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A genetic marker linked to a type of hair loss was found in most patients studied.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

SHISA6 helps maintain certain stem cells in mouse testes by blocking signals that would otherwise cause them to differentiate.

Keratin 17 is important for skin development and may help define skin cell types.

Hidradenitis suppurativa may be a type of autoinflammatory skin disease linked to gene mutations and immune system issues.

Children with classic congenital adrenal hyperplasia have thicker heart fat and more heart and blood vessel risk factors, especially if their condition is not well-controlled.

DHEA boosts bone cell growth and differentiation in elderly stem cells.

Family dynamics affect preschoolers' stress levels, especially DHEA.

Tofacitinib helps improve skin conditions in people with Down syndrome, especially alopecia areata.

Hutchinson-Gilford Progeria Syndrome causes rapid aging due to a gene mutation, with no cure yet, but research may lead to better treatments.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

Finger length ratio is not linked to hirsutism or hormone levels.

MAD2B slows down the growth of skin cells that are important for hair development by interacting with TCF4.

New culture method keeps human skin stem cells more stem-like.

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Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

DHHB from Platycladus orientalis L. promotes hair growth and could be a natural alternative to current treatments.

Hairless protein helps control hair growth by regulating vitamin D receptor activity.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

Adult mice with CBS deficiency show minimal health issues and normal lifespan despite high homocysteine levels.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

DAB labeling effectively identifies collagen type III and PDGFR in horse skin, but may show false positives.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requires high doses of calcium and vitamin D for management.

Laser therapy on human skin affects the HERC6 gene and related genes, influencing many cell processes and requiring careful safety measures.

Hypospadiac rats showed abnormal genital development, useful for studying human hypospadias.