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A 4-year-old girl with a rare lupus condition was successfully treated with oral corticosteroids, leading to full recovery and hair regrowth.

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

A specific RNA increases hair stem cell growth and skin healing by affecting a protein through interaction with a microRNA.

Hair follicle dermal stem cells help control hair growth timing by regulating signals at the hair germ–dermal papilla interface.

A specific gene mutation causes congenital hair loss.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

A specific microRNA, chi-miR-30b-5p, slows down the growth of hair-related cells by affecting the CaMKIIδ gene in cashmere goats.

Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

miR-877-3p can improve cashmere quality by regulating hair growth in goats.

Alopecia areata can cause spotty white areas on nails.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

miR-214-3p helps nerve repair and recovery.

The vellus index is a simple, quick, and reliable method to assess and monitor hair growth, especially in hirsutism.

Some vitamin D analogs can thicken skin and reduce pore size like a common acne treatment, with one analog also affecting skin growth factors.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Prenatal retinoic acid exposure did not affect mouse vibrissal follicle development.

Hair shaft malformation contributes to Central Centrifugal Cicatricial Alopecia.

Hair chromium levels show past nutritional status, not environmental exposure.

lncRNAs may regulate hair follicle development in Hu sheep.

Mandarin duck sail feathers change with seasons due to hormones and genetic regulation.

The man has a genetic skin condition called pachyonychia congenita.

The infant was diagnosed with Rothmund-Thomson syndrome, a rare genetic disorder causing various physical and developmental issues.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

A new mutation in the HR gene causes hair loss in a specific family.

More vellus hairs in frontal scalp indicate early female pattern hair loss.

Pvalb8 is essential for zebrafish hearing and hair cell development, and its mutation causes hearing loss.

LALPS causes non-scarring hair loss along the Blaschko line, with unique trichoscopic findings.