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EGFR helps mouse hair follicles stop growing by reducing certain growth regulators.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Trichohyalin is a protein in hair follicles that helps form hair filaments.

CRF can cause hair loss, but blocking its receptors might prevent this.

The development of breeding tubercles in male zebrafish relies on a specific enzyme that processes hormones.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Formalin-induced pain increases testosterone breakdown in the rat brain and spinal cord.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Tofacitinib effectively improved severe skin symptoms in a patient with Hypohidrotic Ectodermal Dysplasia.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

Removing Ctip2 in skin cells causes skin inflammation similar to atopic dermatitis.

Peficitinib can turn human fibroblasts into cells that help grow hair.

Tamsulosin increases the risk of floppy iris syndrome during cataract surgery.

Armadillo Repeat Only proteins are essential for proper plant growth and response by regulating calcium channels.

Whale genes show changes that help them live in water, like less hair and better flippers.

The FRZB gene slows hair growth in rabbits.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

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

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

The cuneate nucleus has two main neuron types: relay neurons and interneurons.

4PeCDF is highly toxic to male rats, causing weight loss, organ damage, and death.

Epiprofin suppresses parathyroid hormone gene activity, helping regulate calcium levels and could be a treatment target for hyperparathyroidism.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

Csdc2 helps hair growth in cashmere goats by regulating specific genes.

A new gene causes hairlessness and skin cysts in rats.

HuR is essential for Treg function and preventing autoimmunity.

Carpronium chloride increases blood flow by widening small blood vessels.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.