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C M Cohen

Showing results (51-60 of 63) with videos related to

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The Journal of Cell Biology|October 1, 1977
Membrane isolation on polylysine-coated beads. Plasma membrane from HeLa cellsC M Cohen, D I Kalish, B S Jacobson, et al.
Progress in Clinical and Biological Research|January 1, 1984
Functional associations of band 4.1 in the erythrocyte membrane skeleton and their role in inherited membrane skeletal abnormalitiesC M Cohen, R C Langley, S F Foley, et al.
Blood|August 15, 1996
Specific loss of protein kinase activities in senescent erythrocytesH K Jindal, Z Ai, P Gascard, et al.
Biochemistry|January 27, 1976
Introduction of purified hexosaminidase A into Tay-Sachs leukocytes by means of immunoglobulin-coated liposomesC M Cohen, G Weissmann, S Hoffstein, et al.
Genomics|June 15, 1997
The gene encoding protein 4.2 is distinct from the mouse platelet storage pool deficiency mutation pallidB Gwynn, C Korsgren, C M Cohen, et al.
Blood|July 15, 1992
Band 3 Tuscaloosa: Pro327----Arg327 substitution in the cytoplasmic domain of erythrocyte band 3 protein associated with spherocytic hemolytic anemia and partial deficiency of protein 4.2P Jarolim, J Palek, H L Rubin, et al.
Journal of Neurosurgery. Spine|November 6, 2012
Spinal manifestations of spontaneous intracranial hypotensionWouter I Schievink, Ray M Chu, M Marcel Maya, et al.
Biochemistry|March 5, 1996
Human erythrocyte dematin and protein 4.2 (pallidin) are ATP binding proteinsA C Azim, S M Marfatia, C Korsgren, et al.
Nature Genetics|September 1, 1992
The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) geneR A White, L L Peters, L R Adkison, et al.
Brain Research|September 5, 1994
Evidence for the association of protein 4.1 immunoreactive forms with neurofibrillary tangles in Alzheimer's disease brainsR K Sihag, L W Wang, A M Cataldo, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
The Journal of Cell Biology|October 1, 1977
Membrane isolation on polylysine-coated beads. Plasma membrane from HeLa cellsC M Cohen, D I Kalish, B S Jacobson, et al.
Progress in Clinical and Biological Research|January 1, 1984
Functional associations of band 4.1 in the erythrocyte membrane skeleton and their role in inherited membrane skeletal abnormalitiesC M Cohen, R C Langley, S F Foley, et al.
Blood|August 15, 1996
Specific loss of protein kinase activities in senescent erythrocytesH K Jindal, Z Ai, P Gascard, et al.
Biochemistry|January 27, 1976
Introduction of purified hexosaminidase A into Tay-Sachs leukocytes by means of immunoglobulin-coated liposomesC M Cohen, G Weissmann, S Hoffstein, et al.
Genomics|June 15, 1997
The gene encoding protein 4.2 is distinct from the mouse platelet storage pool deficiency mutation pallidB Gwynn, C Korsgren, C M Cohen, et al.
Blood|July 15, 1992
Band 3 Tuscaloosa: Pro327----Arg327 substitution in the cytoplasmic domain of erythrocyte band 3 protein associated with spherocytic hemolytic anemia and partial deficiency of protein 4.2P Jarolim, J Palek, H L Rubin, et al.
Journal of Neurosurgery. Spine|November 6, 2012
Spinal manifestations of spontaneous intracranial hypotensionWouter I Schievink, Ray M Chu, M Marcel Maya, et al.
Biochemistry|March 5, 1996
Human erythrocyte dematin and protein 4.2 (pallidin) are ATP binding proteinsA C Azim, S M Marfatia, C Korsgren, et al.
Nature Genetics|September 1, 1992
The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) geneR A White, L L Peters, L R Adkison, et al.
Brain Research|September 5, 1994
Evidence for the association of protein 4.1 immunoreactive forms with neurofibrillary tangles in Alzheimer's disease brainsR K Sihag, L W Wang, A M Cataldo, et al.
Pageof 7