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Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

Post-finasteride syndrome can cause sexual and systemic side effects, and patients should be informed about these risks.

Scientists can now create skin with hair by reprogramming cells in wounds.

Newly born mesenchymal cells quickly spread out in response to tissue tension during early development.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Mouse touch-sensitive nerve cells adjust their connections based on competition with other similar cells.

Primary cilia affect the size and oil production of eye glands but not the oil's makeup.

Digital games are part of new media but need a deeper look at their complex nature and cultural roots.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

10.5% of sheep in Ismailia, Egypt, had Sarcoptes scabiei, causing skin issues.

Activating β-catenin increases melanocytes and decreases Schwann cells.

Live imaging helps us understand skin immune responses and develop treatments.

Testosterone significantly affects urination differences between male and female mice.

The gene Prss53 affects hair shape and bone development in rabbits.

Commonly used plants in hair products can guide future research and help professionals recommend treatments.

New factors in female hair loss include genetics, hormones, stress, and inflammation; future treatments should also focus on these areas and consider the patient's emotional well-being.

Some treatments like minoxidil, finasteride, and dutasteride are effective for hair loss, but there's no agreed best treatment.

Severe hair loss (androgenetic alopecia) is linked to higher risk of heart disease (cardiovascular atherosclerosis).

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Lack of cystatin M/E causes thin hair and dry skin.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Disrupting β-catenin signaling in certain cells causes anorectal malformations.

The goat hair keratin gene is very similar to sheep's and is strongly expressed in goat hair follicles.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.