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Publications by David N. Louis
Loss of P53 Sensitizes Mice With a Mutation in Ccm1 (KRIT1) to Development of Cerebral Vascular Malformations
American Journal of Pathology
Forensic Medicine
Pathology
Cancer and the Nervous System
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Novel KRIT1/CCM1 Heterozygous Nonsense Mutation (C.715 C>T) Associated With Cerebral and Cerebellar Cavernous Malformations in a Paediatric Patient
BMJ Case Reports
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Novel KRIT1/CCM1 and MGC4607/CCM2 Gene Variants in Chinese Families With Cerebral Cavernous Malformations
Frontiers in Neurology
Neurology
Rap1 and Its Effector KRIT1/CCM1 Regulate -Catenin Signaling
DMM Disease Models and Mechanisms
Immunology
Molecular Biology
Biochemistry
Microbiology
Neuroscience
Medicine
Genetics
Cerebral Cavernous Malformations Proteins Inhibit Rho Kinase to Stabilize Vascular Integrity
Journal of Experimental Medicine
Medicine
Allergy
Immunology
A Human De Novo Mutation inMYH10phenocopies the Loss of Function Mutation in Mice
Rare Diseases
Multiple Cerebral Vascular Malformations and Spontaneous Regression —Case Report—
Neurologia Medico-Chirurgica
Surgery
Neurology
Structural Basis for the Disruption of the Cerebral Cavernous Malformations 2 (CCM2) Interaction With Krev Interaction Trapped 1 (KRIT1) by Disease-Associated Mutations
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Vascular Malformations Part 1 - Normal and Abnormal Vascular Development
South African Journal of Radiology
Radiological
Radiology
Nuclear Medicine
Ultrasound Technology
Imaging
A Loss-Of-Function Mutation in IL-17F Enhances Susceptibility of Mice to Oropharyngeal Candidiasis
