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Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

Androgens like testosterone are important hormones for both men and women, made differently in each sex and affecting the body by regulating genes and quick interactions with cell components.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

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

Proper control of β-catenin activity is crucial for development and preventing diseases like cancer.

Lysophosphatidic acid is important for skin health and disease, and could be a target for new skin disorder treatments.

NF-κB is crucial for different stages and types of hair growth in mice.

The meeting focused on understanding, diagnosing, and finding treatments for irreversible hair loss diseases.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Smoking and drinking worsened hair loss in men with genetic hair loss, while eating and sleeping habits didn't; genetics played a bigger role than environment in hair loss.

Familial factors affect hair loss types in Koreans, with M type in men, L type in women, and paternal factors influencing male hair loss more.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

Wnt7a protein is crucial for development and tissue maintenance and plays varying roles in diseases and potential treatments.

The monkey's hair loss was due to an autoimmune disease, not genetics.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Vitamin A might be a safe extra treatment for dogs with sebaceous adenitis, but more research is needed to prove its effectiveness.

Patients with severe alopecia areata have higher levels of MIF, which decrease after successful treatment.

Some skin diseases and their treatments can negatively affect male fertility.

Various treatments exist for hair loss, but more research is needed for better options.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Diabetes can lead to blindness and skin problems, and managing blood sugar and blood pressure is crucial to prevent these complications.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.

Gintonin-enriched fraction promotes hair growth and could be a potential alopecia treatment.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.