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Overexpression of COX-2 causes early hair loss in mice, but can be prevented with a COX-2 inhibitor.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

SOX10 in hair follicles is linked to inflammation in alopecia areata.

RXRα is crucial for proper immune response and links diet to immune function.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

Researchers found a new mutation causing total hair loss from birth.

Id2 gene helps keep hair follicle stem cells inactive.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

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

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

BMP-2 activates the Dlx3 gene in mouse skin cells, important for hair and skin development.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

The research found that the molecule lncRNA-H19 helps hair follicle cells grow by affecting certain cell pathways in cashmere goats.

Connexin 30 is usually absent in normal skin but can appear in certain skin conditions.

A new gene mutation causes a rare type of hair loss.

Mutations in the Whn gene affect hair keratin gene expression differently.

Pitx2 helps outer root sheath cells differentiate but can't start hair growth on its own.

EZH2 is essential for hair growth and skin cell development.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

A gene mutation in mice causes skin defects and early death.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

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

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

BMP2 and BMPR-IA may stop hair growth while Noggin may encourage it in yak skin.