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The research suggests that immune cells and a specific type of cell death called ferroptosis are involved in Frontal fibrosis alopecia.

Mutations in hKAP1 genes may cause hereditary hair disorders.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

Fos protein is crucial for cell transition to cornification in keratinized tissues.

PDRN is effective and safe for healing wounds and skin issues.

Targeting PTEN can improve healing in venous leg ulcers.

Scientists discovered a new way UVB light increases skin pigmentation through the ATP-P2X7 pathway.

The plant hormone auxin activates the TOR pathway, affecting gene expression related to growth and cell size.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

LncRNA RP11-818024.3 helps hair growth and recovery in hair loss by boosting cell survival and reducing cell death.

p14ARF and p16Ink4a cause hair follicle stem cell aging and dysfunction.

Antizyme reduces tumor growth and normalizes skin cell development affected by MEK.

Monitoring TGF-β and linc-PINT expression may help identify and treat high-risk heart arrhythmia patients.

Janus kinase inhibitors are effective and safe for treating alopecia areata.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

Blocking the JAK/STAT pathway may help reduce skin sensitivity in Xeroderma pigmentosum.

Fibronectin is essential for hair follicle regeneration by supporting stem cells.

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

Neurotrophin-4 increases calcium current in specific mouse neurons through the PI3K pathway.

Ivarmacitinib significantly improved hair regrowth in severe alopecia areata after tofacitinib was less effective.

Certain peptides can prevent hair loss in young rats caused by a cancer drug.

ePUKs could be valuable for regenerative medicine due to their wound healing abilities.

Sorafenib causes skin reactions by increasing the number and activity of skin mast cells.

Mitf plays a key role in melanoma progression and is linked to disease stage.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

Using Janus kinase inhibitors (JAKi) in COVID-19 treatment requires careful consideration due to their immunosuppressive effects.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

The fuzzy gene is crucial for controlling hair growth cycles.