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Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

circRNA-1926 helps goat stem cells turn into hair follicles by affecting miR-148a/b-3p and CDK19.

Neural cell nanovesicles help hair growth by activating key signals.

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

Nociplastic pain is a complex, heritable trait with genetic links to chronic and neuropathic pain.

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

Neural progenitor cell-derived nanovesicles help hair growth by activating a key signaling pathway.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Nestin-expressing blood vessels help skin transplants survive and heal.

The tool iCOUNT helps understand how stem cells divide and affect tissue development and repair.

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

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

The new ddPCR method reliably detects unwanted viruses in CAR-T cell products, ensuring their safety for patients.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

A rare skin growth was successfully removed without recurrence after one year.

Three siblings had both Vohwinkel's disease and congenital alopecia, with no effective treatment.

Epidermal nevi are skin cell clusters linked to various syndromes.

Intralesional chemotherapy with 5-fluorouracil and methotrexate may worsen keratoacanthoma-type skin cancer in transplant patients.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

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

Patients with nevus comedonicus suppurativa should be monitored for diabetes.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

PTCH gene mutations contribute to basal cell carcinoma development.