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The ALADIN score can predict how well patients with alopecia areata will respond to JAK inhibitor treatments.

A young cat had a rare fungal infection caused by Microsporum gypseum.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

Glypican-1 is important for hair follicle blood vessel growth and could be a target for treating hair loss.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

Deleting Gpr54 speeds up hair growth and regeneration.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

Finasteride-treated male rats' offspring had altered glucose metabolism, potentially increasing diabetes risk.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

The KRTAP36-1 gene affects wool quality in Chinese Tan lambs.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Male mice with FGF5 mutations grow longer hair than females.

Researchers found 15 new genetic links to skin traits in Japanese women.

PRP with TM bio-dressing improves skin graft healing in cats.

5α-reductase affects dopamine receptors linked to sensorimotor gating, which may help understand disorders like schizophrenia.

There is no significant link between the MMP-1 rs1799750 polymorphism and androgenetic alopecia in the Indonesian population.

Upadacitinib may effectively treat twenty-nail dystrophy without causing pain.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

WNT10A gene mutations cause short anagen hair syndrome.

A mouse model was created to study hair loss similar to humans.

Allopregnanolone is needed for certain brain processing issues caused by D1 dopamine receptor activation.