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Keratin 2e shows a unique pattern in developing fetal skin, different from other keratins.

Human hair follicle cells can be grown successfully on floating collagen membranes without extra support.

Trichilemmal keratinization is a unique process in hair follicles where the outer root sheath turns into keratin without a specific layer.

New techniques and materials improve sternum reconstruction and patient quality of life.

Changing the direction of cuts can make it easier to put in implants.

The fuzzy gene is crucial for controlling hair growth cycles.

Hair follicle cells can help regenerate teeth.

Desmocollin 1 and 3 have distinct patterns in human tissues, with Dsc1 in specific skin and hair layers and Dsc3 in various epithelial layers.

Sox2-positive dermal papilla cells have unique characteristics and contribute more to skin and hair follicle formation than Sox2-negative cells.

The new method makes it easier to study the whole cochlea from newborn mice and rats in the lab.

Ancient immune and signaling pathways still regulate blood cell development.

Onychomatricoma is a unique nail tumor that mimics the entire nail unit and is not related to other hair-related tumors.

Ascorbyl Tetraisopalmitate penetrates skin better in the stratum corneum than in the infundibulum.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

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

CHI3L1 and CXCL5 proteins help promote hair growth.

An epidermal cyst in the temporal bone can occur as a rare delayed complication after ear surgery.

Charnoly bodies could be a marker for cell damage, and certain nutrients and proteins might prevent them, potentially helping with brain diseases and cancer.

Actin filaments help stabilize and reshape cell membranes.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Fetal wounds heal without scarring because of different biological factors, which could help improve adult wound healing.

This rare genetic disorder causes permanent hair loss and skin bumps from birth.

MEX3A is crucial for maintaining intestinal stem cells in mice.

The southern elephant seal's skin layer helps waterproof the skin by being tightly connected to hair shafts.

α-parvin is necessary for skin and hair growth and for the correct orientation of skin cells.

Trichohyalin helps in hair and skin cell structure and function by binding calcium and linking proteins.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps from birth.

The study concludes that as skin matures from infancy to childhood, there are major changes in cell differentiation, stemness, and growth, leading to a stronger skin barrier in older children.