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New UVA-responsive nanocapsules effectively kill microorganisms in hair follicles when activated by light.

Targeting protein S-palmitoylation could lead to new skin disease treatments.

aPKCλ is crucial for keeping hair follicle stem cells inactive and maintaining normal hair growth.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

Damaged hair follicles make mice more prone to skin inflammation and skin cancer after UV exposure.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

Hutchinson-Gilford Progeria Syndrome causes rapid aging due to a gene mutation, with no cure yet, but research may lead to better treatments.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

HSL treatment speeds up hair growth and reduces oxidative stress in hair follicles of ob/ob mice.

A specific mutation in PA-PLA1α causes abnormal hair growth.

Krtap11-1 is important for hair strength and structure.

The transporter protein SH1446 in Staphylococcus hominis is key to underarm odor production.

Hair keratin-associated proteins are essential for strong hair, with over 80 genes showing specific patterns and variations among people.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Human umbilical cord stem cell vesicles may help treat aging and related diseases.

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

Lack of cystatin M/E causes thin hair and dry skin.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

Loose anagen hair syndrome may be caused by keratin gene mutations.

Stress in hair follicle stem cells causes inflammation in a chronic skin condition through a specific immune response pathway.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Non-immune factors play a significant role in alopecia areata.

A gene variant causes a skin and hair disorder by disrupting protein balance.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

Exosomes from special stem cells help treat ulcerative colitis by reducing inflammation and stress.

Lipase H is important for hair follicle function and shaping hair fibers.

Hairless protein is key for hair growth, cell differences cause gene expression variation, and the N-end rule pathway senses nitric oxide for protein breakdown.