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A higher genetic risk score increases the chance of getting benign prostatic hyperplasia and affects treatment outcomes in Han Chinese men.

Certain gene variants can influence acne risk and severity.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

PCOS shares similar genetic traits across different diagnosis criteria and is linked to other health conditions.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

VEGF and VEGFR-2 genes influence feather maturity, and specific genetic markers can improve chicken breeding.

Androgens may increase arrhythmias in Brugada Syndrome, while Finasteride could reduce them.

Altering SSAT affects fat metabolism and body fat in mice.

The activity of a specific rat enzyme in the prostate and epididymis is highly dependent on the acidity level.

Machine learning can predict how well patients with alopecia areata will respond to certain treatments.

Frontal fibrosing alopecia has occurred in two related male families.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

BioPlex-11 improves DNA profiling from telogen hair roots in forensic work.

Topical immunotherapy with DPCP is most effective for certain alopecia areata types, with success linked to age and disease duration, and influenced by a gene polymorphism.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

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

Combined finasteride and anastrozole therapy effectively treats BPH, influenced by hormone imbalances and genetics.

A 22-year-old woman with a rare genetic condition was successfully treated to develop normal female characteristics and regular menstruation.

Hair loss in certain mice is linked to changes in keratin-related genes.