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Personalized treatment based on detailed tumor analysis successfully managed and reduced the patient's aggressive hair follicle cancer.

Compounds from Pterocarpus indicus may help treat benign prostatic hyperplasia by stopping cell growth.

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

PCE-DP brightens skin and promotes hair growth by enhancing cell growth and reducing melanin uptake.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

The reconstructed skin model from hair follicles functions like human skin in processing chemicals and can be used to test ingredient safety.

PROTACs offer a new, precise way to treat cancer by breaking down harmful proteins.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

A specific gene change in APCDD1 increases the risk of hair loss.

Peptide nanoparticles can effectively deliver CRISPR-Cas9 to target KRAS mutations in cancer.

Some new progesterone derivatives are better at blocking testosterone conversion than a common drug.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

ALRN-6924 may prevent hair loss caused by chemotherapy.

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

Paeoniflorin protects brain cells by involving a specific protein and neurosteroids.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

The DPCP/HPβCD complex improves solubility and anti-inflammatory effects for alopecia areata treatment.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

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

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

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

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

Certain gene variations are found in people with polycystic ovary syndrome.

Finasteride shows promise for preventing prostate cancer, but more research is needed.

The HCR gene contributes to psoriasis risk.

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

Cadd4 effectively reduces cholesterol levels without side effects.