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Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

Testosterone therapy in transgender individuals can increase the risk of erythrocytosis.

Digit ratio likely doesn't predict male hair loss.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

FGF13 gene changes cause excessive hair growth in a rare condition.

Androgenetic alopecia is significantly linked to metabolic syndrome.

Hair pattern in androgenetic alopecia overlaps with scalp and bone demarcations, with distinct gene profiles affecting susceptibility.

Vitiligo and alopecia areata might be early signs of Type 1 Diabetes.

Down Syndrome patients with Alopecia Areata often have hypothyroidism and specific immune abnormalities.

Higher concentration of botulinum toxin A is safe and effective for treating hair loss in men and women.

Measuring the variety in hair thickness can help diagnose male pattern baldness in Korean men.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Gamma-ray exposure improves genome editing efficiency in mice using the i-GONAD method.

Type 2 diabetes may increase the risk of severe hair loss in African American women.

Human and mouse TGase3 enzymes are similar but differ near the activation site, crucial for their function in skin and hair development.

Acne is more common in men with male pattern baldness due to increased hormone levels.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Allergic rhinitis increases hair loss risk, but antihistamines can reduce it.

Serum biomarkers like insulin-like growth factor-1 and vitamin D may help diagnose androgenetic alopecia.

Longer anogenital distance may indicate a higher chance of having polycystic ovary syndrome, and measuring this distance along with hormone levels could improve diagnosis.

hHbl gene is active in hair shaft cells and some pilomatricomas.

Immune changes and specific genes contribute to male hair loss.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Glutamic acid helps increase hair growth in mice.

The patient's hair had unique damage and a lower sulfur-to-nitrogen ratio compared to relatives, but not compared to healthy controls.

The hair keratin variant is mostly found in Caucasians.

A unique enzyme in guinea pig hair follicles helps form protein cross-links in hair.

The ethanol patch test reliably identifies ALDH phenotype.

Genetic testing can help understand male pattern baldness.