Search

everythinglearnresearchcommunity

for

Search:↓

Acute stress increases Y1 receptor gene expression in certain brain areas, but repeated stress does not.

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

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

CUX1 boosts sheep hair cell growth and affects curl patterns.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Cyproterone acetate is used to treat conditions like prostate cancer, early puberty, excessive sexual drive, and female androgenization by blocking male sex hormones.

CAG repeat length in the AR gene is not linked to PCOS risk in Iranian women.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

Cyproterone acetate effectively treats sexual disorders by reducing sexual functions and is generally well-tolerated.

The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

The compound 4c showed strong potential as an anticancer agent.

COX-2 levels change during the hair cycle and affect skin and hair growth.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

Consider rare forms of CAH for accurate diagnosis and treatment.

The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

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

Finasteride is mainly broken down by the enzyme CYP3A4, affecting its levels in the body.

Gene variant linked to prostate cancer, hormone levels, and hair loss.

Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

New genetic variants linked to albinism were found in Pakistani families.

Scientists made all eight versions of a compound called cyoctol, but found it's not an anti-androgen and it fully breaks down in the skin.

CAG repeat polymorphism and prostate zone volume are not reliable markers of long-term androgen sensitivity.

A male with aromatase deficiency improved bone health with estradiol treatment.