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A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Trichothiodystrophy involves brittle hair due to low sulfur amino acids, not a transport defect.

Vitamin D receptor and hairless protein are essential for hair growth.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

DNA methylation of miR-365-1 causes hair follicle stem cell death by affecting DAP3.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

Oxidized trichocyte keratin has a helical dislocation in its structure.

Neuregulin3 affects cell development in the skin and mammary glands.

Lipids from Schizochytrium sp. help prevent hair loss by protecting hair cells from damage and promoting hair growth.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

Different sPLA2 enzymes affect immunity, skin and hair health, reproduction, and may be potential targets for therapy.

Type I and Type II keratin chains can form heterodimers despite sequence differences.

TMPRSS6 is crucial for controlling hepcidin and normal iron absorption.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.

HDAC1 is crucial for skin development and preventing tumors.

New compounds were made that block an enzyme linked to breast cancer better than existing treatments.

Drugs that block GSK-3 show promise for treating various diseases.

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.

LPA3 is crucial for embryo implantation and links LPA to prostaglandin signaling.

ZO-1 helps hair follicle stem cells renew better by changing their structure.

The TRPV3 gene mutation affects hair growth by keeping mice in the growth phase longer, which could help treat hair loss.