-
1
-
-
0026628758
-
Mutations of the red blood cell membrane proteins: From clinical evaluation to detection of the underlying genetic defect
-
Palek J, Sahr KE: Mutations of the red blood cell membrane proteins: From clinical evaluation to detection of the underlying genetic defect. Blood 80:308, 1992
-
(1992)
Blood
, vol.80
, pp. 308
-
-
Palek, J.1
Sahr, K.E.2
-
2
-
-
0023485004
-
Hereditary elliptocytosis, spherocytosis and related disorders: Consequences of a deficiency or a mutation of membrane skeletal proteins
-
Palek J: Hereditary elliptocytosis, spherocytosis and related disorders: Consequences of a deficiency or a mutation of membrane skeletal proteins. Blood Rev 1:147, 1987
-
(1987)
Blood Rev
, vol.1
, pp. 147
-
-
Palek, J.1
-
3
-
-
0021214396
-
Oligomeric states of spectrin in normal erythrocyte membranes: Biochemical and electron microscopic studies
-
Liu SC, Windisch P, Kim S, Palek J: Oligomeric states of spectrin in normal erythrocyte membranes: Biochemical and electron microscopic studies. Cell 37:587, 1984
-
(1984)
Cell
, vol.37
, pp. 587
-
-
Liu, S.C.1
Windisch, P.2
Kim, S.3
Palek, J.4
-
4
-
-
0019321291
-
Association between ankyrin and the cytoplasmic domain of band 3 isolated from the human erythrocyte membrane
-
Bennett V, Stenbuck P: Association between ankyrin and the cytoplasmic domain of band 3 isolated from the human erythrocyte membrane. J Biol Chem 255:6424, 1980
-
(1980)
J Biol Chem
, vol.255
, pp. 6424
-
-
Bennett, V.1
Stenbuck, P.2
-
5
-
-
0023867132
-
Deficiency of protein 4.2 in erythrocytes from a patient with a Coombs negative hemolytic anemia. Evidence for a role of protein 4.2 in stabilizing ankyrin on the membrane
-
Rybicki AC, Heath R, Wolf JL, Lubin B, Schwanz RS: Deficiency of protein 4.2 in erythrocytes from a patient with a Coombs negative hemolytic anemia. Evidence for a role of protein 4.2 in stabilizing ankyrin on the membrane. J Clin Invest 81:893, 1988
-
(1988)
J Clin Invest
, vol.81
, pp. 893
-
-
Rybicki, A.C.1
Heath, R.2
Wolf, J.L.3
Lubin, B.4
Schwanz, R.S.5
-
6
-
-
0021193967
-
Analysis of the ternary interaction of the red cell membrane skeletal proteins spectrin, actin, and 4.1
-
Ohanian V, Wolfe LC, John KM, Pinder JC, Lux SE, Gratzer WB: Analysis of the ternary interaction of the red cell membrane skeletal proteins spectrin, actin, and 4.1. Biochemistry 23:4416, 1984
-
(1984)
Biochemistry
, vol.23
, pp. 4416
-
-
Ohanian, V.1
Wolfe, L.C.2
John, K.M.3
Pinder, J.C.4
Lux, S.E.5
Gratzer, W.B.6
-
7
-
-
0025354418
-
Glycophorin C content of human erythrocyte membrane is regulated by protein 4.1
-
Reid ME, Takakuwa Y, Conboy J, Tchernia G, Mohandas N: Glycophorin C content of human erythrocyte membrane is regulated by protein 4.1. Blood 75:2229, 1990
-
(1990)
Blood
, vol.75
, pp. 2229
-
-
Reid, M.E.1
Takakuwa, Y.2
Conboy, J.3
Tchernia, G.4
Mohandas, N.5
-
8
-
-
1842343276
-
Hemolytic anemias caused by primary defects of red cell membranes
-
Boston, MA, Little, Brown and Company
-
Jandl JH: Hemolytic anemias caused by primary defects of red cell membranes, in Blood: Textbook of Hematology. Boston, MA, Little, Brown and Company, 1987, p 237
-
(1987)
Blood: Textbook of Hematology
, pp. 237
-
-
Jandl, J.H.1
-
9
-
-
0019305526
-
Inherited hemolytic anemia in mice: A review and update
-
