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A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

Alcohol dependence affects stress hormone levels more than childhood maltreatment.

Two genetic variations in Moa buffalo help them adapt to heat.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Heat Shock Proteins are important in the development of Polycystic Ovarian Syndrome and could be targets for new treatments.

The study developed a reliable method to measure active ingredients in hair nourisher products using HPLC.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Hair cortisol may help identify adrenal insufficiency in sickle cell disease patients.

Patients with hidradenitis suppurativa have higher levels of cell-free DNA in their blood.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

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

A new method accurately measures a drug in skin for cancer therapy research.

A genetic hair protein variant is more common in Japanese people and is inherited.

A gene mutation in mice causes severe skin disorder similar to a human condition.

Researchers successfully made new compounds for hormone level tests, but one attempt led to an unexpected product, correcting a past error.

Keratin 17 is important for hair and nail structure and affects pachyonychia congenita symptoms.

The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

Human dermal stem/progenitor cells can divide and differentiate more than hair follicle dermal papilla cells.

GPC1 is important for hair growth by helping blood vessels form around hair follicles.

A specific DNA region controls skin cell gene expression by working with certain proteins.

Skin cells and immune cells change in a skin condition called hidradenitis suppurativa, and a certain treatment can improve these changes.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Certain plasma proteins are linked to prostate cancer risk and could help in early detection and treatment.