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Polarizing light microscopy can easily and reliably diagnose congenital keratinizing disorders like Netherton syndrome.

Four specific keratins in hair follicles help understand hair structure and function.

CD90 is present on specific cells in dog hair follicles.

Different human hair keratin types have unique structures that affect how they dissolve and can be used to create self-tendons.

All Indian dromedary camel breeds have the same KRTAP7 gene affecting hair quality.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

The terpenoid fraction may cause thicker scars by delaying wound healing.

Brandt's hedgehog has thick skin on its back and many glands near its nostrils.

A man's pubic hair infection was treated by shaving and using antifungal medications.

Malassezia fungi in healthy noses can form a "spaghetti-and-meatballs" structure.

A single recessive gene causes sparse hair in certain Japanese White rabbits.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Capitate trichomes have more endoplasmic reticulum and vacuoles, while peltate trichomes have more plastids and larger subcuticular spaces.

Isaria cicadae Miquel rice fermentation extract helps heal wounds and regenerate hair follicles.

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

The study developed a successful mouse model to study skin infections, highlighting the importance of choosing the right fungal strains.

Deleting Crif1 in mouse skin disrupts skin balance and hair growth.

Researchers found genes and microRNAs that control curly fleece in Chinese Tan sheep.

Hunting wild boar can cause fungal infections in dogs.

Hair shaft miR-221 levels can help detect malignant melanoma.

A genetic variant in the KRT25 gene causes tightly curled hair.

Human hair follicle stem cells can help treat bone loss in osteoporosis.

A white-tailed deer fawn in South Dakota was the first cervid found with congenital hypotrichosis, a condition causing sparse or missing hair.

PKM2 is a promising target for heart repair and regeneration.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Somatic BHD mutations are rare in Japanese renal tumors.

PRX01, PRX44, and PRX73 affect root hair growth by interacting with extensins in Arabidopsis.