Search

everythinglearnresearchcommunity

for

Search:↓

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

NKG2D+CD4+ T cells are higher in alopecia areata patients and may be involved in the disease.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

KRT71 gene variants may influence camel hair shape but don't fully explain it.

Akt2 and SGK3 are both important for normal hair growth and development.

Genetic marker rs12558842 strongly linked to male hair loss.

HPV8 E6 gene causes growth of certain skin stem cells.

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

Targeting Keratin 17 may help overcome cancer therapy resistance.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

Skin side effects from CDK4/6 inhibitors in breast cancer patients are generally mild and treatable, allowing most patients to continue treatment.

Ectodysplasin inhibits Wnt signaling to help form hair follicles.

Activated β-catenin affects hair growth and skin thickness, and changes are reversible.

ALRN-6924 can protect hair follicles from chemotherapy damage by temporarily stopping cell division.

The CD44-CD49d complex boosts T cell activation and survival in autoimmune disease.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

Scientists found new and known long non-coding RNAs in mouse hair follicle stem cells that may be important for stem cell function and could be targets for cancer treatment.

The DiLiCre mouse model is an effective tool for precise genome editing using light.

PTCH gene mutations contribute to basal cell carcinoma development.

Sfrp2 increases during hair follicle catagen phase and slows keratinocyte growth.

MicroRNA-302 helps improve the conversion of body cells into stem cells by blocking NR2F2.

A rare gene variant causes hair and nail issues in a family.