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Researchers found four genes that could help diagnose severe alopecia areata early.

Gut flora changes could potentially indicate depression, but more research is needed.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

The study concluded that the arachidonic acid pathway and the protein KRT79 play a role in determining the fineness of cashmere.

Cosmetic procedures can harm hair, but damage can be minimized with knowledge and care; however, once hair is damaged, it cannot be reliably repaired.

New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

A protein called lfTSLP is important in causing allergic and other skin diseases and could be a target for treatment.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

Betacoronaviruses, like COVID-19, may cause hormone system dysfunction and affect disease susceptibility and severity.

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

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

Chemotherapy may cause recurring hair loss due to an autoimmune response.

Epimedium extract helps increase skin pigmentation and could be a new treatment for conditions with reduced pigmentation.

Ginsenoside Rg1 protects mouse skin from UVB damage and helps control inflammation.

Activating TLR5 in the gut can extend lifespan and improve health in aged mice.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

New treatments and diagnostic methods for various animal skin conditions showed promising results.

Early and late matrix progenitors in hair follicles create different cell layers, with early ones forming the companion layer and later ones forming the inner root sheath and hair shaft.

Thyroid function affects skin health, with a complex interaction between the two.

Non-immune factors play a significant role in alopecia areata.

Parathyroid hormones are important for hair growth, but their use in treating hair loss from chemotherapy is still uncertain.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Amyloid deposits linked to a type of protein may cause a unique pattern of hair loss by disrupting hair growth cycles.

Calcium reduces involucrin in rat hair bulbs but doesn't affect filaggrin and Kdap.

Polycystic Ovarian Syndrome is common in overweight urban college girls and may increase the risk of heart and metabolic problems.

Lichen Planopilaris is a hair loss condition best treated early with various medications, including hydroxychloroquine, to prevent permanent baldness.

The meeting covered advances in understanding hair growth, causes of hair loss, and potential treatments.

The workshop discussed the role of a protein called calreticulin in health and disease, its potential as a treatment target, and its possible use as a disease marker.