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D Prasad

Showing results (281-290 of 337) with videos related to

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The Journal of Biological Chemistry|April 29, 2000
Expression and differential polarization of the reduced-folate transporter-1 and the folate receptor alpha in mammalian retinal pigment epitheliumC D Chancy, R Kekuda, W Huang, et al.
Glia|November 11, 2011
Regulation of proton-coupled folate transporter in retinal Müller cells by the antipsoriatic drug monomethylfumarateB Renee Bozard, Paresh P Chothe, Amany Tawfik, et al.
Biochimica Et Biophysica Acta|August 19, 2007
Cloning and functional characterization of human SMCT2 (SLC5A12) and expression pattern of the transporter in kidneyE Gopal, N S Umapathy, P M Martin, et al.
Molecular Genetics and Metabolism|September 22, 2007
Spontaneous development of intestinal and colonic atrophy and inflammation in the carnitine-deficient jvs (OCTN2(-/-)) micePrem S Shekhawat, Sonne R Srinivas, Dietrich Matern, et al.
British Journal of Pharmacology|October 18, 2016
Amino acid transporter SLC6A14 is a novel and effective drug target for pancreatic cancerV Coothankandaswamy, S Cao, Y Xu, et al.
Biochimica Et Biophysica Acta|May 21, 2005
Upregulation of the amino acid transporter ATB0,+ (SLC6A14) in colorectal cancer and metastasis in humansNaren Gupta, Seiji Miyauchi, Robert G Martindale, et al.
The Journal of Biological Chemistry|May 18, 1999
Human placental Na+-dependent multivitamin transporter. Cloning, functional expression, gene structure, and chromosomal localizationH Wang, W Huang, Y J Fei, et al.
Scientific Reports|December 8, 2018
Loss of interneurons and disruption of perineuronal nets in the cerebral cortex following hypoxia-ischaemia in near-term fetal sheepTania M Fowke, Robert Galinsky, Joanne O Davidson, et al.
The Journal of Biological Chemistry|March 24, 1995
Human intestinal H+/peptide cotransporter. Cloning, functional expression, and chromosomal localizationR Liang, Y J Fei, P D Prasad, et al.
Archives of Otolaryngology--Head & Neck Surgery|February 15, 2001
Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13)E M De Leenheer, H H Kunst, W T McGuirt, et al.
Pageof 34

Showing results (281-290 of 337) with videos related to

Sort By:
Pageof 34
The Journal of Biological Chemistry|April 29, 2000
Expression and differential polarization of the reduced-folate transporter-1 and the folate receptor alpha in mammalian retinal pigment epitheliumC D Chancy, R Kekuda, W Huang, et al.
Glia|November 11, 2011
Regulation of proton-coupled folate transporter in retinal Müller cells by the antipsoriatic drug monomethylfumarateB Renee Bozard, Paresh P Chothe, Amany Tawfik, et al.
Biochimica Et Biophysica Acta|August 19, 2007
Cloning and functional characterization of human SMCT2 (SLC5A12) and expression pattern of the transporter in kidneyE Gopal, N S Umapathy, P M Martin, et al.
Molecular Genetics and Metabolism|September 22, 2007
Spontaneous development of intestinal and colonic atrophy and inflammation in the carnitine-deficient jvs (OCTN2(-/-)) micePrem S Shekhawat, Sonne R Srinivas, Dietrich Matern, et al.
British Journal of Pharmacology|October 18, 2016
Amino acid transporter SLC6A14 is a novel and effective drug target for pancreatic cancerV Coothankandaswamy, S Cao, Y Xu, et al.
Biochimica Et Biophysica Acta|May 21, 2005
Upregulation of the amino acid transporter ATB0,+ (SLC6A14) in colorectal cancer and metastasis in humansNaren Gupta, Seiji Miyauchi, Robert G Martindale, et al.
The Journal of Biological Chemistry|May 18, 1999
Human placental Na+-dependent multivitamin transporter. Cloning, functional expression, gene structure, and chromosomal localizationH Wang, W Huang, Y J Fei, et al.
Scientific Reports|December 8, 2018
Loss of interneurons and disruption of perineuronal nets in the cerebral cortex following hypoxia-ischaemia in near-term fetal sheepTania M Fowke, Robert Galinsky, Joanne O Davidson, et al.
The Journal of Biological Chemistry|March 24, 1995
Human intestinal H+/peptide cotransporter. Cloning, functional expression, and chromosomal localizationR Liang, Y J Fei, P D Prasad, et al.
Archives of Otolaryngology--Head & Neck Surgery|February 15, 2001
Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13)E M De Leenheer, H H Kunst, W T McGuirt, et al.
Pageof 34