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Showing results (51-60 of 103) with videos related to

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Microscopy and Microanalysis : the Official Journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada|March 10, 2020
Novel Applications of FIB-SEM-Based ToF-SIMS in Atom Probe Tomography WorkflowsWilliam D A Rickard, Steven M Reddy, David W Saxey, et al.
Arthritis and Rheumatism|July 13, 2004
Dissection of class III major histocompatibility complex haplotypes associated with rheumatoid arthritisJulia L Newton, Sinéad M J Harney, Andrew E Timms, et al.
Nature|May 14, 1992
Profound block in thymocyte development in mice lacking p56lckT J Molina, K Kishihara, D P Siderovski, et al.
Scientific Reports|August 10, 2022
Anti-tumor activity of a T-helper 1 multiantigen vaccine in a murine model of prostate cancerDenise L Cecil, Benjamin Curtis, Ekram Gad, et al.
Scientific Data|June 21, 2020
Transcriptome data of temporal and cingulate cortex in the Rett syndrome brainKimberly A Aldinger, Andrew E Timms, James W MacDonald, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 23, 2023
Rubble pile asteroids are foreverFred Jourdan, Nicholas E Timms, Tomoki Nakamura, et al.
American Journal of Medical Genetics. Part A|June 7, 2016
A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hairKaren W Gripp, Kimberly A Aldinger, James T Bennett, et al.
JCI Insight|September 20, 2019
Genotype correlates with clinical severity in PIK3CA-associated lymphatic malformationsKaitlyn Zenner, Chi Vicky Cheng, Dana M Jensen, et al.
Journal of Immunology (Baltimore, Md. : 1950)|August 26, 1998
Receptor-specific allelic exclusion of TCRV alpha-chains during developmentR Boyd, I Kozieradzki, A Chidgey, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 9, 2020
Mapping the <i>cis</i>-regulatory architecture of the human retina reveals noncoding genetic variation in diseaseTimothy J Cherry, Marty G Yang, David A Harmin, et al.
Pageof 11

Showing results (51-60 of 103) with videos related to

Sort By:
Pageof 11
Microscopy and Microanalysis : the Official Journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada|March 10, 2020
Novel Applications of FIB-SEM-Based ToF-SIMS in Atom Probe Tomography WorkflowsWilliam D A Rickard, Steven M Reddy, David W Saxey, et al.
Arthritis and Rheumatism|July 13, 2004
Dissection of class III major histocompatibility complex haplotypes associated with rheumatoid arthritisJulia L Newton, Sinéad M J Harney, Andrew E Timms, et al.
Nature|May 14, 1992
Profound block in thymocyte development in mice lacking p56lckT J Molina, K Kishihara, D P Siderovski, et al.
Scientific Reports|August 10, 2022
Anti-tumor activity of a T-helper 1 multiantigen vaccine in a murine model of prostate cancerDenise L Cecil, Benjamin Curtis, Ekram Gad, et al.
Scientific Data|June 21, 2020
Transcriptome data of temporal and cingulate cortex in the Rett syndrome brainKimberly A Aldinger, Andrew E Timms, James W MacDonald, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 23, 2023
Rubble pile asteroids are foreverFred Jourdan, Nicholas E Timms, Tomoki Nakamura, et al.
American Journal of Medical Genetics. Part A|June 7, 2016
A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hairKaren W Gripp, Kimberly A Aldinger, James T Bennett, et al.
JCI Insight|September 20, 2019
Genotype correlates with clinical severity in PIK3CA-associated lymphatic malformationsKaitlyn Zenner, Chi Vicky Cheng, Dana M Jensen, et al.
Journal of Immunology (Baltimore, Md. : 1950)|August 26, 1998
Receptor-specific allelic exclusion of TCRV alpha-chains during developmentR Boyd, I Kozieradzki, A Chidgey, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 9, 2020
Mapping the <i>cis</i>-regulatory architecture of the human retina reveals noncoding genetic variation in diseaseTimothy J Cherry, Marty G Yang, David A Harmin, et al.
Pageof 11