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TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

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

The protein Gnαs is found more in black mice than white mice and may influence their coat color.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

Akt2 and SGK3 are both important for normal hair growth and development.

High LGR5 levels in glioblastoma indicate poor prognosis and are essential for cancer stem cell survival.

Increased PPARGC1α relates to hair thinning in common baldness.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

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

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

Editing the FGF5 gene in sheep increases fine wool growth.

Removing Sprouty genes in mice causes various hormone-related issues but does not increase cancer risk by one year of age.

AGC2-1 protein is essential for root hair growth in Arabidopsis.

ERG increases SOX9, promoting prostate cancer growth and invasion.

Certain gene variations are found in people with polycystic ovary syndrome.

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

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

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

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

Steroid sulfatase in hair follicles may be a target for treating hair loss.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

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

SQSTM1 gene issues may increase the risk of alopecia areata.

Researchers found 15 new genetic links to skin traits in Japanese women.

Overexpressing the epigen gene in mice leads to enlarged sebaceous glands and greasy fur.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.