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Development (Cambridge, England)
|
June 10, 2011
Dynamic control of head mesoderm patterning
Ingo Bothe, Gennadiy Tenin, Adelola Oseni, et al.
Data in Brief
|
December 19, 2022
Data on cardiac lncRNA <i>STX18-AS1</i> expression in developing human hearts and function during <i>in vitro</i> hESC-cardiomyocyte differentiation
Yingjuan Liu, Mun-Kit Choy, Sabu Abraham, et al.
Circulation. Genomic and Precision Medicine
|
October 16, 2019
Integration of Large-Scale Genomic Data Sources With Evolutionary History Reveals Novel Genetic Loci for Congenital Heart Disease
Elisavet Fotiou, Simon Williams, Alexandra Martin-Geary, et al.
Plos One
|
October 1, 2014
Erbb2 is required for cardiac atrial electrical activity during development
Gennadiy Tenin, Christopher Clowes, Kathryn Wolton, et al.
European Journal of Human Genetics : EJHG
|
April 25, 2020
Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1-BP2) deletion in the UK Biobank
Simon G Williams, Apostol Nakev, Hui Guo, et al.
The Application of Clinical Genetics
|
May 6, 2020
Association of Cholinergic Muscarinic M4 Receptor Gene Polymorphism with Schizophrenia
Ivan V Pozhidaev, Anastasiia S Boiko, Anton J M Loonen, et al.
Plos Genetics
|
October 31, 2017
Non-muscle myosin IIB (Myh10) is required for epicardial function and coronary vessel formation during mammalian development
Liam A Ridge, Karen Mitchell, Ali Al-Anbaki, et al.
Human Molecular Genetics
|
May 19, 2017
Induced pluripotent stem cell modelling of HLHS underlines the contribution of dysfunctional NOTCH signalling to impaired cardiogenesis
Chunbo Yang, Yaobo Xu, Min Yu, et al.
Biorxiv : the Preprint Server for Biology
|
June 12, 2025
The RNA splicing factor PRPF8 is required for left-right organiser cilia function and determination of cardiac left-right asymmetry via regulation of Arl13b splicing
Fangfei Jiang, Michael Boylan, Dale W Maxwell, et al.
Cell Reports. Medicine
|
March 4, 2022
Genetic resiliency associated with dominant lethal <i>TPM1</i> mutation causing atrial septal defect with high heritability
Polakit Teekakirikul, Wenjuan Zhu, Xinxiu Xu, et al.
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Showing results (1-10 of 10) with videos related to
Sort By:
Page
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Development (Cambridge, England)
|
June 10, 2011
Dynamic control of head mesoderm patterning
Ingo Bothe, Gennadiy Tenin, Adelola Oseni, et al.
Data in Brief
|
December 19, 2022
Data on cardiac lncRNA <i>STX18-AS1</i> expression in developing human hearts and function during <i>in vitro</i> hESC-cardiomyocyte differentiation
Yingjuan Liu, Mun-Kit Choy, Sabu Abraham, et al.
Circulation. Genomic and Precision Medicine
|
October 16, 2019
Integration of Large-Scale Genomic Data Sources With Evolutionary History Reveals Novel Genetic Loci for Congenital Heart Disease
Elisavet Fotiou, Simon Williams, Alexandra Martin-Geary, et al.
Plos One
|
October 1, 2014
Erbb2 is required for cardiac atrial electrical activity during development
Gennadiy Tenin, Christopher Clowes, Kathryn Wolton, et al.
European Journal of Human Genetics : EJHG
|
April 25, 2020
Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1-BP2) deletion in the UK Biobank
Simon G Williams, Apostol Nakev, Hui Guo, et al.
The Application of Clinical Genetics
|
May 6, 2020
Association of Cholinergic Muscarinic M4 Receptor Gene Polymorphism with Schizophrenia
Ivan V Pozhidaev, Anastasiia S Boiko, Anton J M Loonen, et al.
Plos Genetics
|
October 31, 2017
Non-muscle myosin IIB (Myh10) is required for epicardial function and coronary vessel formation during mammalian development
Liam A Ridge, Karen Mitchell, Ali Al-Anbaki, et al.
Human Molecular Genetics
|
May 19, 2017
Induced pluripotent stem cell modelling of HLHS underlines the contribution of dysfunctional NOTCH signalling to impaired cardiogenesis
Chunbo Yang, Yaobo Xu, Min Yu, et al.
Biorxiv : the Preprint Server for Biology
|
June 12, 2025
The RNA splicing factor PRPF8 is required for left-right organiser cilia function and determination of cardiac left-right asymmetry via regulation of Arl13b splicing
Fangfei Jiang, Michael Boylan, Dale W Maxwell, et al.
Cell Reports. Medicine
|
March 4, 2022
Genetic resiliency associated with dominant lethal <i>TPM1</i> mutation causing atrial septal defect with high heritability
Polakit Teekakirikul, Wenjuan Zhu, Xinxiu Xu, et al.
Page
of 1