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Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Hydrogen peroxide in hair dye can cause hair loss.

RSPO1 could help create new diabetes treatments by increasing pancreatic β cells.

Prostate cells have proteins that bind to specific hormones, which can increase protein production when activated by these hormones.

Targeting ornithine decarboxylase can help prevent skin cancer.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

ELL is crucial for gene transcription related to skin cell growth.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

1,25-(OH)2D3 helps hair grow by blocking certain harmful signals.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

A reliable model for screening type II 5α-reductase inhibitors was created and validated.

TCHHL1 is a protein important for hair growth, found in hair follicles.

People with Alopecia Areata have higher oxidative stress and different enzyme activities compared to healthy individuals.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

Biotin helps regulate proteins in the blood, which may explain its role in hair growth.

Rapamycin may help treat Leigh syndrome by targeting protein kinase C.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

A specific gene mutation causes severe skin and nail issues and hair loss.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

Ornithine decarboxylase is crucial for human hair growth and the hair cycle.

Hormonal imbalances, including high prolactin and thyroid issues, contribute to hair growth problems in women.

A new gene mutation is linked to monilethrix in the studied family.

Researchers found potential urine markers for polycystic ovary syndrome, including testosterone-glucuronide and 11α-hydroxyprogesterone, which may help diagnose the condition.

Increased HSD11B1 enzyme expression is linked to higher body fat and insulin resistance.

5αR inhibitors help slow early prostate cancer cell growth, suggesting combined treatments are needed.

Key enzymes control androgen levels, affecting hormone activity and potential treatments.

Colchicine can inhibit hair growth by affecting cell activity and protein expression in hair follicles.