M J BENNETT - JoVE Visualize

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Progress in Clinical and Biological Research|January 1, 1992

Detection and quantitation of acylcarnitines in plasma and blood spots from patients with inborn errors of fatty acid oxidationE Schmidt-Sommerfeld, D Penn, M Duran, et al.

Clinical Chemistry|February 1, 1992

When do gut flora in the newborn produce 3-phenylpropionic acid? Implications for early diagnosis of medium-chain acyl-CoA dehydrogenase deficiencyM J Bennett, A Bhala, S F Poirier, et al.

Steroids|January 1, 1997

Structure and function of 3 alpha-hydroxysteroid dehydrogenaseT M Penning, M J Bennett, S Smith-Hoog, et al.

The EMBO Journal|April 16, 1999

AUX1 regulates root gravitropism in Arabidopsis by facilitating auxin uptake within root apical tissuesA Marchant, J Kargul, S T May, et al.

Clinical Chemistry|August 1, 1995

Inborn errors of metabolism diagnosed in sudden death cases by acylcarnitine analysis of postmortem bileM S Rashed, P T Ozand, M J Bennett, et al.

Pediatric Research|August 14, 1998

Analysis of carnitine esters by radio-high performance liquid chromatography in cultured skin fibroblasts from patients with mitochondrial fatty acid oxidation disordersE Schmidt-Sommerfeld, P J Bobrowski, D Penn, et al.

Gene Therapy|February 1, 1996

Structural and functional analysis of cationic transfection lipids: the hydrophobic domainR P Balasubramaniam, M J Bennett, A M Aberle, et al.

Biochemical and Biophysical Research Communications|February 24, 1997

Assignment of the human peroxisomal branched-chain acyl-CoA oxidase gene to chromosome 3p21.1-p14.2 by rodent/human somatic cell hybridizationN N Moghrabi, S L Naylor, P P Van Veldhoven, et al.

The Journal of Biological Chemistry|October 12, 2000

Comparison of the interactions of transferrin receptor and transferrin receptor 2 with transferrin and the hereditary hemochromatosis protein HFEA P West, M J Bennett, V M Sellers, et al.

Pediatric Research|July 1, 1993

Renal handling of carnitine in secondary carnitine deficiency disordersC A Stanley, G T Berry, M J Bennett, et al.

Pageof 25

Showing results (171-180 of 245) with videos related to

Sort By:

Pageof 25

Progress in Clinical and Biological Research|January 1, 1992

Detection and quantitation of acylcarnitines in plasma and blood spots from patients with inborn errors of fatty acid oxidationE Schmidt-Sommerfeld, D Penn, M Duran, et al.

Clinical Chemistry|February 1, 1992

When do gut flora in the newborn produce 3-phenylpropionic acid? Implications for early diagnosis of medium-chain acyl-CoA dehydrogenase deficiencyM J Bennett, A Bhala, S F Poirier, et al.

Steroids|January 1, 1997

Structure and function of 3 alpha-hydroxysteroid dehydrogenaseT M Penning, M J Bennett, S Smith-Hoog, et al.

The EMBO Journal|April 16, 1999

AUX1 regulates root gravitropism in Arabidopsis by facilitating auxin uptake within root apical tissuesA Marchant, J Kargul, S T May, et al.

Clinical Chemistry|August 1, 1995

Inborn errors of metabolism diagnosed in sudden death cases by acylcarnitine analysis of postmortem bileM S Rashed, P T Ozand, M J Bennett, et al.

Pediatric Research|August 14, 1998

Analysis of carnitine esters by radio-high performance liquid chromatography in cultured skin fibroblasts from patients with mitochondrial fatty acid oxidation disordersE Schmidt-Sommerfeld, P J Bobrowski, D Penn, et al.

Gene Therapy|February 1, 1996

Structural and functional analysis of cationic transfection lipids: the hydrophobic domainR P Balasubramaniam, M J Bennett, A M Aberle, et al.

Biochemical and Biophysical Research Communications|February 24, 1997

Assignment of the human peroxisomal branched-chain acyl-CoA oxidase gene to chromosome 3p21.1-p14.2 by rodent/human somatic cell hybridizationN N Moghrabi, S L Naylor, P P Van Veldhoven, et al.

The Journal of Biological Chemistry|October 12, 2000

Comparison of the interactions of transferrin receptor and transferrin receptor 2 with transferrin and the hereditary hemochromatosis protein HFEA P West, M J Bennett, V M Sellers, et al.

Pediatric Research|July 1, 1993

Renal handling of carnitine in secondary carnitine deficiency disordersC A Stanley, G T Berry, M J Bennett, et al.

Pageof 25