Search research articles
Contact Us
Filters
Showing results (51-60 of 63) with videos related to
Page
of 7
Sort By:
The Journal of Cell Biology
|
October 1, 1977
Membrane isolation on polylysine-coated beads. Plasma membrane from HeLa cells
C 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 abnormalities
C M Cohen, R C Langley, S F Foley, et al.
Blood
|
August 15, 1996
Specific loss of protein kinase activities in senescent erythrocytes
H 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 liposomes
C 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 pallid
B 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 4.2
P Jarolim, J Palek, H L Rubin, et al.
Journal of Neurosurgery. Spine
|
November 6, 2012
Spinal manifestations of spontaneous intracranial hypotension
Wouter 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 proteins
A 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) gene
R 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 brains
R K Sihag, L W Wang, A M Cataldo, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 63) with videos related to
Sort By:
Page
of 7
The Journal of Cell Biology
|
October 1, 1977
Membrane isolation on polylysine-coated beads. Plasma membrane from HeLa cells
C 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 abnormalities
C M Cohen, R C Langley, S F Foley, et al.
Blood
|
August 15, 1996
Specific loss of protein kinase activities in senescent erythrocytes
H 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 liposomes
C 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 pallid
B 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 4.2
P Jarolim, J Palek, H L Rubin, et al.
Journal of Neurosurgery. Spine
|
November 6, 2012
Spinal manifestations of spontaneous intracranial hypotension
Wouter 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 proteins
A 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) gene
R 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 brains
R K Sihag, L W Wang, A M Cataldo, et al.
Page
of 7