorders.

The protein AtRXR3 limits root hair growth in Arabidopsis, affecting phosphorus uptake.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Early genetic testing and new therapies like secukinumab are crucial for managing Netherton syndrome effectively.

The study created a mouse model to better understand hair follicle stem cells' role in hair growth and repair.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

EP 2 receptor is essential for heart repair by helping macrophages work properly.

TLR2 helps control hair growth and regeneration, and its reduction with age or obesity can impair hair growth.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Blocking the androgen receptor in skin cells reduces their growth response to male hormones, suggesting a possible treatment for skin conditions linked to androgens.

Dysplastic nevi have unique gene expressions, making them distinct from common melanocytic nevi.

A person with a new mutation in the SCN1A gene developed brain inflammation after COVID-19.

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

RpoS helps Borrelia burgdorferi survive in hosts and adapt to different environments.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

The FOS gene helps hair growth in Tan sheep.