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

The 4C32 gene may help in mouse skin development and differentiation.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

Two genetic variations in Moa buffalo help them adapt to heat.

PDRN from salmon may slow skin aging by improving skin quality and reducing inflammation.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

Compounds from Eclipta prostrata L. plant have diabetes and obesity-fighting properties and reduce inflammation.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Triphenylphosphine oxide can increase oil production and reduce inflammation in skin cells without affecting TRPM5.

Lack of TG2 increases fat storage and lowers cell cleanup in skin oil cells.

Triptolide effectively and safely reduces actinic keratosis lesions in mice.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

Certain gene variants are linked to a higher risk of polycystic ovary syndrome, hair loss, and obesity in women from western Saudi Arabia.

Protease Nexin-1 is found in human hair growth cells and is affected by male hormones.

A new genetic variant in the EEF2K gene may contribute to polycystic ovary syndrome.

FOL-005 peptide may help treat excessive hair growth safely.

An allele of the KRTAP13-2 gene may improve wool quality in sheep.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Certain genetic variations are linked to hair loss in Mexican men.

Researchers found 19 genes important for root hair growth in a plant called Arabidopsis.

Loss of Dnmt3a and Dnmt3b increases aggressive skin tumors by affecting PPAR-γ.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Researchers created a cell line to study hair growth and found specific genes affected by dihydrotestosterone.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.