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Men's hair loss is caused by hormones and genes, and can be treated with medication and surgery, while graying is due to aging and has no prevention except dyeing.

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

A male with aromatase deficiency improved bone health with estradiol treatment.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

Fibroblasts, cells usually linked to tissue repair, also help regenerate various organs and their ability decreases with age. Turning adult fibroblasts back to a younger state could be a new treatment approach.

Non-coding RNAs play key roles in the hair growth cycle of Angora rabbits.

Prostaglandin E2 affects human platelet activity in complex ways that could lead to personalized heart disease treatments.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

New treatments for immune disorders caused by FOXN1 deficiency are promising.

Melatonin helps Cashmere goats grow more hair by affecting certain genes and cell pathways.

Loss of keratin K2 causes skin problems and inflammation.

Patient-derived melanocytes can potentially treat vitiligo by restoring skin pigmentation.

Placental growth factor may help treat hair loss.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

Late pregnancy helps repair brain damage in rats due to the GABAergic system.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

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.

The gene p53 is crucial for removing damaged cells to allow for healthy tissue renewal.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

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

Wounds heal without scarring in early development but later result in scars, and studying Wnt signaling could help control scarring.

DNA methylation changes are linked to hair growth cycles in goats.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

The document concludes that understanding the anatomical changes of the ageing face is important for effective rejuvenation treatments.

Allergic reactions to blood thinners are rare but can be serious, requiring careful management and alternative treatments.

New compounds were found to help increase hair growth and decrease hair loss.

The conclusion is that androgenetic alopecia and senescent alopecia have unique gene changes, suggesting different causes and potential treatments for these hair loss types.

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.