Results 111 to 120 of about 1,245,456 (166)

A Clinical Genetics-Driven Dual Diagnosis of Prader-Willi Syndrome Due to Mosaic Maternal UPD(15) and <i>NOTCH3</i>-Related CADASIL. [PDF]

open access: yesGenes (Basel)
Bogliardi FM   +10 more
europepmc   +1 more source

A novel missense variant Cys559Gly in <i>NOTCH3</i> in CADASIL family and vascular lesions in patients with migraine. [PDF]

open access: yesPostep Psychiatr Neurol
Jastrzębski K   +4 more
europepmc   +1 more source

Targeting notch signaling pathway in esophageal cancer: from molecular insights to therapies. [PDF]

open access: yesOncol Rev
Bhattacharyya S   +6 more
europepmc   +1 more source

NICD3 mediates pro-angiogenic effects through SMAD3/TGFBI axis in colorectal cancer. [PDF]

open access: yesCell Death Dis
An R   +14 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy