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

Food deprivation increases MST enzyme in the brain, possibly affecting energy balance.

Poor maternal nutrition can lead to fewer wool follicles in Chinese Merino sheep.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

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

Mettl3 is essential for normal tissue development and self-renewal by regulating gene expression.

Caloric restriction improves skin and fur structure but can cause muscle loss and movement issues.

Natural feedstuffs help reduce muscular dystrophy in rabbits more than selenium or vitamin E alone.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

MOF controls skin development by regulating genes for mitochondria and cilia.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

DNMT1 helps turn hair follicle stem cells into fat cells by blocking a specific microRNA.

MFN2 mutations cause mitochondrial problems, leading to more upper body fat and lower leptin levels.

TMPRSS6 is crucial for controlling hepcidin and normal iron absorption.

Bezafibrate treatment improved skin and spleen health in aging mice but didn't extend lifespan.

MK-0773 is a moderate inhibitor of the SRD5A2 enzyme.

Proper diet management is crucial for phenylketonuria patients to avoid severe health issues.

DNA methylation likely doesn't cause different lambskin patterns in Hu sheep.

Defective protein folding due to a mutation is key in ANE syndrome.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Lethal-milk mice produce zinc-deficient milk, causing health issues in pups unless supplemented with zinc.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

Targeting METTL1 may help slow papillary thyroid cancer growth and spread.

LncRNA MSTRG.14227.1 hinders hair follicle development in cashmere goats, affecting cashmere quality.

Low selenium levels can extend lifespan but worsen health issues.

Mycophenolate mofetil is a good alternative for autoimmune hepatitis patients who can't tolerate azathioprine.