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M Moulds

Showing results (71-80 of 118) with videos related to

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Vox Sanguinis|January 1, 1987
Swa: a subdivisionM Contreras, P Teesdale, M Moulds, et al.
Transfusion|September 12, 2013
New RHCE variant alleles encoding the D- - phenotypeGorka Ochoa-Garay, Joann M Moulds, Jacqueline Cote, et al.
Experimental and Clinical Immunogenetics|March 11, 1999
Reference typing report for complement component C4G Mauff, B Luther, P M Schneider, et al.
Molecular Immunology|March 4, 2000
The C3b/C4b receptor (CR1, CD35) on erythrocytes: methods for study of the polymorphismsJ H Cohen, J P Atkinson, L B Klickstein, et al.
Transfusion|December 7, 2017
Whole-exome sequencing of sickle cell disease patients with hyperhemolysis syndrome suggests a role for rare variation in disease predispositionSavannah Mwesigwa, Joann M Moulds, Alice Chen, et al.
Tissue Antigens|November 1, 1995
HLA-class II alleles and C4 null genes in Greeks with systemic lupus erythematosusJ D Reveille, F C Arnett, M L Olsen, et al.
Genes and Immunity|December 4, 2004
A complement receptor-1 polymorphism with high frequency in malaria endemic regions of Asia but not AfricaB N Thomas, B Donvito, I Cockburn, et al.
Annals of Human Genetics|August 16, 2006
Mitochondrial DNA variation in Mauritania and Mali and their genetic relationship to other Western Africa populationsA M González, V M Cabrera, J M Larruga, et al.
Transfusion|April 16, 2013
Three novel alleles in the Kell blood group system resulting in the Knull phenotype and the first in a Native AmericanJoann M Moulds, Rosemary Persa, Darbi Rierson, et al.
Pediatric Blood & Cancer|June 9, 2015
Paroxysmal cold hemoglobinuria due to an IgA Donath-Landsteiner antibodyNicholas S Whipple, Dawn A B Moreau, JoAnn M Moulds, et al.
Pageof 12

Showing results (71-80 of 118) with videos related to

Sort By:
Pageof 12
Vox Sanguinis|January 1, 1987
Swa: a subdivisionM Contreras, P Teesdale, M Moulds, et al.
Transfusion|September 12, 2013
New RHCE variant alleles encoding the D- - phenotypeGorka Ochoa-Garay, Joann M Moulds, Jacqueline Cote, et al.
Experimental and Clinical Immunogenetics|March 11, 1999
Reference typing report for complement component C4G Mauff, B Luther, P M Schneider, et al.
Molecular Immunology|March 4, 2000
The C3b/C4b receptor (CR1, CD35) on erythrocytes: methods for study of the polymorphismsJ H Cohen, J P Atkinson, L B Klickstein, et al.
Transfusion|December 7, 2017
Whole-exome sequencing of sickle cell disease patients with hyperhemolysis syndrome suggests a role for rare variation in disease predispositionSavannah Mwesigwa, Joann M Moulds, Alice Chen, et al.
Tissue Antigens|November 1, 1995
HLA-class II alleles and C4 null genes in Greeks with systemic lupus erythematosusJ D Reveille, F C Arnett, M L Olsen, et al.
Genes and Immunity|December 4, 2004
A complement receptor-1 polymorphism with high frequency in malaria endemic regions of Asia but not AfricaB N Thomas, B Donvito, I Cockburn, et al.
Annals of Human Genetics|August 16, 2006
Mitochondrial DNA variation in Mauritania and Mali and their genetic relationship to other Western Africa populationsA M González, V M Cabrera, J M Larruga, et al.
Transfusion|April 16, 2013
Three novel alleles in the Kell blood group system resulting in the Knull phenotype and the first in a Native AmericanJoann M Moulds, Rosemary Persa, Darbi Rierson, et al.
Pediatric Blood & Cancer|June 9, 2015
Paroxysmal cold hemoglobinuria due to an IgA Donath-Landsteiner antibodyNicholas S Whipple, Dawn A B Moreau, JoAnn M Moulds, et al.
Pageof 12