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Methylene blue staining effectively highlights detailed nerve structures in rat fur.

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

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

ETS2 drives cancer progression in squamous cell carcinoma and is linked to poor patient outcomes.

The new patch made of cell matrix and a polymer improves wound healing and supports blood vessel growth.

Minoxidil increases cell layer permeability by reducing tight junction proteins and raising ROS levels.

QLT0267 stops hair follicle cell growth and movement.

Sebaceous glands help study fatty acid transporters and binding proteins.

Overexpression of COX-2 in mice skin causes abnormal skin and hair development.

lncRNAs significantly influence koi carp skin color.

Basal cell carcinomas may use IDO to protect themselves from the immune system.

Nonmelanoma skin cancers have higher levels of certain osteopontin variants than normal skin.

KY19382 speeds up wound healing by activating a specific cell signaling pathway.

Fgf20 is crucial for hair follicle formation by influencing cell movement and growth.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

The hair defect is due to abnormal inner root sheath keratinization.

Corin helps control salt and sweat release in sweat glands.

The conclusion is that a new method combining magnetic tweezers and traction force microscopy may help understand skin cell interactions and diseases.

A specific RNA increases hair stem cell growth and skin healing by affecting a protein through interaction with a microRNA.

Human basal cell carcinomas and squamous cell carcinomas have unique gene expression patterns not fully mirrored in mouse models.

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.

A specific group of skin stem cells was found to help maintain hair follicle cells.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

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

PRX102 is essential for rice root hair growth by helping transport substances to the tips.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.