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Sox9 levels in brain stem cells affect whether they stay as stem cells or become neurons.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

A specific gene mutation causes a severe skin disorder in a family.

The study identified diverse cell types and gene expressions in ovarian steroid cell tumors, improving understanding of this rare tumor.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

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

BBS7 is essential for maintaining healthy gums and teeth.

A specific gene mutation causes Olmsted syndrome.

AQB reduces harmful skin changes in systemic sclerosis.

Obstructive sleep apnea can be hereditary and linked to a genetic mutation in the COL1A2 gene.

Certain gene variations may increase the risk of PCOS in South Indian women.

BBS7 is crucial for maintaining healthy gums by regulating important signaling pathways.

A new mouse mutation causes skin and hair defects due to a gene change.

Targeting SOX proteins may improve cancer treatment by restoring immune function.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

OCT4B1 and SOX-2 levels are higher in Crohn's and ulcerative colitis patients, possibly aiding tissue repair.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

Seven genes are highly expressed in both germ-line and hematopoietic stem cells.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

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

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

S100A4 promotes aggressive ovarian cancer and is a potential treatment target.

The enzyme steroid sulfatase is linked to breast cancer and other conditions, and inhibitors are being developed for treatment.

BBS7 is essential for healthy gums by supporting cell function and blood flow.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.