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 …
revealed that NOTCH signaling is an evolutionarily conserved pathway. NOTCH receptors …
Cadasil
Cerebral autosomal dominant arteriopathy with subcortical infarcts and
leucoencephalopathy (CADASIL) is the most common heritable cause of stroke 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
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 …
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 …
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 …
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 …
leukoencephalopathy (CADASIL) is an increasingly recognized autosomal dominant …
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients
Background CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts
and leucoencephalopathy) is commonly overlooked or misdiagnosed owing to its recent …
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 …
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 …
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 …
arteriopathy), which leads to stroke and dementia in humans. CADASIL arteriopathy is …