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P R Harrison

Showing results (71-80 of 79) with videos related to

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Journal of Medical Genetics|May 1, 1996
Acute intermittent porphyria caused by defective splicing of porphobilinogen deaminase RNA: a synonymous codon mutation at -22 bp from the 5' splice site causes skipping of exon 3D H Llewellyn, G A Scobie, A J Urquhart, et al.
Human Genetics|October 1, 1990
Acute intermittent porphyria caused by a C----T mutation that produces a stop codon in the porphobilinogen deaminase geneG A Scobie, D H Llewellyn, A J Urquhart, et al.
Biomedica Biochimica Acta|January 1, 1990
Regulation of erythroid-specific gene expressionP R Harrison, M Plumb, J Frampton, et al.
Journal of Cell Science. Supplement|January 1, 1988
cis and trans control of erythroid cell-specific gene expression during erythropoiesisP R Harrison, M Plumb, J Frampton, et al.
Leukemia|April 1, 1997
Molecular mechanisms involved in long-term maintenance of erythroleukaemia cells by stromal cellsP R Harrison, R J Nibbs, C Bartholomew, et al.
Gene|June 30, 1989
The complete sequence of the rabbit erythroid cell-specific 15-lipoxygenase mRNA: comparison of the predicted amino acid sequence of the erythrocyte lipoxygenase with other lipoxygenasesJ Fleming, B J Thiele, J Chester, et al.
Advances in Experimental Medicine and Biology|January 1, 1982
Analysis of red blood cell differentiationP R Harrison, N Affara, P S Goldfarb, et al.
Lancet (London, England)|September 26, 1987
DNA polymorphism of human porphobilinogen deaminase gene in acute intermittent porphyriaD H Llewellyn, G H Elder, N A Kalsheker, et al.
Leukemia|October 27, 1997
The role of soluble growth factors in inducing transient growth and clonal extinction of stroma cell dependent erythroblastic leukemia cellsK Itoh, J Friel, C Laker, et al.
Pageof 8

Showing results (71-80 of 79) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 79 results.
Journal of Medical Genetics|May 1, 1996
Acute intermittent porphyria caused by defective splicing of porphobilinogen deaminase RNA: a synonymous codon mutation at -22 bp from the 5' splice site causes skipping of exon 3D H Llewellyn, G A Scobie, A J Urquhart, et al.
Human Genetics|October 1, 1990
Acute intermittent porphyria caused by a C----T mutation that produces a stop codon in the porphobilinogen deaminase geneG A Scobie, D H Llewellyn, A J Urquhart, et al.
Biomedica Biochimica Acta|January 1, 1990
Regulation of erythroid-specific gene expressionP R Harrison, M Plumb, J Frampton, et al.
Journal of Cell Science. Supplement|January 1, 1988
cis and trans control of erythroid cell-specific gene expression during erythropoiesisP R Harrison, M Plumb, J Frampton, et al.
Leukemia|April 1, 1997
Molecular mechanisms involved in long-term maintenance of erythroleukaemia cells by stromal cellsP R Harrison, R J Nibbs, C Bartholomew, et al.
Gene|June 30, 1989
The complete sequence of the rabbit erythroid cell-specific 15-lipoxygenase mRNA: comparison of the predicted amino acid sequence of the erythrocyte lipoxygenase with other lipoxygenasesJ Fleming, B J Thiele, J Chester, et al.
Advances in Experimental Medicine and Biology|January 1, 1982
Analysis of red blood cell differentiationP R Harrison, N Affara, P S Goldfarb, et al.
Lancet (London, England)|September 26, 1987
DNA polymorphism of human porphobilinogen deaminase gene in acute intermittent porphyriaD H Llewellyn, G H Elder, N A Kalsheker, et al.
Leukemia|October 27, 1997
The role of soluble growth factors in inducing transient growth and clonal extinction of stroma cell dependent erythroblastic leukemia cellsK Itoh, J Friel, C Laker, et al.
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