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S Chong

Showing results (521-530 of 976) with videos related to

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Clinical Chemistry|September 7, 2013
Methylation-specific triplet-primed PCR and melting curve analysis as a rapid screening tool for identifying actionable FMR1 genotypesClara R L Teo, Indhu-Shree Rajan-Babu, Hai-Yang Law, et al.
Annals of Plastic Surgery|March 15, 2014
Biomechanical comparison of different suturing techniques in rabbit medial gastrocnemius muscle laceration repairMin He, Sandeep J Sebastin, Aaron W T Gan, et al.
World Journal of Surgery|July 16, 2016
Innovative Patient Safety Curriculum Using iPAD Game (PASSED) Improved Patient Safety Concepts in Undergraduate Medical StudentsA W C Kow, B L S Ang, C S Chong, et al.
Lancet (London, England)|September 17, 1988
Clinical heterogeneity of central pontine myelinolysisC P Bearcroft, K Metcalfe, M I McCarthy, et al.
European Journal of Haematology|January 8, 2013
Evidence of differential selection for the -α(3.7) and -α(4.2) single-α-globin gene deletions within the same populationZhi Min Yap, Kar Mun Sun, Clara R L Teo, et al.
Journal of Virology|January 7, 1998
Hepatitis G virus encodes protease activities which can effect processing of the virus putative nonstructural proteinsA S Belyaev, S Chong, A Novikov, et al.
Cellular Immunology|April 15, 1991
Ability of cell-sized beads bearing tumor cell membrane proteins to stimulate LAK cells to secrete interferon-gamma and tumor necrosis factor-alphaA S Chong, J K Pinkard, K S Lam, et al.
Immunological Investigations|October 1, 1990
Regulation of tumor necrosis factor secretion in leukocytes from alpha-1-antitrypsin deficient humansP Scuderi, P R Finley, B Y Shon, et al.
The Pharmacogenomics Journal|June 1, 2011
An update on ABCB1 pharmacogenetics: insights from a 3D model into the location and evolutionary conservation of residues corresponding to SNPs associated with drug pharmacokineticsS J Wolf, M Bachtiar, J Wang, et al.
Human Molecular Genetics|February 1, 1997
Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndromeC Lo Nigro, C S Chong, A C Smith, et al.
Pageof 98

Showing results (521-530 of 976) with videos related to

Sort By:
Pageof 98
Clinical Chemistry|September 7, 2013
Methylation-specific triplet-primed PCR and melting curve analysis as a rapid screening tool for identifying actionable FMR1 genotypesClara R L Teo, Indhu-Shree Rajan-Babu, Hai-Yang Law, et al.
Annals of Plastic Surgery|March 15, 2014
Biomechanical comparison of different suturing techniques in rabbit medial gastrocnemius muscle laceration repairMin He, Sandeep J Sebastin, Aaron W T Gan, et al.
World Journal of Surgery|July 16, 2016
Innovative Patient Safety Curriculum Using iPAD Game (PASSED) Improved Patient Safety Concepts in Undergraduate Medical StudentsA W C Kow, B L S Ang, C S Chong, et al.
Lancet (London, England)|September 17, 1988
Clinical heterogeneity of central pontine myelinolysisC P Bearcroft, K Metcalfe, M I McCarthy, et al.
European Journal of Haematology|January 8, 2013
Evidence of differential selection for the -α(3.7) and -α(4.2) single-α-globin gene deletions within the same populationZhi Min Yap, Kar Mun Sun, Clara R L Teo, et al.
Journal of Virology|January 7, 1998
Hepatitis G virus encodes protease activities which can effect processing of the virus putative nonstructural proteinsA S Belyaev, S Chong, A Novikov, et al.
Cellular Immunology|April 15, 1991
Ability of cell-sized beads bearing tumor cell membrane proteins to stimulate LAK cells to secrete interferon-gamma and tumor necrosis factor-alphaA S Chong, J K Pinkard, K S Lam, et al.
Immunological Investigations|October 1, 1990
Regulation of tumor necrosis factor secretion in leukocytes from alpha-1-antitrypsin deficient humansP Scuderi, P R Finley, B Y Shon, et al.
The Pharmacogenomics Journal|June 1, 2011
An update on ABCB1 pharmacogenetics: insights from a 3D model into the location and evolutionary conservation of residues corresponding to SNPs associated with drug pharmacokineticsS J Wolf, M Bachtiar, J Wang, et al.
Human Molecular Genetics|February 1, 1997
Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndromeC Lo Nigro, C S Chong, A C Smith, et al.
Pageof 98