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C Papp

Showing results (181-190 of 227) with videos related to

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American Journal of Respiratory Cell and Molecular Biology|June 10, 2017
A Novel In Vitro Human Granuloma Model of Sarcoidosis and Latent Tuberculosis InfectionElliott D Crouser, Peter White, Evelyn Guirado Caceres, et al.
BMC Systems Biology|November 7, 2008
Integrated weighted gene co-expression network analysis with an application to chronic fatigue syndromeAngela P Presson, Eric M Sobel, Jeanette C Papp, et al.
American Journal of Human Genetics|July 1, 1995
Spectrum of small mutations in the dystrophin coding regionT W Prior, C Bartolo, D K Pearl, et al.
Human Mutation|January 1, 1993
Exon 44 nonsense mutation in two-Duchenne muscular dystrophy brothers detected by heteroduplex analysisT W Prior, A C Papp, P J Snyder, et al.
Human Molecular Genetics|March 1, 1993
Identification of two point mutations and a one base deletion in exon 19 of the dystrophin gene by heteroduplex formationT W Prior, A C Papp, P J Snyder, et al.
Nature Genetics|August 1, 1993
A missense mutation in the dystrophin gene in a Duchenne muscular dystrophy patientT W Prior, A C Papp, P J Snyder, et al.
American Journal of Human Genetics|January 7, 2023
Unsupervised discovery of ancestry-informative markers and genetic admixture proportions in biobank-scale datasetsSeyoon Ko, Benjamin B Chu, Daniel Peterson, et al.
Journal of Medical Genetics|April 1, 1996
A novel splice site mutation in a Becker muscular dystrophy patientC Bartolo, A C Papp, P J Snyder, et al.
Annals of the New York Academy of Sciences|September 30, 1994
The role of progestationally regulated stromal cell tissue factor and type-1 plasminogen activator inhibitor (PAI-1) in endometrial hemostasis and menstruationC J Lockwood, G Krikun, C Papp, et al.
American Journal of Medical Genetics|March 1, 1994
Heteroduplex analysis of the dystrophin gene: application to point mutation and carrier detectionT W Prior, A C Papp, P J Snyder, et al.
Pageof 23

Showing results (181-190 of 227) with videos related to

Sort By:
Pageof 23
American Journal of Respiratory Cell and Molecular Biology|June 10, 2017
A Novel In Vitro Human Granuloma Model of Sarcoidosis and Latent Tuberculosis InfectionElliott D Crouser, Peter White, Evelyn Guirado Caceres, et al.
BMC Systems Biology|November 7, 2008
Integrated weighted gene co-expression network analysis with an application to chronic fatigue syndromeAngela P Presson, Eric M Sobel, Jeanette C Papp, et al.
American Journal of Human Genetics|July 1, 1995
Spectrum of small mutations in the dystrophin coding regionT W Prior, C Bartolo, D K Pearl, et al.
Human Mutation|January 1, 1993
Exon 44 nonsense mutation in two-Duchenne muscular dystrophy brothers detected by heteroduplex analysisT W Prior, A C Papp, P J Snyder, et al.
Human Molecular Genetics|March 1, 1993
Identification of two point mutations and a one base deletion in exon 19 of the dystrophin gene by heteroduplex formationT W Prior, A C Papp, P J Snyder, et al.
Nature Genetics|August 1, 1993
A missense mutation in the dystrophin gene in a Duchenne muscular dystrophy patientT W Prior, A C Papp, P J Snyder, et al.
American Journal of Human Genetics|January 7, 2023
Unsupervised discovery of ancestry-informative markers and genetic admixture proportions in biobank-scale datasetsSeyoon Ko, Benjamin B Chu, Daniel Peterson, et al.
Journal of Medical Genetics|April 1, 1996
A novel splice site mutation in a Becker muscular dystrophy patientC Bartolo, A C Papp, P J Snyder, et al.
Annals of the New York Academy of Sciences|September 30, 1994
The role of progestationally regulated stromal cell tissue factor and type-1 plasminogen activator inhibitor (PAI-1) in endometrial hemostasis and menstruationC J Lockwood, G Krikun, C Papp, et al.
American Journal of Medical Genetics|March 1, 1994
Heteroduplex analysis of the dystrophin gene: application to point mutation and carrier detectionT W Prior, A C Papp, P J Snyder, et al.
Pageof 23