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

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

Rushton's hyaline bodies form from hair keratin and blood substances.

A reliable model for screening type II 5α-reductase inhibitors was created and validated.

Caffeine can damage hearing cells and affect hearing recovery after ear trauma.

Human scalp hair follicles can produce hormones and have a system similar to a brain-body communication network.

Removing GRK2 in skin cells causes hair loss similar to immune-related alopecia.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

Blocking GABA(A) receptors increases neuron sensitivity, showing GABA and glycine have different roles in pain.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Mice without active or present vitamin D receptors maintain normal blood sugar control and islet gene expression when calcium levels are normal.

Aδ-LTMRs have complex synapses with glycine, while Aβ-LTMRs have simpler ones.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

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

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

Blocking a protein called prostaglandin D2 might help treat hair loss.

Histamine and its enzyme may help start hair regrowth.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

The TRPV3 channel structure changes linked to severe itch and hyperkeratosis were identified using cryo-EM.

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

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Skin cells and certain hair follicle areas produce hemoglobin, which may help protect against oxidative stress like UV damage.

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

Caffeine may help reduce stress-induced hair loss.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

AGC2-1 protein is essential for root hair growth in Arabidopsis.

Retinoic acid production and signaling in hair follicles are regulated by location and timing, affecting hair growth and cycling.