Bernstein SE: Inherited hemolytic anemia in mice: A review and update. Lab Anim Sci 30:197, 1980
-
(1980)
Lab Anim Sci
, vol.30
, pp. 197
-
-
Bernstein, S.E.1
-
10
-
-
0345567963
-
Marrow transplantation in newborn mice with hereditary spherocytosis: A model system
-
Motulsky AG, Anderson R, Sparkes RS, Huestis RH: Marrow transplantation in newborn mice with hereditary spherocytosis: A model system. Trans Assoc Am Phys 1xxv:64, 1962
-
(1962)
Trans Assoc Am Phys
, vol.125
, pp. 64
-
-
Motulsky, A.G.1
Anderson, R.2
Sparkes, R.S.3
Huestis, R.H.4
-
11
-
-
0021704597
-
Spectrin deficient inherited hemolytic anemias in the mouse: Characterization by spectrin synthesis and mRNA activity in reticulocytes
-
Bodine DM, Birkenmeier CS, Barker JE: Spectrin deficient inherited hemolytic anemias in the mouse: Characterization by spectrin synthesis and mRNA activity in reticulocytes. Cell 37:721, 1984
-
(1984)
Cell
, vol.37
, pp. 721
-
-
Bodine, D.M.1
Birkenmeier, C.S.2
Barker, J.E.3
-
12
-
-
0028149097
-
The murine mutation jaundice is caused by replacement of an arginine with a stop codon in the mRNA encoding the ninth repeat of β-spectrin
-
Bloom ML, Kaysser TM, Birkenmeier CS, Barker JE: The murine mutation jaundice is caused by replacement of an arginine with a stop codon in the mRNA encoding the ninth repeat of β-spectrin. Proc Natl Acad Sci 91:10099, 1994
-
(1994)
Proc Natl Acad Sci
, vol.91
, pp. 10099
-
-
Bloom, M.L.1
Kaysser, T.M.2
Birkenmeier, C.S.3
Barker, J.E.4
-
13
-
-
77957210812
-
A mutation causing neonatal jaundice in the house mouse
-
Stevens LC, MacKensen JA, Bernstein SE: A mutation causing neonatal jaundice in the house mouse. J Hered 50:35, 1959
-
(1959)
J Hered
, vol.50
, pp. 35
-
-
Stevens, L.C.1
MacKensen, J.A.2
Bernstein, S.E.3
-
14
-
-
0023760729
-
Chromosomal location of three spectrin genes: Relationship to the inherited hemolytic anemias of mouse and man
-
Birkenmeier CS, McFarland SE, Barker JE: Chromosomal location of three spectrin genes: Relationship to the inherited hemolytic anemias of mouse and man. Proc Natl Acad Sci USA 85:8121, 1988
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 8121
-
-
Birkenmeier, C.S.1
McFarland, S.E.2
Barker, J.E.3
-
15
-
-
1842342295
-
A new mutation (sph) causing neonatal jaundice in the house mouse
-
Teasdale JM, Miller JR: A new mutation (sph) causing neonatal jaundice in the house mouse. Can J Genet Cytol 4:219, 1962
-
(1962)
Can J Genet Cytol
, vol.4
, pp. 219
-
-
Teasdale, J.M.1
Miller, J.R.2
-
16
-
-
0025719950
-
Deficiency of alpha-spectrin synthesis in burst-forming units-erythroid in lethal hereditary spherocytosis
-
Whitfield CF, Follweiler JB, Lopresti ML, Miller BA: Deficiency of alpha-spectrin synthesis in burst-forming units-erythroid in lethal hereditary spherocytosis. Blood 78:3043, 1991
-
(1991)
Blood
, vol.78
, pp. 3043
-
-
Whitfield, C.F.1
Follweiler, J.B.2
Lopresti, M.L.3
Miller, B.A.4
-
17
-
-
1842393681
-
Band 3 Coimbra: A variant associated with dominant hereditary spherocytosis and band 3 deficiency
-
abstr
-
Alloisio N, Texier P, Forissier M, Ribeiro ML, Morle L, Bozon M, Bursaux E, Maulet P, Tanner MJA, Delaunay J: Band 3 Coimbra: A variant associated with dominant hereditary spherocytosis and band 3 deficiency. Blood 82:4a, 1993 (suppl, abstr)
-
(1993)
Blood
, vol.82
, Issue.SUPPL.
