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Hannu Kalimo

Showing results (71-80 of 83) with videos related to

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Journal of Medical Genetics|June 14, 2012
Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy geneMaria Kousi, Verneri Anttila, Angela Schulz, et al.
Brain Pathology (Zurich, Switzerland)|April 22, 2008
Heparan sulfate accumulation with Abeta deposits in Alzheimer's disease and Tg2576 mice is contributed by glial cellsPaul O'Callaghan, Elina Sandwall, Jin-Ping Li, et al.
Brain Pathology (Zurich, Switzerland)|February 8, 2013
Quantitative vascular pathology and phenotyping familial and sporadic cerebral small vessel diseasesLucinda J L Craggs, Christian Hagel, Gregor Kuhlenbaeumer, et al.
Acta Neuropathologica|January 13, 2010
Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2Anna Vihola, Linda L Bachinski, Mario Sirito, et al.
Acta Neuropathologica Communications|November 21, 2013
The Arctic AβPP mutation leads to Alzheimer's disease pathology with highly variable topographic deposition of differentially truncated AβHannu Kalimo, Maciej Lalowski, Nenad Bogdanovic, et al.
Nature Genetics|November 12, 2005
The gene disrupted in Marinesco-Sjögren syndrome encodes SIL1, an HSPA5 cochaperoneAnna-Kaisa Anttonen, Ibrahim Mahjneh, Riikka H Hämäläinen, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 11, 2011
Hypomorphic Notch 3 alleles link Notch signaling to ischemic cerebral small-vessel diseaseJoseph F Arboleda-Velasquez, Jan Manent, Jeong Hyun Lee, et al.
Journal of Neuro-Oncology|November 18, 2005
Antioxidant enzymes in oligodendroglial brain tumors: association with proliferation, apoptotic activity and survivalSally Järvelä, Järvelä Sally, Helena Bragge, et al.
Journal of Neurochemistry|February 1, 2013
Monoclonal antibodies selective for α-synuclein oligomers/protofibrils recognize brain pathology in Lewy body disorders and α-synuclein transgenic mice with the disease-causing A30P mutationTherese Fagerqvist, Veronica Lindström, Eva Nordström, et al.
Acta Neuropathologica|January 15, 2013
VMA21 deficiency prevents vacuolar ATPase assembly and causes autophagic vacuolar myopathyNivetha Ramachandran, Iulia Munteanu, Peixiang Wang, et al.
Pageof 9

Showing results (71-80 of 83) with videos related to

Sort By:
Pageof 9
Journal of Medical Genetics|June 14, 2012
Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy geneMaria Kousi, Verneri Anttila, Angela Schulz, et al.
Brain Pathology (Zurich, Switzerland)|April 22, 2008
Heparan sulfate accumulation with Abeta deposits in Alzheimer's disease and Tg2576 mice is contributed by glial cellsPaul O'Callaghan, Elina Sandwall, Jin-Ping Li, et al.
Brain Pathology (Zurich, Switzerland)|February 8, 2013
Quantitative vascular pathology and phenotyping familial and sporadic cerebral small vessel diseasesLucinda J L Craggs, Christian Hagel, Gregor Kuhlenbaeumer, et al.
Acta Neuropathologica|January 13, 2010
Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2Anna Vihola, Linda L Bachinski, Mario Sirito, et al.
Acta Neuropathologica Communications|November 21, 2013
The Arctic AβPP mutation leads to Alzheimer's disease pathology with highly variable topographic deposition of differentially truncated AβHannu Kalimo, Maciej Lalowski, Nenad Bogdanovic, et al.
Nature Genetics|November 12, 2005
The gene disrupted in Marinesco-Sjögren syndrome encodes SIL1, an HSPA5 cochaperoneAnna-Kaisa Anttonen, Ibrahim Mahjneh, Riikka H Hämäläinen, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 11, 2011
Hypomorphic Notch 3 alleles link Notch signaling to ischemic cerebral small-vessel diseaseJoseph F Arboleda-Velasquez, Jan Manent, Jeong Hyun Lee, et al.
Journal of Neuro-Oncology|November 18, 2005
Antioxidant enzymes in oligodendroglial brain tumors: association with proliferation, apoptotic activity and survivalSally Järvelä, Järvelä Sally, Helena Bragge, et al.
Journal of Neurochemistry|February 1, 2013
Monoclonal antibodies selective for α-synuclein oligomers/protofibrils recognize brain pathology in Lewy body disorders and α-synuclein transgenic mice with the disease-causing A30P mutationTherese Fagerqvist, Veronica Lindström, Eva Nordström, et al.
Acta Neuropathologica|January 15, 2013
VMA21 deficiency prevents vacuolar ATPase assembly and causes autophagic vacuolar myopathyNivetha Ramachandran, Iulia Munteanu, Peixiang Wang, et al.
Pageof 9