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SASH1 gene mutations are linked to various inherited skin pigmentation disorders.

The SYP123-VAMP727 complex is important for transporting materials that harden the root hair shank in Arabidopsis.

Scientists found new, better-working inhibitors for a hormone-related enzyme.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

Dog hair follicle stem cells can turn into fat cells.

Kaempferol helps skin stem cells grow and may improve skin thickness due to its 3-OH group.

Removing STAT5 from 3D-cultured human skin cells reduces their ability to grow hair.

Ginsenoside Rd may help improve skin aging by increasing collagen in the skin.

Different cells affect hair follicle blood vessels, endothelial cells react differently to inflammation and oxidized fats, and prasugrel better protects heart vessels during a procedure than clopidogrel.

Prasugrel is better than clopidogrel at preventing heart damage and improving blood flow in small heart vessels during heart artery procedures.

DKK4 can be used to improve wool quality in Zhexi Angora rabbits.

DPP4-positive fibroblasts play a major role in producing proteins that lead to skin fibrosis.

Transgenic sheep embryos with a specific promoter were successfully created, but more research is needed for gene expression in hair follicles.

Sheep have a unique gene, KAP8-2, that humans don't have, which may affect wool properties.

CD98hc's role in skin health decreases with age.

The ZIP13 variant is linked to abnormal hair quality.

FCER1A and RGS1 may help diagnose and treat systemic lupus erythematosus.

A protein called sFRP4 can partly inhibit hair growth.

Keratin-associated proteins help link filaments and affect keratin's strength.

A specific gene mutation causes a severe skin disorder in a family.

Human hair proteins have similar cysteine and glycine levels to skin proteins.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

HSP90 and lamin A/C are crucial for hair growth and could be targets for treating hair loss.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.