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Rhodococcus equi causes severe pneumonia in young foals, and effective vaccines are needed due to foals' weak immune responses.

Janus kinase inhibitors may effectively treat resistant scalp conditions like folliculitis decalvans and dissecting cellulitis.

5α-reductases increase epitestosterone's effect on androgen receptors.

Tofacitinib can be effective in treating hair loss caused by alopecia areata.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

A rare genetic disease causes rickets and often hair loss in young children, which can improve with specific treatments.

Using tretinoin and hydroquinone can speed up the fading of skin pigmentation.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

Tailoring facelift techniques to individual needs improves patient satisfaction.

GI197111X is best dissolved in Capmul MCM for trials.

Most hair loss in captive rhesus macaques is likely due to environmental and behavioral factors.

A 3-year-old with vitamin D-resistant rickets and severe hair loss died despite treatment, highlighting the need for improved management of the condition.

A medicine called tofacitinib worked to treat a hair loss condition linked with a muscle and skin disease.

An 8-year-old boy with Recklinghausen's Disease shows various symptoms and is from a family with close genetic ties.

SARMs show promise but need more evidence to prove they're better than traditional androgens.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Blocking certain immune signals can reduce skin damage from radiation therapy.

Growth hormone therapy can improve symptoms and growth in children with Vitamin-D Dependent Rickets Type-2.

Recombinant collagen with nicotinamide boosts hair growth and health.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

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

Blocking mTORC1 activity with rapamycin could help increase hair pigmentation and growth, potentially reversing gray hair.

Androgens like testosterone increase colon muscle contractions by affecting calcium pathways.

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

ARHGEF3 is essential for proper hair follicle development in mice.

Retinoids are important for treating skin conditions but should be used with caution due to serious side effects and risks during pregnancy.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.