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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.

DHT affects bone growth by altering gene activity in osteoblasts, potentially complicating steroid use.

Finasteride exposure affects gene expression and anogenital distance in male rat fetuses.

The research found that the gene activity in mouse skin stem cells changes significantly as they age.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

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

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Using CRISPR for gene editing in the body is promising but needs better delivery methods to be more efficient and specific.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

The conclusion is that we need more effective hair loss treatments than the current ones, and these could include new drugs, gene and stem cell therapy, hormones, and scalp cooling, but they all need thorough safety testing.

Beard and scalp hair cells have different gene expressions, which may affect beard growth characteristics.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Nanotechnology is improving drug delivery and targeting, with promising applications in cancer treatment, gene therapy, and cosmetics, but challenges remain in ensuring precise delivery and safety.

The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

Injecting CHIR-99021 into goose embryos improves feather growth by changing gene activity and energy processes.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

The Hairless gene is crucial for hair cell development, affecting whether skin cells become hair or skin and oil gland cells.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Mice with a mutated Dsg3 gene showed severe symptoms but not the typical blistering of pemphigus vulgaris.

Obese mice with a leptin gene mutation have a longer resting phase in their hair cycle, which may help understand certain hair loss conditions.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

Differences in gene expression and methylation patterns found in AGA patients suggest potential targets for future treatments.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Keratin gene expression helps understand different types of skin cells and their development, and should be used carefully as biological markers.

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.