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S-M Pulst

Showing results (71-80 of 106) with videos related to

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Annals of Neurology|November 18, 2000
Parkin is associated with actin filaments in neuronal and nonneural cellsD P Huynh, D R Scoles, T H Ho, et al.
Human Molecular Genetics|June 1, 1994
Mutations of the neurofibromatosis type 2 gene and lack of the gene product in vestibular schwannomasJ Sainz, D P Huynh, K Figueroa, et al.
Human Molecular Genetics|October 1, 1993
Dinucleotide repeat polymorphism at the D22S351 locusJ Sainz, M Rasmussen, A Nechiporuk, et al.
Human Genetics|June 1, 1991
Exclusion of linkage to the pericentromeric region of chromosome 21 in the Canadian pedigree with familial Alzheimer diseaseS M Pulst, P Fain, V Cohn, et al.
Neurology|November 18, 1998
Clinical and genetic analysis of a distinct autosomal dominant spinocerebellar ataxiaR P Grewal, E Tayag, K P Figueroa, et al.
Neurology|November 24, 1999
Familial multisystem degeneration with parkinsonism associated with the 11778 mitochondrial DNA mutationD K Simon, S M Pulst, J P Sutton, et al.
American Journal of Ophthalmology|November 1, 1995
Ocular abnormalities in neurofibromatosis 2N K Ragge, M E Baser, J Klein, et al.
Genetic Analysis : Biomolecular Engineering|October 1, 1995
Construction and utility of a human chromosome 22-specific Fosmid libraryU J Kim, H Shizuya, J Sainz, et al.
Human Molecular Genetics|June 22, 2000
The neurofibromatosis 2 tumor suppressor protein interacts with hepatocyte growth factor-regulated tyrosine kinase substrateD R Scoles, D P Huynh, M S Chen, et al.
Human Molecular Genetics|April 4, 2001
The NF2 interactor, hepatocyte growth factor-regulated tyrosine kinase substrate (HRS), associates with merlin in the "open" conformation and suppresses cell growth and motilityD H Gutmann, C A Haipek, S P Burke, et al.
Pageof 11

Showing results (71-80 of 106) with videos related to

Sort By:
Pageof 11
Annals of Neurology|November 18, 2000
Parkin is associated with actin filaments in neuronal and nonneural cellsD P Huynh, D R Scoles, T H Ho, et al.
Human Molecular Genetics|June 1, 1994
Mutations of the neurofibromatosis type 2 gene and lack of the gene product in vestibular schwannomasJ Sainz, D P Huynh, K Figueroa, et al.
Human Molecular Genetics|October 1, 1993
Dinucleotide repeat polymorphism at the D22S351 locusJ Sainz, M Rasmussen, A Nechiporuk, et al.
Human Genetics|June 1, 1991
Exclusion of linkage to the pericentromeric region of chromosome 21 in the Canadian pedigree with familial Alzheimer diseaseS M Pulst, P Fain, V Cohn, et al.
Neurology|November 18, 1998
Clinical and genetic analysis of a distinct autosomal dominant spinocerebellar ataxiaR P Grewal, E Tayag, K P Figueroa, et al.
Neurology|November 24, 1999
Familial multisystem degeneration with parkinsonism associated with the 11778 mitochondrial DNA mutationD K Simon, S M Pulst, J P Sutton, et al.
American Journal of Ophthalmology|November 1, 1995
Ocular abnormalities in neurofibromatosis 2N K Ragge, M E Baser, J Klein, et al.
Genetic Analysis : Biomolecular Engineering|October 1, 1995
Construction and utility of a human chromosome 22-specific Fosmid libraryU J Kim, H Shizuya, J Sainz, et al.
Human Molecular Genetics|June 22, 2000
The neurofibromatosis 2 tumor suppressor protein interacts with hepatocyte growth factor-regulated tyrosine kinase substrateD R Scoles, D P Huynh, M S Chen, et al.
Human Molecular Genetics|April 4, 2001
The NF2 interactor, hepatocyte growth factor-regulated tyrosine kinase substrate (HRS), associates with merlin in the "open" conformation and suppresses cell growth and motilityD H Gutmann, C A Haipek, S P Burke, et al.
Pageof 11