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LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.

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A new mutation in the KRT86 gene causes monilethrix in a Han family.

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Pattern mode isolation improves the reliability and predictability of Turing patterns.

Arabidopsis Formin 2 stabilizes actin filaments, affecting cell-to-cell movement and virus susceptibility.

Pvalb8 is essential for zebrafish hearing and hair cell development, and its mutation causes hearing loss.

New findings suggest potential treatments for melanoma, hyperpigmentation, hair defects, and multiple sclerosis, and show skin microbiome changes don't cause atopic dermatitis.

A specific metabolite, not a receptor protein, triggers the production of certain kidney enzymes, but this process is disrupted in mice with a mutation causing testicular feminization.

PRSS35 enzyme may help start skin tumors and could be a target for cancer treatment.

LL-37 helps stem cells grow and move, aiding tissue regeneration and hair growth.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

Mutations in the LIPH gene cause woolly hair in a child.

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Trichophyton mentagrophytes genotype VII is a sexually transmitted fungus causing skin issues, mainly among men who have sex with men in Europe, and requires quick treatment.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

Ban Tu Wan, a Chinese herbal supplement, can cause severe liver damage.

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A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

The TT genotype of a specific SNP in sheep is linked to better wool quality.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

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Blocking the JAK/STAT pathway may help reduce skin sensitivity in Xeroderma pigmentosum.

Trps1 plays a key role in hair follicle development and cycling.

The DiLiCre mouse model is an effective tool for precise genome editing using light.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.