Search

everythinglearnresearchcommunity

for

Search:↓

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

Hair loss and aging are caused by the breakdown of a key protein in hair stem cells.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Certain bacteria from the Citrullus colocynthis plant may be a new source of antibiotics to fight drug-resistant diseases.

The transporter protein SH1446 in Staphylococcus hominis is key to underarm odor production.

3D culture helps maintain hair growth cells better than 2D culture and identifies key genes for potential hair loss treatments.

New understanding of hair loss could lead to better treatments.

ERG increases SOX9, promoting prostate cancer growth and invasion.

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

Mitochondrial therapy and platelet-rich plasma therapy both stimulated hair regrowth in aging mice, with mitochondrial therapy showing similar effectiveness to plasma therapy.

Finasteride causes temporary cell death in BPH tissues.

Tadalafil and Finasteride may help treat aggressive melanoma.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Niacin derivatives may increase hair fullness in women with hair loss.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

Some women with excess hair growth have a hormone condition that can't be diagnosed by blood or urine tests alone.

The technology can help diagnose and subtype autoimmune diseases by identifying specific autoantibodies.

A specific mutation known for causing cancer is also found to cause a skin condition in a young girl.

Genes affect cytokine production, which can influence chronic diseases, and certain interventions may help prevent related molecular damage.

Obesity changes androgen levels in women with PCOS, leading to higher testosterone relative to androstenedione.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Certain genetic variants and pathways are linked to hair loss.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

Mutations in the KRT85 gene cause hair and nail problems.

FGF5 gene mutations cause long hair in domestic cats.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.