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I Tein

Showing results (1-10 of 39) with videos related to

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Journal of Inherited Metabolic Disease|August 2, 2003
Carnitine transport: pathophysiology and metabolism of known molecular defectsI Tein
Pediatric Research|January 7, 2000
Metabolic disease in the fetus predisposes to maternal hepatic complications of pregnancyI Tein
Seminars in Perinatology|May 20, 1999
Neonatal metabolic myopathiesI Tein
Seminars in Pediatric Neurology|June 1, 1996
Metabolic myopathiesI Tein
Archives of Neurology|March 1, 1985
Possible valproate teratogenicityI Tein, D L MacGregor
Biochemical and Biophysical Research Communications|November 2, 1999
GFP-Human high-affinity carnitine transporter OCTN2 protein: subcellular localization and functional restoration of carnitine uptake in mutant cell lines with the carnitine transporter defectA M Lamhonwah, I Tein
Biochemical and Biophysical Research Communications|October 28, 1994
Reversal of valproic acid-associated impairment of carnitine uptake in cultured human skin fibroblastsI Tein, Z W Xie
Biochemical and Biophysical Research Communications|November 25, 1998
Carnitine uptake defect: frameshift mutations in the human plasmalemmal carnitine transporter geneA M Lamhonwah, I Tein
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 30, 1996
The human plasmalemmal carnitine transporter defect is expressed in cultured lymphoblasts: a new non-invasive method for diagnosisI Tein, Z W Xie
Critical Care Medicine|October 1, 1984
Increased intracranial pressure associated with N-acetylcysteine inhalation therapyJ Venturelli, I Tein, R Hollenberg
Pageof 4

Showing results (1-10 of 39) with videos related to

Sort By:
Pageof 4
Journal of Inherited Metabolic Disease|August 2, 2003
Carnitine transport: pathophysiology and metabolism of known molecular defectsI Tein
Pediatric Research|January 7, 2000
Metabolic disease in the fetus predisposes to maternal hepatic complications of pregnancyI Tein
Seminars in Perinatology|May 20, 1999
Neonatal metabolic myopathiesI Tein
Seminars in Pediatric Neurology|June 1, 1996
Metabolic myopathiesI Tein
Archives of Neurology|March 1, 1985
Possible valproate teratogenicityI Tein, D L MacGregor
Biochemical and Biophysical Research Communications|November 2, 1999
GFP-Human high-affinity carnitine transporter OCTN2 protein: subcellular localization and functional restoration of carnitine uptake in mutant cell lines with the carnitine transporter defectA M Lamhonwah, I Tein
Biochemical and Biophysical Research Communications|October 28, 1994
Reversal of valproic acid-associated impairment of carnitine uptake in cultured human skin fibroblastsI Tein, Z W Xie
Biochemical and Biophysical Research Communications|November 25, 1998
Carnitine uptake defect: frameshift mutations in the human plasmalemmal carnitine transporter geneA M Lamhonwah, I Tein
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 30, 1996
The human plasmalemmal carnitine transporter defect is expressed in cultured lymphoblasts: a new non-invasive method for diagnosisI Tein, Z W Xie
Critical Care Medicine|October 1, 1984
Increased intracranial pressure associated with N-acetylcysteine inhalation therapyJ Venturelli, I Tein, R Hollenberg
Pageof 4