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Finasteride, at doses of 5mg or higher, may negatively affect male fertility by reducing the expression of certain genes involved in sperm production.

A gene mutation in Lama3 is linked to a common type of hair loss.

The LAMTOR3 gene is involved in cashmere goat hair growth and is affected by certain treatments and other genes.

PROTACs offer a new, precise way to treat cancer by breaking down harmful proteins.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

AH-001 could be a safer and more effective treatment for hair loss.

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

The E2 protein affects gene activity in hair follicles of mice.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

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

The QuantAnts machines can find cancer markers and create CRISPR targets for them.

A gene mutation in mice causes severe skin disorder similar to a human condition.

Loss of Dnmt3a and Dnmt3b increases aggressive skin tumors by affecting PPAR-γ.

The lentiviral array can monitor and predict gene activity during stem cell differentiation.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

Neuregulin3 affects cell development in the skin and mammary glands.

Mdm2 is crucial for controlling p53 to maintain healthy cells and prevent tumors.

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

Hair follicle samples effectively show how well the drug MK-0752 targets and engages with the Notch pathway.

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

Enhanced stem cells from the placenta can help treat Graves' eye disease by stopping fat cell growth.

PRC1 influences skin stem cell development by both turning genes on and off, affecting hair growth and skin cell types.

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

MAEG helps in mouse hair follicle development by aiding cell adhesion.

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