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J A Irving

Showing results (21-30 of 30) with videos related to

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Leukemia|May 21, 1998
Collection of Philadelphia-negative peripheral blood progenitor cells in unselected patients with chronic granulocytic leukaemia. Northern Regional Haematology GroupA Lennard, N Storey, A M Dickinson, et al.
Leukemia|June 9, 1999
Analysis of CD34 populations in mobilised peripheral blood stem cell harvests and in bone marrow by fluorescent in situ hybridisation for the bcr/abl gene fusion in patients with chronic granulocytic leukaemiaJ A Irving, A Lennard, N Storey, et al.
Genomics|January 25, 2000
Human ovalbumin serpin evolution: phylogenic analysis, gene organization, and identification of new PI8-related genes suggest that two interchromosomal and several intrachromosomal duplications generated the gene clusters at 18q21-q23 and 6p25F L Scott, H J Eyre, M Lioumi, et al.
DNA and Cell Biology|April 21, 2001
Sequence, organization, chromosomal localization, and alternative splicing of the human serine protease inhibitor gene hurpin (PI13) which is upregulated in psoriasisH F Abts, T Welss, S Scheuring, et al.
Cellular and Molecular Life Sciences : CMLS|February 11, 2004
Human clade B serpins (ov-serpins) belong to a cohort of evolutionarily dispersed intracellular proteinase inhibitor clades that protect cells from promiscuous proteolysisG A Silverman, J C Whisstock, D J Askew, et al.
Medical and Pediatric Oncology|February 5, 2000
Population-based study of the pattern of molecular markers of minimal residual disease in childhood and adult acute lymphoblastic leukemia: an assessment of the practical difficulty of representative sampling for trial purposes. Northern Region Haematology GroupP G Middleton, J Norden, D Levett, et al.
Biochemistry|June 14, 2000
Simple modifications of the serpin reactive site loop convert SCCA2 into a cysteine proteinase inhibitor: a critical role for the P3' proline in facilitating RSL cleavageC Luke, C Schick, C Tsu, et al.
Bone Marrow Transplantation|May 17, 2016
Xenograft-directed personalized therapy for a patient with post-transplant relapse of ALLT N Trahair, R B Lock, R Sutton, et al.
The Journal of Biological Chemistry|July 4, 2001
The serpins are an expanding superfamily of structurally similar but functionally diverse proteins. Evolution, mechanism of inhibition, novel functions, and a revised nomenclatureG A Silverman, P I Bird, R W Carrell, et al.
Leukemia|October 4, 2016
A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1J Vijayakrishnan, R Kumar, M Y R Henrion, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Leukemia|May 21, 1998
Collection of Philadelphia-negative peripheral blood progenitor cells in unselected patients with chronic granulocytic leukaemia. Northern Regional Haematology GroupA Lennard, N Storey, A M Dickinson, et al.
Leukemia|June 9, 1999
Analysis of CD34 populations in mobilised peripheral blood stem cell harvests and in bone marrow by fluorescent in situ hybridisation for the bcr/abl gene fusion in patients with chronic granulocytic leukaemiaJ A Irving, A Lennard, N Storey, et al.
Genomics|January 25, 2000
Human ovalbumin serpin evolution: phylogenic analysis, gene organization, and identification of new PI8-related genes suggest that two interchromosomal and several intrachromosomal duplications generated the gene clusters at 18q21-q23 and 6p25F L Scott, H J Eyre, M Lioumi, et al.
DNA and Cell Biology|April 21, 2001
Sequence, organization, chromosomal localization, and alternative splicing of the human serine protease inhibitor gene hurpin (PI13) which is upregulated in psoriasisH F Abts, T Welss, S Scheuring, et al.
Cellular and Molecular Life Sciences : CMLS|February 11, 2004
Human clade B serpins (ov-serpins) belong to a cohort of evolutionarily dispersed intracellular proteinase inhibitor clades that protect cells from promiscuous proteolysisG A Silverman, J C Whisstock, D J Askew, et al.
Medical and Pediatric Oncology|February 5, 2000
Population-based study of the pattern of molecular markers of minimal residual disease in childhood and adult acute lymphoblastic leukemia: an assessment of the practical difficulty of representative sampling for trial purposes. Northern Region Haematology GroupP G Middleton, J Norden, D Levett, et al.
Biochemistry|June 14, 2000
Simple modifications of the serpin reactive site loop convert SCCA2 into a cysteine proteinase inhibitor: a critical role for the P3' proline in facilitating RSL cleavageC Luke, C Schick, C Tsu, et al.
Bone Marrow Transplantation|May 17, 2016
Xenograft-directed personalized therapy for a patient with post-transplant relapse of ALLT N Trahair, R B Lock, R Sutton, et al.
The Journal of Biological Chemistry|July 4, 2001
The serpins are an expanding superfamily of structurally similar but functionally diverse proteins. Evolution, mechanism of inhibition, novel functions, and a revised nomenclatureG A Silverman, P I Bird, R W Carrell, et al.
Leukemia|October 4, 2016
A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1J Vijayakrishnan, R Kumar, M Y R Henrion, et al.
Pageof 3