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The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

People with Down's syndrome are more likely to have syringomas.

Steroid sulfatase is important for activating hormones that affect memory, brain function, and certain diseases, and could be a target for treating hormone-related disorders.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

A new gene variant causes glucocorticoid resistance in a mother and son.

Certain MC4R gene variants are linked to higher BMI in obese women with PCOS but do not cause PCOS.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

Different sPLA2 enzymes affect immunity, skin and hair health, reproduction, and may be potential targets for therapy.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

Some mutant mice have hair with abnormal cross-linking, mainly in the cuticle, not affecting other hair parts.

Male and female bodies respond differently to stress, influenced by hormones and development stages, with implications for stress-related diseases.

Nanog gene boosts stem cells, helps hair growth, and may treat hair loss.

Baldness in men with prostate cancer is linked to higher levels of certain sex hormones, but chest hair density is not.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

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

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

The study found key factors in the cause of hidradenitis suppurativa, its link to other diseases, and identified existing drugs that could potentially treat it.

The document concludes that more research is needed to fully understand the causes of PCOS.

Skin problems in COVID-19 patients are rare and may be due to the body's complex immune response or blood clotting issues.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Use finasteride, dutasteride, and minoxidil for hair loss treatment.

Beta-HPV and MCPyV are linked to certain skin cancers, with ongoing research and vaccine development.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

The conclusion is that future hair loss treatments should target the root causes of hair thinning, not just promote hair growth.

Selecting specific KRTAP26-1 gene variants can improve wool quality in sheep.

Male and female skin differ due to hormones, affecting conditions like hair loss, acne, and skin cancer, and suggesting a need for gender-specific treatments.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.