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T Warren

Showing results (341-350 of 471) with videos related to

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American Journal of Human Genetics|February 24, 2009
Replication stress induces genome-wide copy number changes in human cells that resemble polymorphic and pathogenic variantsMartin F Arlt, Jennifer G Mulle, Valerie M Schaibley, et al.
Transplantation|March 5, 2019
Antibody-suppressor CD8+ T Cells Require CXCR5Jason M Zimmerer, Bryce A Ringwald, Steven M Elzein, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 2002
Molecular and biochemical characterization of two P450 enzymes in the ecdysteroidogenic pathway of Drosophila melanogasterJames T Warren, Anna Petryk, Guillermo Marques, et al.
Frontiers in Behavioral Neuroscience|November 5, 2014
Generalization of fear-potentiated startle in the presence of auditory cues: a parametric analysisSeth Davin Norrholm, Tanja Jovanovic, Maria A Briscione, et al.
Anticancer Research|September 29, 2020
Clinical Efficacy of Tumor Treating Fields for Newly Diagnosed GlioblastomaYang Liu, Myla S Strawderman, Kwanza T Warren, et al.
Journal of Oral and Maxillofacial Surgery : Official Journal of the American Association of Oral and Maxillofacial Surgeons|April 19, 2017
Buffered 1% Lidocaine With Epinephrine Can Be as Effective as Nonbuffered 2% Lidocaine With Epinephrine for Maxillary Field BlockJames A Phero, Victor T Warren, Anson G Fisher, et al.
Science (New York, N.Y.)|May 24, 1991
Fragile X genotype characterized by an unstable region of DNAS Yu, M Pritchard, E Kremer, et al.
Molecular Biology of the Cell|October 22, 2002
Novel proteins linking the actin cytoskeleton to the endocytic machinery in Saccharomyces cerevisiaeH Dewar, D T Warren, F C Gardiner, et al.
Nature Neuroscience|January 3, 2004
Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathwayPeng Jin, Daniela C Zarnescu, Stephanie Ceman, et al.
Nature Genetics|February 1, 1997
Characterization of the full fragile X syndrome mutation in fetal gametesH E Malter, J C Iber, R Willemsen, et al.
Pageof 48

Showing results (341-350 of 471) with videos related to

Sort By:
Pageof 48
American Journal of Human Genetics|February 24, 2009
Replication stress induces genome-wide copy number changes in human cells that resemble polymorphic and pathogenic variantsMartin F Arlt, Jennifer G Mulle, Valerie M Schaibley, et al.
Transplantation|March 5, 2019
Antibody-suppressor CD8+ T Cells Require CXCR5Jason M Zimmerer, Bryce A Ringwald, Steven M Elzein, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 2002
Molecular and biochemical characterization of two P450 enzymes in the ecdysteroidogenic pathway of Drosophila melanogasterJames T Warren, Anna Petryk, Guillermo Marques, et al.
Frontiers in Behavioral Neuroscience|November 5, 2014
Generalization of fear-potentiated startle in the presence of auditory cues: a parametric analysisSeth Davin Norrholm, Tanja Jovanovic, Maria A Briscione, et al.
Anticancer Research|September 29, 2020
Clinical Efficacy of Tumor Treating Fields for Newly Diagnosed GlioblastomaYang Liu, Myla S Strawderman, Kwanza T Warren, et al.
Journal of Oral and Maxillofacial Surgery : Official Journal of the American Association of Oral and Maxillofacial Surgeons|April 19, 2017
Buffered 1% Lidocaine With Epinephrine Can Be as Effective as Nonbuffered 2% Lidocaine With Epinephrine for Maxillary Field BlockJames A Phero, Victor T Warren, Anson G Fisher, et al.
Science (New York, N.Y.)|May 24, 1991
Fragile X genotype characterized by an unstable region of DNAS Yu, M Pritchard, E Kremer, et al.
Molecular Biology of the Cell|October 22, 2002
Novel proteins linking the actin cytoskeleton to the endocytic machinery in Saccharomyces cerevisiaeH Dewar, D T Warren, F C Gardiner, et al.
Nature Neuroscience|January 3, 2004
Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathwayPeng Jin, Daniela C Zarnescu, Stephanie Ceman, et al.
Nature Genetics|February 1, 1997
Characterization of the full fragile X syndrome mutation in fetal gametesH E Malter, J C Iber, R Willemsen, et al.
Pageof 48