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Overexpression of SSAT in mice causes hair loss, liver damage, and sensitivity to polyamine analogues.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Increasing SSAT makes skin more prone to cancer.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Overexpressing SSAT enzyme reduces prostate tumor growth in mice.

Mutations in the Sgk3 gene cause fuzzy hair in mice.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

CRISPR/Cas9 editing in spinach affects root hair growth by altering specific genes.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Hydrogen sulfide disrupts protein function and root hair growth in plants by modifying proteins.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

The scraggly mutation causes hair loss and skin defects in mice.

TRPV3 gene mutations cause Olmsted syndrome symptoms, but severity varies.

A gene mutation in mice causes skin defects and early death.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

SSO helps in skin protection and keratinization.

The study created a mouse model that survives longer and shows fewer symptoms of pemphigus vulgaris.

Msx2 deficiency in mice leads to bone growth and organ development problems.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

Mutant Cx43 causes slower wound healing and hair growth issues in ODDD.

Overexpressing Dsg3 in mice skin causes excessive cell growth and abnormal skin development.

PRX01, PRX44, and PRX73 are essential for root hair growth in Arabidopsis thaliana.