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The document concludes that the skin's immune system is complex, involving interactions with hair follicles, nerves, and microbes, and can protect or cause disease, offering targets for new treatments.

Telomere damage affects skin and hair follicle stem cells by messing up important growth signals.

Blocking Wnt/β-catenin signaling with EGF receptor is necessary for proper hair growth.

Proper control of β-catenin activity is crucial for development and preventing diseases like cancer.

Thymus transplantation successfully restored immune function in infants with FOXN1 deficiency.

The summit aimed to speed up finding treatments for alopecia areata.

Basement membrane changes are crucial for hair follicle development.

Mesenchymal stromal cells may help treat severe COVID-19, but more research is needed to confirm their effectiveness.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

DNA methylation and long non-coding RNAs are key in controlling hair growth in Cashmere goats.

SLFC can improve scalp health and reduce sensitive scalp symptoms.

Scientists have created a new hair loss treatment using ultrasound to deliver gene-editing particles, which resulted in up to 90% hair regrowth in mice.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

The BMP2 gene is more active in the early growth phase of Cashmere goat hair and may affect hair regeneration and textile production.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Steroid Sulfatase inhibitors show promise in treating hormone-dependent disorders like cancers, hair loss, and acne, with 667COUMATE being a potential candidate for breast cancer treatment trials.

A protein from fat-derived stem cells, DKK1, is linked to hair loss and blocking it may help treat alopecia areata.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Certain gene variations are linked to the thickness of cashmere goat hair.

New single-cell analysis techniques are improving our understanding of stem cells and could help in treating diseases.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.