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

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

StemMACS media is better for growing therapeutic stem cells.

Finasteride reduces prostate size and DHT in male mastomys but not in females.

Adding fetal calf serum to the medium kept Merkel cells alive and changed their shape.

Monilethrix causes brittle hair and hair loss, and it runs in families.

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

Spiny mice regenerate skin better than laboratory mice due to larger hair bulges, more stem cells, and different collagen ratios.

Mice with a specific BRCA1 mutation have a higher risk of tumors, especially in the uterus and ovaries.

Diagnosing and managing monilethrix is harder when it occurs with other hair loss conditions.

Diagnosing and managing monilethrix is harder when it occurs with other hair loss conditions.

Hyperaesthetic leucotrichia in horses causes painful, recurring skin lesions and hair color changes, especially in Arabian and American paint horses.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Milia, SM, and EVHC may be related conditions, not separate ones.

Diagnosing and treating monilethrix is challenging when it occurs with other hair disorders.

Chemotherapy can cause hair changes similar to alopecia areata, which might lead to misdiagnosis.

Certain skin proteins can form anchoring structures without the protein AMACO.

Hairless mice have longer hair follicles and abnormal structures during the catagen phase.

DcR3 helps heal wounds and regrow hair by changing macrophages to a repair-focused type.

New mutations in the DSG4 gene cause a rare hair condition.

Microarray analysis helps find hidden chromosomal changes in patients with intellectual disabilities and birth defects.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The document concludes that MGRN1 affects mouse fur color by interfering with a receptor's signaling, but its full role in the body is still unknown.

The conclusion is that a new method combining magnetic tweezers and traction force microscopy may help understand skin cell interactions and diseases.

Male hormones and reduced plakoglobin can impair heart electrical function and increase arrhythmia risk in males.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.