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A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Mice lacking steroid 5α-reductase 2 show less aggression and better impulse control.

H19 boosts hair growth potential by activating Wnt signaling, possibly helping treat hair loss.

A woman's mature cystic teratoma caused her virilization by producing testosterone.

A woman's increased facial hair and hair loss were caused by a rare ovarian tumor, cured by surgery.

The treatment was not recommended due to limited effectiveness and significant side effects.

Loss of the Y chromosome and UTY gene activity increases cancer risk in men.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.

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

Higher IL-17A and IL-23 levels are linked to alopecia areata severity and could help in tracking and treating the disease.

This enzyme helps metabolize fatty acids and isoleucine, and could be key in treating neurological diseases and certain cancers.

Alopecia areata severity is linked to increased TH1 and TH2 activity.

Targeted cytokine treatments may help with alopecia areata, but more research is needed.

Metabolic syndrome is linked to skin diseases, requiring integrated treatment and monitoring.

Stem cell treatment from umbilical cords reduces symptoms of atopic dermatitis and may help hair growth.

Atopic dermatitis may trigger alopecia areata, and early treatment can help prevent severe cases.

Upadacitinib is safe and effective for treating alopecia areata and atopic dermatitis in children.

The name Janus is fitting for JAK inhibitors as they revolutionize dermatology treatments.

Eurycoma longifolia extract may help increase testosterone levels and reduce andropause symptoms.

Certain CD8+ T cells attack hair follicles in alopecia areata, suggesting they could be targeted for treatment.

Most 46XX CAH patients have female identity, but a few identify as male and may need treatment and surgery.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

LPA3 signaling in the uterus is crucial for placental formation and fetal development.

A boy's early puberty caused by a testicular tumor returned to normal after surgery.

A mutant FERONIA gene affects root hair growth at high temperatures.

IL-26 has antimicrobial and pro-inflammatory effects in the chronic skin condition Hidradenitis Suppurativa.