Search

everythinglearnresearchcommunity

for

Search:↓

The research found that the molecule lncRNA-H19 helps hair follicle cells grow by affecting certain cell pathways in cashmere goats.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

A substance called miR-1246 may help treat severe hair loss by reducing certain immune cell activities.

Damaged hair follicle stem cells may leave the skin to help maintain youthfulness.

Sox2 controls hair color by affecting pigment production in hair follicles.

Retinoic acid and DMSO improve gene delivery to mouse skin for potential hair and skin disease treatment.

Monilethrix causes brittle hair and hair loss, and it runs in families.

miR‑339‑5p can slow down hair follicle stem cell differentiation by targeting DLX5.

Human hair follicles have a unique metabolism that changes between growth stages and may contribute to baldness.

Retinoids can help treat skin pigmentation disorders by affecting melanin production.

Copper therapy improved health and enzyme activity in mice with copper deficiency.

Glutamine helps macrophages reduce inflammation and improve wound healing.

Food deprivation increases MST enzyme in the brain, possibly affecting energy balance.

H19 may help cause PCOS by affecting CTGF levels, suggesting a new treatment target.

Male hormones control a specific gene in hamster skin, with different hormones having varying effects.

Somatostatin may help protect hair follicles from immune attacks.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

MXD@CP could be a promising new topical treatment for hair loss.

Minoxidil analogs can be improved for hair growth inhibition by modifying specific parts of their structure.

Higher protein diets with DL-methionine improve mink hair growth and fur quality.

Overactive sonic hedgehog signaling worsens uterine scarring by reducing cell recycling.

Mitochondrial problems in tooth cells lead to bad enamel and dentin development in mice.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

A 6-year-old girl was diagnosed with a rare hair disorder called monilethrix.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.