-
-
Alloisio, N.1
Texier, P.2
Forissier, M.3
Ribeiro, M.L.4
Morle, L.5
Bozon, M.6
Bursaux, E.7
Maulet, P.8
Tanner, M.J.A.9
Delaunay, J.10
-
18
-
-
0021914750
-
Partial deficiency of erythrocyte spectrin in hereditary spherocytosis
-
Agre P, Casella JF, Zinkham WH, McMilian C, Bennett V: Partial deficiency of erythrocyte spectrin in hereditary spherocytosis. Nature 314:380, 1985
-
(1985)
Nature
, vol.314
, pp. 380
-
-
Agre, P.1
Casella, J.F.2
Zinkham, W.H.3
McMilian, C.4
Bennett, V.5
-
19
-
-
0020083327
-
Deficient red-cell spectrin in severe, recessively inherited spherocytosis
-
Agre P, Orringer EP, Bennett V: Deficient red-cell spectrin in severe, recessively inherited spherocytosis. N Engl J Med 306:1155, 1982
-
(1982)
N Engl J Med
, vol.306
, pp. 1155
-
-
Agre, P.1
Orringer, E.P.2
Bennett, V.3
-
20
-
-
0023873493
-
Partial ankyrin and spectrin deficiency in severe, atypical hereditary spherocytosis
-
Coetzer TL, Lawler J, Liu SC, Prchal JT, Gualtieri RJ, Brain MC, Dacie JV, Palek J: Partial ankyrin and spectrin deficiency in severe, atypical hereditary spherocytosis. N Engl J Med 318:230, 1988
-
(1988)
N Engl J Med
, vol.318
, pp. 230
-
-
Coetzer, T.L.1
Lawler, J.2
Liu, S.C.3
Prchal, J.T.4
Gualtieri, R.J.5
Brain, M.C.6
Dacie, J.V.7
Palek, J.8
-
21
-
-
0028927524
-
Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte β-spectrin gene
-
Gallagher PG, Weed SA, Tse WT, Benoit L, Morrow JS, Marchesi SL, Mohandas N, Forget BG: Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte β-spectrin gene. J Clin Invest 95:1174, 1995
-
(1995)
J Clin Invest
, vol.95
, pp. 1174
-
-
Gallagher, P.G.1
Weed, S.A.2
Tse, W.T.3
Benoit, L.4
Morrow, J.S.5
Marchesi, S.L.6
Mohandas, N.7
Forget, B.G.8
-
22
-
-
0022916675
-
Inheritance pattern and clinical response to splenectomy as a reflection of erythrocyte spectrin deficiency in hereditary spherocytosis
-
Agre P, Asimos A, Casella JF, McMillan C: Inheritance pattern and clinical response to splenectomy as a reflection of erythrocyte spectrin deficiency in hereditary spherocytosis. N Engl J Med 315:1579, 1986
-
(1986)
N Engl J Med
, vol.315
, pp. 1579
-
-
Agre, P.1
Asimos, A.2
Casella, J.F.3
McMillan, C.4
-
23
-
-
0344705852
-
Hereditary spherocytosis in the deer mouse. Its similarity to the human disease
-
Anderson R, Huestis RR, Motulsky AG: Hereditary spherocytosis in the deer mouse. Its similarity to the human disease. Blood 15:491, 1960
-
(1960)
Blood
, vol.15
, pp. 491
-
-
Anderson, R.1
Huestis, R.R.2
Motulsky, A.G.3
-
24
-
-
0024311439
-
Marrow transplantation in the treatment of a murine heritable hemolytic anemia
-
Barker JE, McFarland-Starr EC: Marrow transplantation in the treatment of a murine heritable hemolytic anemia. Blood 73:2014, 1989
-
(1989)
Blood
, vol.73
, pp. 2014
-
-
Barker, J.E.1
McFarland-Starr, E.C.2
-
25
-
-
0024428496
-
Bone marrow replacement in the treatment of hemolytic disease in mice
-
Bernstein SE, Deveau SA: Bone marrow replacement in the treatment of hemolytic disease in mice. Exp Hematol 17:1004, 1989
-
(1989)
Exp Hematol
, vol.17
, pp. 1004
-
-
Bernstein, S.E.1
Deveau, S.A.2
-
26
-
-
0027258694
-
Treatment of murine mucopolysaccharidosis type VII by syngeneic bone marrow transplantation in neonates
