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Andrew E Timms

Showing results (11-20 of 47) with videos related to

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Cancer Prevention Research (Philadelphia, Pa.)|May 19, 2019
The Effect of Mouse Strain, Sex, and Carcinogen Dose on Toxicity and the Development of Lung Dysplasia and Squamous Cell Carcinomas in MiceLaura Riolobos, Ekram A Gad, Piper M Treuting, 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.
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.
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.
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.
Bone|March 11, 2015
Osteoblast differentiation profiles define sex specific gene expression patterns in craniosynostosisSarah S Park, Richard P Beyer, Matthew D Smyth, et al.
Developmental Cell|March 18, 2022
Cell-specific cis-regulatory elements and mechanisms of non-coding genetic disease in human retina and retinal organoidsEric D Thomas, Andrew E Timms, Sarah Giles, et al.
JAMA Psychiatry|April 5, 2013
Support for the N-methyl-D-aspartate receptor hypofunction hypothesis of schizophrenia from exome sequencing in multiplex familiesAndrew E Timms, Michael O Dorschner, Jeremy Wechsler, et al.
Pageof 5

Showing results (11-20 of 47) with videos related to

Sort By:
Pageof 5
Cancer Prevention Research (Philadelphia, Pa.)|May 19, 2019
The Effect of Mouse Strain, Sex, and Carcinogen Dose on Toxicity and the Development of Lung Dysplasia and Squamous Cell Carcinomas in MiceLaura Riolobos, Ekram A Gad, Piper M Treuting, 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.
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.
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.
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.
Bone|March 11, 2015
Osteoblast differentiation profiles define sex specific gene expression patterns in craniosynostosisSarah S Park, Richard P Beyer, Matthew D Smyth, et al.
Developmental Cell|March 18, 2022
Cell-specific cis-regulatory elements and mechanisms of non-coding genetic disease in human retina and retinal organoidsEric D Thomas, Andrew E Timms, Sarah Giles, et al.
JAMA Psychiatry|April 5, 2013
Support for the N-methyl-D-aspartate receptor hypofunction hypothesis of schizophrenia from exome sequencing in multiplex familiesAndrew E Timms, Michael O Dorschner, Jeremy Wechsler, et al.
Pageof 5