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Frontiers in Molecular Neuroscience
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February 2, 2019
Fragile-X Syndrome Is Associated With NMDA Receptor Hypofunction and Reduced Dendritic Complexity in Mature Dentate Granule Cells
Suk-Yu Yau, Luis Bettio, Jason Chiu, et al.
Current Protocols in Human Genetics
|
April 23, 2008
DNA mutation detection using denaturing high-performance liquid chromatography (DHPLC)
Bing Yu, Nicole A Sawyer, Christine Chiu, et al.
International Journal of Cardiology
|
June 5, 2007
Postmortem molecular analysis of KCNQ1 and SCN5A genes in sudden unexplained death in young Australians
Alessandra Doolan, Neil Langlois, Christine Chiu, et al.
American Heart Journal
|
February 9, 2002
Use of an implantable loop recorder in the evaluation of children with congenital heart disease
Shubhayan Sanatani, Alejandro Peirone, Christine Chiu, et al.
Journal of Molecular and Cellular Cardiology
|
July 28, 2007
Genetic screening of calcium regulation genes in familial hypertrophic cardiomyopathy
Christine Chiu, Molly Tebo, Jodie Ingles, et al.
Chinese Medical Journal
|
March 16, 2007
QT hysteresis in long-QT syndrome children with exercise testing
Dong-sheng Gao, Wei-yi Fang, Christine Chiu-Man, et al.
Journal of Molecular and Cellular Cardiology
|
July 12, 2008
Sex hormone receptor gene variation associated with phenotype in male hypertrophic cardiomyopathy patients
Joanne M Lind, Christine Chiu, Jodie Ingles, et al.
Geophysical Research Letters
|
December 30, 2022
Near-Cloud Aerosol Retrieval Using Machine Learning Techniques, and Implied Direct Radiative Effects
C Kevin Yang, J Christine Chiu, Alexander Marshak, et al.
Geophysical Research Letters
|
March 8, 2021
Observational Constraints on Warm Cloud Microphysical Processes Using Machine Learning and Optimization Techniques
J Christine Chiu, C Kevin Yang, Peter Jan van Leeuwen, et al.
Journal of Molecular and Cellular Cardiology
|
February 9, 2005
Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: clinical, genetic and functional consequences
Alessandra Doolan, Molly Tebo, Jodie Ingles, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 25) with videos related to
Sort By:
Page
of 3
Frontiers in Molecular Neuroscience
|
February 2, 2019
Fragile-X Syndrome Is Associated With NMDA Receptor Hypofunction and Reduced Dendritic Complexity in Mature Dentate Granule Cells
Suk-Yu Yau, Luis Bettio, Jason Chiu, et al.
Current Protocols in Human Genetics
|
April 23, 2008
DNA mutation detection using denaturing high-performance liquid chromatography (DHPLC)
Bing Yu, Nicole A Sawyer, Christine Chiu, et al.
International Journal of Cardiology
|
June 5, 2007
Postmortem molecular analysis of KCNQ1 and SCN5A genes in sudden unexplained death in young Australians
Alessandra Doolan, Neil Langlois, Christine Chiu, et al.
American Heart Journal
|
February 9, 2002
Use of an implantable loop recorder in the evaluation of children with congenital heart disease
Shubhayan Sanatani, Alejandro Peirone, Christine Chiu, et al.
Journal of Molecular and Cellular Cardiology
|
July 28, 2007
Genetic screening of calcium regulation genes in familial hypertrophic cardiomyopathy
Christine Chiu, Molly Tebo, Jodie Ingles, et al.
Chinese Medical Journal
|
March 16, 2007
QT hysteresis in long-QT syndrome children with exercise testing
Dong-sheng Gao, Wei-yi Fang, Christine Chiu-Man, et al.
Journal of Molecular and Cellular Cardiology
|
July 12, 2008
Sex hormone receptor gene variation associated with phenotype in male hypertrophic cardiomyopathy patients
Joanne M Lind, Christine Chiu, Jodie Ingles, et al.
Geophysical Research Letters
|
December 30, 2022
Near-Cloud Aerosol Retrieval Using Machine Learning Techniques, and Implied Direct Radiative Effects
C Kevin Yang, J Christine Chiu, Alexander Marshak, et al.
Geophysical Research Letters
|
March 8, 2021
Observational Constraints on Warm Cloud Microphysical Processes Using Machine Learning and Optimization Techniques
J Christine Chiu, C Kevin Yang, Peter Jan van Leeuwen, et al.
Journal of Molecular and Cellular Cardiology
|
February 9, 2005
Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: clinical, genetic and functional consequences
Alessandra Doolan, Molly Tebo, Jodie Ingles, et al.
Page
of 3