-
Sands MS, Barker JE, Vogler C, Levy B, Gwynn B, Galvin N, Sly WS, Birkenmeier EH: Treatment of murine mucopolysaccharidosis type VII by syngeneic bone marrow transplantation in neonates. Lab Invest 68:676, 1993
-
(1993)
Lab Invest
, vol.68
, pp. 676
-
-
Sands, M.S.1
Barker, J.E.2
Vogler, C.3
Levy, B.4
Gwynn, B.5
Galvin, N.6
Sly, W.S.7
Birkenmeier, E.H.8
-
27
-
-
0026044081
-
Purkinje cell degeneration associated with erythroid ankyrin deficiency in nb/nb mice
-
Peters LL, Birkenmeier CS, Bronson RT, White RA, Lux SE, Otto E, Bennett V, Higgins A, Barker JE: Purkinje cell degeneration associated with erythroid ankyrin deficiency in nb/nb mice. J Cell Biol 114:1233, 1991
-
(1991)
J Cell Biol
, vol.114
, pp. 1233
-
-
Peters, L.L.1
Birkenmeier, C.S.2
Bronson, R.T.3
White, R.A.4
Lux, S.E.5
Otto, E.6
Bennett, V.7
Higgins, A.8
Barker, J.E.9
-
28
-
-
0025250561
-
Beta spectrin in human skeletal muscle. Tissue-specific differential processing of 3′ beta spectrin pre-mRNA generates a beta spectrin isoform with a unique carboxyl terminus
-
Winkelmann JC, Costa FF, Linzie BL, Forget BG: Beta spectrin in human skeletal muscle. Tissue-specific differential processing of 3′ beta spectrin pre-mRNA generates a beta spectrin isoform with a unique carboxyl terminus. J Biol Chem 265:20449, 1990
-
(1990)
J Biol Chem
, vol.265
, pp. 20449
-
-
Winkelmann, J.C.1
Costa, F.F.2
Linzie, B.L.3
Forget, B.G.4
-
29
-
-
0022454882
-
Brain spectrin(240/ 235) and brain spectrin(240/235E): Two distinct spectrin subtypes with different locations within mammalian neural cells
-
Riederer BM, Zagon IS, Goodman SR: Brain spectrin(240/ 235) and brain spectrin(240/235E): Two distinct spectrin subtypes with different locations within mammalian neural cells. J Cell Biol 102:2088, 1986
-
(1986)
J Cell Biol
, vol.102
, pp. 2088
-
-
Riederer, B.M.1
Zagon, I.S.2
Goodman, S.R.3
-
30
-
-
0027371802
-
Complete nucleotide sequence of the murine erythroid beta spectrin cDNA, and tissue specific expression in normal and jaundiced mice
-
Bloom ML, Birkenmeier CS, Barker JE: Complete nucleotide sequence of the murine erythroid beta spectrin cDNA, and tissue specific expression in normal and jaundiced mice. Blood 82:2906, 1993
-
(1993)
Blood
, vol.82
, pp. 2906
-
-
Bloom, M.L.1
Birkenmeier, C.S.2
Barker, J.E.3
-
31
-
-
0026711133
-
Dystrophin colocalizes with beta-spectrin in distinct subsarcolemmal domains in mammalian skeletal muscle
-
Porter GA, Dmytrenko GM, Winkelmann JC, Bloch RJ: Dystrophin colocalizes with beta-spectrin in distinct subsarcolemmal domains in mammalian skeletal muscle. J Cell Biol 117:997, 1992
-
(1992)
J Cell Biol
, vol.117
, pp. 997
-
-
Porter, G.A.1
Dmytrenko, G.M.2
Winkelmann, J.C.3
Bloch, R.J.4
-
32
-
-
0026772911
-
Human cardiac and skeletal muscle spectrins: Differential expression and localization
-
Vybiral T, Winkelmann JC, Roberts R, Joe E, Casey DL, Williams JK, Epstein HF: Human cardiac and skeletal muscle spectrins: Differential expression and localization. Cell Motil Cytoskeleton 21:293, 1992
-
(1992)
Cell Motil Cytoskeleton
, vol.21
, pp. 293
-
-
Vybiral, T.1
Winkelmann, J.C.2
Roberts, R.3
Joe, E.4
Casey, D.L.5
Williams, J.K.6
