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Microbial-derived polydeoxyribonucleotide is a better and more sustainable alternative to salmon-based versions for healing and immune support.

Finasteride improves prostate cancer prediction by adjusting kallikrein marker levels.

Cytokeratin 19 and cytokeratin 15 are key markers for monitoring the quality and self-renewing potential of engineered skin.

Mutations in the SNRPE gene cause hereditary hair loss.

K25, K27, and K28 are found in all inner root sheath layers of hair, while K26 is only in the cuticle.

Reconstructed skin models are useful for studying how skin processes certain chemicals.

Certain gene changes and hormone levels are linked to female hair loss.

SGK1 is important in cancer growth and treatment resistance, and targeting it could improve therapies.

New methods efficiently isolate dermal papilla cells from hair follicles, preserving their characteristics better than traditional methods.

Mouse skin cells can become sperm-like cells in the lab.

A rare genetic mutation in the EGFR gene caused severe skin issues and other health problems in a Slovakian girl, who is now 4 years old and receiving care.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

The research found that people's hair proteins vary by individual and body part, with some differences between ethnic groups, which could help in forensics.

The BASP classification is a detailed system for categorizing hair loss in both men and women, but it may be complex for beginners and not fully suitable for grading female hair loss.

The research found a link between certain molecular features and the biological activity of BC3, which can help identify or create new active compounds.

Genetic variation in the KRTAP15-1 gene affects wool yield in sheep.

KAP6 genes are conserved across species and active in hair follicles.

qPCR is effective for quickly diagnosing fungal infections in horses.

Solid-state NMR can effectively study keratin structure and treatment effects in fur.

Multiphoton microscopy effectively images mouse skin layers and structures.

Smoking and certain health conditions like thyroid disease may make palmoplantar pustulosis harder to treat.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

The research found that a protein called caveolin-1 is reduced in psoriasis, but reintroducing it can help alleviate some psoriasis symptoms.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.