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Gene knockout mice developed scars similar to human hypertrophic scars, useful for studying scar progression.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

Abnormal gene expression related to keratin causes hair loss in certain mice.

Overexpressing ovine β-catenin in mice skin increases hair follicle density and growth.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

PINK1 is important for controlling gut immune responses linked to early Parkinson's disease.

The error was corrected without affecting the study's results.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

B6.Cg-Tyr c−2J Hr hr /J mice have a stronger delayed sunburn reaction and are good for UV research.

Removing Sprouty genes in mice causes various hormone-related issues but does not increase cancer risk by one year of age.

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

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

Targeting ATM could help manage heart cell enlargement due to pressure overload.

Bim and Puma proteins are found in developing mouse hair follicles and are involved in more than just cell death.

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

Aire mutation reduces alopecia areata, while Notch4 mutation prevents it in mice.

Minoxidil treatment improves heart defects in a DiGeorge syndrome model.

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

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

The SHJH hr mice with a mutated Hr gene show signs of faster skin aging due to poor antioxidative protection.

Tsc2-deficient stem cells can help understand and treat TSC-related tumors.

A mouse model was created to study hair loss similar to humans.

A new genetic mutation was found causing hair and eye issues in a boy.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

The same gene mutation can cause different symptoms in family members.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Mouse keratin 6 genes evolved independently from human ones and are regulated differently.

Mitochondrial Complex I reduces inflammation and increases bone breakdown by affecting certain immune cells.