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

Volltext

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

Volltext

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

Volltext

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.

Volltext

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

Volltext

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

Volltext

THE BIOCHEMICAL BASIS FOR THE DIFFERENTIAL SENSITIVITY OF INTESTINAL MUCOSA AND BONE MARROW TO 6-THIOGUANINE von MARCHESI, S L, SARTORELLI, A C

Volltext

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

Volltext

Magnesium Starvation of Aerobacter aerogenes III. Protein Metabolism von Marchesi, Sally L., Kennell, David

Volltext

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

Volltext

Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. II, Determination of molecular genetic origins of rearrangements von CONBOY, J, MARCHESI, S, KIM, R, AGRE, P, KAN, Y. W, MOHANDAS, N

Volltext

Immunological Studies of Factor VIII in Haemophilia and von Willebrand's Disease von GRALNICK, HARVEY R, COLLER, BARRY S, MARCHESI, SALLY L

Volltext

Poikilocytic Hereditary Elliptocytosis Associated With Spectrin Alexandria: An al/50b Kd Variant That Is Caused by a Single Amino Acid Deletion von Gallagher, Patrick G., Roberts, William E., Benoit, Lori, Speicher, David W., Marchesi, Sally L., Forget, Bernard G.

Volltext

Immunofluorescent Identification of Human Megakaryocyte Colonies Using an Antiplatelet Glycoprotein Antiserum von Mazur, Eric M., Hoffman, Ronald, Chasis, Joel, Marchesi, Sally, Bruno, Edward

Volltext

Heterogeneity of the Molecular Basis of Hereditary Pyropoikilocytosis and Hereditary Elliptocytosis Associated With Increased Levels of the Spectrin von Floyd, Patricia B., Gallagher, Patrick G., Valentino, Leonard A., Davis, Melvin, Marchesi, Sally L., Forget, Bernard G.

Volltext

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

Volltext

Intravascular Coagulation in Acute Leukemia: Clinical and Subclinical Abnormalities von Gralnick, Harvey R., Marchesi, Sally, Givelber, Harry

Volltext

Studies on the purification and characterization of human factor VIII von Marchesi, Sally L., Shulman, N. Raphael, Gralnick, Harvey R.

Volltext

Platelets: Production, Function, Transfusion, and Storage von Marchesi, Sally L.

Volltext

Influence of Plasma Source on T-Lymphocyte Subpopulations in Hemophiliacs Using Factor VIII Concentrate von Cable, R G, Hoyer, L, Marchesi, S, Mukherji, B, Morse, E E, Saxton, P

Volltext