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P Marynen

Showing results (151-160 of 185) with videos related to

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Blood|April 1, 1996
The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemiaS Raynaud, H Cave, M Baens, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Limited expansion of the (CAG)n repeat of the Huntington gene: a premutation (?)E Legius, H Cuppens, H Dierick, et al.
Diabetologia|August 1, 1994
Association of particular HLA class II alleles, haplotypes and genotypes with susceptibility to IDDM in the Belgian populationI Buyse, L A Sandkuyl, M Zamani Ghabanbasani, et al.
Leukemia Research|May 6, 1999
Identification of multiple copies of a 20q-chromosome in a case of myelodysplastic syndrome: a FISH studyD Falzetti, J R Vermeesch, T L Hood, et al.
Leukemia|June 10, 2005
FOXP1, a gene highly expressed in a subset of diffuse large B-cell lymphoma, is recurrently targeted by genomic aberrationsI Wlodarska, E Veyt, P De Paepe, et al.
Blood|March 7, 1998
Fluorescence in situ hybridization characterization of new translocations involving TEL (ETV6) in a wide spectrum of hematologic malignanciesI Wlodarska, R La Starza, M Baens, et al.
Leukemia|January 28, 2005
NUP214-ABL1 amplification in t(5;14)/HOX11L2-positive ALL present with several forms and may have a prognostic significanceP Ballerini, M Busson, S Fasola, et al.
Human Genetics|September 1, 1990
Association between XV2c/CS7/KM19/D9 haplotypes and the delta F508 mutation. A study of 57 Belgian familiesH Cuppens, E Legius, P Cabello, et al.
Blood|March 9, 2000
Inv(2)(p23q35) in anaplastic large-cell lymphoma induces constitutive anaplastic lymphoma kinase (ALK) tyrosine kinase activation by fusion to ATIC, an enzyme involved in purine nucleotide biosynthesisZ Ma, J Cools, P Marynen, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 26, 1996
Molecular characterization of the human peroxisomal branched-chain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of the protein in Zellweger syndromeE Baumgart, J C Vanhooren, M Fransen, et al.
Pageof 19

Showing results (151-160 of 185) with videos related to

Sort By:
Pageof 19
Blood|April 1, 1996
The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemiaS Raynaud, H Cave, M Baens, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Limited expansion of the (CAG)n repeat of the Huntington gene: a premutation (?)E Legius, H Cuppens, H Dierick, et al.
Diabetologia|August 1, 1994
Association of particular HLA class II alleles, haplotypes and genotypes with susceptibility to IDDM in the Belgian populationI Buyse, L A Sandkuyl, M Zamani Ghabanbasani, et al.
Leukemia Research|May 6, 1999
Identification of multiple copies of a 20q-chromosome in a case of myelodysplastic syndrome: a FISH studyD Falzetti, J R Vermeesch, T L Hood, et al.
Leukemia|June 10, 2005
FOXP1, a gene highly expressed in a subset of diffuse large B-cell lymphoma, is recurrently targeted by genomic aberrationsI Wlodarska, E Veyt, P De Paepe, et al.
Blood|March 7, 1998
Fluorescence in situ hybridization characterization of new translocations involving TEL (ETV6) in a wide spectrum of hematologic malignanciesI Wlodarska, R La Starza, M Baens, et al.
Leukemia|January 28, 2005
NUP214-ABL1 amplification in t(5;14)/HOX11L2-positive ALL present with several forms and may have a prognostic significanceP Ballerini, M Busson, S Fasola, et al.
Human Genetics|September 1, 1990
Association between XV2c/CS7/KM19/D9 haplotypes and the delta F508 mutation. A study of 57 Belgian familiesH Cuppens, E Legius, P Cabello, et al.
Blood|March 9, 2000
Inv(2)(p23q35) in anaplastic large-cell lymphoma induces constitutive anaplastic lymphoma kinase (ALK) tyrosine kinase activation by fusion to ATIC, an enzyme involved in purine nucleotide biosynthesisZ Ma, J Cools, P Marynen, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 26, 1996
Molecular characterization of the human peroxisomal branched-chain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of the protein in Zellweger syndromeE Baumgart, J C Vanhooren, M Fransen, et al.
Pageof 19