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Gyapay

Showing results (71-80 of 92) with videos related to

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Genome Research|December 10, 1998
Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14qC Paternotte, D Rudnicki, C Fizames, et al.
Science (New York, N.Y.)|February 14, 2009
Polydnaviruses of braconid wasps derive from an ancestral nudivirusAnnie Bézier, Marc Annaheim, Juline Herbinière, et al.
BMC Biology|July 25, 2020
Genomic architecture of endogenous ichnoviruses reveals distinct evolutionary pathways leading to virus domestication in parasitic waspsFabrice Legeai, Bernardo F Santos, Stéphanie Robin, et al.
Nature|March 10, 2001
A physical map of human chromosome 14T Brüls, G Gyapay, J L Petit, et al.
Molecular Systems Biology|March 6, 2008
A complete collection of single-gene deletion mutants of Acinetobacter baylyi ADP1Véronique de Berardinis, David Vallenet, Vanina Castelli, et al.
European Journal of Human Genetics : EJHG|January 20, 2012
KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutationsStephan Klebe, Alexander Lossos, Hamid Azzedine, et al.
Journal of Experimental Botany|October 20, 2017
Deciphering the Theobroma cacao self-incompatibility system: from genomics to diagnostic markers for self-compatibilityClaire Lanaud, Olivier Fouet, Thierry Legavre, et al.
Neurogenetics|December 14, 1999
Linkage analysis of candidate myelin genes in familial multiple sclerosisE Seboun, J R Oksenberg, A Rombos, et al.
Nature Genetics|August 1, 1996
A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics GroupJ L Haines, M Ter-Minassian, A Bazyk, et al.
Human Mutation|August 7, 2010
High-throughput sequencing of a 4.1 Mb linkage interval reveals FLVCR2 deletions and mutations in lethal cerebral vasculopathySophie Thomas, Ferechté Encha-Razavi, Louise Devisme, et al.
Pageof 10

Showing results (71-80 of 92) with videos related to

Sort By:
Pageof 10
Genome Research|December 10, 1998
Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14qC Paternotte, D Rudnicki, C Fizames, et al.
Science (New York, N.Y.)|February 14, 2009
Polydnaviruses of braconid wasps derive from an ancestral nudivirusAnnie Bézier, Marc Annaheim, Juline Herbinière, et al.
BMC Biology|July 25, 2020
Genomic architecture of endogenous ichnoviruses reveals distinct evolutionary pathways leading to virus domestication in parasitic waspsFabrice Legeai, Bernardo F Santos, Stéphanie Robin, et al.
Nature|March 10, 2001
A physical map of human chromosome 14T Brüls, G Gyapay, J L Petit, et al.
Molecular Systems Biology|March 6, 2008
A complete collection of single-gene deletion mutants of Acinetobacter baylyi ADP1Véronique de Berardinis, David Vallenet, Vanina Castelli, et al.
European Journal of Human Genetics : EJHG|January 20, 2012
KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutationsStephan Klebe, Alexander Lossos, Hamid Azzedine, et al.
Journal of Experimental Botany|October 20, 2017
Deciphering the Theobroma cacao self-incompatibility system: from genomics to diagnostic markers for self-compatibilityClaire Lanaud, Olivier Fouet, Thierry Legavre, et al.
Neurogenetics|December 14, 1999
Linkage analysis of candidate myelin genes in familial multiple sclerosisE Seboun, J R Oksenberg, A Rombos, et al.
Nature Genetics|August 1, 1996
A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics GroupJ L Haines, M Ter-Minassian, A Bazyk, et al.
Human Mutation|August 7, 2010
High-throughput sequencing of a 4.1 Mb linkage interval reveals FLVCR2 deletions and mutations in lethal cerebral vasculopathySophie Thomas, Ferechté Encha-Razavi, Louise Devisme, et al.
Pageof 10