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A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

GI198745 is more potent and longer-lasting than finasteride, potentially better for treating hair loss.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

Finding functions for unknown GPCRs is hard but key for making new drugs.

Inhibiting HSP90 increases cell adaptability and survival under stress.

Sry may regulate fatty acid metabolism and shows different expression levels in rat tissues.

Mutations in the enzyme don't significantly change how it binds to its specific substances.

Increased 11β-HSD1 activity in skin may contribute to aging and could be targeted to reduce aging effects.

Mouse profilaggrin helps in skin cell differentiation and may be involved in calcium signaling.

TRH stimulates human hair growth and extends the hair growth phase.

The enzyme for activating vitamin D is found in many body tissues, not just the kidneys.

The Oat mouse model shows mild retinal degeneration, useful for testing treatments.

Prostate cells have proteins that bind to specific hormones, which can increase protein production when activated by these hormones.

LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

Neurosteroids regulate synaptic inhibition in the spinal cord and may help manage spinal pain.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

Steroid-binding globulins have important roles beyond just transporting steroids.

HNG helps hair grow by keeping hair in the growth phase longer.

Goserelin and oestradiol treatment slightly improved hairiness but did not significantly change sebum production or hair characteristics in mildly hirsute women.

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

TCHHL1 is a protein important for hair growth, found in hair follicles.

HLA can be linked to autoimmune hepatitis.

The activity of a specific rat enzyme in the prostate and epididymis is highly dependent on the acidity level.

A gene variation is linked to hair thickness in Asians.

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

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

Gene knockout mice developed scars similar to human hypertrophic scars, useful for studying scar progression.

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.