Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

Zfp157 is active in many mouse tissues during development and in specific adult cells.

Clq deficiency is linked to systemic lupus erythematosus symptoms.

Msx2 and Foxn1 are both crucial for hair growth and health.

DNA methylation of miR-365-1 causes hair follicle stem cell death by affecting DAP3.

Sonic hedgehog signaling is needed for the development of touch-receptor cells in the skin, and the loss of Polycomb repressive complex 2 can lead to more of these cells.

Targeting CD169+ skin macrophages may help treat psoriasis.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

Loss of Dnmt3a and Dnmt3b increases aggressive skin tumors by affecting PPAR-γ.

Gorab deficiency speeds up skin aging by disrupting protein regulation and reducing collagen.

Homozygous K5Cre transgenic mice have wavy hair and faster cancer progression.

Combining L-cysteine, NAC, and a MET inhibitor significantly kills cervical cancer cells.

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

Krox20 (Egr2) is important for the function of epithelial stem cells.

Mice with human fetal thymic tissue and stem cells developed symptoms similar to chronic graft-versus-host disease.

A new keratin gene was found in mice, explaining hair growth.

A new keratin 6 type in mice explains why some mice without certain keratin genes still have normal hair and nails.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

Fz3 and Fz6 can partially replace each other in tissue polarity and axon guidance.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

Sox9 levels in brain stem cells affect whether they stay as stem cells or become neurons.

TNF alpha in skin cells causes weight loss, hair and fat issues, and skin inflammation in mice.

Human cathepsin V can replace mouse cathepsin L to maintain normal skin and hair in mice.

Gene expression, especially Dkk4, is key to cat color patterns.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

The retinoid receptor antagonist effectively disrupts vitamin A-related development in embryos.

Disrupting Notch signaling in blood vessels increases scarring during wound healing in mice.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.