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Syphilis is becoming more common and remains a major health problem due to challenges in prevention and treatment.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

Drug metabolism affects how long a drug works, its interactions, activation, and toxicity, and is influenced by genetics, diet, illness, and other drugs.

Genetic counselors should be culturally skilled and aware of transgender patients' unique health risks and needs.

Certain long non-coding RNAs in cashmere goats affect hair growth when treated with a specific growth factor.

Insulin resistance and obesity are key factors in the development and worsening of polycystic ovary syndrome, and lifestyle changes are important for managing it.

The gene KAP22-1 affects wool yield and fiber shape in sheep.

Androgens like testosterone are important hormones for both men and women, made differently in each sex and affecting the body by regulating genes and quick interactions with cell components.

Early hair loss may indicate risk of insulin resistance.

High testosterone increases heart disease risk in women with PCOS.

American men are older, more obese, and have longer infertility than Canadian men.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

The cause of Frontal Fibrosing Alopecia is unclear, diagnosis involves clinical evaluation and various treatments exist, but their effectiveness is uncertain.

A gluten-free diet significantly improves skin and health issues in people with dermatitis herpetiformis, a skin condition linked to celiac disease.

Skin grafts are effective for chronic leg ulcers, especially autologous split-thickness grafts for venous ulcers, but more data is needed for diabetic ulcers.

The document concludes that lifestyle changes and medical treatments can significantly reduce symptoms of Hidradenitis Suppurativa, a chronic skin condition.

Small molecule drugs show promise for advancing regenerative medicine but still face development challenges.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.

Pediatric endocrinologists should provide early fertility counseling and preservation options to young patients at risk of infertility.

Alopecia areata, a type of hair loss, is likely an autoimmune disease with a genetic link, but its exact cause is still unknown.

Most women with hirsutism or androgenic alopecia had polycystic ovaries, especially if they had irregular periods.

The summit concluded that new treatments like Jak inhibitors show promise for Alopecia Areata and personalized approaches are needed.

Finasteride treats baldness but may cause lasting sexual side effects.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

New genes and pathways are important for testosterone production and male sexual development.