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The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

5α-reductase is essential for male sexual development and its inhibitors have potential in treating various conditions related to hormone action.

Mutant mice help researchers understand hair growth and related genetic factors.

There are still challenges in diagnosing and treating chronic skin diseases, but there is hope for future improvements.

Blocking the prolactin receptor might help treat various diseases, but more research is needed.

Adrenal disorders can cause lasting brain and behavior issues in children.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

New treatments for relapsing multiple sclerosis are more effective and convenient but have higher risks of serious side effects.

A boy with severe immune deficiency and Epstein-Barr virus died from high-grade B-cell lymphoma.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

Photobiomodulation therapy significantly increases hair density and growth for androgenic alopecia, but more research is needed to confirm safety.

PROTO1 and PROTO2 protect against hearing damage.

Mitochondrial reactive oxygen species are essential for skin and hair development.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

The review suggests that a special cell-derived treatment shows promise for various skin conditions and hair growth but needs more research for confirmation.

Oral lichen planus is a chronic disease causing mouth discomfort and sometimes needs immunosuppressive treatment.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Light therapy can stimulate hair growth and is more effective when started early, but more research is needed on its long-term effects and optimal use.

SLE patients with Evans syndrome often show blood issues and need careful monitoring and treatment.

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.

Deleting the EDAR gene in Cashmere goats affects genes and proteins related to hair growth.

Some viruses can cause cancer by changing cell processes and avoiding the immune system; vaccines and targeted treatments help reduce these cancers.

ISCK03 stops melanin production in human melanoma cells and lightens skin color in mice and guinea pigs.

Patients with GATA2 deficiency show early skin symptoms that help diagnose the condition.

Thymus transplantation successfully restored immune function in infants with FOXN1 deficiency.

The conclusion is that different blood diseases cause specific oral symptoms and require varied treatments to manage these symptoms and improve patient health.

Alopecia areata involves both innate and adaptive immunity, with specific genes linked to the disease.

Oncogenic K-ras causes rapid cancerous changes in the mouth's lining.