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The fuzzy gene is crucial for controlling hair growth cycles.

ZmSPL10, ZmSPL14, and ZmSPL26 genes are essential for forming maize structures needed for pollen capture and kernel production.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

EP 2 receptor is essential for heart repair by helping macrophages work properly.

Blocking BACE1 and BACE2 enzymes causes hair color loss in mice.

PINK1 is important for controlling gut immune responses linked to early Parkinson's disease.

Too much AKR1C3 enzyme causes resistance to finasteride by increasing testosterone.

KRTAP genes evolved early in mammals, leading to diverse hair traits.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

Apocynin may protect skin cells from aging and damage caused by UVB light.

Setipiprant did not significantly improve hair growth in men with hair loss.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

A specific gene mutation causes congenital hair loss.

White lupin uses specific genes to grow root hairs and access phosphorus when it's scarce.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

Astraglus polysaccharide may help hair growth by boosting follicle stem cell activity.

A girl with a rare skin condition improved after one month of treatment with acitretin.

Keratin 15 expression in skin cells is regulated by two mechanisms involving PKC/AP-1 and FOXM1.

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

PD‐L1 and PD‐L2 may not effectively control immune activation in alopecia areata.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Retinoic acid-binding proteins in skin are regulated by β-catenin and Notch signalling.

SSEA-4 can distinguish between eccrine and apocrine sweat gland ducts.

4-Aminopyridine gel speeds up burn wound healing and improves skin regeneration.

Frog skin cells need the protein desmoplakin for proper development and cell layer formation.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

VILLIN4 helps root hair growth by organizing actin with calcium.