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The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

The piRNA pathway genes are crucial in early development and may influence sex differentiation through hormone regulation.

The N gene affects the protein makeup of mouse hair.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

Four new genes related to sheep wool were discovered, showing genetic diversity.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

Genetic factors influence growth and brain development in children.

OsPHR2 gene in rice enhances root growth and phosphorus accumulation.

The same gene mutation can cause different symptoms in family members.

New genetic variants linked to albinism were found in Pakistani families.

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

Hair loss gene linked to prostate issues.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Noncoding RNAs help determine cashmere quality in goats.

New topical treatment using spherical nucleic acids shows promise in reducing psoriasis inflammation.

The ND1 gene of the Asian black bear Sichuan subspecies is similar to other bear species.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

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

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

TMPRSS2 affects COVID-19 severity and treatment options.

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.

Woodhouse-Sakati syndrome shows varied symptoms and genetic differences within families.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.