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The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

The study found that Tourette Syndrome may be linked to certain immune system processes and synaptic signaling.

Key genes and pathways involved in thyroid eye disease were identified, aiding potential treatment and diagnosis.

Cannabidivarin (CBDV) helps new brain cells grow and develop in a specific brain area through a certain receptor.

A boy with early puberty and laughing seizures was treated, stopping seizures and slowing puberty.

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

An 8-year-old boy with neurofibromatosis type one also has rare hair and eye disorders.

A new microneedle patch helps repair spinal cord injuries by reducing scarring and promoting nerve growth.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Early surgical intervention and a multidisciplinary approach are crucial for managing complex cardio-obstetric patients.

Scube3 gene affects mouse embryo growth in multiple areas, but needs more research.

Extracellular vesicles may help prevent and repair spine disc degeneration.

Gene therapy, especially using atoh1, shows promise for creating functional sensory hair cells in the inner ear, but dosing and side effects need to be managed for clinical application.

A transwoman developed a brain tumor after nine years of hormone therapy, suggesting a possible link between the treatment and tumor development.

Hair follicles can be used to easily create neurons and glial cells for potential nerve repair.

Amyand's hernia treatment is complex and depends on literature and surgeon's experience.

Trichofolliculoma was found in a person with amniotic band syndrome for the first time.

A 7-year-old girl had unusually long eyelashes with no known cause or related health issues.

Melanocytes from human fetal hair follicles were successfully cultured, showing potential for hair disease research and clinical use.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Early detection and treatment of Menkes disease with copper injections are crucial for better outcomes.

The study found that tight junctions reach the top layer of the skin's stratum granulosum, not just the second top layer as previously thought.

Certain astrocytes can protect the brain and improve recovery after a stroke, and a hair loss drug might reduce cancer spread.

Early diagnosis and teamwork are crucial for managing ILVASC effectively.

Zebrafish skin regeneration relies on cell behaviors and reactive oxygen species, with antioxidants reducing and hydrogen peroxide increasing regeneration.

AMN can cause bladder problems due to nerve damage.

Titanflow improves male urinary health by strengthening the detrusor muscle and enhancing urine flow.

DEC cells show promise as a safe and effective treatment for Duchenne muscular dystrophy.

Reducing neurosteroid levels worsens brain injury in fetal sheep.

Dupilumab effectively controls symptoms in infants with Netherton syndrome.