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A new DSG4 gene mutation causes hair defects in a young girl.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

Allopregnanolone changes gene expression in glioblastoma cells.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

3D culture helps maintain hair growth cells better than 2D culture and identifies key genes for potential hair loss treatments.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

VEGF and VEGFR-2 genes influence feather maturity, and specific genetic markers can improve chicken breeding.

A specific gene change in APCDD1 increases the risk of hair loss.

HSPC016 gene is important for hair growth.

Higher STAT3 levels are found in hair loss areas, but not linked to hair loss severity.

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

FP-1 is a key protein in rat hair growth, active only during the growth phase.

Human adrenals and gonads have a unique enzyme for steroid hormone production.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

The study found potential new DNA patterns in fertility genes, but further testing is needed.

CDP is crucial for lung and hair follicle cell development.

GasderminA3 is important for normal hair cycle transitions by controlling Wnt signaling.

Plet-1 protein helps hair follicle cells move and stick to tissues.

High TSPEAR levels in colorectal cancer predict worse outcomes.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

PRC2 is not essential for hair follicle stem cell maintenance or hair growth.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

Losing both ERBB2 and ERBB3 receptors in mice causes significant skin problems and inflammation.