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Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

Young women with nonclassic congenital adrenal hyperplasia may experience worse sexual function and mild depression compared to healthy women.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

We need better ways to test and understand SARMs to make safer and more effective treatments.

Finasteride caused blisters on hands and feet.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

Children with classic congenital adrenal hyperplasia have thicker heart fat and are at higher risk for heart problems and early atherosclerosis.

Lipedematous alopecia involves a thickened scalp and hair loss, with limited effective treatments available.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

MC4R gene variants not linked to female hair loss.

Tofacitinib and ruxolitinib are effective and safe for treating various autoimmune skin and joint disorders.

Gintonin-enriched fraction promotes hair growth and could be a potential alopecia treatment.

Vismodegib is effective for basal cell carcinoma but has severe side effects.

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.

Damaged hair follicles make mice more prone to skin inflammation and skin cancer after UV exposure.

Modified stem cells that overexpress a specific protein can improve hair growth and reduce hair abnormalities in mice.

A five-month-old boy with Omenn syndrome successfully recovered after a stem cell transplant with reduced intensity conditioning.

A man developed a skin reaction from metronidazole, which improved after stopping the drug and starting steroids.

A genetic marker linked to a type of hair loss was found in most patients studied.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Key genes linked to hair growth and cancer were identified in hairless mice.

t-Flavanone helps improve male pattern hair loss by making hair roots stronger.

Simvastatin may help manage symptoms in women with non-classic congenital adrenal hyperplasia by lowering cholesterol and certain hormone levels.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

A woman's hair turned gray and fell out after starting a cancer drug called imatinib mesylate.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

Knowing how skin works and its diseases helps doctors diagnose and treat skin conditions better.