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The review concludes that innovations in regenerative medicine, tissue engineering, and developmental biology are essential for effective tissue repair and organ transplants.

Cell polarity signaling controls tissue mechanics and cell fate, with complex interactions and varying pathways across species.

Overexpressing ovine β-catenin in mice skin increases hair follicle density and growth.

Removing the VDR gene in skin cells reduces their growth and affects hair-related genes.

New CRISPR/Cas9 variants and nanotechnology-based delivery methods are improving cancer treatment, but choosing the best variant and overcoming certain limitations remain challenges.

Nanoparticles may improve caffeine delivery for hair growth, offering a potential alternative to minoxidil for hair loss treatment.

Stem cells, PRP, and exosomes show promise in treating skin conditions but face regulatory and safety challenges.

Melatonin improved secondary hair growth in goats but didn't affect primary hair density or litter size.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

New tools show that in fish, NPY increases feeding and somatostatin decreases it.

Copper treatments increase copper in all tissues, but brindled female mice accumulate much more copper in their kidneys without clinical effects, unlike brindled male mice where brain copper deficiency is clinically significant.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

A mother's diet at conception can cause lasting genetic changes in her child.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

Mutant mice help researchers understand hair growth and related genetic factors.

Aromatase gene variation may increase female hair loss risk.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Products should be called 'sperm-safe' only after thorough, well-designed tests.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

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

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

Hirsutism is excessive male-pattern hair growth in women, often caused by hormonal imbalances, and requires ongoing treatment to manage.

The review found no clear link between vitamin D receptor gene variations and polycystic ovary syndrome.

The spiny mouse is a unique menstruating rodent that can help us understand menstruation and reproductive disorders.

FoxN1 gene is essential for proper thymus structure and preventing hair loss.

The type 3 IP3 receptor is important for controlling hair loss and growth.

A gene called Gk5 controls lipid production in the skin and affects hair growth.