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The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

New cells are added to the hair's dermal papilla during the active growth phase.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

New cancer treatments are less harmful to hair but can still cause hair loss, color, shape, and growth changes.

Yellow dots look different in various hair loss conditions and can help diagnose them.

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 2004 hair research meeting presented new findings on hair cell differentiation, genetic factors in hair loss, hair pigmentation, and potential targeted therapies.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Alopecia areata is an autoimmune disease causing patchy hair loss, often with other autoimmune disorders, but its exact causes are unknown.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

Alopecia areata can cause unpredictable hair loss, and treatments like corticosteroids and minoxidil may help but have varying side effects.

IFN-γ and IL-2 are important for T cell activation in hair loss in mice.

Hair microscopy is useful for diagnosing certain hair loss conditions but has limitations and must be interpreted carefully.

Malassezia yeast linked to hair loss; ketoconazole helps treat it.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

Alopecia areata is an autoimmune condition causing hair loss, influenced by genetics, stress, and diet, and may be prevented by a high soy oil diet.

Hair loss and aging are caused by the breakdown of a key protein in hair stem cells.

Finasteride treats enlarged prostate and hair loss, but may cause side effects in some patients.

Animal models have helped understand hair loss from alopecia areata and find new treatments.

EDA2R gene linked to hair loss.

Hair color loss can indicate the effectiveness of a drug targeting the KIT protein in mice and humans.

Asian hair loss differs from Europeans; consider individual needs and psychological well-being for treatment.

Hair loss requires customized treatments based on its various causes and types.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

Finasteride shows promise for treating hair loss and excessive hair growth, but more research is needed to confirm its effectiveness and safety.

New hair loss treatments may include topical medications, injections, and improved transplant methods.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

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