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Modern lifestyles, including poor diet, stress, and long-term use of certain medications, hinder the body's ability to heal from inflammation, leading to chronic diseases.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

A mother's PPARγ is crucial for preventing harmful milk that can cause inflammation and growth problems in babies.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

The circadian clock is crucial for tissue renewal and regeneration, affecting stem cell functions and having implications for health and disease.

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

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

Hair mineral analysis might help diagnose diseases early, but standard methods are needed.

A certain smell receptor in hair follicles can affect hair growth when activated by a synthetic sandalwood scent.

The TGF-β family helps control how cells change and move, affecting skin, hair, and organ development.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

Vitamin D3 affects cell differentiation in specific skin areas.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

Tiny needles with valproic acid can effectively regrow hair.

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Stress increases certain chemicals in the skin and nerves, which might worsen skin conditions.

Cancer development is like natural selection, involving mutated cells and environmental factors.

Scientists found a way to grow human hair cells in a lab that can create new hair when transplanted.

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

Vitamin D receptor is crucial for starting hair growth after birth.

Patients with Bohring-Opitz syndrome and ASXL1 mutations need regular kidney ultrasounds to check for tumors.

Loose Anagen Hair Syndrome is a hereditary condition causing hair loss in children due to abnormal hair follicles.

FOXN1 gene variants cause low T cells and immune issues from birth.

K16 can partially replace K14 but causes hair loss and skin issues.

People often struggle to consistently use contraceptives and other medications, and long-acting options might be better for those who want to avoid daily doses.

Maintaining the right amount of retinoic acid is crucial for healthy hair and skin.

Mothers and newborns with dental fillings had higher mercury in their hair, but getting fillings during pregnancy didn't raise mercury levels further.

Regenerative pharmacology, which combines drugs with regenerative medicine, shows promise for repairing damaged body parts and needs more interdisciplinary research.