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

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

The E2 protein affects gene activity in hair follicles of mice.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

Researchers found a non-functional sheep keratin gene due to mutations.

Mice hair follicles take in the amino acid cystine.

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

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

The improved genome of the African spiny mouse helps study its tissue regeneration.

Spiny mice have resilient, large mitochondria that help them regenerate tissue.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

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

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

A compound named ZCZ90 can increase muscle spindle firing, potentially helping treat muscle spasms and hypertension.

A gene mutation in mice causes severe skin disorder similar to a human condition.

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

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

Sheep cells were successfully modified to include a spider silk protein gene.

RpoS helps Borrelia burgdorferi survive in hosts and adapt to different environments.

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

SR-ECDi helps better understand and map the chiroptical properties of solid chiral materials.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

Spiny keratoderma may be ectopic hair formation on palms and soles.

Researchers developed a new type of memory using antiferromagnets that is stable, not disrupted by magnets, and works at room temperature.

The TRPV3 channel structure changes linked to severe itch and hyperkeratosis were identified using cryo-EM.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.