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The document concludes that a new biosensor can efficiently detect prostate cancer cells and that standardized referrals help find significant cancers effectively.

CEC levels may be a useful marker for predicting prostate cancer progression.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

The Rotterdam Study investigates diseases in older adults and has produced many research findings.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

The study found that in Latin America, ancestry varies by location, influences physical traits, and affects how people perceive their own heritage.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

The Rotterdam Study aims to understand various diseases in older adults.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Tight junctions are key for skin protection and controlling what gets absorbed or passes through the skin.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

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

Animal models have helped understand hair loss from alopecia areata and find new treatments.

A new gene, JMJD1C, may affect testosterone levels in men.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

Male pattern hair loss caused by follicular miniaturization; early diagnosis and treatment can reduce psychological burden.

A gene called HDAC9 might be a new factor in male-pattern baldness.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Genetic variations affecting skin structure play a key role in severe acne.

Current treatments for male pattern baldness include minoxidil and finasteride, with new options being developed.

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

Dutasteride makes alcohol less sedating and may lead to less drinking in men.

Genetic marker rs12558842 strongly linked to male hair loss.

Hair loss risk is influenced by multiple genes.

No link found between new male baldness genes and female hair loss.

No link found between specific genes and female pattern hair loss.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.