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Chad A Shaw

Showing results (21-30 of 171) with videos related to

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Plos Genetics|July 26, 2019
Functionalization of CD36 cardiovascular disease and expression associated variants by interdisciplinary high throughput analysisNamrata Madan, Andrew R Ghazi, Xianguo Kong, et al.
Thrombosis and Haemostasis|March 3, 2017
Identification of a functional genetic variant driving racially dimorphic platelet gene expression of the thrombin receptor regulator, PCTPXianguo Kong, Lukas M Simon, Michael Holinstat, et al.
BMC Medical Genetics|November 29, 2011
High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsyLarissa R Stewart, April L Hall, Sung-Hae L Kang, et al.
Human Molecular Genetics|June 16, 2006
Role of genomic architecture in PLP1 duplication causing Pelizaeus-Merzbacher diseaseJennifer A Lee, Ken Inoue, Sau W Cheung, et al.
Bioinformatics (Oxford, England)|July 28, 2018
Design tools for MPRA experimentsAndrew R Ghazi, Edward S Chen, David M Henke, et al.
Plos One|June 29, 2017
Correction: Sequence variability of the respiratory syncytial virus (RSV) fusion gene among contemporary and historical genotypes of RSV/A and RSV/BAnne M Hause, David M Henke, Vasanthi Avadhanula, et al.
Plos Biology|August 7, 2007
Aging hematopoietic stem cells decline in function and exhibit epigenetic dysregulationStuart M Chambers, Chad A Shaw, Catherine Gatza, et al.
European Journal of Human Genetics : EJHG|December 6, 2022
High molecular diagnostic yields and novel phenotypic expansions involving syndromic anorectal malformationsRaymond Belanger Deloge, Xiaonan Zhao, Pamela N Luna, et al.
Plos One|April 18, 2017
Sequence variability of the respiratory syncytial virus (RSV) fusion gene among contemporary and historical genotypes of RSV/A and RSV/BAnne M Hause, David M Henke, Vasanthi Avadhanula, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 15, 2015
MeCP2 binds to non-CG methylated DNA as neurons mature, influencing transcription and the timing of onset for Rett syndromeLin Chen, Kaifu Chen, Laura A Lavery, et al.
Pageof 18

Showing results (21-30 of 171) with videos related to

Sort By:
Pageof 18
Plos Genetics|July 26, 2019
Functionalization of CD36 cardiovascular disease and expression associated variants by interdisciplinary high throughput analysisNamrata Madan, Andrew R Ghazi, Xianguo Kong, et al.
Thrombosis and Haemostasis|March 3, 2017
Identification of a functional genetic variant driving racially dimorphic platelet gene expression of the thrombin receptor regulator, PCTPXianguo Kong, Lukas M Simon, Michael Holinstat, et al.
BMC Medical Genetics|November 29, 2011
High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsyLarissa R Stewart, April L Hall, Sung-Hae L Kang, et al.
Human Molecular Genetics|June 16, 2006
Role of genomic architecture in PLP1 duplication causing Pelizaeus-Merzbacher diseaseJennifer A Lee, Ken Inoue, Sau W Cheung, et al.
Bioinformatics (Oxford, England)|July 28, 2018
Design tools for MPRA experimentsAndrew R Ghazi, Edward S Chen, David M Henke, et al.
Plos One|June 29, 2017
Correction: Sequence variability of the respiratory syncytial virus (RSV) fusion gene among contemporary and historical genotypes of RSV/A and RSV/BAnne M Hause, David M Henke, Vasanthi Avadhanula, et al.
Plos Biology|August 7, 2007
Aging hematopoietic stem cells decline in function and exhibit epigenetic dysregulationStuart M Chambers, Chad A Shaw, Catherine Gatza, et al.
European Journal of Human Genetics : EJHG|December 6, 2022
High molecular diagnostic yields and novel phenotypic expansions involving syndromic anorectal malformationsRaymond Belanger Deloge, Xiaonan Zhao, Pamela N Luna, et al.
Plos One|April 18, 2017
Sequence variability of the respiratory syncytial virus (RSV) fusion gene among contemporary and historical genotypes of RSV/A and RSV/BAnne M Hause, David M Henke, Vasanthi Avadhanula, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 15, 2015
MeCP2 binds to non-CG methylated DNA as neurons mature, influencing transcription and the timing of onset for Rett syndromeLin Chen, Kaifu Chen, Laura A Lavery, et al.
Pageof 18