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Testosterone is linked to cardiovascular risk factors and stroke, but its exact role is unclear.

Certain gene variants can influence acne risk and severity.

A specific gene change is linked to severe hair loss.

New genetic variants linked to inherited ichthyoses were identified, offering insights for potential gene therapy.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Seven new genetic risk areas for prostate cancer were found.

Polygenic risk scores can predict the risk and outcomes of benign prostatic hyperplasia.

A new gene mutation causes a rare type of hair loss.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

MITF+ melanoma patients are more likely to have multiple melanomas and unique skin patterns.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Men with high genetic risk for Polycystic Ovary Syndrome (PCOS) have increased chances of obesity, type 2 diabetes, heart disease, and hair loss, showing PCOS risk factors can affect both genders.

Two specific genetic markers increase the risk of hair loss in Asian populations.

Lichen planopilaris may have a genetic link.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Female relatives of PCOS patients have a higher chance of showing PCOS symptoms.

Mice with a specific BRCA1 mutation have a higher risk of tumors, especially in the uterus and ovaries.

Researchers found a gene mutation responsible for a rare hair loss condition.