Epstein, H.F.7
-
33
-
-
0027525225
-
The 270 kDa splice variant of erythrocyte β-spectrin (βIΣ2) segregates in vivo and in vitro to specific domains of cerebellar neurons
-
Malchiodi-Albedi F, Ceccarini M, Winkelmann JC, Morrow JS, Petrucci TC: The 270 kDa splice variant of erythrocyte β-spectrin (βIΣ2) segregates in vivo and in vitro to specific domains of cerebellar neurons. J Cell Sci 106:67, 1993
-
(1993)
J Cell Sci
, vol.106
, pp. 67
-
-
Malchiodi-Albedi, F.1
Ceccarini, M.2
Winkelmann, J.C.3
Morrow, J.S.4
Petrucci, T.C.5
-
35
-
-
0028324606
-
Engraftment of human peripheral blood lymphocytes in normal strains of mice
-
Lubin I, Segall H, Marcus H, David M, Kulova L, Steinitz M, Erlich P, Gan J, Reisner Y: Engraftment of human peripheral blood lymphocytes in normal strains of mice. Blood 83:2368, 1994
-
(1994)
Blood
, vol.83
, pp. 2368
-
-
Lubin, I.1
Segall, H.2
Marcus, H.3
David, M.4
Kulova, L.5
Steinitz, M.6
Erlich, P.7
Gan, J.8
Reisner, Y.9
-
36
-
-
0005066970
-
Assignment of genes to regions of mouse chromosomes
-
Eicher EM, Washbum LL; Assignment of genes to regions of mouse chromosomes. Proc Natl Acad Sci USA 75:946, 1978
-
(1978)
Proc Natl Acad Sci USA
, vol.75
, pp. 946
-
-
Eicher, E.M.1
Washbum, L.L.2
-
37
-
-
0014342920
-
Erythropoiesis in the spleen and bone marrow of the pregnant mouse
-
Fowler JH, Nash DJ: Erythropoiesis in the spleen and bone marrow of the pregnant mouse. Dev Biol 18:331, 1968
-
(1968)
Dev Biol
, vol.18
, pp. 331
-
-
Fowler, J.H.1
Nash, D.J.2
-
38
-
-
0003006629
-
Blood and blood formation
-
Green EL (ed) New York, NY, Dover Publications
-
Russell ES, Bernstein SE: Blood and blood formation, in Green EL (ed): Biology of the laboratory mouse (Ed 2). New York, NY, Dover Publications, 1966, p 365
-
(1966)
Biology of the Laboratory Mouse (Ed 2)
, pp. 365
-
-
Russell, E.S.1
Bernstein, S.E.2
-
39
-
-
1842355976
-
Hemolytic anemias
-
Boston, MA, Blackwell Scientific Publications
-
Jandl JH: Hemolytic anemias, in: Blood: Pathophysiology. Boston, MA, Blackwell Scientific Publications, 1991, p 153
-
(1991)
Blood: Pathophysiology
, pp. 153
-
-
Jandl, J.H.1
-
40
-
-
0027438310
-
Spectrin cagliari: An ALA-GLY substitution in helix 2 of β-spectrin repeat 17 that severely disrupts the structure and self association of the erythrocyte spectrin heterodimer
-
Sahr KE, Coetzer TL, Moy LS, Derick LH, Chishti AH, Jarolim P, Lorenzo F, Miraglia del Guidice E, Iolascon A, Gallanello R, Cao A, Delaunay J, Liu S-C, Palek J: Spectrin cagliari: An ALA-GLY substitution in helix 2 of β-spectrin repeat 17 that severely disrupts the structure and self association of the erythrocyte spectrin heterodimer. J Biol Chem 268:22656, 1993
-
(1993)
J Biol Chem
, vol.268
, pp. 22656
-
-
Sahr, K.E.1
Coetzer, T.L.2
Moy, L.S.3
Derick, L.H.4
Chishti, A.H.5
Jarolim, P.6
Lorenzo, F.7
Miraglia Del Guidice, E.8
Iolascon, A.9
Gallanello, R.10
Cao, A.11
Delaunay, J.12
Liu, S.-C.13
Palek, J.14
-
41
-
-
0024993498
-
Point mutation in the β-spectrin gene associated with αI/74 hereditary elliptocytosis
-
Tse WE, LeComte M-C, Costa FF, Garbarz M, Feo C, Boivin P, Dhermy D, Forget BG: Point mutation in the β-spectrin gene associated with αI/74 hereditary elliptocytosis. J Clin Invest 86:909, 1990
