Search

everythinglearnresearchcommunity

for

Search:↓

Mice without the p21 gene can fully regenerate injured ears due to reduced Sdf1 increase and leukocyte recruitment, suggesting new ways to induce tissue regeneration in mammals.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

UTMD with diclofenac and Doxil® improves cancer treatment by boosting immune response and reducing tumor-supporting cells.

Blocking CD44 can reduce leukocyte migration in autoimmune skin diseases.

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

Blocking the CXCR3 receptor reduces T cell accumulation in the skin and prevents hair loss in mice.

Lgr6+ cells are important for tissue repair and could be a target for treating cancer and other diseases.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

BST2 is highly expressed in certain immune cells in alopecia areata, suggesting a role in the disease.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

CS12192 effectively treats alopecia areata with better safety than current options.

P-cadherin is crucial for hair follicle pigmentation but not skin pigmentation.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

K6/ODC transgenic mice are effective for quickly identifying cancer-causing chemicals.

VDAC2 promotes cell death in cashmere goat hair follicles through the P53 pathway.

Basonuclin may help control ribosomal RNA gene activity in skin cells.

PTCH gene mutations contribute to basal cell carcinoma development.

Certain genetic markers may increase or decrease prostate cancer risk.

CD4+ skin cells may be precursors to basal cell carcinoma.

CDKN2AIP gene is less active in nevus sebaceous, affecting related RNA networks.

TCF/Lef1 is essential for skin barrier function by regulating lipid metabolism.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

Selective breeding can enhance immunity in dairy cattle.

Hair follicles help skin immune recovery after UVB exposure.

Increased ODC expression makes normally tumor-resistant mice more prone to tumor development.

RACB in barley is crucial for cell polarity and nucleus positioning, aiding fungal infection.