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The hair follicle dermal sheath is essential for hair shedding and needs to communicate with the outer root sheath for normal hair growth cycles.

Giant axonal neuropathy changes the structure of keratin in human hair, making it stiffer and stronger.

Different hair cleaning methods caused varying levels of damage to the hair's outer layer.

The dye quickly penetrates hair follicles, mainly through the gap, not the surrounding skin.

Trichothiodystrophy is a condition with brittle hair and various physical and mental issues due to low sulfur in proteins.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Sebum helps protect human skin from microbes.

A gene mutation in mice causes skin defects and early death.

The study concludes that the EDA2R gene is activated by p53 during chemotherapy but is not necessary for chemotherapy-induced hair loss.

A patient with total hair loss developed vitiligo after using a treatment called DCP.

Dermoscopy helps diagnose unusual skin lesions like osteonevus of Nanta and can prevent misdiagnosis of serious conditions.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

Naked-mouse hair lacks certain proteins and has less soluble fibril.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

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A 17-year-old with Netherton syndrome has dry, itchy skin, brittle hair, and high IgE levels, treated with antihistamines and emollients.

Lacking cyclin D3 reduces skin cancer growth without affecting normal skin cell growth.

Squalene-based carriers improve delivery of a treatment to hair follicles for alopecia areata.

Desmocollin 1 is essential for strong skin and proper skin function.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Non-classical 21-hydroxylase deficiency can be missed in newborn screenings and should be considered in cases of early puberty or virilization.

Special scalp and hair examination techniques can identify hair problems.

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

Type IV collagen chains vary in different parts of human skin, with specific patterns linked to melanocytes.

The new delivery method for dutasteride is more effective and has fewer side effects.

Injecting specific oligonucleotides can change hair growth and structure by altering a gene.

Damaged hair follicles make mice more prone to skin inflammation and skin cancer after UV exposure.