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MCHR2 gene duplications may be linked to alopecia areata.

Certain genes are linked to the risk of developing Alopecia Areata.

The rs6152 allele is not a good marker for baldness in the Indonesian population, but family history, age, gender, high blood pressure, and body weight are linked to the risk.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Activating Tgr5 may help treat hair loss and bone loss.

Genetic testing can diagnose hair loss linked to DSG4 gene variants.

Increased ODC expression makes normally tumor-resistant mice more prone to tumor development.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

A new mouse mutation causes skin and hair defects due to a gene change.

New genetic mutations causing hair loss were found in a Chinese family.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Genetic profiling can improve androgenetic alopecia treatment by predicting drug response and minimizing side effects.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.

The KRTAP19-5 gene affects wool curvature in Chinese Tan sheep, with Variant B reducing curvature.

C-scores can help predict gain-of-function and loss-of-function mutations.

The rs1128977 gene variant may affect cholesterol and body measurements.

The ACE1 gene variant doesn't affect long-COVID symptoms.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Tgm2 helps stabilize dying cells and aids fibroblast attachment to the extracellular matrix.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.