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Oncogene
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April 4, 2017
Sox2 is dispensable for primary melanoma and metastasis formation
S M Schaefer, C Segalada, P F Cheng, et al.
The Journal of Clinical Investigation
|
January 3, 2014
OTX2 loss causes rod differentiation defect in CRX-associated congenital blindness
Jerome E Roger, Avinash Hiriyanna, Norimoto Gotoh, et al.
Medrxiv : the Preprint Server for Health Sciences
|
October 24, 2023
Shared genetic basis informs the roles of polyunsaturated fatty acids in brain disorders
Huifang Xu, Yitang Sun, Michael Francis, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
May 9, 2001
Enhancement of Sindbis virus self-replicating RNA vaccine potency by linkage of Mycobacterium tuberculosis heat shock protein 70 gene to an antigen gene
W F Cheng, C F Hung, C Y Chai, et al.
The Review of Scientific Instruments
|
August 3, 2021
Upgrade of vacuum ultraviolet spectroscopy system on J-TEXT tokamak
X Y Zhang, W J Qing, X L Zhang, et al.
AJNR. American Journal of Neuroradiology
|
June 19, 2003
Brain MR imaging in neonatal hyperammonemic encephalopathy resulting from proximal urea cycle disorders
Jun-ichi Takanashi, A James Barkovich, Sabrina F Cheng, et al.
Epidemiology and Infection
|
August 6, 1998
Rotavirus infection in Hong Kong: epidemiology and estimates of disease burden
P K Chan, J S Tam, E A Nelson, et al.
Gut
|
May 13, 2005
ATP8B1 mutations in British cases with intrahepatic cholestasis of pregnancy
R Müllenbach, A Bennett, N Tetlow, et al.
Nature Communications
|
January 24, 2018
Publisher Correction: The low affinity neurotrophin receptor CD271 regulates phenotype switching in melanoma
Gaetana Restivo, Johanna Diener, Phil F Cheng, et al.
Nature Communications
|
December 8, 2017
low neurotrophin receptor CD271 regulates phenotype switching in melanoma
Gaetana Restivo, Johanna Diener, Phil F Cheng, et al.
Page
of 147
Search research articles
Search
Showing results (1011-1020 of 1,465) with videos related to
Sort By:
Page
of 147
Oncogene
|
April 4, 2017
Sox2 is dispensable for primary melanoma and metastasis formation
S M Schaefer, C Segalada, P F Cheng, et al.
The Journal of Clinical Investigation
|
January 3, 2014
OTX2 loss causes rod differentiation defect in CRX-associated congenital blindness
Jerome E Roger, Avinash Hiriyanna, Norimoto Gotoh, et al.
Medrxiv : the Preprint Server for Health Sciences
|
October 24, 2023
Shared genetic basis informs the roles of polyunsaturated fatty acids in brain disorders
Huifang Xu, Yitang Sun, Michael Francis, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
May 9, 2001
Enhancement of Sindbis virus self-replicating RNA vaccine potency by linkage of Mycobacterium tuberculosis heat shock protein 70 gene to an antigen gene
W F Cheng, C F Hung, C Y Chai, et al.
The Review of Scientific Instruments
|
August 3, 2021
Upgrade of vacuum ultraviolet spectroscopy system on J-TEXT tokamak
X Y Zhang, W J Qing, X L Zhang, et al.
AJNR. American Journal of Neuroradiology
|
June 19, 2003
Brain MR imaging in neonatal hyperammonemic encephalopathy resulting from proximal urea cycle disorders
Jun-ichi Takanashi, A James Barkovich, Sabrina F Cheng, et al.
Epidemiology and Infection
|
August 6, 1998
Rotavirus infection in Hong Kong: epidemiology and estimates of disease burden
P K Chan, J S Tam, E A Nelson, et al.
Gut
|
May 13, 2005
ATP8B1 mutations in British cases with intrahepatic cholestasis of pregnancy
R Müllenbach, A Bennett, N Tetlow, et al.
Nature Communications
|
January 24, 2018
Publisher Correction: The low affinity neurotrophin receptor CD271 regulates phenotype switching in melanoma
Gaetana Restivo, Johanna Diener, Phil F Cheng, et al.
Nature Communications
|
December 8, 2017
low neurotrophin receptor CD271 regulates phenotype switching in melanoma
Gaetana Restivo, Johanna Diener, Phil F Cheng, et al.
Page
of 147