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The African spiny mouse heals skin without scarring due to different protein activity compared to the common house mouse, which heals with scarring.

The study found that women with hyperandrogenic PCOS have higher levels of AKT1 and AKT2 proteins in their cells, which may lead to cell dysfunction.

Blocking neurosteroid production can lead to more seizures and faster epilepsy onset in rats.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

Menopause causes significant changes in the vaginal introitus, but less so in the labia majora, which may lead to symptoms of vaginal atrophy.

Some growth factors, while important for normal body functions, can cause diseases when not regulated properly.

The research identifies genes linked to wool quality in sheep and provides insights to improve wool production.

Cashmere and milk goats have different hair growth cycles and gene expressions, which could help improve wool production.

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

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

Different forms of FGF5 either promote or inhibit hair growth.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

ERβ has potential in treating prostate cancer and neurodegenerative diseases, but human studies are needed before clinical use.

Henna helps wounds heal faster and better.

FGF13 gene changes cause excessive hair growth in a rare condition.

Antiviral drugs, especially daclatasvir, may be a new treatment for a rare skin disease, improving survival and reducing symptoms in mice.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

Significant progress was made in understanding PXE, but effective treatments are still needed.

Both cell and non-cell parts are important for rat whisker follicle regrowth.

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

Insulin resistance and obesity are key factors in the development and worsening of polycystic ovary syndrome, and lifestyle changes are important for managing it.

Melatonin is important for skin health and protection, and can be made by the skin or applied to it.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

Hair proteins in preschool children and their mothers could indicate developmental changes and health status.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Variant G of the KRTAP20-1 gene improves wool curliness in Chinese Tan sheep.

Melatonin improves tomato root growth and plant health at certain levels by affecting genes and hormones but can damage roots at high levels.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

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