Search

everythinglearnresearchcommunity

for

Search:↓

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

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.

Early diagnosis and teamwork are crucial for managing ILVASC effectively.

The vitamin D receptor can work without its usual activating molecule.

Avicennia marina leaf extract can fight Vancomycin-resistant bacteria.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

Severe CCCA may be biologically and clinically different from milder forms.

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

Adalimumab helped control a child's severe eye disease when other treatments failed.

Vitamin D receptor is essential for healthy bones and skin.

Astressin-B can reverse and prevent hair loss in stressed mice.

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

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Oxytocin receptor changes in hair cells may help identify autism, especially in males.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

New probes were created to effectively measure specific enzymes involved in fat metabolism, which could help develop new drugs.

CCC1 is essential for pH balance and normal cell function in plants.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

TRPV channels are important in osteoarthritis and could be key to new treatments.

A compound named ZCZ90 can increase muscle spindle firing, potentially helping treat muscle spasms and hypertension.

A boy with severe Vitamin D-resistant rickets did not respond to treatment and lacked a common symptom, suggesting a need for alternative treatments.

Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.