Skin and Sural Nerve Biopsies: Ultrastructural Findings in the First Genetically Confirmed Cases of CADASIL in Serbia

Pathogenesis of CADASIL

(2010) Anne Joutel   BIOESSAYS

Functional Coupling between the Extracellular Matrix and Nuclear Lamina by Wnt Signaling in Progeria

(2010) Lidia Hernandez et al.   DEVELOPMENTAL CELL

Laminopathies and lamin-associated signaling pathways

(2010) Nadir M. Maraldi et al.   JOURNAL OF CELLULAR BIOCHEMISTRY

Puma is required for p53-induced depletion of adult stem cells

(2010) Dongping Liu et al.   NATURE CELL BIOLOGY

Defective Lamin A-Rb Signaling in Hutchinson-Gilford Progeria Syndrome and Reversal by Farnesyltransferase Inhibition

(2010) Jackleen Marji et al.   PLoS One

Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients

(2009) Saara Tikka et al.   BRAIN

Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain

(2009) Marie Monet-Leprêtre et al.   BRAIN

Mutations in NOTCH3 cause the formation and retention of aggregates in the endoplasmic reticulum, leading to impaired cell proliferation

(2009) Keikichi Takahashi et al.   HUMAN MOLECULAR GENETICS

Role of A-type lamins in signaling, transcription, and chromatin organization

(2009) Vicente Andrés et al.   JOURNAL OF CELL BIOLOGY

Nerve conduction studies in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

(2009) Sa-Yoon Kang et al.   JOURNAL OF NEUROLOGY

Behavioural and psychological symptoms in vascular dementia; differences between small- and large-vessel disease

(2009) S. S. Staekenborg et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

CADASIL

(2009) Hugues Chabriat et al.   LANCET NEUROLOGY

Apathy: A major symptom in CADASIL

(2009) S. Reyes et al.   NEUROLOGY

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy with severe factor XII deficiency

(2009) Pavlovic Aleksandra et al.   NEUROLOGY INDIA

Ultrastructural analysis of small blood vessels in skin biopsies in CADASIL

(2008) Vesna Lackovic et al.   Archives of Biological Sciences

Activating NOTCH3 mutation in a patient with small-vessel-disease of the Brain

(2008) Charles Fouillade et al.   HUMAN MUTATION

CADASIL: Extended polymorphisms and mutational analysis of the NOTCH3 gene

(2008) C. Ungaro et al.   JOURNAL OF NEUROSCIENCE RESEARCH

Lamin A-dependent misregulation of adult stem cells associated with accelerated ageing

(2008) Paola Scaffidi et al.   NATURE CELL BIOLOGY

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): Three case reports from Serbia

(2008) Jasna Zidverc-Trajkovic et al.   Srpski Arhiv za Celokupno Lekarstvo