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The oral supplement improved hair loss in patients with telogen effluvium.

SH-SY5Y cell lysate is effective for diagnosing Satoyoshi syndrome.

A specific gene mutation causes severe skin and nail issues and hair loss.

Alloxan diabetes, methylthiouracil, cortisone, and adrenaline affect how white mice hair follicles use glucose and cystine and their cell division.

Necl2 affects skin cell behavior and slows wound healing.

Researchers developed a method to identify and analyze cyclosporin compounds and their structures effectively.

Hair proteins have weak spots in their α-helical segments.

Trichohyalin in sheep hair follicles may help with structure and calcium binding.

New lipid/fiber microplexes improve mRNA therapy for degenerative diseases by enhancing cell function and treatment effectiveness.

Excessive selenium in supplements can cause hair loss and nail issues.

LSD1 is essential for healthy skin development and creating the skin's protective barrier.

A young man had a rare case of hair cysts on his elbows, which was hard to diagnose and treat.

L-cysteine and ultrasound successfully improved rabbit hair fibers for industrial use.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

S100A4 promotes aggressive ovarian cancer and is a potential treatment target.

Terbinafine effectively treated kerion celsi despite disrupted immune responses.

Three related Persian cats have a rare, likely hereditary skin condition causing hair loss and poor coat quality, with limited treatment options.

The protein's size was reduced, but more work is needed to confirm its function.

Prussian Blue causes hair cuticles to detach, weakening the hair.

A lotion with tretinoin, minoxidil, and betamethasone valerate helped treat a woman's skin infection.

Eruptive vellus hair cysts are rare, benign skin lesions that are hard to treat.

Contaminated wheat caused hair loss and other symptoms due to high selenium, but washing it with alkaline water helped.

A special diet can fix hair problems in argininosuccinase deficiency.

The woman has scurvy and needs more vitamin C.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

Hypertrichosis (excessive hair growth) can help diagnose superficial epidermolytic ichthyosis.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.