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A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

Scientists discovered two versions of a new human hair keratin gene.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

PLA2R1 overexpression harms kidney cells by stopping their growth cycle.

Keratins are important for skin cell health and their problems can cause diseases.

Mutations in specific genes cause different types of ectodermal dysplasias.

Mutations in the KRT85 gene cause hair and nail problems.

The KRTAP gene family helps understand hair evolution and hair disorders.

Certain immune system genes are linked to a higher risk of psoriasis and psoriatic arthritis, while others may offer protection.

The human K5 promoter controls specific gene expression in skin cells, with key regulatory elements near the TATA box.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

KRTAP2-3 could help predict cancer recurrence by identifying specific cancer cells.

Mutations in the hairless gene cause a rare form of permanent hair loss.

The Bsk mutation doesn't involve keratin gene recombination and its cause is unknown.

Hair loss gene linked to prostate issues.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

Prostaglandins and the enzyme AKR1C3 could play a role in skin cancer and hair loss, and further research is needed to understand these mechanisms.

AKR1D1 controls glucocorticoid levels and receptor activity in liver cells.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

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

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

BRG1 is essential for skin cells to move and heal wounds properly.

Krtap11-1 is important for hair strength and structure.

RAR-gamma 1 is important for normal skin maintenance and differentiation.

The EDAR gene greatly affects hair thickness in Asian populations.