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Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

Epigenetic changes in blood cells may contribute to alopecia areata.

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

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

KRTAP28-1 gene can help breed sheep with finer wool.

A new DSG4 gene mutation causes hair defects in a young girl.

EREG therapy may help treat hair loss by promoting hair growth.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Certain immune-related proteins are higher in people with alopecia and their healthy relatives, hinting at a genetic link.

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

More research is needed to understand the genetic causes of Alopecia areata to develop better treatments.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

Removing REDD1 in mice increases skin fat by making fat cells larger and more numerous.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

RNA editing significantly affects hair growth and follicle cycling in the Tianzhu white yak.

A new method helps diagnose alopecia areata using specific gene markers and could guide targeted treatments.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

Mutations in the KRT85 gene cause hair and nail problems.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

Increasing isoleucine intake improved skin and health issues in an infant with maple syrup urine disease.

Machine learning can predict how well patients with alopecia areata will respond to certain treatments.

Blood tests can help understand the genetic differences in people with alopecia areata, including how severe it is and if it's inherited.

The study developed a mouse model for Alopecia Areata that responds to treatment, useful for future research.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Ambras syndrome's genetic cause is unknown, as it isn't linked to androgen levels.

Acrodermatitis enteropathica can be linked to dental issues, so thorough dental exams are important.