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Liver damage in PCOS is linked to iron overload and cell death due to the miR-761-hepcidin/GPX4 pathway.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

FGF-7 helps hair grow by activating hair follicles and is a promising target for hair loss treatments.

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

A new gene mutation causes a rare type of hair loss.

OsRopGEF3 is crucial for rice root hair growth and ROS production.

GLI2 activates GLI1, promoting skin tumor growth and hair development.

RORA plays a key role in controlling seasonal hair molting by affecting hair follicle cell activity.

The hr gene is linked to hair loss in Valle del Belice sheep.

Half of the patients treated with a specific drug for skin cancer experienced hair loss not related to the drug's dosage.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

Certain miRNAs might be involved in a hair loss condition called frontal fibrosing alopecia and could possibly help in its diagnosis.

MYB30 and EIN3 work against each other to control root hair growth and phosphorus uptake in plants when phosphate is low.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

Kidney cancer cells without folliculin are more sensitive to radiation due to increased self-eating cell death.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

Key genes and pathways, including Wnt, NF-Kappa, and JAK-STAT, are crucial for starting Pashmina fiber growth in goats.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Birt–Hogg–Dubé Syndrome requires genetic testing for accurate diagnosis due to its similarities with tuberous sclerosis.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

Sheep cells were successfully modified to include a spider silk protein gene.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Vav2 changes how hair follicle stem cells' genes work as they age, which might improve regeneration but also raise cancer risk.

Early changes in skin gene expression can predict later bone mass loss after radiation exposure.