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

The F2 hair tonic with shallot extract is effective and stable for hair growth.

Vaccines and targeting TrxR variants can help prevent cancer and reduce metastasis.

Gorab deficiency speeds up skin aging by disrupting protein regulation and reducing collagen.

Overexpression of PTHrP in chondrocytes causes short-limbed dwarfism and delayed bone formation in mice.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

BRG1 is essential for skin cells to move and heal wounds properly.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

CRAC channels are crucial for the development and function of specialized immune cells, preventing severe inflammation and autoimmune diseases.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

The DiLiCre mouse model is an effective tool for precise genome editing using light.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

LPA 4 helps control blood and lymph vessel development in zebrafish.

Mice with enhanced regeneration abilities may help develop new regenerative medicine therapies.

ERK activation spreads between cells in mouse skin, linked to cell division and influenced by TPA and EGF receptors.

Par3 protein is essential for skin cell balance and stability.

Retinoic acid-binding proteins in skin are regulated by β-catenin and Notch signalling.

RHUPUS should be considered in children with deforming arthritis.

The most common sign of aging at the gene level is more Ectodysplasin A2 Receptor (EDA2R) being made.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

The study suggests that changes in immune system receptors and their interaction with a cell component may be important in the development of a type of hair loss condition.

PROTACs offer new ways to treat hard-to-target diseases, with promising drugs for cancer in advanced trials.

Axolotls regenerate their spinal cord through a signal that recruits cells, influenced by cell sensitivity and signal spread.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

HVDRR is caused by VDR gene mutations, leading to vitamin D resistance, treatable with high calcium doses, but alopecia remains permanent.

Efficient delivery systems are needed for the clinical use of CRISPR-Cas9 gene editing.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

A protein in plants needs to bind two lipids to help with root hair growth, and this process is similar across different plant species.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.