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A group has developed therapies that show promise for treating cancer and various other conditions.

Dogs with dermatomyositis, especially Collies and Shetland Sheepdogs, need better treatments for their skin and muscle inflammation.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

Male hormones may play a role in the development of heart disease, and more research is needed to understand their effects.

Childhood obesity is rising globally due to various factors, and early prevention and healthy lifestyle changes are crucial.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

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

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

Most women with excess hair growth have an underlying hormonal issue, often treated with medication and hair removal methods.

Patients with certain skin symptoms and high ANA titers should be monitored for potential systemic lupus.

Men generally have more severe COVID-19 cases and higher death rates than women due to biological differences.

People with PCOS, especially if obese, often have NAFLD, linked to obesity, insulin resistance, and high androgen levels.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

5α‐reductase isozymes are crucial for prostate development and health, and targeting them can help prevent and treat prostate issues.

Pregnancy can increase lupus activity, but careful planning and treatment can improve outcomes.

EDA2R gene linked to hair loss.

Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Lymphocytes, especially CD8+ T cells, play a key role in causing alopecia areata, and targeting them may lead to new treatments.

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

The document concludes that hair transplantation and gene therapy may be important for future hair loss treatment.

The skin's ability to produce hormones is linked to various skin conditions, and better understanding this process could lead to new treatments.

Low-potency steroids can cause serious side effects in people with skin conditions like Netherton syndrome.

Marie Antoinette syndrome causes sudden hair whitening, but its exact cause is unknown.

DHT's role in hair loss is important, but measuring its level for diagnosis is questionable.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

The gene p53 is crucial for removing damaged cells to allow for healthy tissue renewal.

Mutations in certain receptors can cause diseases and offer new treatment options.

Researchers created a mouse model of a type of rickets that does not cause hair loss.