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Showing results (111-120 of 118) with videos related to

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Vox Sanguinis|January 1, 1976
Linkage of gene for C2 deficiency and the major histocompatibility complex MHC in man. Family study of a further caseN K Day, P Rubinstein, D Case, et al.
The Journal of Biological Chemistry|April 5, 2000
Cloning and expression of the histo-blood group Pk UDP-galactose: Ga1beta-4G1cbeta1-cer alpha1, 4-galactosyltransferase. Molecular genetic basis of the p phenotypeR Steffensen, K Carlier, J Wiels, et al.
The Journal of Experimental Medicine|August 1, 1975
Mixed lymphocyte culture determinants and C2 deficiency: LD-7a associated with C2 deficiency in four familiesS M Fu, R Stern, H G Kunkel, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1974
Two separate genes controlling stimulation in mixed lymphocyte reaction in manB Dupont, R A Good, G S Hansen, et al.
British Journal of Haematology|September 30, 1998
Shift from Rh-positive to Rh-negative phenotype caused by a somatic mutation within the RHD gene in a patient with chronic myelocytic leukaemiaB Chérif-Zahar, V Bony, R Steffensen, et al.
Vox Sanguinis|November 16, 2006
A population-based binational register for monitoring long-term outcome and possible disease concordance among blood donors and recipientsG Edgren, H Hjalgrim, T N Tran, et al.
Tissue Antigens|January 1, 1971
The recombination fraction of the HL-A systemA Svejgaard, A Bratlie, P J Hedin, et al.
The New England Journal of Medicine|December 15, 1977
Reconstitution in severe combined immunodeficiency by transplantation of marrow from an unrelated donorR J O'Reilly, B Dupont, S Pahwa, et al.
Pageof 12

Showing results (111-120 of 118) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 118 results.
Vox Sanguinis|January 1, 1976
Linkage of gene for C2 deficiency and the major histocompatibility complex MHC in man. Family study of a further caseN K Day, P Rubinstein, D Case, et al.
The Journal of Biological Chemistry|April 5, 2000
Cloning and expression of the histo-blood group Pk UDP-galactose: Ga1beta-4G1cbeta1-cer alpha1, 4-galactosyltransferase. Molecular genetic basis of the p phenotypeR Steffensen, K Carlier, J Wiels, et al.
The Journal of Experimental Medicine|August 1, 1975
Mixed lymphocyte culture determinants and C2 deficiency: LD-7a associated with C2 deficiency in four familiesS M Fu, R Stern, H G Kunkel, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1974
Two separate genes controlling stimulation in mixed lymphocyte reaction in manB Dupont, R A Good, G S Hansen, et al.
British Journal of Haematology|September 30, 1998
Shift from Rh-positive to Rh-negative phenotype caused by a somatic mutation within the RHD gene in a patient with chronic myelocytic leukaemiaB Chérif-Zahar, V Bony, R Steffensen, et al.
Vox Sanguinis|November 16, 2006
A population-based binational register for monitoring long-term outcome and possible disease concordance among blood donors and recipientsG Edgren, H Hjalgrim, T N Tran, et al.
Tissue Antigens|January 1, 1971
The recombination fraction of the HL-A systemA Svejgaard, A Bratlie, P J Hedin, et al.
The New England Journal of Medicine|December 15, 1977
Reconstitution in severe combined immunodeficiency by transplantation of marrow from an unrelated donorR J O'Reilly, B Dupont, S Pahwa, et al.
Pageof 12