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The supplement with amino acids, iron, selenium, and marine hydrolyzed collagen improved hair growth more than drug treatment alone, with most people tolerating it well.

People with chronic hair loss often have lower Vitamin B12 levels.

The marine protein complex, Viviscal®, was found to effectively reduce hair loss and improve hair, skin, and nails quality in women.

Genetic manipulations that extend lifespan in mice may not work as effectively in humans.

JAK inhibitors show promise for treating skin conditions like eczema, hair loss, and psoriasis.

Alopecia areata is an autoimmune disease where T cells attack hair follicles.

Notch signalling helps skin cells differentiate and prevents tumors.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Acitretin is effective for severe skin conditions but has significant side effects and requires careful monitoring.

Trichohyalin is modified by enzymes to form strong structures in hair cells.

NK cells play a role in skin diseases like eczema and psoriasis.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

Lack of Ctip2 in skin cells delays wound healing and disrupts hair follicle stem cell markers in mice.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Thallium, mercury, selenium, and colchicine strongly cause hair loss.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Platelet-rich plasma shows potential for hair loss and skin rejuvenation but needs more research for widespread use.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Telogen Effluvium is a condition causing excessive hair loss due to stress, illness, drugs, or hormonal changes, and can be treated with specific products or naturally resolves after 3-4 years.

Hair cystine levels may indicate protein malnutrition, but more research is needed.

Cronkhite-Canada syndrome is a rare, non-inherited condition causing various symptoms like polyps, hair loss, and weight loss.

Oxidative stress plays a significant role in alopecia areata, and new treatments may include JAK inhibitors and antioxidants.

Simvastatin/ezetimibe may help some patients with severe alopecia areata regrow hair.

The C-terminal tail of AHF/trichohyalin is essential for organizing keratin filaments in keratinocytes.

Fox genes are important for hair growth and development in cashmere goats.

Alopecia areata caused a boy's hair to regrow straight instead of curly, but the exact reason is unknown.