Gene encoding the human beta-hexosaminidase beta chain: extensive homology of intron placement in the alpha- and beta-chain genes.

Por Proia, R L
Publicado em 1988

cDNA clone for the alpha-chain of human beta-hexosaminidase: deficiency of alpha-chain mRNA in Ashkenazi Tay-Sachs fibroblasts.

Por Myerowitz, R, Proia, R L
Publicado em 1984

Tay-Sachs disease in Moroccan Jews: deletion of a phenylalanine in the alpha-subunit of beta-hexosaminidase.

Por Navon, R, Proia, R L
Publicado em 1991

Synthesis of beta-hexosaminidase in cell-free translation and in intact fibroblasts: an insoluble precursor alpha chain in a rare form of Tay-Sachs disease.

Por Proia, R L, Neufeld, E F
Publicado em 1982

The molecular basis of HEXA mRNA deficiency caused by the most common Tay-Sachs disease mutation.

Por Boles, D J, Proia, R L
Publicado em 1995

Identification and rapid detection of three Tay-Sachs mutations in the Moroccan Jewish population.

Por Drucker, L, Proia, R L, Navon, R
Publicado em 1992

Membrane receptors for bacterial toxins.

Por Eidels, L, Proia, R L, Hart, D A
Publicado em 1983

Diphtheria toxin-binding glycoproteins on hamster cells: candidates for diphtheria toxin receptors.

Por Proia, R L, Eidels, L, Hart, D A
Publicado em 1979

Interaction of diphtheria toxin with phosphorylated molecules.

Por Proia, R L, Hart, D A, Eidels, L
Publicado em 1979

Inactivation or elimination of potentially trypanolytic, complement-activating immune complexes by pathogenic trypanosomes.

Por Balber, A E, Bangs, J D, Jones, S M, Proia, R L
Publicado em 1979

Ashkenazi-Jewish and non-Jewish adult GM2 gangliosidosis patients share a common genetic defect.

Por Navon, R, Kolodny, E H, Mitsumoto, H, Thomas, G H, Proia, R L
Publicado em 1990

Immunoprecipitation and partial characterization of diphtheria toxin-binding glycoproteins from surface of guinea pig cells.

Por Proia, R L, Hart, D A, Holmes, R K, Holmes, K V, Eidels, L
Publicado em 1979

Targeted disruption of the Hexa gene results in mice with biochemical and pathologic features of Tay-Sachs disease.

Por Yamanaka, S, Johnson, M D, Grinberg, A, Westphal, H, Crawley, J N, Taniike, M, Suzuki, K, Proia, R L
Publicado em 1994

Bone marrow transplantation prolongs life span and ameliorates neurologic manifestations in Sandhoff disease mice.

Por Norflus, F, Tifft, C J, McDonald, M P, Goldstein, G, Crawley, J N, Hoffmann, A, Sandhoff, K, Suzuki, K, Proia, R L
Publicado em 1998