Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

LHX2 is essential for hair follicle development, controlled by NF-κB and TGFβ2 signaling.

Runx3 helps determine hair shape.

Cathepsin L deficiency causes hair and skin issues in mice.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

Egfl6 is not needed for zebrafish face development.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

Rac1 is crucial for normal hair structure and pigmentation.

A missing mK6irs1 gene causes hair loss in mice.

PTHrP is important for bone formation and may be targeted for osteoporosis treatment and longevity therapies.

Mice with extra PKCδ resist chemical-induced skin cancer but not UV-induced.

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

Agouti protein affects melanocortin receptors through competitive antagonism and receptor down-regulation.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

CRAC channels are crucial for the development and function of specialized immune cells, preventing severe inflammation and autoimmune diseases.

Overexpression of LRIG3 in skin causes hair loss.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

FoxN1 gene is crucial for proper thymus structure and normal skin appearance.

The PP2A-B55α protein is essential for brain and skin development in embryos.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

Blocking Wnt signaling in young mice causes thymus shrinkage and cell loss, but recovery is possible when the block is removed.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

Antizyme slows skin tumor growth by reducing cell growth in mice.

Mutations in the Sgk3 gene cause fuzzy hair in mice.

Overexpressing 14-3-3σ in mice skin reduces cell growth and hair density.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Small molecules KY19382 and KY19334 may help treat skin cancer by reducing CDK1 levels and blocking harmful cell signals.