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Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

New treatments for Hepatitis C show promise but need more research to confirm their safety and effectiveness for clinical use.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

A specific RNA modification in cashmere goats helps activate hair growth-related stem cells.

Circ 0020938 slows down hair growth in cashmere goats.

FOXN1 gene variants cause low T cells and immune issues from birth.

Higher CO2 levels help a cyanobacterium grow better by boosting photosynthesis and carbon uptake.

Modified β-catenin can cause different effects in mouse skin cells, leading to cysts or tumors depending on the cell type.

A genetic variant in goats is linked to cashmere growth.

The gene URB is more active in human hair growth cells and responds to a hair-related hormone.

17β-estradiol lowers polyamine oxidase levels in breast cancer cells through estrogen receptor 2.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

IL-19 and IL-24 help cells respond to DNA damage and could be targeted for cancer and age-related disease treatments.

Cashmere quality differences are due to gene expression variations affecting hair development and adaptation to cold.

The engineered yeast strain BLYAS can quickly and sensitively detect androgenic chemicals.

The protein's size was reduced, but more work is needed to confirm its function.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

FOXN1 is crucial for thymus development and immune response in Xenopus laevis.

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

CXXC5 is a protein that prevents hair growth and could be a target for hair loss treatment.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

CCL5 is important for the hair growth potential of human dermal papilla cells.

The marker 5-hmC changes in hair follicle stem cells when they start to grow.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

LTBP1 is a key regulator in diseases and a potential target for new treatments.

The TIP1 gene is crucial for normal plant cell growth in Arabidopsis.

ETS2 drives cancer progression in squamous cell carcinoma and is linked to poor patient outcomes.