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Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Male pattern hair loss is genetic and influenced by hormones, with treatments like minoxidil and surgery available.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

The article concludes that the wool follicle is a valuable model for studying tissue interactions and has potential for genetic improvements in wool production.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

FFA's causes may include environmental triggers and genetic factors.

Alopecia Areata has no guaranteed treatment for hair regrowth, but options like corticosteroids and minoxidil are used, with future research focusing on genetic and immune therapies.

Stress and alcohol affect brain chemicals differently in rats, mice, and humans, influenced by genetic differences.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Alopecia areata, a type of hair loss, is likely an autoimmune disease with a genetic link, but its exact cause is still unknown.

The current understanding of frontal fibrosing alopecia involves immune, genetic, hormonal factors, and possibly environmental triggers, but more research is needed for effective treatments.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Certain IL-18 gene variations may increase the risk of alopecia areata.

A mother and daughter with similar hair loss conditions and identical HLA types suggest a genetic link between the conditions.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Women with hirsutism have different levels of omentin-1, which may be linked to the condition and its genetic aspects.

Genetic differences within ethnic groups may affect prostate cancer treatment effectiveness.

New models predict male pattern baldness better than old ones but still need improvement.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

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

Alopecia areata causes sudden hair loss, has genetic links, and can be managed but not cured.