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Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

Thyrotropin-Releasing Hormone helps heal wounds in frog and human skin.

The 14-3-3σ gene is essential for preventing hair loss.

Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Alopecia areata patients have higher levels of certain immune receptors, suggesting new treatment possibilities.

A rabbit gene important for hair development was identified and detailed.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

Changing YBX1 protein activity affects skin stem cell function and aging.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

Inhibiting the PI3K/Akt pathway may help prevent radiation-induced liver injury.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

The vitamin D receptor can regulate genes and affect hair and hormone levels without its usual activator.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

Exosomal miR-222-3p reduces melanin production in rabbits by targeting the SOX10 gene.

A specific gene mutation causes a severe skin disorder in a family.

Sox9 levels in brain stem cells affect whether they stay as stem cells or become neurons.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

The new aptamer TAGX-0003 shows promise as an effective treatment for hair loss disorder alopecia areata.

ASH2L is essential for skin and hair development.

The Celsr1 gene is crucial for normal hair patterning in mice.

A missing mK6irs1 gene causes hair loss in mice.

AMPK activation may reduce melanoma risk in red-haired individuals.

Skin cell types develop when specific genes are turned on by removing certain chemical tags from DNA.

Removing part of the vitamin D receptor stops vitamin D from working properly.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Fixing DNA errors is crucial to prevent skin cancer.

MPZL3 protein helps keep sebaceous gland size and cell growth in check.