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Concentrated nanofat helps mice grow hair by activating skin cells and may be used to treat hair loss.

FLCN helps control iron levels in cells.

NFIC helps rat dental cells grow and turn into bone-like cells.

Familial dyskeratotic comedones are a rare, inherited skin condition that is hard to treat but may improve slightly with topical retinoids and urea cream.

Recurrent NICF is a rare skin condition with unclear causes, involving follicle inflammation and crystal deposits.

OCIAD2 and DCN genes affect hair growth in goats by having opposite effects on a growth signaling pathway and inhibiting each other.

Corni Fructus extract may help manage benign prostatic hyperplasia by reducing prostate cell growth and inflammation.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

Decorin helps hair growth by influencing specific cell signals.

The calcineurin/NFAT pathway plays a significant role in the development and growth of a type of skin cancer called cutaneous squamous cell carcinoma.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Familial dyskeratotic comedones are a rare, benign skin disorder that is hard to treat.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

A specific RNA, circNlgn, contributes to heart damage and scarring caused by the cancer drug doxorubicin.

Targeting NCoR1 can help treat heart enlargement and dysfunction.

Neural crest-derived progenitor cells in the cornea could help treat corneal issues without transplants.

NonClassic Congenital Adrenal Hyperplasia is a less severe form of a genetic disorder affecting adrenal gland function.

The protein CCN2 controls hair growth by affecting hair follicle formation and stem cell activity in mice.

circCFAP20DC helps goat ovarian cells grow, aiding follicle development.

Nuclear Factor I-C is important for controlling hair growth by affecting the TGF-β1 pathway.

Early diagnosis and multidisciplinary care are crucial for managing CNOT3 syndrome.

Corneodesmosin is essential for skin and hair health, and its dysfunction can lead to skin and hair disorders.

Deleting the CDSN gene causes severe skin and hair problems, leading to death.

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

Decorin helps keep hair follicle stem cells and may prevent age-related hair loss.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

N-Cadherin is crucial in scar formation, offering potential for scar prevention therapies.

Long-term use of calcineurin inhibitors in transplant patients can cause hormone issues that can be managed with proper care.

The Blood Glucose Management Service improved patient safety and outcomes in managing blood sugar in hospitalized patients.