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A protein called FERONIA helps control root hair growth in response to cold and low nitrogen by activating nutrient-sensing pathways in a plant called Arabidopsis.

People with alopecia areata have higher levels of RBP4 protein and antibodies against it.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Frontal fibrosing alopecia has occurred in two related male families.

Keratin 14 is uniquely found in a specific group of placental cells.

A KRT32 gene variant causes loose anagen hair syndrome.

Mice without the Sept4/ARTS gene heal wounds better due to more stem cells that don't die easily.

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

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

New androgen receptor modulators show promise for treating diseases like prostate cancer and muscle wasting.

Certain genetic markers can indicate a person's risk of developing prostate cancer.

ATR04-484 ointment shows promise for treating skin issues from cancer therapies.

A 12-year-old boy with PAIS successfully developed male characteristics using high-dose testosterone and anastrozole.

RORA affects hair follicle stem cells' structure and movement, potentially helping treat hair loss.

Vitamin D receptor and hairless protein are essential for hair growth.

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

rPanglaoDB helps study rare cell types by merging RNA data, confirming fibrocytes' role in healing.

The E2 protein affects gene activity in hair follicles of mice.

LEF-1 boosts cell growth in goat hair follicles, aiding cashmere production.

The K14 promoter is more active in skin cells than the K5 promoter.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

Sfrp2 increases during hair follicle catagen phase and slows keratinocyte growth.

Acinetobacter strain A1-4-2 can safely clean water pollutants.

NcoA4 may have roles beyond helping control gene activity, possibly affecting cell behavior and stability.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.