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Nucleic Acids Research
|
April 1, 2005
Efficient and seamless DNA recombineering using a thymidylate synthase A selection system in Escherichia coli
Queenie N Y Wong, Vivian C W Ng, Marie C M Lin, et al.
Journal of Microencapsulation
|
July 26, 2003
Release of paclitaxel from polylactide-co-glycolide (PLGA) microparticles and discs under irradiation
J Wang, C W Ng, K Y Win, et al.
Epilepsia
|
September 17, 2013
Seizure predisposition after perinatal hypoxia: effects of subsequent age and of an epilepsy predisposing gene mutation
A Soren Leonard, S Nabeel Hyder, Brad J Kolls, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine
|
October 11, 2017
Prevalence of Cardiac Arrhythmias in Asian Patients With Obstructive Sleep Apnea: A Singapore Sleep Center Experience
Wei Li Neo, Adele C W Ng, Mahalakshmi Rangabashyam, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
August 26, 2019
The presence of Aspergillus fumigatus is associated with worse respiratory quality of life in cystic fibrosis
Gina Hong, Kevin Alby, Sharon C W Ng, et al.
Protein and Peptide Letters
|
June 22, 2016
Activities of Venom Proteins and Peptides with Possible Therapeutic Applications from Bees and WASPS
Xiujuan Ye, Suzhen Guan, Jiwen Liu, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society
|
September 28, 2010
A splice-site mutation leads to haploinsufficiency of EXT2 mRNA for a dominant trait in a large family with multiple osteochondromas
Liu Yang, Wing Sum Hui, Wilson C W Chan, et al.
American Journal of Human Genetics
|
December 21, 2010
Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis
Eva Klopocki, Silke Lohan, Francesco Brancati, et al.
Diabetes/Metabolism Research and Reviews
|
January 21, 2020
Circulating branched-chain amino acids and incident heart failure in type 2 diabetes: The Hong Kong Diabetes Register
Lee-Ling Lim, Eric S H Lau, Erik Fung, et al.
Human Molecular Genetics
|
April 4, 2007
COL10A1 nonsense and frame-shift mutations have a gain-of-function effect on the growth plate in human and mouse metaphyseal chondrodysplasia type Schmid
Matthew S P Ho, Kwok Yeung Tsang, Rebecca L K Lo, et al.
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of 9
Search research articles
Search
Showing results (21-30 of 87) with videos related to
Sort By:
Page
of 9
Nucleic Acids Research
|
April 1, 2005
Efficient and seamless DNA recombineering using a thymidylate synthase A selection system in Escherichia coli
Queenie N Y Wong, Vivian C W Ng, Marie C M Lin, et al.
Journal of Microencapsulation
|
July 26, 2003
Release of paclitaxel from polylactide-co-glycolide (PLGA) microparticles and discs under irradiation
J Wang, C W Ng, K Y Win, et al.
Epilepsia
|
September 17, 2013
Seizure predisposition after perinatal hypoxia: effects of subsequent age and of an epilepsy predisposing gene mutation
A Soren Leonard, S Nabeel Hyder, Brad J Kolls, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine
|
October 11, 2017
Prevalence of Cardiac Arrhythmias in Asian Patients With Obstructive Sleep Apnea: A Singapore Sleep Center Experience
Wei Li Neo, Adele C W Ng, Mahalakshmi Rangabashyam, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
August 26, 2019
The presence of Aspergillus fumigatus is associated with worse respiratory quality of life in cystic fibrosis
Gina Hong, Kevin Alby, Sharon C W Ng, et al.
Protein and Peptide Letters
|
June 22, 2016
Activities of Venom Proteins and Peptides with Possible Therapeutic Applications from Bees and WASPS
Xiujuan Ye, Suzhen Guan, Jiwen Liu, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society
|
September 28, 2010
A splice-site mutation leads to haploinsufficiency of EXT2 mRNA for a dominant trait in a large family with multiple osteochondromas
Liu Yang, Wing Sum Hui, Wilson C W Chan, et al.
American Journal of Human Genetics
|
December 21, 2010
Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis
Eva Klopocki, Silke Lohan, Francesco Brancati, et al.
Diabetes/Metabolism Research and Reviews
|
January 21, 2020
Circulating branched-chain amino acids and incident heart failure in type 2 diabetes: The Hong Kong Diabetes Register
Lee-Ling Lim, Eric S H Lau, Erik Fung, et al.
Human Molecular Genetics
|
April 4, 2007
COL10A1 nonsense and frame-shift mutations have a gain-of-function effect on the growth plate in human and mouse metaphyseal chondrodysplasia type Schmid
Matthew S P Ho, Kwok Yeung Tsang, Rebecca L K Lo, et al.
Page
of 9