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Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

An 8-year-old boy's early puberty was caused by a rare hormone-secreting brain tumor, which was successfully treated with surgery.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

A man with itchy skin lesions and weight loss was diagnosed with a rare skin condition linked to a pancreatic tumor.

Myotonic Dystrophy may age cells faster, and drugs that target aging could be potential treatments.

Long-standing benign tumors can become cancerous, especially in people with weakened immune systems.

A man's rare adrenal tumor caused feminization and white hair, was removed surgically, and improved after treatment.

A 29-year-old man had a jaw plaque diagnosed as follicular mucinosis, linked to nestin-positive hair follicle stem cells.

A 9-year-old girl developed type 1 diabetes and alopecia after being treated for a rare kidney disease.

A 19-month-old boy with a rare hair disorder showed mild improvement with treatment, but his family chose gentle hair care due to limited success.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive stomach cancer.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

Finasteride may help treat childhood brain tumors by activating certain genes.

A rare pancreatic tumor caused a woman's male-like features, treated successfully with surgery and medication.

A cat with a rare pancreatic tumor and diabetes died despite treatment, showing similar symptoms to a human condition.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

The man had pretibial myxedema and hyperthyroidism, causing skin changes and thyroid issues.

A boy's early puberty caused by a testicular tumor returned to normal after surgery.

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

Introducing the OTC gene improved symptoms in mice with OTC deficiency.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

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

ErbB2 signaling is crucial for skin cell growth and cancer development in mice.

Rothmund-Thomson syndrome type 2 can cause chronic, poorly healing wounds.

A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.