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Age, smoking, and lower BMI increase facial wrinkles; men wrinkle more than women, except in old age; pale skin and certain hormonal factors can protect against wrinkles.

Certain genes are more active during wound healing in axolotl and Acomys, which could help develop materials that improve human wound healing and regeneration.

New genetic locations explain much of hair color variation in Europeans.

ALRV5XR is the most effective hair regrowth treatment at 24 weeks.

Patients with mycosis fungoides have a higher risk of heart disease.

The document suggests a possible link between Crohn's disease and Johne's disease and calls for more research.

Minoxidil helps some bald men, but most lose hair again when stopping.

Scalp pain is a common symptom in people with active hair loss from telogen effluvium.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

The PDGF/PDGFR pathway is a potential drug target with mixed success in treating various diseases, including some cancers and fibrosis.

The enzyme 25 Hydroxyvitamin D 1 α-Hydroxylase is essential for healthy skin and recovery after skin damage.

Hormones, especially androgens, play a key role in acne, which can be a symptom of systemic diseases like PCOS and may require targeted treatment.

Msx2 and Foxn1 are both crucial for hair growth and health.

HIV can cause unusual and severe skin problems that are hard to treat.

Different species and human skin models vary in their skin enzyme activities, with pig skin and some models closely matching human skin, useful for safety assessments and understanding the skin's protective roles.

Pregnancy can change skin disease severity, with some conditions improving and others worsening, and treatment should balance benefits and fetal safety.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Hormonal treatment is effective for women with acne not helped by usual treatments, especially if they have hormonal imbalances.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Thioglycolate lotions are the most popular method for permanent waving and hair straightening.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

No link found between Coxsackie viruses and pemphigus.

Women with nonclassic 21-hydroxylase deficiency can have successful pregnancies through IVF, with certain factors affecting their chances.

A man with testotoxicosis was fertile despite low FSH levels, suggesting high testosterone may allow sperm production without FSH.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Children need early diagnosis and treatment for iron-deficiency anemia to prevent learning problems and promote health.

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

Genetic mutations can affect female sexual development, requiring personalized medical care.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

Hormone treatments for transgender individuals generally improve mental health and physical transition, with some health risks that require medical supervision.