Search

everythinglearnresearchcommunity

for

Search:↓

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Apocynin may protect skin cells from aging and damage caused by UVB light.

Cinnamomi cortex may help treat prostate enlargement by reducing related proteins.

High-dose radiation speeds up aging in skin stem cells.

The method effectively identifies and measures seven banned substances in cosmetics.

A specific gene mutation causes woolly hair and hair loss.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

Human skin can produce steroids from cholesterol.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

New genes and pathways are important for testosterone production and male sexual development.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Women with non-classical congenital adrenal hyperplasia have higher levels of certain steroids, which can be reduced by treatment.

A unique gene mutation was found in a family with monilethrix.

A genetic variant in the KRT25 gene causes tightly curled hair.

CB-03-04 shows promise as a treatment for prostate issues due to its strong anti-androgen effects.

Certain drugs that block specific enzymes can help treat prostate diseases.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Certain enzymes react strongly with some hormones in rat skin during hair growth, mainly in sebaceous glands and hair sheaths.

The document explains how to make a compound called 3.BETA.-Benzoyloxy-4-pregnen-16.ALPHA.,17.ALPHA.-epoxy-6,20-dione and describes its crystal structure.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.