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The research found that PCOS has common genetic factors regardless of how it is diagnosed and is linked to metabolic and reproductive issues.

Fat cells help recruit healing cells and build skin structure during wound healing.

Oestrogens are key for bone growth during puberty in both boys and girls.

Blood vessels and specific genes help turn cartilage into bone when bones heal.

Male pattern baldness involves genetics, hormones, and needs better treatments.

Lower SHBG levels may increase the risk of PCOS.

Fat tissue stem cells may help increase hair growth.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

The method effectively detects banned substances in urine for sports antidoping.

New cells are added to the hair's dermal papilla during the active growth phase.

ESR2 gene variations may be linked to female pattern hair loss.

Dutasteride is more efficient than finasteride, but individual results vary.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Androgens affect bone and fat cell development differently based on the cells' embryonic origin.

The document concludes that diagnosing PCOS in teenagers is difficult and should focus on specific hormone levels and menstrual irregularities, while also considering treatment for symptoms and related health issues.

Estrogens are key for bone growth spurts in both boys and girls and affect growth into adulthood.

A new non-invasive method can analyze skin mRNA to understand skin diseases better.

Hormonal imbalances may play a role in frontal fibrosing alopecia, and antiandrogenic drugs combined with steroids are currently the most effective treatment.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

Women treated with X-ray for scalp fungus as children had a higher chance of hair loss, especially with higher radiation doses and severe fungus infections.

Polycomb Repressive Complex 2 is not needed for hair regeneration.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

Both classical and L-type atypical BSE from cattle can infect goats with different incubation times, and tests can distinguish between the two strains.

DNA can predict physical traits like eye and hair color accurately, especially in Europeans, but predicting other traits and in diverse populations needs more research.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Genetic variations affect dutasteride treatment response for male pattern hair loss.