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Mouse profilaggrin helps in skin cell differentiation and may be involved in calcium signaling.

Allopregnanolone changes gene expression in glioblastoma cells.

Self-amplifying RNA could be a better option for protein replacement therapy with lower doses and lasting effects, but delivering it into cells is still challenging.

Cells lacking the Bax protein can outcompete others, leading to better tissue repair and hair growth.

Efficient delivery systems are needed for the clinical use of CRISPR-Cas9 gene editing.

Different species use the same genes for tooth regeneration.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

Certain genes affect udder shape in Holstein cows, important for health and milk production.

Certain natural and synthetic compounds may help treat inflammatory skin diseases by targeting a specific signaling pathway.

Advancements in nanoformulations for CRISPR-Cas9 genome editing can respond to specific triggers for controlled gene editing, showing promise in treating incurable diseases, but challenges like precision and system design complexity still need to be addressed.

ATP-sensitive K+ channel subunits, particularly Sur2A, play a significant role in various cancers.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

FKBP10 and FBN2 are key proteins for hair growth in cashmere goats.

Excessive blue light harms eye cells and disrupts sleep patterns.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

Certain gene variations are linked to the thickness of cashmere goat hair.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

New patents include innovations in skin and hair care, disease treatment, plant stress tolerance, and protein purification.

Plant roots respond to fungus smells by possibly using certain proteins and a plant hormone to change root growth, but more research is needed.

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

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

Sex steroids affect the MafB gene differently in male and female hamsters.

Humans lost body hair relatively recently in evolution.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Macrophages help heal nerves by aiding the maturation of Schwann cells and are important for nerve repair.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.