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Gene variation affects prostate issues and hair loss.

Human skin cells contain Protease Nexin-1, and male hormones can decrease its levels, potentially affecting hair growth.

Forsythiaside A helps protect cells and liver from damage by reducing oxidative stress and boosting antioxidants.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

CAP1 helps Arabidopsis plants grow better under ammonium stress.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Some hair protein genes evolved early and were adapted for use in hair follicles.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

A protein complex called mTORC1 likely affects when hair growth starts in mice.

ILK is essential for proper hair follicle development and structure.

Inhibiting PDE8A may help treat hair loss by boosting fat cell growth and hair regeneration.

A protein in plants needs to bind two lipids to help with root hair growth, and this process is similar across different plant species.

PDGF and its receptors are crucial for stem cell growth and function.

The atlas maps maize peptides, showing complex regulation and varied roles across tissues and stages.

Certain skin proteins can form anchoring structures without the protein AMACO.

Compounds from Pterocarpus indicus may help treat benign prostatic hyperplasia by stopping cell growth.

CD2 might be a new treatment target for patchy alopecia areata.

Reduced matriptase activity causes skin and hair issues in both humans and mice.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

TIP39 and PTH2R help control calcium levels and skin cell development.

Metformin helps hair growth by affecting cell signals related to hair follicle development.

ME1 and PPAR signaling may influence hair loss in androgenetic alopecia.

CXCR2 in skin cells promotes tumor growth.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Blocking casein kinase 1 in skin cells can help melanocyte precursors move better, potentially helping with conditions like vitiligo or gray hair.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

A peptide from hair follicle stem cells can boost hair growth.

A protein called ectodysplasin-A2 increases a hair growth inhibitor in balding cells, which could be a target for hair loss treatment.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.