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GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.

Pumpkin Seed Oil in niosomes may help treat hair loss and improve hair growth.

Inhaling medicine may reduce side effects and improve treatment for a major lung cancer type.

Trichoscopy shows hair diameter variability, vellus hairs, and the peripilar sign are key indicators for diagnosing Androgenetic Alopecia.

Uterine transplants for transgender women are feasible but need more research.

The trial aims to test if spironolactone is an effective acne treatment for women without the side effects of current treatments.

The review concludes that innovations in regenerative medicine, tissue engineering, and developmental biology are essential for effective tissue repair and organ transplants.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Human hair shows promise for non-invasive medical testing, but more research is needed to standardize its use.

Keratin proteins are crucial for hair structure and strength.

Organoids help study and treat genetic diseases, offering personalized medicine and therapy testing.

Testosterone significantly affects sexual desire in both men and women, but its impact on women is more complex and influenced by psychological factors.

Plant roots respond to fungus smells by possibly using certain proteins and a plant hormone to change root growth, but more research is needed.

Sirolimus and propranolol may reduce abnormal cell growth and improve lymphatic malformations in children.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Feather patterns form through genetic and epigenetic controls, with cells self-organizing into periodic patterns.

A specific genetic deletion in goats affects cashmere yield and thickness.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

Understanding skin structure and development helps diagnose and treat skin disorders.

Gene therapy, especially using atoh1, shows promise for creating functional sensory hair cells in the inner ear, but dosing and side effects need to be managed for clinical application.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.