Search

everythinglearnresearchcommunity

for

Search:↓

Frontal fibrosing alopecia often occurs after menopause, with delayed diagnosis and possible links to certain medications and conditions.

Androgens reduce THY1 in skin cells, leading to less fat, more fibrosis, and worse healing in males.

Tofacitinib effectively treated a woman's complex autoimmune and autoinflammatory disorders.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

Women with diffuse hair loss often have lower iron and vitamin D levels, but their thyroid function is typically normal.

The fer-ts mutation in plants prevents root hair growth at high temperatures.

Tofacitinib improved ulcerative colitis, skin ulcers, and hair loss in a patient who didn't respond well to other treatments.

Certain drugs and supplements may contribute to hair loss in the frontal hairline in older women.

Tofacitinib successfully treated a woman's severe symptoms from a rare autoimmune condition.

Riboflavin is essential for health and growth, and its deficiency causes serious health issues.

Recent advances show zebrafish can model anemia, Alx4 affects craniofacial and hair development, and mTORC1 is crucial for retinal development.

Tofacitinib is a promising treatment for children with rheumatic diseases.

Tofacitinib citrate improved nail dystrophy and pain in patients with alopecia universalis without causing side effects.

Zinc is vital for health, and its deficiency can worsen gastrointestinal and liver diseases.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

Mice without active or present vitamin D receptors maintain normal blood sugar control and islet gene expression when calcium levels are normal.

Tofacitinib improved hair and nail conditions in a teen with alopecia areata.

Defective T cell metabolism can cause early skin aging and poor hair follicle stem cell function.

The research developed new fortilin protein constructs for potential heart disease treatments.

Forsythiaside A helps reduce brain damage from lack of blood flow by activating certain protective pathways.

Local testosterone treatment improved sexual desire in a female with fragile X syndrome.

ACKR2 helps prevent skin scarring and hair loss by controlling inflammation.

Iron contributes to skin fibrosis in nephrogenic systemic fibrosis.

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

Frontal fibrosing alopecia shows increased inflammation and JAK-STAT pathway activity without reduced hair proteins.