Search

everythinglearnresearchcommunity

for

Search:↓

Increasing COX-2 in mouse skin causes bigger sebaceous glands and thinner hair, but stopping COX-2 can reverse hair thinning.

Beta-trace protein may help diagnose and predict treatment response in certain nerve disorders.

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

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Patients with Alopecia areata have fewer specific immune cells that normally regulate the immune system, which may contribute to the condition.

Overexpressing IGF-1 in mice leads to skin abnormalities and tumors.

New findings suggest potential treatments for melanoma, hyperpigmentation, hair defects, and multiple sclerosis, and show skin microbiome changes don't cause atopic dermatitis.

Skin grafts on mice can cause an immune response leading to hair loss, useful for studying human hair loss conditions.

Trichothiodystrophy involves brittle hair due to low sulfur amino acids, not a transport defect.

The Hairless gene is crucial for healthy skin and hair growth.

Male-to-female skin grafts in mice are rejected due to sex-linked antigens.

Triphenylphosphine oxide can increase oil production and reduce inflammation in skin cells without affecting TRPM5.

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

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Mice without the IL-6 gene had more hair growth after injury due to higher activity of a related protein, Stat3.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

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

G-1 promotes hair growth in female mice by activating specific signaling pathways.

Abnormal keratin expression in mice causes severe oral issues, affecting feeding.

Lhx2 helps retinal cells respond to signals for eye development.

CRISPR gene editing reduces harmful molecules in cells from Emery–Dreifuss Muscular Dystrophy patients.

Two mouse mutants have defective hair cuticle cross-linking.

Mouse models help understand alopecia areata and find treatments.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

DGAT1 enzyme is crucial for healthy skin and hair by regulating retinoid levels.