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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 Infection
Elliott 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 syndrome
Angela 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 region
T 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 analysis
T 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 formation
T 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 patient
T 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 datasets
Seyoon 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 patient
C 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 menstruation
C 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 detection
T W Prior, A C Papp, P J Snyder, et al.
Page
of 23
Search research articles
Search
Showing results (181-190 of 227) with videos related to
Sort By:
Page
of 23
American Journal of Respiratory Cell and Molecular Biology
|
June 10, 2017
A Novel In Vitro Human Granuloma Model of Sarcoidosis and Latent Tuberculosis Infection
Elliott 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 syndrome
Angela 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 region
T 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 analysis
T 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 formation
T 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 patient
T 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 datasets
Seyoon 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 patient
C 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 menstruation
C 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 detection
T W Prior, A C Papp, P J Snyder, et al.
Page
of 23