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Elizabeth C Schramm

Showing results (1-10 of 11) with videos related to

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Euphytica: Netherlands Journal of Plant Breeding|November 29, 2014
Wheat ABA-insensitive mutants result in reduced grain dormancyElizabeth C Schramm, Sven K Nelson, Camille M Steber
Annual Review of Pathology|December 14, 2016
Complement Dysregulation and Disease: Insights from Contemporary GeneticsM Kathryn Liszewski, Anuja Java, Elizabeth C Schramm, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|December 6, 2012
Increased ABA sensitivity results in higher seed dormancy in soft white spring wheat cultivar 'Zak'Elizabeth C Schramm, Sven K Nelson, Kimberlee K Kidwell, et al.
Molecular Immunology|July 19, 2014
Genetic variants in the complement system predisposing to age-related macular degeneration: a reviewElizabeth C Schramm, Simon J Clark, Michael P Triebwasser, et al.
Journal of Plant Registrations|January 13, 2015
Registration of Zak <i>ERA8</i> Soft White Spring Wheat Germplasm with Enhanced Response to ABA and Increased Seed DormancyShantel A Martinez, Elizabeth C Schramm, Tracy J Harris, et al.
Investigative Ophthalmology & Visual Science|October 27, 2015
Rare Variants in the Functional Domains of Complement Factor H Are Associated With Age-Related Macular DegenerationMichael P Triebwasser, Elisha D O Roberson, Yi Yu, et al.
Human Molecular Genetics|March 20, 2015
Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levelsDavid Kavanagh, Yi Yu, Elizabeth C Schramm, et al.
Journal of the American Society of Nephrology : JASN|October 17, 2015
A Familial C3GN Secondary to Defective C3 Regulation by Complement Receptor 1 and Complement Factor HSophie Chauvet, Lubka T Roumenina, Sarah Bruneau, et al.
Analytical Biochemistry|February 10, 2015
A quantitative lateral flow assay to detect complement activation in bloodElizabeth C Schramm, Nick R Staten, Zhouning Zhang, et al.
Human Molecular Genetics|May 22, 2014
Whole-exome sequencing identifies rare, functional CFH variants in families with macular degenerationYi Yu, Michael P Triebwasser, Edwin K S Wong, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Euphytica: Netherlands Journal of Plant Breeding|November 29, 2014
Wheat ABA-insensitive mutants result in reduced grain dormancyElizabeth C Schramm, Sven K Nelson, Camille M Steber
Annual Review of Pathology|December 14, 2016
Complement Dysregulation and Disease: Insights from Contemporary GeneticsM Kathryn Liszewski, Anuja Java, Elizabeth C Schramm, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|December 6, 2012
Increased ABA sensitivity results in higher seed dormancy in soft white spring wheat cultivar 'Zak'Elizabeth C Schramm, Sven K Nelson, Kimberlee K Kidwell, et al.
Molecular Immunology|July 19, 2014
Genetic variants in the complement system predisposing to age-related macular degeneration: a reviewElizabeth C Schramm, Simon J Clark, Michael P Triebwasser, et al.
Journal of Plant Registrations|January 13, 2015
Registration of Zak <i>ERA8</i> Soft White Spring Wheat Germplasm with Enhanced Response to ABA and Increased Seed DormancyShantel A Martinez, Elizabeth C Schramm, Tracy J Harris, et al.
Investigative Ophthalmology & Visual Science|October 27, 2015
Rare Variants in the Functional Domains of Complement Factor H Are Associated With Age-Related Macular DegenerationMichael P Triebwasser, Elisha D O Roberson, Yi Yu, et al.
Human Molecular Genetics|March 20, 2015
Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levelsDavid Kavanagh, Yi Yu, Elizabeth C Schramm, et al.
Journal of the American Society of Nephrology : JASN|October 17, 2015
A Familial C3GN Secondary to Defective C3 Regulation by Complement Receptor 1 and Complement Factor HSophie Chauvet, Lubka T Roumenina, Sarah Bruneau, et al.
Analytical Biochemistry|February 10, 2015
A quantitative lateral flow assay to detect complement activation in bloodElizabeth C Schramm, Nick R Staten, Zhouning Zhang, et al.
Human Molecular Genetics|May 22, 2014
Whole-exome sequencing identifies rare, functional CFH variants in families with macular degenerationYi Yu, Michael P Triebwasser, Edwin K S Wong, et al.
Pageof 2