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Early diagnosis and aggressive treatment are crucial for better outcomes in lymphomatoid granulomatosis.

The document concludes that PCOS has a strong genetic component, but more research is needed to fully understand the specific genes involved.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

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

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

The protein Gnαs is found more in black mice than white mice and may influence their coat color.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

Alopecia X in dogs is a cosmetic issue, not a hormonal disorder, and harmful treatments should be avoided.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

Obesity is linked to various skin problems and may increase the risk of skin cancer.

Androgens can both stimulate and cause hair loss, and understanding their effects is key to treating hair disorders.

Genetics and hormones play a role in male and female hair loss, but more research is needed to fully understand it.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Kawasaki Disease is rare and often missed in adults, who show different symptoms than children, and may benefit from early treatment.

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

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

S5αR inhibitors might help treat schizophrenia and other mental disorders but need more research.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

Asian hair loss differs from Europeans; consider individual needs and psychological well-being for treatment.

Men are more likely to get infectious skin diseases, while women are more prone to autoimmune and pigment-related skin conditions, influenced by biological and environmental factors.

Drug repositioning is becoming more targeted and efficient with new technologies, offering personalized treatment options and growing interest in the field.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

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

Stress and alcohol affect brain chemicals differently in rats, mice, and humans, influenced by genetic differences.

Signaling pathways are crucial for hair growth in goats.

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

The VEGF +405G allele may increase the risk of PCOS in South Indian women.