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IL-17 plays a key role in severe hair loss in chronic alopecia areata.

Grasp protein helps maintain skin health after UVB exposure.

Certain immune cells worsen post-surgery gut paralysis by activating a specific immune response.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.

Certain gut bacteria can lower androgen levels in male mice.

Turning off the Lhx2 gene in mouse embryos leads to slower wound healing and scars.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Gut bacteria can lower androgen levels in male mice.

Desmoglein 1 can partly make up for the loss of Desmoglein 3 in hair adhesion but not in mucous membranes.

Transferrin receptor expression increases iron in mouse skin cells without causing damage.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

CXCL7 is essential for muscle repair by aiding early neutrophil infiltration.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Increasing TSPO in the brain reduces anxiety and depression.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

Controlled delivery of specific RNA and IL-4 restored hair growth in mice with autoimmune alopecia.

Krtap11-1 is important for hair strength and structure.

The E2 protein affects gene activity in hair follicles of mice.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

Increasing Treg cells in the skin does not cure hair loss from alopecia areata in mice.

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

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.

Alopecia in VDR knockout mice is due to a defect in hair cycle initiation, not keratinocyte issues.

LHX2 is essential for hair follicle development, controlled by NF-κB and TGFβ2 signaling.

Progranulin overexpression leads to shorter, thinner hair and increased cell death in mouse hair follicles.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.