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Using polyethylenimine-DNA to deliver the hTERT gene can stimulate hair growth and may be useful in treating hair loss, but there could be potential cancer risks.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

Activating TRPMLs helps human cells important for hair growth and increases hair growth in mice.

PTHrP is higher in certain dog tumors and may act as a local growth factor.

TR3 is mainly found in hair follicle stem cells and may be involved in hair loss.

Targeting the TRPV4 channel may help treat intestinal diseases.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

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.

Hyaluronan from Has2 is important for proper wound healing and hair follicle development.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

Higher CRHR1 levels in AA patients lead to increased inflammation.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

A genetic marker linked to a type of hair loss was found in most patients studied.

Mutant cells in hair follicles are influenced by their location and interactions with surrounding cells.

The hairless (hr) gene is essential for normal hair follicle function and its mutation leads to hair loss.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Aryl hydrocarbon receptor overexpression found in miniaturized hair follicles in female hair loss.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Serotonin helps wounds heal faster.

The skin produces and responds to thyroid-stimulating hormone, which is controlled by other thyroid-related hormones.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

PCAT1 and HOTAIR levels are lower in people with androgenic alopecia.

The Hairless gene is crucial for healthy skin and hair growth.

Gene variant linked to prostate cancer, hormone levels, and hair loss.

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