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Iron deficiency worsens inflammatory skin diseases by disrupting iron balance and increasing inflammation.

Lung and liver macrophages protect our tissues and their dysfunction can cause various diseases.

Fatp4 is crucial for healthy skin development and function.

Macrophage iron release is crucial for hair growth and wound healing.

Iron chelators can effectively reduce hair loss and improve hair growth in autoimmune alopecia.

Estrogen can temporarily slow down hair growth but this can be reversed.

Iron deficiency in menstruating women causes many health issues beyond anemia and needs early detection and treatment.

Polycystic ovary syndrome and iron overload share similar symptoms and can be potentially treated with blood removal, diet changes, and probiotics.

Exposure to certain metals may worsen attention-related behaviors in adolescents, with stronger effects in females.

Bead-jet printing of stem cells improves muscle and hair regeneration.

Combining sugarcane fiber and enzymes reduces hairballs in cats.

A woman was diagnosed with porphyria cutanea tarda and improved with phlebotomy and lifestyle changes.

The Spherical Skin Model improves drug and cosmetic testing by accurately mimicking human skin for efficient compound screening.

Iron supplements may improve hair loss satisfaction even if initial iron levels are normal.

The HFE hair transplant method is effective, safe, and provides natural-looking results with quick recovery for men with hair loss.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

The hr gene is linked to hair loss in Valle del Belice sheep.

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

Knockout mice showed anemia and hair loss, suggesting other ways exist for iron absorption.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

A genetic marker linked to a type of hair loss was found in most patients studied.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Women with excessive hair growth or polycystic ovary disease may more often carry a gene variant for 21 hydroxylase deficiency.

The hairless (hr) gene is essential for normal hair follicle function and its mutation leads to hair loss.

A new mutation in the HR gene causes hair loss in a specific family.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

A gene mutation causes monilethrix in a Chinese family.