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C G Mullighan

Showing results (11-20 of 31) with videos related to

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Gut|June 9, 1998
A rapid method of haplotyping HFE mutations and linkage disequilibrium in a Caucasoid populationC G Mullighan, M Bunce, G C Fanning, et al.
Clinical and Experimental Immunology|July 27, 2001
Assessment of male CVID patients for mutations in the Btk gene: how many have been misdiagnosed?S A Weston, M L Prasad, C G Mullighan, et al.
Tissue Antigens|March 24, 1998
Rapid haplotyping of mutations in the Duffy gene using the polymerase chain reaction and sequence-specific primersC G Mullighan, S E Marshall, G C Fanning, et al.
Annals of the Rheumatic Diseases|December 16, 2003
Fas gene promoter polymorphisms in primary Sjögren's syndromeC G Mullighan, S Heatley, S Lester, et al.
Leukemia|June 29, 2007
Pediatric acute myeloid leukemia with NPM1 mutations is characterized by a gene expression profile with dysregulated HOX gene expression distinct from MLL-rearranged leukemiasC G Mullighan, A Kennedy, X Zhou, et al.
Genes and Immunity|February 22, 2003
Variation in immune response genes and chronic Q fever. Concepts: preliminary test with post-Q fever fatigue syndromeK J Helbig, S L Heatley, R J Harris, et al.
Journal of Clinical Immunology|September 1, 1996
Human cytomegalovirus infection is not increased in common variable immunodeficiencyC G Mullighan, S J Read, A G Bird, et al.
Kidney International|October 24, 2000
Glutathione S-transferase polymorphisms and skin cancer after renal transplantationS E Marshall, C Bordea, N A Haldar, et al.
Kidney International|May 7, 1999
Adhesion molecule polymorphisms in chronic renal allograft failureA J McLaren, S E Marshall, N A Haldar, et al.
Oncogene|March 14, 2007
Genome-wide single-nucleotide polymorphism analysis in juvenile myelomonocytic leukemia identifies uniparental disomy surrounding the NF1 locus in cases associated with neurofibromatosis but not in cases with mutant RAS or PTPN11C Flotho, D Steinemann, C G Mullighan, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
Gut|June 9, 1998
A rapid method of haplotyping HFE mutations and linkage disequilibrium in a Caucasoid populationC G Mullighan, M Bunce, G C Fanning, et al.
Clinical and Experimental Immunology|July 27, 2001
Assessment of male CVID patients for mutations in the Btk gene: how many have been misdiagnosed?S A Weston, M L Prasad, C G Mullighan, et al.
Tissue Antigens|March 24, 1998
Rapid haplotyping of mutations in the Duffy gene using the polymerase chain reaction and sequence-specific primersC G Mullighan, S E Marshall, G C Fanning, et al.
Annals of the Rheumatic Diseases|December 16, 2003
Fas gene promoter polymorphisms in primary Sjögren's syndromeC G Mullighan, S Heatley, S Lester, et al.
Leukemia|June 29, 2007
Pediatric acute myeloid leukemia with NPM1 mutations is characterized by a gene expression profile with dysregulated HOX gene expression distinct from MLL-rearranged leukemiasC G Mullighan, A Kennedy, X Zhou, et al.
Genes and Immunity|February 22, 2003
Variation in immune response genes and chronic Q fever. Concepts: preliminary test with post-Q fever fatigue syndromeK J Helbig, S L Heatley, R J Harris, et al.
Journal of Clinical Immunology|September 1, 1996
Human cytomegalovirus infection is not increased in common variable immunodeficiencyC G Mullighan, S J Read, A G Bird, et al.
Kidney International|October 24, 2000
Glutathione S-transferase polymorphisms and skin cancer after renal transplantationS E Marshall, C Bordea, N A Haldar, et al.
Kidney International|May 7, 1999
Adhesion molecule polymorphisms in chronic renal allograft failureA J McLaren, S E Marshall, N A Haldar, et al.
Oncogene|March 14, 2007
Genome-wide single-nucleotide polymorphism analysis in juvenile myelomonocytic leukemia identifies uniparental disomy surrounding the NF1 locus in cases associated with neurofibromatosis but not in cases with mutant RAS or PTPN11C Flotho, D Steinemann, C G Mullighan, et al.
Pageof 4