R J Desnick|S R Thorpe|M B Fiddler - JoVE Visualize

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The Journal of Biological Chemistry|November 25, 1985

Loci of catabolism of beta-very low density lipoprotein in vivo delineated with a residualizing label, 125I-dilactitol tyramineA Daugherty, S R Thorpe, L G Lange, et al.

Cancer Research|July 15, 1995

Effects of radiolabeling monoclonal antibodies with a residualizing iodine radiolabel on the accretion of radioisotope in tumorsR Stein, D M Goldenberg, S R Thorpe, et al.

Scandinavian Journal of Immunology|December 1, 1990

Site of catabolism of autologous and heterologous IgA in non-human primatesZ Moldoveanu, I Moro, J Radl, et al.

American Journal of Human Genetics|March 3, 1999

Diaphyseal medullary stenosis with malignant fibrous histiocytoma: a hereditary bone dysplasia/cancer syndrome maps to 9p21-22J A Martignetti, R J Desnick, E Aliprandis, et al.

Clinical Genetics|August 1, 1984

Reduced plasma concentrations of total, low density lipoprotein and high density lipoprotein cholesterol in patients with Gaucher type I diseaseH Ginsberg, G A Grabowski, J C Gibson, et al.

Proceedings of the National Academy of Sciences of the United States of America|September 1, 1981

Regional gene assignment of human porphobilinogen deaminase and esterase A4 to chromosome 11q23 leads to 11qterA L Wang, F X Arredondo-Vega, P F Giampietro, et al.

JAMA|October 23, 1997

Prenatal genetic carrier testing using triple disease screeningC M Eng, C Schechter, J Robinowitz, et al.

FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 12, 2000

Infusion of recombinant human acid sphingomyelinase into niemann-pick disease mice leads to visceral, but not neurological, correction of the pathophysiologyS R Miranda, X He, C M Simonaro, et al.

Human Molecular Genetics|October 1, 1994

Fabry disease: twenty-three mutations including sense and antisense CpG alterations and identification of a deletional hot-spot in the alpha-galactosidase A geneC M Eng, D J Niehaus, A L Enriquez, et al.

Human Genetics|May 1, 1991

Regional assignment of the human uroporphyrinogen III synthase (UROS) gene to chromosome 10q25.2----q26.3K H Astrin, C A Warner, H W Yoo, et al.

Pageof 40

Showing results (261-270 of 399) with videos related to

Sort By:

Pageof 40

The Journal of Biological Chemistry|November 25, 1985

Loci of catabolism of beta-very low density lipoprotein in vivo delineated with a residualizing label, 125I-dilactitol tyramineA Daugherty, S R Thorpe, L G Lange, et al.

Cancer Research|July 15, 1995

Effects of radiolabeling monoclonal antibodies with a residualizing iodine radiolabel on the accretion of radioisotope in tumorsR Stein, D M Goldenberg, S R Thorpe, et al.

Scandinavian Journal of Immunology|December 1, 1990

Site of catabolism of autologous and heterologous IgA in non-human primatesZ Moldoveanu, I Moro, J Radl, et al.

American Journal of Human Genetics|March 3, 1999

Diaphyseal medullary stenosis with malignant fibrous histiocytoma: a hereditary bone dysplasia/cancer syndrome maps to 9p21-22J A Martignetti, R J Desnick, E Aliprandis, et al.

Clinical Genetics|August 1, 1984

Reduced plasma concentrations of total, low density lipoprotein and high density lipoprotein cholesterol in patients with Gaucher type I diseaseH Ginsberg, G A Grabowski, J C Gibson, et al.

Proceedings of the National Academy of Sciences of the United States of America|September 1, 1981

Regional gene assignment of human porphobilinogen deaminase and esterase A4 to chromosome 11q23 leads to 11qterA L Wang, F X Arredondo-Vega, P F Giampietro, et al.

JAMA|October 23, 1997

Prenatal genetic carrier testing using triple disease screeningC M Eng, C Schechter, J Robinowitz, et al.

FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 12, 2000

Infusion of recombinant human acid sphingomyelinase into niemann-pick disease mice leads to visceral, but not neurological, correction of the pathophysiologyS R Miranda, X He, C M Simonaro, et al.

Human Molecular Genetics|October 1, 1994

Fabry disease: twenty-three mutations including sense and antisense CpG alterations and identification of a deletional hot-spot in the alpha-galactosidase A geneC M Eng, D J Niehaus, A L Enriquez, et al.

Human Genetics|May 1, 1991

Regional assignment of the human uroporphyrinogen III synthase (UROS) gene to chromosome 10q25.2----q26.3K H Astrin, C A Warner, H W Yoo, et al.

Pageof 40