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A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

A patient's gum problems worsened after using cyclosporine for a scalp condition, but improved with a lower dose.

A specific gene mutation causes long hair in Angora rabbits.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Substances from Chinese medicines show promise for immune support and disease prevention, but the way they are processed affects their effectiveness.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Researchers developed a model to predict how well certain compounds can block an enzyme related to hair loss and prostate issues, suggesting a 50 mg dose of finasteride might be effective based on lab and body data.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

Some people with pattern hair loss may also have scalp inflammation and scarring similar to lichen planopilaris.

New compounds similar to cromakalim were less effective at inhibiting insulin release but improved in solubility and one acted as a calcium entry blocker, not a potassium channel opener.

The Rotterdam Study aims to understand various diseases in older adults.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

New compounds were made that effectively block enzymes related to prostate issues and hair loss.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

Macroalgae compounds offer sustainable, effective benefits for cosmetics.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

A mouse gene mutation increases the risk of skin cancer.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Understanding wool keratin-associated proteins in sheep can help improve wool quality through selective breeding.

Male hormones worsen kidney transplant damage, but blocking them helps.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Stem cell niches are adaptable and key for tissue maintenance and repair.

Zinc supplementation may help improve treatment outcomes for chronic hepatitis C.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.