Search

everythinglearnresearchcommunity

for

Search:↓

Children with classic congenital adrenal hyperplasia have thicker heart fat and more heart and blood vessel risk factors, especially if their condition is not well-controlled.

Adipocyte-derived stem cell conditioned media is effective and safe for treating hair loss caused by hormones.

SIPHL1 from tomato enhances plants' response to low phosphate levels.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

BIMA grafting can be safely done in females with careful preparation.

A protein called HMGB1 helps hair grow by affecting prostaglandin metabolism.

Green OLED light improves stem cell effectiveness for better wound healing.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

Red LED light boosts cell activity and growth, aiding wound healing and blood vessel repair.

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

PCE-DP brightens skin and promotes hair growth by enhancing cell growth and reducing melanin uptake.

Fat tissue stem cells show promise for repairing different body tissues and are being tested in clinical trials.

Researchers converted human embryonic stem cells into trophoblast stem cells using specific transcription factors.

AHR ligands could treat inflammatory skin diseases.

Indian Hedgehog helps control skin cell growth and protects against aggressive skin cancer.

Thy-1 protein helps improve blood flow and wound healing in the skin.

Higher RBP4 levels found in people with two types of hair loss.

Squaric acid dibutylester can cause severe skin reactions in people with allergies.

Tanning ability is linked to specific DNA changes in skin genes.

Abrocitinib, a JAK inhibitor, may help treat atopic dermatitis and alopecia universalis together.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Epigenetic changes in blood cells may contribute to alopecia areata.