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R D Koler

Showing results (11-20 of 40) with videos related to

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The Journal of Clinical Investigation|October 1, 1976
Red cell age-related changes of hemoglobins AIa+b and AIc in normal and diabetic subjectsJ F Fitzgibbons, R D Koler, R T Jones
Advances in Experimental Medicine and Biology|January 1, 1972
Hemoglobin Casper G8 106 leu leads to pro: further evidence that hemoglobin mutations are not randomR T Jones, R D Koler, M Duerst, et al.
Annals of Human Genetics|May 1, 1971
Genetics of haemoglobin H and alpha-thalassaemiaR D Koler, R T Jones, P Wasi, et al.
Hemoglobin|January 1, 1976
Hemoglobin Willamette (alpha2beta2 51Pro replaced by Apg (D2)) a new abnormal human hemoglobinR T Jones, R D Koler, M L Duerst, et al.
Hemoglobin|January 1, 1980
Physiologic and genetic alterations in human red cell DPGMR D Koler, M R McClung, L L Peterson, et al.
Biochemistry|November 4, 1975
Isolation and functional characterization of hemoglobin Casper: beta106(G8) Leu replaced by ProH Wajcman, G Gacon, D Labie, et al.
American Journal of Diseases of Children (1960)|July 1, 1980
Juvenile chronic granulocytic leukemia: emphasis on cutaneous manifestations and underlying neurofibromatosisJ A Mays, R C Neerhout, G C Bagby, et al.
The Medical Journal of Australia|June 26, 1971
Haemoglobin Norfolk: another example in SydneyS Gordon, E Powell, R D Koler, et al.
American Journal of Human Genetics|May 1, 1979
Hemolytic anemia due to pyruvate kinase deficiency: characterization of the enzymatic activity from eight patientsJ A Black, M B Rittenberg, R H Bigley, et al.
Cell|July 1, 1975
Synthesis of erythrocyte-specific proteins in cultured friend leukemia cellsD Kabat, C C Sherton, L H Evans, et al.
Pageof 4

Showing results (11-20 of 40) with videos related to

Sort By:
Pageof 4
The Journal of Clinical Investigation|October 1, 1976
Red cell age-related changes of hemoglobins AIa+b and AIc in normal and diabetic subjectsJ F Fitzgibbons, R D Koler, R T Jones
Advances in Experimental Medicine and Biology|January 1, 1972
Hemoglobin Casper G8 106 leu leads to pro: further evidence that hemoglobin mutations are not randomR T Jones, R D Koler, M Duerst, et al.
Annals of Human Genetics|May 1, 1971
Genetics of haemoglobin H and alpha-thalassaemiaR D Koler, R T Jones, P Wasi, et al.
Hemoglobin|January 1, 1976
Hemoglobin Willamette (alpha2beta2 51Pro replaced by Apg (D2)) a new abnormal human hemoglobinR T Jones, R D Koler, M L Duerst, et al.
Hemoglobin|January 1, 1980
Physiologic and genetic alterations in human red cell DPGMR D Koler, M R McClung, L L Peterson, et al.
Biochemistry|November 4, 1975
Isolation and functional characterization of hemoglobin Casper: beta106(G8) Leu replaced by ProH Wajcman, G Gacon, D Labie, et al.
American Journal of Diseases of Children (1960)|July 1, 1980
Juvenile chronic granulocytic leukemia: emphasis on cutaneous manifestations and underlying neurofibromatosisJ A Mays, R C Neerhout, G C Bagby, et al.
The Medical Journal of Australia|June 26, 1971
Haemoglobin Norfolk: another example in SydneyS Gordon, E Powell, R D Koler, et al.
American Journal of Human Genetics|May 1, 1979
Hemolytic anemia due to pyruvate kinase deficiency: characterization of the enzymatic activity from eight patientsJ A Black, M B Rittenberg, R H Bigley, et al.
Cell|July 1, 1975
Synthesis of erythrocyte-specific proteins in cultured friend leukemia cellsD Kabat, C C Sherton, L H Evans, et al.
Pageof 4