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Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

IL-33 is linked to hair follicle damage in psoriasis and could be a treatment target for hair loss in this condition.

Lower levels of certain genes in hair cells improve hair loss treatment outcomes.

Constant-release melatonin reduces SOX21 gene expression in goats during the hair follicle resting phase.

Certain proteins are significantly increased in the skin of people with hidradenitis suppurativa.

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

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.

Increasing SSAT makes skin more prone to cancer.

Annexin A2 isoform 2 helps dermal papillae cells grow, affecting hair growth.

A new mouse mutation causes skin and hair defects due to a gene change.

TRF1 is crucial for creating and maintaining stem cells and marks both pluripotent and adult stem cells.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

MLO proteins help regulate calcium and ROS levels, promoting root hair growth in Arabidopsis.

Long non-coding RNAs help regulate wool fineness in Gansu alpine fine-wool sheep.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Aging in one type of stem cell can cause aging-like changes in various organs.

miR-5110 affects alpaca pigmentation by altering specific gene expressions.

Activating TLR3 improves the healing and immune properties of periodontal ligament stem cells.

Stem cell differentiation involves gradual chromatin changes and dynamic gene activity.

GLABRA2 represses root hair formation by inhibiting a specific gene.

Quiescent cells have increased mitochondrial activity and ECM gene expression, but reduced glycolysis.

Activating the hexosamine pathway can improve skin health and increase hair follicle stem cells.

Researchers created a new mouse model for studying scleroderma.

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

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Several genes, including Hox-7A, Stra6, and Lim-1, are involved in normal palate formation.

LncRNA MTC boosts growth of goat skin cells, improving cashmere quality.