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Zfp157 is active in many mouse tissues during development and in specific adult cells.

S1PR1 helps control inflammation in blood vessel cells by affecting gene activity differently in various cell types and locations.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

miRNA-211 reduces melanin in Cashmere goats by suppressing AP1S2.

SQSTM1 gene issues may increase the risk of alopecia areata.

Sphingosine 1-phosphate affects inflammation and gene expression in different aorta cells.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

TRF1 is crucial for creating and maintaining stem cells and marks both pluripotent and adult stem cells.

TRM21 helps control flavonoid production and root hair growth in Arabidopsis thaliana.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

MicroRNA-200 prevents sebaceous gland development by inhibiting SOX9 and cell cycle progression.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

Lrig1 marks a unique group of stem cells in mouse skin that can become different skin cell types.

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

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

MEX3A is crucial for maintaining intestinal stem cells in mice.

Low-dose DMSO may help treat castration-resistant prostate cancer by reducing key cancer cell receptors.

The rs1128977 gene variant may affect cholesterol and body measurements.

DcR3 helps heal wounds and regrow hair by changing macrophages to a repair-focused type.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.