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A Lindblom

Showing results (111-120 of 135) with videos related to

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Genes, Chromosomes & Cancer|July 1, 1995
High allele loss rates at 17q12-q21 in breast and ovarian tumors from BRCAl-linked families. The Breast Cancer Linkage ConsortiumR S Cornelis, S L Neuhausen, O Johansson, et al.
Journal of Medical Genetics|January 20, 2004
Screening for genomic rearrangements of the MMR genes must be included in the routine diagnosis of HNPCCF Di Fiore, F Charbonnier, C Martin, et al.
Breast Cancer Research : BCR|April 18, 2001
Low frequency of E-cadherin alterations in familial breast cancerS Salahshor, L Haixin, H Huo, et al.
Nature|March 17, 1994
Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancerC E Bronner, S M Baker, P T Morrison, et al.
Molecular Biology of the Cell|February 1, 1994
Distinct and overlapping ligand specificities of the alpha 3A beta 1 and alpha 6A beta 1 integrins: recognition of laminin isoformsG O Delwel, A A de Melker, F Hogervorst, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 2001
Frameshift-mutation-derived peptides as tumor-specific antigens in inherited and spontaneous colorectal cancerI Saeterdal, J Bjørheim, K Lislerud, et al.
Mutation Research|September 3, 1998
Mutation analyses of KRAS exon 1 comparing three different techniques: temporal temperature gradient electrophoresis, constant denaturant capillary electrophoresis and allele specific polymerase chain reactionJ Bjørheim, S Lystad, A Lindblom, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 9, 2013
Results from a large multinational clinical trial (guardian™3) using prophylactic treatment with turoctocog alfa in paediatric patients with severe haemophilia A: safety, efficacy and pharmacokineticsR Kulkarni, F A Karim, S Glamocanin, et al.
Journal of Medical Genetics|January 8, 2008
A frame-shift mutation of PMS2 is a widespread cause of Lynch syndromeM Clendenning, L Senter, H Hampel, et al.
Cancer Research|November 3, 2001
The role of hPMS1 and hPMS2 in predisposing to colorectal cancerT Liu, H Yan, S Kuismanen, et al.
Pageof 14

Showing results (111-120 of 135) with videos related to

Sort By:
Pageof 14
Genes, Chromosomes & Cancer|July 1, 1995
High allele loss rates at 17q12-q21 in breast and ovarian tumors from BRCAl-linked families. The Breast Cancer Linkage ConsortiumR S Cornelis, S L Neuhausen, O Johansson, et al.
Journal of Medical Genetics|January 20, 2004
Screening for genomic rearrangements of the MMR genes must be included in the routine diagnosis of HNPCCF Di Fiore, F Charbonnier, C Martin, et al.
Breast Cancer Research : BCR|April 18, 2001
Low frequency of E-cadherin alterations in familial breast cancerS Salahshor, L Haixin, H Huo, et al.
Nature|March 17, 1994
Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancerC E Bronner, S M Baker, P T Morrison, et al.
Molecular Biology of the Cell|February 1, 1994
Distinct and overlapping ligand specificities of the alpha 3A beta 1 and alpha 6A beta 1 integrins: recognition of laminin isoformsG O Delwel, A A de Melker, F Hogervorst, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 2001
Frameshift-mutation-derived peptides as tumor-specific antigens in inherited and spontaneous colorectal cancerI Saeterdal, J Bjørheim, K Lislerud, et al.
Mutation Research|September 3, 1998
Mutation analyses of KRAS exon 1 comparing three different techniques: temporal temperature gradient electrophoresis, constant denaturant capillary electrophoresis and allele specific polymerase chain reactionJ Bjørheim, S Lystad, A Lindblom, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 9, 2013
Results from a large multinational clinical trial (guardian™3) using prophylactic treatment with turoctocog alfa in paediatric patients with severe haemophilia A: safety, efficacy and pharmacokineticsR Kulkarni, F A Karim, S Glamocanin, et al.
Journal of Medical Genetics|January 8, 2008
A frame-shift mutation of PMS2 is a widespread cause of Lynch syndromeM Clendenning, L Senter, H Hampel, et al.
Cancer Research|November 3, 2001
The role of hPMS1 and hPMS2 in predisposing to colorectal cancerT Liu, H Yan, S Kuismanen, et al.
Pageof 14