-
(1990)
J Clin Invest
, vol.86
, pp. 909
-
-
Tse, W.E.1
LeComte, M.-C.2
Costa, F.F.3
Garbarz, M.4
Feo, C.5
Boivin, P.6
Dhermy, D.7
Forget, B.G.8
-
42
-
-
0031017565
-
Mutation of a highly conserved residue of β1 spectrin associated with fatal and near-fatal neonatal hemolytic anemia
-
Gallagher PG, Petruzzi MJ, Weed SA, Zhang Z, Marchesi SL, Mohandas N, Morrow JS, Forget BG: Mutation of a highly conserved residue of β1 spectrin associated with fatal and near-fatal neonatal hemolytic anemia. J Clin Invest 99:267, 1997
-
(1997)
J Clin Invest
, vol.99
, pp. 267
-
-
Gallagher, P.G.1
Petruzzi, M.J.2
Weed, S.A.3
Zhang, Z.4
Marchesi, S.L.5
Mohandas, N.6
Morrow, J.S.7
Forget, B.G.8
-
43
-
-
0020613846
-
Infection with parvovirus-like virus and aplastic crisis in chronic hemolytic anemia
-
Rao KRP, Patel AR, Anderson MJ, Hodgson J, Jones SE, Pattison JR: Infection with parvovirus-like virus and aplastic crisis in chronic hemolytic anemia. Ann Intern Med 98:930, 1983
-
(1983)
Ann Intern Med
, vol.98
, pp. 930
-
-
Rao, K.R.P.1
Patel, A.R.2
Anderson, M.J.3
Hodgson, J.4
Jones, S.E.5
Pattison, J.R.6
-
44
-
-
0038712935
-
The aplastic crisis in sickle-cell anaemia
-
Maclver JE, Parker-Williams EJ: The aplastic crisis in sickle-cell anaemia. Lancet 1:1086, 1961
-
(1961)
Lancet
, vol.1
, pp. 1086
-
-
Maclver, J.E.1
Parker-Williams, E.J.2
-
45
-
-
0022587420
-
Six cases of hereditary spherocytosis revealed by human parvovirus infection
-
Lefrere JJ, Courouce A-M, Girot R, Bertrand Y, Soulier J-P: Six cases of hereditary spherocytosis revealed by human parvovirus infection. Br J Haematol 62:653, 1986
-
(1986)
Br J Haematol
, vol.62
, pp. 653
-
-
Lefrere, J.J.1
Courouce, A.-M.2
Girot, R.3
Bertrand, Y.4
Soulier, J.-P.5
-
46
-
-
0018873397
-
Transient aplastic crisis in hereditary spherocytosis
-
Maser G, Mieli G, Petrone M, Porcelli P: Transient aplastic crisis in hereditary spherocytosis. Acta Haematol 63:28, 1980
-
(1980)
Acta Haematol
, vol.63
, pp. 28
-
-
Maser, G.1
Mieli, G.2
Petrone, M.3
Porcelli, P.4
-
48
-
-
1842359814
-
Renal hemosiderosis in the hemolytic anemias: Diagnosis by means of needle biopsy
-
Leonardi P, Ruol A: Renal hemosiderosis in the hemolytic anemias: Diagnosis by means of needle biopsy. Blood 16:1029, 1960
-
(1960)
Blood
, vol.16
, pp. 1029
-
-
Leonardi, P.1
Ruol, A.2
-
50
-
-
0029953791
-
The lethal hemolytic mutation in βIσ2 spectrin Providence yields a null phenotype in neonatal skeletal muscle
-
Weed SA, Stabach PR, Oyer CE, Gallagher PG, Morrow JS: The lethal hemolytic mutation in βIσ2 spectrin Providence yields a null phenotype in neonatal skeletal muscle. Lab Invest 74:1117, 1996
-
(1996)
Lab Invest
, vol.74
, pp. 1117
-
-
Weed, S.A.1
Stabach, P.R.2
Oyer, C.E.3
Gallagher, P.G.4
Morrow, J.S.5
-
51
-
-
0028017579
-
Erythroid-specific processing of human β spectrin I pre-mRNA
-
Chu Z-L, Wickrema A, Krantz SB, Winkelmann JC: Erythroid-specific processing of human β spectrin I pre-mRNA. Blood 84:1992, 1994
-
(1994)
Blood
, vol.84
, pp. 1992
-
-
Chu, Z.-L.1
Wickrema, A.2
Krantz, S.B.3
Winkelmann, J.C.4
-
52
-
-
0027304398
-
Identification of novel pleckstrin homology (PH) domains provides a hypothesis for PH domain function
