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Understanding how acne develops in different diseases could lead to new treatments.

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.

Skin organoids help improve wound healing and tissue repair.

Editing the FGF5 gene in sheep increases fine wool growth.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

Fibroblast Growth Factors (FGFs) are important for tissue repair and regeneration, influencing cell behavior and other factors involved in healing, and are crucial in processes like wound healing, bone repair, and hair growth.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

The document concludes that various signaling pathways and genetic factors are crucial for chicken feather development, affecting poultry quality.

DFMO treatment improves hair growth, muscle tone, and development in Bachmann-Bupp syndrome patients.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Hair loss in men might be linked to changes in cell energy factories.

Restoring mitochondrial function in mice reversed their skin wrinkling and hair loss.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Disrupted cholesterol production impairs hair follicle stem cells, leading to hair loss.

Melatonin, a hormone, can help protect skin from aging by reducing stress, inflammation, and damage, and may also help treat hair loss in women.

Finasteride can cause sexual problems and depression in young men.

Azathioprine may help treat severe alopecia areata, but more research is needed.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Hypothyroidism may cause certain types of hair loss.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

Alopecia Areata is a complex, unpredictable autoimmune hair loss condition with limited treatment options and a significant psychological impact.