Notch signaling pathway: architecture, disease, and therapeutics

B Zhou, W Lin, Y Long, Y Yang, H Zhang… - Signal transduction and …, 2022 - nature.com
The NOTCH gene was identified approximately 110 years ago. Classical studies have
revealed that NOTCH signaling is an evolutionarily conserved pathway. NOTCH receptors …

Cadasil

H Chabriat, A Joutel, M Dichgans… - The Lancet …, 2009 - thelancet.com
Cerebral autosomal dominant arteriopathy with subcortical infarcts and
leucoencephalopathy (CADASIL) is the most common heritable cause of stroke and …

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

A Joutel, C Corpechot, A Ducros, K Vahedi, H Chabriat… - Nature, 1996 - nature.com
STROKE is the third leading cause of death, and vascular dementia the second cause of
dementia after Alzheimer's disease. CADASIL (for cerebral autosomal dominant arteriopathy …

Pathogenesis of leukoaraiosis: a review

L Pantoni, JH Garcia - Stroke, 1997 - Am Heart Assoc
Background Changes in the cerebral hemispheric white matter, detectable with increasing
frequency by modern neuroimaging methods, are associated with aging and conceivably …

[PDF][PDF] Inflammation, apoptosis and autophagy as critical players in vascular dementia.

XX Wang, B Zhang, R **a, QY Jia - European Review for …, 2020 - europeanreview.org
Vascular dementia is the second-most cause of dementia, characterized by cerebral infarcts,
white matter lesions, myelin loss and often amyloid angiopathy. Hence, vascular damage is …

The phenotypic spectrum of CADASIL: clinical findings in 102 cases

M Dichgans, M Mayer, I Uttner, R Brüning… - Annals of …, 1998 - Wiley Online Library
Cerebral autosomal dominant arteriopathy with subcortical infarcts and
leukoencephalopathy (CADASIL) is an increasingly recognized autosomal dominant …

Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients

A Joutel, K Vahedi, C Corpechot, A Troesch… - The Lancet, 1997 - thelancet.com
Background CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts
and leucoencephalopathy) is commonly overlooked or misdiagnosed owing to its recent …

Clinical spectrum of CADASIL: a study of 7 families

H Chabriat, K Vahedi, MG Bousser, MT Iba-Zizen… - The Lancet, 1995 - Elsevier
Cerebral autosomal dominant arteriopathy with subcortical infarcts and
leukoencephalopathy (CADASIL) is an inherited arterial disease of the brain recently …

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12

E Tournier-Lasserve, A Joutel, J Melki… - Nature …, 1993 - nature.com
Cerebral autosomal dominant arteriopathy with subcortical infarcts and
leukoencephalopathy (CADASIL) has been recently reported as a cause of stroke. It is …

The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients

A Joutel, F Andreux, S Gaulis… - The Journal of …, 2000 - Am Soc Clin Investig
Mutations in Notch3 cause CADASIL (cerebral autosomal dominant adult onset
arteriopathy), which leads to stroke and dementia in humans. CADASIL arteriopathy is …