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Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Two mouse mutations cause similar hair loss despite different skin changes.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Certain bacteria can boost lentil growth and improve soil used for farming.

Polycomb Repressive Complex 2 is not needed for hair regeneration.

Dermal EZH2 controls skin cell development and hair growth in mice.

Notch1 signaling is crucial for improving wound healing and skin regeneration by affecting stem cell behavior.

SOX9 helps determine stem cell roles by interacting with DNA and proteins that control gene activity.

Runx genes are important for stem cell regulation and their roles in aging and disease need more research.

The Itpr3 gene causes a specific hair pattern in mice.

Environmental factors like diet and vitamin levels, especially Vitamin D, can affect autoimmune diseases differently, with lifestyle changes potentially improving outcomes.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

Rapamycin may help treat Leigh syndrome by targeting protein kinase C.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

The research reveals how early embryonic mouse skin develops from simple to complex structures, identifying various cell types and their roles in this process.

Vav2 and Vav3 proteins help control skin stem cell numbers and activity in both healthy and cancerous cells.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

Mechanical forces are crucial for shaping cells and forming tissues during development.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

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

Stem cells help remove dead cells to keep tissues healthy by balancing cell replacement and clearance.