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W R McCombie

Showing results (21-30 of 45) with videos related to

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Annals of Neurology|March 1, 1992
Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European originL G Goldfarb, P Brown, M Haltia, et al.
DNA Sequence : the Journal of DNA Sequencing and Mapping|January 1, 1992
Sequencing and analysis of genomic fragments from the NF1 locusA Martin-Gallardo, D A Marchuk, J Gocayne, et al.
Genomics|March 15, 2001
Identification of mesoderm development (mesd) candidate genes by comparative mapping and genome sequence analysisM E Wines, L Lee, M S Katari, et al.
Neurology|February 1, 1994
Iatrogenic Creutzfeldt-Jakob disease: an example of the interplay between ancient genes and modern medicineP Brown, L Cervenáková, L G Goldfarb, et al.
FEBS Letters|September 25, 1989
Cloning, sequence analysis and chromosome localization of a Drosophila muscarinic acetylcholine receptorT Onai, M G FitzGerald, S Arakawa, et al.
Nature Genetics|August 1, 1992
Expressed genes, Alu repeats and polymorphisms in cosmids sequenced from chromosome 4p16.3W R McCombie, A Martin-Gallardo, J D Gocayne, et al.
Neurology|February 11, 1992
Atypical Creutzfeldt-Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor geneP Brown, L G Goldfarb, W R McCombie, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 11, 1991
Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP geneL G Goldfarb, P Brown, W R McCombie, et al.
Nature Genetics|May 1, 1992
Caenorhabditis elegans expressed sequence tags identify gene families and potential disease gene homologuesW R McCombie, M D Adams, J M Kelley, et al.
Nature Genetics|April 1, 1992
Automated DNA sequencing and analysis of 106 kilobases from human chromosome 19q13.3A Martin-Gallardo, W R McCombie, J D Gocayne, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
Annals of Neurology|March 1, 1992
Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European originL G Goldfarb, P Brown, M Haltia, et al.
DNA Sequence : the Journal of DNA Sequencing and Mapping|January 1, 1992
Sequencing and analysis of genomic fragments from the NF1 locusA Martin-Gallardo, D A Marchuk, J Gocayne, et al.
Genomics|March 15, 2001
Identification of mesoderm development (mesd) candidate genes by comparative mapping and genome sequence analysisM E Wines, L Lee, M S Katari, et al.
Neurology|February 1, 1994
Iatrogenic Creutzfeldt-Jakob disease: an example of the interplay between ancient genes and modern medicineP Brown, L Cervenáková, L G Goldfarb, et al.
FEBS Letters|September 25, 1989
Cloning, sequence analysis and chromosome localization of a Drosophila muscarinic acetylcholine receptorT Onai, M G FitzGerald, S Arakawa, et al.
Nature Genetics|August 1, 1992
Expressed genes, Alu repeats and polymorphisms in cosmids sequenced from chromosome 4p16.3W R McCombie, A Martin-Gallardo, J D Gocayne, et al.
Neurology|February 11, 1992
Atypical Creutzfeldt-Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor geneP Brown, L G Goldfarb, W R McCombie, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 11, 1991
Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP geneL G Goldfarb, P Brown, W R McCombie, et al.
Nature Genetics|May 1, 1992
Caenorhabditis elegans expressed sequence tags identify gene families and potential disease gene homologuesW R McCombie, M D Adams, J M Kelley, et al.
Nature Genetics|April 1, 1992
Automated DNA sequencing and analysis of 106 kilobases from human chromosome 19q13.3A Martin-Gallardo, W R McCombie, J D Gocayne, et al.
Pageof 5