Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8 von Lux, Samuel E., Tse, William T., Menninger, Joan C., John, Kathryn M., Harris, Peter, Shalev, Oded, Chilcote, Robert R., Marchesi, Sally L., Watkins, Paul C., Bennett, Vann, Mclntosh, Sue, Collins, Francis S., Francke, Uta, Ward, David C., Forget, Bernard G.

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Sequence and exon-intron organization of the DNA encoding the αI domain of human spectrin: application to the study of mutations causing hereditary elliptocytosis von SAHR, K. E, TOBE, T, SCARPA, A, LAUGHINGHOUSE, K, MARCHESI, S. L, AGRE, P, LINNENBACH, A. J, MARCHESI, V. T, FORGET, B. G

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Mutant forms of spectrin α-subunits in hereditary elliptocytosis von MARCHESI, S. L, LETSINGER, J. T, SPEICHER, D. W, MARCHESI, V. T, AGRE, P, HYUN, B, GULATI, G

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Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. I, Biochemical identification of rearrangements in the spectrin/actin binding domain and functi... von MARCHESI, S. L, CONBOY, J, AGRE, P, LETSINGER, J. T, MARCHESI, V. T, SPEICHER, D. W, MOHANDAS, N

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Amino‐acid substitution in α‐spectrin commonly coinherited with nondominant hereditary spherocytosis von Tse, William T., Gallagher, Patrick G., Jenkins, Patricia B., Wang, Yongping, Benoit, Lori, Speicher, David, Winkelmann, John C., Agre, Peter, Forget, Bernard G., Marchesi, Sally L.

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Molecular basis and haplotyping of the αII domain polymorphisms of spectrin : Application to the study of hereditary elliptocytosis and pyropoikilocytosis von GALLAGHER, P. G, KOTULA, L, WANG, Y, MARCHESI, S. L, CURTIS, P. J, SPEICHER, D. W, FORGET, B. G

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Physical and chemical properties of a protein isolated from red cell membranes von Marchesi, Sally L, Steers, Edward, Marchesi, V. T, Tillack, T. W

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Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin αI/74-kilodalton tryptic peptid... von FLOYD, P. B, GALLAGHER, P. G, VALENTINO, L. A, DAVIS, M, MARCHESI, S. L, FORGET, B. G

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Common structural polymorphisms in human erythrocyte spectrin von KNOWLES, W. J, BOLOGNA, M. L, CHASIS, J. A, MARCHESI, S. L, MARCHESI, V. T

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Poikilocytic hereditary elliptocytosis associated with spectrin Alexandria : an αI/50b Kd variant that is caused by a single amino acid deletion von GALLAGHER, P. G, ROBERTS, W. E, BENOIT, L, SPEICHER, D. W, MARCHESI, S. L, FORGET, B. G

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Abnormal Spectrin in Hereditary Elliptocytosis von Marchesi, Sally L., Knowles, William J., Morrow, Jon S., Bologna, Marcia, Marchesi, Vincent T.

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Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene von Gallagher, P G, Weed, S A, Tse, W T, Benoit, L, Morrow, J S, Marchesi, S L, Mohandas, N, Forget, B G

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Molecular basis and haplotyping of the alphaII domain polymorphisms of spectrin: application to the study of hereditary elliptocytosis and pyropoikilocytosis von Gallagher, P G, Kotula, L, Wang, Y, Marchesi, S L, Curtis, P J, Speicher, D W, Forget, B G

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Magnesium starvation of Aerobacter aerogenes. 3. Protein metabolism von Marchesi, S L, Kennell, D

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A comparative study of spectrin: A protein isolated from red blood cell membranes von Tillack, T.W., Marchesi, S.L., Marchesi, V.T., Steers, E.

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Abnormal spectrin in hereditary elliptocytosis von Marchesi, SL, Knowles, WJ, Morrow, JS, Bologna, M, Marchesi, VT

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Studies on the purification and characterization of human factor 8 von Marchesi, S L, Shulman, N R, Gralnick, H R

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Urinary fibrin split products in lupus nephritis. Correlation with other parameters of renal disease von Marchesi, S. L., Aptekar, R. G., Steinberg, A. D., Gralnick, H. R., Decker, J. L.

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Isolation of human platelet glycoproteins von Marchesi, Sally L., Chasis, Joel A.

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THEORETICAL APPROACH TO MOLECULAR BIOLOGY OF FACTOR VIII: HETEROGENEITY OF THE MOLECULE von Gralnick, Harvey R., Marchesi, Sally L., Coller, Barry S.

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