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Rapamycin treatment helps reduce brain inflammation and symptoms of mitochondrial disease by blocking specific pathways in mice.

PRC2 is not essential for hair follicle stem cell maintenance or hair growth.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Lrig1 marks a unique group of stem cells in mouse skin that can become different skin cell types.

Neurotrophin-4 increases calcium current in specific mouse neurons through the PI3K pathway.

Type 1/17 inflammation in psoriasis increases skin cell growth due to a molecule that could be a new treatment target.

White lupin uses specific genes to grow root hairs and access phosphorus when it's scarce.

PH-762 shows promise in treating skin cancer by effectively targeting and silencing PD-1 in tumors with minimal side effects.

Ishophloroglucin A from Ishige okamurae may be a natural alternative for treating hair loss by inhibiting 5α-reductase and promoting hair growth.

Sheep breeds show different keratin gene expression in the groin, linked to hair follicle density.

miR-3606-3p reduces skin fibrosis by blocking key signaling pathways.

Peps help Arabidopsis plants grow more root hairs by affecting specific genes and calcium signaling.

Sphingosine 1-phosphate affects inflammation and gene expression in different aorta cells.

Dicer is crucial for hair growth in mice.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

RNase L suppresses regeneration in mammals.

K15 and Id3 are important in hair follicle regeneration, with K15 increasing in early stages and Id3 responding later.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

A potential treatment for atopic dermatitis could be to increase PADI1 expression to improve skin barrier function.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

IL-18 signaling helps mature Tregs move into the thymus.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

GRHL3 is important for controlling gene activity in skin cells during different stages of their development.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

EGFR helps control how hair grows and forms without needing p53 protein.