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MCHR2 gene duplications may be linked to alopecia areata.

Mutations in the WNT10A gene cause Short Anagen Hair syndrome and increase the risk of male pattern hair loss.

A person with Werner syndrome was initially thought to just have female pattern hair loss.

A pet rabbit in Korea was successfully treated for sarcoptic mange with Ivermectin.

MK-0773 safely increased muscle mass but did not improve muscle strength or function in elderly women with sarcopenia.

MK-5108 is safe and shows potential against tumors, especially alone.

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.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Photobiomodulation increased hair count in men with hair loss after 5 weeks, with no further increase after 10 weeks.

CCC1 is essential for ion balance and proper plant cell function.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

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COVID-19 can cause a temporary hair loss condition.

A 17-year-old in Saudi Arabia was diagnosed with a rare skin condition causing red-brown facial patches.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

SHPro® improved urinary symptoms and erectile function in men and is safe.

Certain changes in the VEGF gene can increase or decrease the risk of polycystic ovary syndrome.

Cyclohexyl salicylate may help hair growth and treat hair loss.

Two new mutations in the AR gene linked to severe androgen insensitivity were found.

miR-203a-3p helps hair follicle stem cells become specialized by targeting Smad1.

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There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.