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Melatonin can increase cashmere yield by altering gene expression and restarting the growth cycle early.

Mothers have more hair proteins than their children, with age-related differences in protein patterns, and some proteins in hair could indicate early childhood development.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

The document is a detailed medical reference on skin and genetic disorders.

The gene Prss53 affects hair shape and bone development in rabbits.

Acne can be managed with various treatments and requires psychological support due to its emotional impact.

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

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

Stem cells regenerate tissues and their behavior varies by environment, suggesting the hematopoietic system model may need revision.

The document concludes that proper recognition and treatment of skin appendage disorders are important for management.

Skin stem cells are crucial for maintaining and repairing skin, with potential for treating skin disorders and improving wound healing.

Human skin has multiple layers and functions, with key roles in protection, temperature control, and appearance.

Hair health is influenced by genetics, aging, and environmental factors, with proper care needed to maintain it.

Diabetic patients often have ingrown nails due to obesity, high blood pressure, past injuries, bad nail trimming, nail fungus, weak foot pulse, and weak knee reflex.

Iron supplements may reverse premature graying in iron-deficient individuals; ingrown nails are common in diabetics with certain risk factors; topical finasteride may reduce scalp DHT as effectively as oral finasteride; monilethrix treatment is challenging but some medications can help.

Iron supplements may reverse premature hair graying caused by iron deficiency.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

Eating a balanced diet with the right vitamins and minerals is important for healthy hair, but too many supplements can be harmful.

The document concludes that managing skin conditions during pregnancy is important and requires specialized care.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

The 2006 editorial concluded that immunotherapy was advancing with new drugs, focusing on specific biological therapies and convenient oral treatments, and highlighted the importance of partnerships and new regulations in the field.

Alopecia areata in infants may be more common than previously thought.

The document concludes that accurate diagnosis and understanding the type of hair disorder are crucial for treating hair loss in children.

Skin issues can indicate immune system problems.

GRK2 is essential for healthy hair follicle function, and its absence can lead to hair loss and cysts.