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Chemokine signaling is important for hair development.

Men are more likely to get infectious skin diseases, while women are more prone to autoimmune and pigment-related skin conditions, influenced by biological and environmental factors.

Wnt signaling is important for development and cell regulation but can cause diseases like cancer when not working properly.

Regenerative pharmacology, which combines drugs with regenerative medicine, shows promise for repairing damaged body parts and needs more interdisciplinary research.

The conclusion is that understanding how feathers and hairs pattern can help in developing hair regeneration treatments.

The document concludes that future heart disease research should account for sex-specific differences to improve diagnosis, treatment, and outcomes.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

Thyroid hormone affects skin health, with too little causing rough, pale skin and too much leading to smooth, thin skin, and may also impact wound healing and skin conditions.

Genetic variations affecting skin structure play a key role in severe acne.

People with atopic dermatitis are more likely to develop other skin conditions due to shared genetics and immune pathways.

RACB in barley is crucial for cell polarity and nucleus positioning, aiding fungal infection.

The skin is the largest organ, protecting the body, regulating temperature, and producing hormones.

Finger length ratios are not linked to the number of specific gene repeats affecting testosterone sensitivity.

Hirsutism can be caused by various conditions besides PCOS, and it's important to treat the underlying issue and manage symptoms with medication and cosmetic approaches.

Low serum complement levels in SLE patients don't always match with disease flares; monitoring C3 and C4 is useful, but cell-bound complement products might better indicate disease activity.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

Macrophages help hair growth after injury through CX3CR1 and TGF-β1.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Androgens may influence T cells, contributing to higher autoimmune liver disease risk in women.

Hydrogen peroxide and monoethanolamine in hair dye can cause dermatitis and hair loss.

Women with polycystic ovary syndrome tend to have a longer anogenital distance.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

STAT5 activation is crucial for starting the hair growth phase.

Psychotropic medications can cause skin reactions, including severe conditions like SJS and TEN, and it's important for psychiatrists to recognize and manage these side effects.

New treatments for PCOS focus on insulin resistance and reducing testosterone levels, along with traditional hormone therapies.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Oral zinc sulphate reduces dark hair color in mice.