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The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

Injecting lentiviral vectors into early gestation mice effectively targets skin stem cells for potential gene therapy.

Rat vibrissae structure relates to their sensory function.

Two siblings were diagnosed with Trichothiodystrophy, identified by brittle hair and low sulfur content.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

RAR-gamma 1 is important for normal skin maintenance and differentiation.

Prenatal diagnosis of trichothiodystrophy is possible in the second trimester using fetal eyebrow biopsy, with sulfur content analysis being more reliable.

PROTACs show promise in cancer treatment by effectively degrading specific harmful proteins.

CaV1.2 helps activate hair follicle stem cells without calcium flux.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

CXCR2 in skin cells promotes tumor growth.

Resveratrol shows health benefits but faces challenges in effectiveness and regulation.

New research suggests that skin cell renewal may not require a special type of cell previously thought to be essential.

FLCN helps control iron levels in cells.

Cinacalcet may help treat hereditary vitamin D resistant rickets safely.

New compounds effective against SARS-CoV-2 variants were identified using a rapid testing method with human lung cells.

Mice without active or present vitamin D receptors maintain normal blood sugar control and islet gene expression when calcium levels are normal.

Tralokinumab effectively improved atopic dermatitis symptoms in most patients, but some stopped due to side effects like hair loss.

A gene mutation causes monilethrix in a Chinese family.

Tph cells are linked to the severity of systemic lupus erythematosus.

Arabidopsis Formin 2 stabilizes actin filaments, affecting cell-to-cell movement and virus susceptibility.

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

A specific gene mutation causes different hair defects in Indian monilethrix families.

The vitamin D receptor is essential for skin stem cells to grow, move, and become different cell types needed for skin healing.

Trichoscopy helps accurately diagnose temporal triangular alopecia.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.