-
Shaw G: Identification of novel pleckstrin homology (PH) domains provides a hypothesis for PH domain function. Biochem Biophys Res Commun 195:1145, 1993
-
(1993)
Biochem Biophys Res Commun
, vol.195
, pp. 1145
-
-
Shaw, G.1
-
53
-
-
0023151831
-
Brain spectrin(240/ 235) and brain spectrin(240/235E): Differential expression during mouse brain development
-
Riederer BM, Zagon IS, Goodman SR: Brain spectrin(240/ 235) and brain spectrin(240/235E): Differential expression during mouse brain development. J Neurosci 7:864, 1987
-
(1987)
J Neurosci
, vol.7
, pp. 864
-
-
Riederer, B.M.1
Zagon, I.S.2
Goodman, S.R.3
-
54
-
-
0024548732
-
An unusual beta-spectrin associated with clustered acetylcholine receptors
-
Bloch RJ, Morrow JS: An unusual beta-spectrin associated with clustered acetylcholine receptors. J Cell Biol 108:481, 1989
-
(1989)
J Cell Biol
, vol.108
, pp. 481
-
-
Bloch, R.J.1
Morrow, J.S.2
-
55
-
-
0029965715
-
Microangiopathic glomerulopathy in children with sickle cell anemia
-
Vogler C, Wood E, Lane P, Ellis E, Cole B, Thorpe C: Microangiopathic glomerulopathy in children with sickle cell anemia. Pediatr Pathol Lab Med 16:275, 1996
-
(1996)
Pediatr Pathol Lab Med
, vol.16
, pp. 275
-
-
Vogler, C.1
Wood, E.2
Lane, P.3
Ellis, E.4
Cole, B.5
Thorpe, C.6
-
56
-
-
0019750063
-
The Budd-Chiari syndrome in paroxysmal nocturnal hemoglobinuria-revisited
-
Leibowitz A, Hartmann RC: The Budd-Chiari syndrome in paroxysmal nocturnal hemoglobinuria-revisited. Br J Haematol 49:659, 1981
-
(1981)
Br J Haematol
, vol.49
, pp. 659
-
-
Leibowitz, A.1
Hartmann, R.C.2
-
57
-
-
0015442003
-
Thrombosis in paroxysmal nocturnal hemoglobinuria with particular reference to progressive, diffuse hepatic venous thrombosis
-
Peytrmann R, Rhodes RS, Hartmann RC: Thrombosis in paroxysmal nocturnal hemoglobinuria with particular reference to progressive, diffuse hepatic venous thrombosis. Ser Haematol 5:115, 1972
-
(1972)
Ser Haematol
, vol.5
, pp. 115
-
-
Peytrmann, R.1
Rhodes, R.S.2
Hartmann, R.C.3
-
58
-
-
0026099699
-
Beyond hemoglobin polymerization: The red blood cell membrane and sickle disease pathophysiology
-
Hebbel RP: Beyond hemoglobin polymerization: The red blood cell membrane and sickle disease pathophysiology. Blood 77:214, 1991
-
(1991)
Blood
, vol.77
, pp. 214
-
-
Hebbel, R.P.1
-
59
-
-
0031043059
-
Pathophysiologic implications of membrane phospholipid asymmetry in blood cells
-
Zwaal RFA, Schroit AJ: Pathophysiologic implications of membrane phospholipid asymmetry in blood cells. Blood 89:1121, 1997
-
(1997)
Blood
, vol.89
, pp. 1121
-
-
Zwaal, R.F.A.1
Schroit, A.J.2
-
60
-
-
0027458442
-
The distribution of erythrocyte phospholipids in hereditary spherocytosis demonstrates a minimal role for erythrocyte spectrin on phospholipid diffusion and asymmetry
-
Kuypers FA, Lubin BH, Yee M, Agre P, Devaux PF, Geldwerth D: The distribution of erythrocyte phospholipids in hereditary spherocytosis demonstrates a minimal role for erythrocyte spectrin on phospholipid diffusion and asymmetry. Blood 81:1051, 1993
-
(1993)
Blood
, vol.81
, pp. 1051
-
-
Kuypers, F.A.1
Lubin, B.H.2
Yee, M.3
Agre, P.4
Devaux, P.F.5
Geldwerth, D.6
|