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Technique creates 3D cell spheroids for hair-follicle regeneration.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

The new wound dressing promotes cell growth and healing, absorbs wound fluids well, and is biocompatible.

aPKCλ is crucial for keeping hair follicle stem cells inactive and maintaining normal hair growth.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Understanding skin structure and function is key to managing skin diseases and improving quality of life.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

Platycarya strobilacea extract significantly improves hair growth and follicle health.

Chicken feather gene mutation helps understand human hair disorders.

K15 gene is mainly active in the basal layers of hair follicles and epithelia, aiding early skin cell development.

sPLA2-X is crucial for normal hair growth and follicle health.

A six-year-old girl with extra hair on her elbows was treated with hair removal methods.

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

The film-trigger applicator improves microneedle skin delivery and drug efficiency using simple finger force.

GLABRA2 represses root hair formation by inhibiting a specific gene.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

Cat paws have complex touch sensors for detailed sensory processing.

Hair follicle dermal stem cells help control hair growth timing by regulating signals at the hair germ–dermal papilla interface.

Disulfide bonds are crucial for hair structure during keratinization.

Cystic panfolliculoma is a rare, harmless tumor that can be confused with other skin tumors.

Platelet-rich plasma with a new carrier significantly increases hair thickness without serious side effects.

A 2-year-old boy was diagnosed with a rare genetic condition causing fragile hair, intellectual issues, and short stature.

The two-step enzyme digestion method is the best for isolating axillary dermal papilla cells.

Abnormal keratin expression in mice causes severe oral issues, affecting feeding.

TrichoScan helps identify subtle hair thinning in women with androgenetic alopecia.

Dermal papilla cells from human hair follicles form unique structures and don't live as long as other skin cells in lab conditions.

Researchers developed a method to grow hair follicle cells for transplantation using a special chip.

Plica polonica is a rare condition where hair becomes irreversibly tangled, and the treatment is to cut the matted hair.

The human scalp has different types of pigment cells in hair follicles with varying abilities to produce pigment.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.