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notch3 protein, human
(compound)
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Genetic Markers
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Curated Studies
Most Correlated Studies
T-cell acute lymphoblastic leukemia TALL-1 cells treated with compound E or anti-NOTCH3 antibody
NOTCH3 knockdown in non-transformed esophageal cells
Multipotent mesenchymal stromal cells: TGFβ3/BMP2 induced chondrogenesis
Ovarian cancer OVCAR8 cells treated with recombinant protein relaxin-2 (RLN2)
Prostate carcinoma PC-3 cells expressing ESR2 variants
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Literature
Most Relevant Literature
Influence of different spectra of NOTCH3 variants on the clinical phenotype of CADASIL - experience …
NOTCH3 C201R variant causes cerebral autosomal dominant arteriopathy with subcortical infarcts and l…
NOTCH3 mutations in a cohort of Portuguese patients within CADASIL spectrum phenotype.
Notch3: A New Culprit in Fibrotic Lung Disease.
Prominent juxtacortical white matter lesion hallmarks NOTCH3-related intracerebral haemorrhage.
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There were no clinical trials for notch3 protein, human
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