[HTML][HTML] Notch3 signaling and aggregation as targets for the treatment of CADASIL and other NOTCH3-associated small-vessel diseases

D Schoemaker, JF Arboleda-Velasquez - The American Journal of …, 2021 - Elsevier
Mutations in the NOTCH3 gene can lead to small-vessel disease in humans, including the
well-characterized cerebral autosomal dominant arteriopathy with subcortical infarcts and …

Notch3 Signaling and Aggregation as Targets for the Treatment of CADASIL and Other NOTCH3-Associated Small-Vessel Diseases

D Schoemaker… - The American journal …, 2021 - pubmed.ncbi.nlm.nih.gov
Mutations in the NOTCH3 gene can lead to small-vessel disease in humans, including the
well-characterized cerebral autosomal dominant arteriopathy with subcortical infarcts and …

[HTML][HTML] Notch3 Signaling and Aggregation as Targets for the Treatment of CADASIL and Other NOTCH3-Associated Small-Vessel Diseases

D Schoemaker… - The American Journal of …, 2021 - ncbi.nlm.nih.gov
Mutations in the NOTCH3 gene can lead to small-vessel disease in humans, including the
well-characterized cerebral autosomal dominant arteriopathy with subcortical infarcts and …

Notch3 Signaling and Aggregation as Targets for the Treatment of CADASIL and Other NOTCH3-Associated Small-Vessel Diseases

D Schoemaker, JF Arboleda-Velasquez - The American Journal of Pathology, 2021 - ASIP
Mutations in the NOTCH3 gene can lead to small-vessel disease in humans, including the
well-characterized cerebral autosomal dominant arteriopathy with subcortical infarcts and …

Notch3 Signaling and Aggregation as Targets for the Treatment of CADASIL and Other NOTCH3-Associated Small-Vessel Diseases.

D Schoemaker… - The American Journal of …, 2021 - europepmc.org
Mutations in the NOTCH3 gene can lead to small-vessel disease in humans, including the
well-characterized cerebral autosomal dominant arteriopathy with subcortical infarcts and …

[引用][C] Notch3 Signaling and Aggregation as Targets for the Treatment of CADASIL and Other NOTCH3-Associated Small-Vessel Diseases

D Schoemaker… - The American Journal of …, 2021 - europepmc.org
Mutations in theNOTCH3 gene can lead to small-vessel disease in humans, including the
well-characterized cerebral autosomal dominant arteriopathy with subcortical infarcts and …