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The research found that postmortem root bands in hair are likely caused by the breakdown of a specific part of the hair's inner structure after death.

Scientists successfully grew mini hair follicles using human skin cells, which could help treat baldness.

Curly hair may be caused by a muscle contraction, and muscle relaxants might help treat it.

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.

KRT17 may be a new target for endometrial cancer treatment because it helps cancer cells move and form new blood vessels.

BMP signaling is essential for the development of touch domes.

The enzyme 25 Hydroxyvitamin D 1 α-Hydroxylase is essential for healthy skin and recovery after skin damage.

Understanding intermediate filaments helps explain hair health and related diseases.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

Type 2 diabetes slows down skin and hair renewal by blocking important stem cell activation in mice.

Understanding keratinization is crucial for treating skin conditions like ichthyoses and psoriasis.

A man with skin and hair symptoms improved partially with specific treatment.

A new hydrogel with stem cells from human umbilical cords improves skin wound healing and reduces inflammation.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

Changes in keratin make hair follicles stiffer.

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

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Eating collagen peptides may help with skin and hair growth.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

The hair masks are safe, stable, and effective for hair care.

New treatments targeting specific genes show promise for treating keratin disorders.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Keratin 15 is not a reliable sole marker for identifying epidermal stem cells because it's found in various cell types.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Hair keratin-associated proteins are essential for strong hair, with over 80 genes showing specific patterns and variations among people.

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

Prolactin affects the production of different keratins in human hair, which could lead to new treatments for skin and hair disorders.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

K16 can partially replace K14 but causes hair loss and skin issues.

Keratin peptides can change hair shape gently without harsh chemicals.