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Clinical Chemistry
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September 7, 2013
Methylation-specific triplet-primed PCR and melting curve analysis as a rapid screening tool for identifying actionable FMR1 genotypes
Clara 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 repair
Min 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 Students
A W C Kow, B L S Ang, C S Chong, et al.
Lancet (London, England)
|
September 17, 1988
Clinical heterogeneity of central pontine myelinolysis
C 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 population
Zhi 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 proteins
A 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-alpha
A 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 humans
P 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 pharmacokinetics
S 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 syndrome
C Lo Nigro, C S Chong, A C Smith, et al.
Page
of 98
Search research articles
Search
Showing results (521-530 of 976) with videos related to
Sort By:
Page
of 98
Clinical Chemistry
|
September 7, 2013
Methylation-specific triplet-primed PCR and melting curve analysis as a rapid screening tool for identifying actionable FMR1 genotypes
Clara 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 repair
Min 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 Students
A W C Kow, B L S Ang, C S Chong, et al.
Lancet (London, England)
|
September 17, 1988
Clinical heterogeneity of central pontine myelinolysis
C 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 population
Zhi 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 proteins
A 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-alpha
A 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 humans
P 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 pharmacokinetics
S 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 syndrome
C Lo Nigro, C S Chong, A C Smith, et al.
Page
of 98