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Hydrogel with M2-derived exosomes improves wound healing by slowly releasing exosomes that help reduce inflammation and promote tissue repair.

The UK's EDS National Diagnostic Service found that early diagnosis, lifestyle advice, and regular check-ups are crucial for managing vascular Ehlers-Danlos syndrome. A combination of losartan and bisoprolol can reduce vascular events, improving survival and quality of life.

Wharton’s Jelly stem cells from the umbilical cord improve skin healing and hair growth without scarring.

Men who start losing hair at age 30 may have a lower risk of prostate cancer.

The document concludes that hormonal biomarkers are key for diagnosing hyperandrogenemia in women and hypogonadism in men.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Male-pattern hair loss is largely influenced by genetics, with key genes identified.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

The scalp fat tissue of men with hair loss shows changes in gene activity that may contribute to their condition.

Researchers found genes linked to hair growth cycles in Inner Mongolia cashmere goats, which could help understand and treat hair loss.

Certain DNA regions in alpacas are linked to fiber diameter.

CAP1 decreases the expression of a hair-related protein in young Tan sheep's skin.

Ethnicity affects how polycystic ovary syndrome shows up in women, with white women having higher metabolic risks but less diabetes, and South Asian women showing more androgenic symptoms and being younger at presentation.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Neuregulin3 affects cell development in the skin and mammary glands.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

Lower SMAD2/3 activation predicts more severe skin cancer.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Certain skin proteins can form anchoring structures without the protein AMACO.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

New understanding and treatments for hair loss are improving, but more research is needed.

A genetic variant linked to hair thinning in Japanese women was found.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

P-cadherin is crucial for hair follicle pigmentation but not skin pigmentation.