C B Poole|D I Crane - JoVE Visualize

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European Journal of Immunology|August 1, 1985

Production and characterization of antibody probes directed at constant regions of the alpha and beta subunit of the human T cell receptorM Fabbi, O Acuto, A Bensussan, et al.

Gene|September 1, 1990

Nucleotide sequence of the phage lambda gt11 SacI-KpnI lacZ regionL S Moran, C V Maina, C B Poole, et al.

Experimental Parasitology|September 1, 1993

Brugia malayi and Brugia pahangi: synthetic biotin labeling of oligonucleotide probes for use in species-specific detection assaysS A Williams, C B Poole, D Landry, et al.

American Journal of Human Genetics|August 12, 1999

PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disordersY Liu, J Björkman, A Urquhart, et al.

European Journal of Pediatrics|November 1, 1992

Ultrastructure and immunocytochemistry of hepatic peroxisomes in rhizomelic chondrodysplasia punctataJ L Hughes, A Poulos, D I Crane, et al.

Archives of Biochemistry and Biophysics|August 1, 1990

Immunocytochemical studies on the localization of 5-aminolevulinate synthase in rat liverM Rohde, G Srivastava, D B Rylatt, et al.

Molecular and Biochemical Parasitology|November 12, 1996

Carboxy-terminal sequence divergence and processing of the polyprotein antigen from Dirofilaria immitisC B Poole, L J Hornstra, J S Benner, et al.

The Journal of Cell Biology|October 1, 1996

Pex13p is an SH3 protein of the peroxisome membrane and a docking factor for the predominantly cytoplasmic PTs1 receptorS J Gould, J E Kalish, J C Morrell, et al.

Human Genetics|September 10, 1999

A common PEX1 frameshift mutation in patients with disorders of peroxisome biogenesis correlates with the severe Zellweger syndrome phenotypeM A Maxwell, P V Nelson, S J Chin, et al.

The Journal of Experimental Medicine|June 1, 1985

Molecular analysis of T cell receptor (Ti) variable region (V) gene expression. Evidence that a single Ti beta V gene family can be used in formation of V domains on phenotypically and functionally diverse T cell populationsO Acuto, T J Campen, H D Royer, et al.

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Showing results (31-40 of 46) with videos related to

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Pageof 5

European Journal of Immunology|August 1, 1985

Production and characterization of antibody probes directed at constant regions of the alpha and beta subunit of the human T cell receptorM Fabbi, O Acuto, A Bensussan, et al.

Gene|September 1, 1990

Nucleotide sequence of the phage lambda gt11 SacI-KpnI lacZ regionL S Moran, C V Maina, C B Poole, et al.

Experimental Parasitology|September 1, 1993

Brugia malayi and Brugia pahangi: synthetic biotin labeling of oligonucleotide probes for use in species-specific detection assaysS A Williams, C B Poole, D Landry, et al.

American Journal of Human Genetics|August 12, 1999

PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disordersY Liu, J Björkman, A Urquhart, et al.

European Journal of Pediatrics|November 1, 1992

Ultrastructure and immunocytochemistry of hepatic peroxisomes in rhizomelic chondrodysplasia punctataJ L Hughes, A Poulos, D I Crane, et al.

Archives of Biochemistry and Biophysics|August 1, 1990

Immunocytochemical studies on the localization of 5-aminolevulinate synthase in rat liverM Rohde, G Srivastava, D B Rylatt, et al.

Molecular and Biochemical Parasitology|November 12, 1996

Carboxy-terminal sequence divergence and processing of the polyprotein antigen from Dirofilaria immitisC B Poole, L J Hornstra, J S Benner, et al.

The Journal of Cell Biology|October 1, 1996

Pex13p is an SH3 protein of the peroxisome membrane and a docking factor for the predominantly cytoplasmic PTs1 receptorS J Gould, J E Kalish, J C Morrell, et al.

Human Genetics|September 10, 1999

A common PEX1 frameshift mutation in patients with disorders of peroxisome biogenesis correlates with the severe Zellweger syndrome phenotypeM A Maxwell, P V Nelson, S J Chin, et al.

The Journal of Experimental Medicine|June 1, 1985

Molecular analysis of T cell receptor (Ti) variable region (V) gene expression. Evidence that a single Ti beta V gene family can be used in formation of V domains on phenotypically and functionally diverse T cell populationsO Acuto, T J Campen, H D Royer, et al.

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