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E Gal

Showing results (31-40 of 66) with videos related to

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International Archives of Allergy and Applied Immunology|January 1, 1988
Western immunoblotting of cereal proteins with monoclonal antibodies to wheat gliadin to investigate coeliac diseaseA R Freedman, G Galfre, E Gal, et al.
The American Journal of Medicine|December 1, 1983
Normolipemic subcutaneous xanthomatosisR Fleischmajer, E J Schaefer, A E Gal, et al.
Presse Medicale (Paris, France : 1983)|February 15, 1997
[Autochthonous viral hepatitis E in Languedoc-Roussillon]P Corne, S Yeche, E Gal, et al.
Acta Cytologica|September 29, 2001
Granulomatous inflammation of the breast in a pregnant woman: report of a case with fine needle aspiration diagnosisA W Poniecka, P Krasuski, E Gal, et al.
Chemistry and Physics of Lipids|December 15, 1986
Animal and cellular models of sphingolipid storage disorders of humansA E Gal, A L Weis, J M Quirk, et al.
The Journal of Biological Chemistry|August 10, 1973
Isolation and characterization of glucocerebrosidase from human placental tissueP G Pentchev, R O Brady, S R Hibbert, et al.
The Journal of Biological Chemistry|June 10, 1974
Isolation and relationship of human hexosaminidasesJ F Tallman, R O Brady, J M Quirk, et al.
Birth Defects Original Article Series|January 1, 1980
Status of enzyme replacement therapy for Gaucher diseaseR O Brady, J A Barranger, A E Gal, et al.
Analytical Biochemistry|May 1, 1979
The distribution of glucocerebroside in the liver of patients with Gaucher's diseaseA E Gal, P G Pentchev, J A Barranger, et al.
The New England Journal of Medicine|November 7, 1974
Replacement therapy for inherited enzyme deficiency. Use of purified glucocerebrosidase in Gaucher's diseaseR O Brady, P G Pentchev, A E Gal, et al.
Pageof 7

Showing results (31-40 of 66) with videos related to

Sort By:
Pageof 7
International Archives of Allergy and Applied Immunology|January 1, 1988
Western immunoblotting of cereal proteins with monoclonal antibodies to wheat gliadin to investigate coeliac diseaseA R Freedman, G Galfre, E Gal, et al.
The American Journal of Medicine|December 1, 1983
Normolipemic subcutaneous xanthomatosisR Fleischmajer, E J Schaefer, A E Gal, et al.
Presse Medicale (Paris, France : 1983)|February 15, 1997
[Autochthonous viral hepatitis E in Languedoc-Roussillon]P Corne, S Yeche, E Gal, et al.
Acta Cytologica|September 29, 2001
Granulomatous inflammation of the breast in a pregnant woman: report of a case with fine needle aspiration diagnosisA W Poniecka, P Krasuski, E Gal, et al.
Chemistry and Physics of Lipids|December 15, 1986
Animal and cellular models of sphingolipid storage disorders of humansA E Gal, A L Weis, J M Quirk, et al.
The Journal of Biological Chemistry|August 10, 1973
Isolation and characterization of glucocerebrosidase from human placental tissueP G Pentchev, R O Brady, S R Hibbert, et al.
The Journal of Biological Chemistry|June 10, 1974
Isolation and relationship of human hexosaminidasesJ F Tallman, R O Brady, J M Quirk, et al.
Birth Defects Original Article Series|January 1, 1980
Status of enzyme replacement therapy for Gaucher diseaseR O Brady, J A Barranger, A E Gal, et al.
Analytical Biochemistry|May 1, 1979
The distribution of glucocerebroside in the liver of patients with Gaucher's diseaseA E Gal, P G Pentchev, J A Barranger, et al.
The New England Journal of Medicine|November 7, 1974
Replacement therapy for inherited enzyme deficiency. Use of purified glucocerebrosidase in Gaucher's diseaseR O Brady, P G Pentchev, A E Gal, et al.
Pageof 7