Search

everythinglearnresearchcommunity

for

Search:↓

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

A new compound with strong antiandrogenic effects was found, potentially useful for treating conditions like acne and prostate cancer.

The compound was successfully made and shows potential for treating prostate cancer.

Early diagnosis and treatment of hereditary hemochromatosis can prevent serious complications.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

CAP1/Prss8 does not activate PAR2 or inhibit PN-1.

Finasteride metabolism varies by age, sex, and P450 inducers, with males processing it faster.

Tebentafusp-tebn improves survival rates in uveal melanoma patients but has common side effects like rash and fatigue.

Loss of Pten in certain hair follicle stem cells increases skin cancer risk.

Liver damage in PCOS is linked to iron overload and cell death due to the miR-761-hepcidin/GPX4 pathway.

The nano-carrier makes etoposide safer and more effective against lung cancer.

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

Finasteride dosages should be adjusted based on CYP3A5 genotype and liver function to avoid side effects.

Smaller substituents at C-17 enhance the inhibitory activity of progesterone derivatives on 5alpha-reductase.

GBP1 is a key target for treating Epstein-Barr virus-related kidney cancer, and finasteride may help.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

miR-200c-3p could help diagnose and treat alopecia areata.

The P133R mutation in AKR1D1 enzyme causes harmful bile acid buildup, explaining related health issues.

Adding TERT and BMI1 to certain skin cells can improve their ability to create hair follicles in mice.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

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

No link found between aromatase gene and female hair loss.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

Early diagnosis and treatment of NCCAH can improve symptoms and fertility.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.