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Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

The dog had sebaceous adenitis, treated with ciclosporin, leading to some hair regrowth.

CD44 variant changes start alopecia areata, but don't maintain it.

The stump-tailed macaque is a good model for studying human hair loss, but it's expensive and hard to find, while rodent models are promising for understanding hair growth and finding new treatments.

Dogs could be good models for studying human hair growth and hair loss.

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

Hair cortisol reliably indicates stress in rabbits.

Murine cytomegalovirus does not cause alopecia areata in these mice.

The dog likely has a canine alopecia X-like disorder.

CARI ONE helps start hair growth and makes hair follicles bigger and more numerous.

Carbon dots from Cinnamomum burmannii leaves can promote hair growth and regeneration.

miR-200c-3p could help diagnose and treat alopecia areata.

Haarpower® did not significantly reduce excessive shedding in dogs.

New treatments and early diagnosis methods for permanent hair loss due to scar tissue are important for managing its psychological effects.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

Melanocyte-associated antigens may play a key role in alopecia areata and could be targets for new treatments.

A woman with a rare adrenal tumor and hormonal disorder had improved testosterone levels after surgery, but her menstrual irregularities continued.

A mixed breed dog with skin issues improved significantly after treatment and needs to avoid dampness and certain bath products to prevent it from coming back.

The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Mutation in hairless gene may increase hair loss risk.

Mutation in hairless gene may increase hair loss risk.

A substance called TCQA could potentially darken hair by activating certain genes and increasing melanin.

NonClassic Congenital Adrenal Hyperplasia is a less severe form of a genetic disorder affecting adrenal gland function.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

Hair loss led to the diagnosis of Cushing's disease in a patient, showing that hair loss can be a sign of hormonal disorders.