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J Prieur

Showing results (61-70 of 122) with videos related to

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Laboratory Animal Science|February 1, 1979
Partial oculocutaneous albinism in Mystromys albicaudatus: nonhomology with the Chediak-Higashi syndromeD J Prieur, H M Olson, D M Young
The American Journal of Pathology|December 1, 1991
Ovine GM-1 gangliosidosisD J Prieur, A J Ahern-Rindell, R D Murnane
The American Journal of Pathology|October 1, 1989
Lectin histochemistry of an ovine lysosomal storage disease with deficiencies of beta-galactosidase and alpha-neuraminidaseR D Murnane, A J Ahern-Rindell, D J Prieur
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|November 1, 1991
Ultrastructural lesions of ovine GM1 gangliosidosisR D Murnane, A J Ahern-Rindell, D J Prieur
Somatic Cell and Molecular Genetics|November 1, 1989
Interspecific genetic complementation analysis of human and sheep fibroblasts with beta-galactosidase deficiencyA J Ahern-Rindell, R D Murnane, D J Prieur
Biochemical Genetics|December 1, 1988
Beta-galactosidase activity in fibroblasts and tissues from sheep with a lysosomal storage diseaseA J Ahern-Rindell, R D Murnane, D J Prieur
American Journal of Hematology|November 1, 1981
Evaluation of the platelet storage pool deficiency in the feline counterpart of the Chediak-Higashi syndromeK M Meyers, C L Seachord, H Holmsen, et al.
Acta Gastro-Enterologica Belgica|March 1, 1979
[Hermans's syndrome and gastric cancer (author's transl)]P Rampal, C Karsenty, J Prieur, et al.
Journal of Clinical Microbiology|August 1, 1985
Serum susceptibility of Haemophilus somnus from bovine clinical cases and carriersL B Corbeil, K Blau, D J Prieur, et al.
Veterinary Pathology|May 23, 1998
Clinical and morphologic features of mucopolysaccharidosis type II in a dog: naturally occurring model of Hunter syndromeM J Wilkerson, D C Lewis, S L Marks, et al.
Pageof 13

Showing results (61-70 of 122) with videos related to

Sort By:
Pageof 13
Laboratory Animal Science|February 1, 1979
Partial oculocutaneous albinism in Mystromys albicaudatus: nonhomology with the Chediak-Higashi syndromeD J Prieur, H M Olson, D M Young
The American Journal of Pathology|December 1, 1991
Ovine GM-1 gangliosidosisD J Prieur, A J Ahern-Rindell, R D Murnane
The American Journal of Pathology|October 1, 1989
Lectin histochemistry of an ovine lysosomal storage disease with deficiencies of beta-galactosidase and alpha-neuraminidaseR D Murnane, A J Ahern-Rindell, D J Prieur
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|November 1, 1991
Ultrastructural lesions of ovine GM1 gangliosidosisR D Murnane, A J Ahern-Rindell, D J Prieur
Somatic Cell and Molecular Genetics|November 1, 1989
Interspecific genetic complementation analysis of human and sheep fibroblasts with beta-galactosidase deficiencyA J Ahern-Rindell, R D Murnane, D J Prieur
Biochemical Genetics|December 1, 1988
Beta-galactosidase activity in fibroblasts and tissues from sheep with a lysosomal storage diseaseA J Ahern-Rindell, R D Murnane, D J Prieur
American Journal of Hematology|November 1, 1981
Evaluation of the platelet storage pool deficiency in the feline counterpart of the Chediak-Higashi syndromeK M Meyers, C L Seachord, H Holmsen, et al.
Acta Gastro-Enterologica Belgica|March 1, 1979
[Hermans's syndrome and gastric cancer (author's transl)]P Rampal, C Karsenty, J Prieur, et al.
Journal of Clinical Microbiology|August 1, 1985
Serum susceptibility of Haemophilus somnus from bovine clinical cases and carriersL B Corbeil, K Blau, D J Prieur, et al.
Veterinary Pathology|May 23, 1998
Clinical and morphologic features of mucopolysaccharidosis type II in a dog: naturally occurring model of Hunter syndromeM J Wilkerson, D C Lewis, S L Marks, et al.
Pageof 13