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Journal of Chromatography. B, Biomedical Sciences and Applications
|
October 5, 2001
Quantification of naltrexone and 6,beta-naltrexol in plasma and milk using gas chromatography-mass spectrometry. Application to studies in the lactating sheep
C F Chan, G M Chiswell, R Bencini, et al.
Neuroimage
|
February 2, 2006
Mapping radiation dose distribution on the fractional anisotropy map: applications in the assessment of treatment-induced white matter injury
Deqiang Qiu, Lucullus H T Leung, Dora L W Kwong, et al.
Pediatric Blood & Cancer
|
December 14, 2004
Cortical laminar necrosis in childhood intracranial germ cell tumor survivors
Pek-Lan Khong, Kim-Ching Ng, Dora L W Kwong, et al.
Human Movement Science
|
April 6, 2004
An experimentally confirmed statistical model on arm movement
M F Chan, D R Giddings, C S Chandler, et al.
Oncotarget
|
October 21, 2017
Mitochondrial genome variation and prostate cancer: a review of the mutational landscape and application to clinical management
Anton M F Kalsbeek, Eva K F Chan, Niall M Corcoran, et al.
Journal of Cutaneous Pathology
|
August 11, 2017
Development of RET mutant cutaneous angiosarcoma during BRAF inhibitor therapy
Julia Dai, Christian A Kunder, Emily Y Chu, et al.
Endocrine Development
|
February 9, 2013
ACTH resistance: genes and mechanisms
E Meimaridou, C R Hughes, J Kowalczyk, et al.
Biochimica Et Biophysica Acta
|
December 14, 1987
Novel aspects of vitamin A metabolism in the dog: distribution of lipoprotein retinyl esters in vitamin A-deprived and cholesterol-fed animals
D E Wilson, J Hejazi, N L Elstad, et al.
Anti-Cancer Drugs
|
October 11, 2003
Induction of colon cancer cell death by 7-hydroxystaurosporine (UCN-01) is associated with increased p38 MAPK and decreased Bcl-xL
Ursula P F Chan, Janet F Y Lee, S H Wang, et al.
European Journal of Endocrinology
|
November 12, 2009
Isolated Addison's disease is unlikely to be caused by mutations in MC2R, MRAP or STAR, three genes responsible for familial glucocorticoid deficiency
R P Dias, L F Chan, L A Metherell, et al.
Page
of 138
Search research articles
Search
Showing results (711-720 of 1,377) with videos related to
Sort By:
Page
of 138
Journal of Chromatography. B, Biomedical Sciences and Applications
|
October 5, 2001
Quantification of naltrexone and 6,beta-naltrexol in plasma and milk using gas chromatography-mass spectrometry. Application to studies in the lactating sheep
C F Chan, G M Chiswell, R Bencini, et al.
Neuroimage
|
February 2, 2006
Mapping radiation dose distribution on the fractional anisotropy map: applications in the assessment of treatment-induced white matter injury
Deqiang Qiu, Lucullus H T Leung, Dora L W Kwong, et al.
Pediatric Blood & Cancer
|
December 14, 2004
Cortical laminar necrosis in childhood intracranial germ cell tumor survivors
Pek-Lan Khong, Kim-Ching Ng, Dora L W Kwong, et al.
Human Movement Science
|
April 6, 2004
An experimentally confirmed statistical model on arm movement
M F Chan, D R Giddings, C S Chandler, et al.
Oncotarget
|
October 21, 2017
Mitochondrial genome variation and prostate cancer: a review of the mutational landscape and application to clinical management
Anton M F Kalsbeek, Eva K F Chan, Niall M Corcoran, et al.
Journal of Cutaneous Pathology
|
August 11, 2017
Development of RET mutant cutaneous angiosarcoma during BRAF inhibitor therapy
Julia Dai, Christian A Kunder, Emily Y Chu, et al.
Endocrine Development
|
February 9, 2013
ACTH resistance: genes and mechanisms
E Meimaridou, C R Hughes, J Kowalczyk, et al.
Biochimica Et Biophysica Acta
|
December 14, 1987
Novel aspects of vitamin A metabolism in the dog: distribution of lipoprotein retinyl esters in vitamin A-deprived and cholesterol-fed animals
D E Wilson, J Hejazi, N L Elstad, et al.
Anti-Cancer Drugs
|
October 11, 2003
Induction of colon cancer cell death by 7-hydroxystaurosporine (UCN-01) is associated with increased p38 MAPK and decreased Bcl-xL
Ursula P F Chan, Janet F Y Lee, S H Wang, et al.
European Journal of Endocrinology
|
November 12, 2009
Isolated Addison's disease is unlikely to be caused by mutations in MC2R, MRAP or STAR, three genes responsible for familial glucocorticoid deficiency
R P Dias, L F Chan, L A Metherell, et al.
Page
of 138