Full-length sequence of the cDNA for human erythroid beta-spectrin.Winkelmann J.C., Chang J.G., Tse W.T., Scarpa A.L., Marchesi V.T., Forget B.G.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS 1 AND 3), VARIANTS ASN-439 AND ASP-1151CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Biol. Chem. 265:11827-11832 (1990)Cited in1
The DNA sequence and analysis of human chromosome 14.Heilig R., Eckenberg R., Petit J.-L., Fonknechten N., Da Silva C., Cattolico L., Levy M., Barbe V., De Berardinis V.[...], Weissenbach J.View abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNature 421:601-607 (2003)Cited in99+99+
Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a splice site mutation.Garbarz M., Tse W.T., Gallagher P.G., Picat C., Lecomte M.C., Galibert F., Dhermy D., Forget B.G.View abstractCited forPARTIAL NUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS 1 AND 3), ALTERNATIVE SPLICINGCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Clin. Invest. 88:76-81 (1991)Cited in1
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 J.C., Costa F.F., Linzie B.L., Forget B.G.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] OF 1055-2137 (ISOFORM 2), VARIANT ASP-1151TissueSkeletal muscleCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Biol. Chem. 265:20449-20454 (1990)Cited in1
A splice site mutation of the beta-spectrin gene causing exon skipping in hereditary elliptocytosis associated with a truncated beta-spectrin chain.Gallagher P.G., Tse W.T., Costa F., Scarpa A., Boivin P., Delaunay J., Forget B.G.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] OF 2002-2137 (ISOFORM 1)CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Biol. Chem. 266:15154-15159 (1991)Cited in1
Identification of an unusual deletion within homologous repeats of human reticulocyte beta-spectrin and probable peptide polymorphism.Yoon S.H., Kentros C.G., Prchal J.T.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] OF 928-1756 (ISOFORMS 1/2/3), VARIANT ASP-1151CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCGene 91:297-302 (1990)Cited in1
Molecular cloning of the cDNA for human erythrocyte beta-spectrin.Winkelmann J.C., Leto T.L., Watkins P.C., Eddy R., Shows T.B., Linnenbach A.J., Sahr K.E., Kathuria N., Marchesi V.T., Forget B.G.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] OF 1334-1432 (ISOFORMS 1/2/3), NUCLEOTIDE SEQUENCE [MRNA] OF 1909-2137 (ISOFORM 1), VARIANT ARG-1374CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCBlood 72:328-334 (1988)Cited in1
Isolation and characterization of cDNA clones for human erythrocyte beta- spectrin.Prchal J.T., Morley B.J., Yoon S.-H., Coetzer T.L., Palek J., Conboy J.G., Kan Y.W.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] OF 1209-1482 (ISOFORMS 1/2/3)CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 84:7468-7472 (1987)Cited in1
Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides.Gevaert K., Goethals M., Martens L., Van Damme J., Staes A., Thomas G.R., Vandekerckhove J.View abstractCited forPROTEIN SEQUENCE OF 2-18TissuePlateletCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNat. Biotechnol. 21:566-569 (2003)Cited in99+
Erythrocyte spectrin is comprised of many homologous triple helical segments.Speicher D.W., Marchesi V.T.View abstractCited forDOMAINSCategoriesFamily & DomainsSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNature 311:177-180 (1984)Cited in2
In vivo phosphorylation of human erythrocyte spectrin occurs in a sequential manner.Tang H.Y., Speicher D.W.View abstractCited forPHOSPHORYLATION AT THR-2110; SER-2114; SER-2117; SER-2123; SER-2125 AND SER-2128CategoriesPTM / ProcessingSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCBiochemistry 43:4251-4262 (2004)Cited in1
Novel beta-spectrin mutations in hereditary spherocytosis associated with decreased levels of mRNA.Maciag M., Plochocka D., Adamowicz-Salach A., Burzynska B.View abstractCited forINVOLVEMENT IN SPH2CategoriesDisease & VariantsSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCBr. J. Haematol. 146:326-332 (2009)Cited in1
Initial characterization of the human central proteome.Burkard T.R., Planyavsky M., Kaupe I., Breitwieser F.P., Buerckstuemmer T., Bennett K.L., Superti-Furga G., Colinge J.View abstractCited forIDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS]CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCBMC Syst. Biol. 5:17-17 (2011)Cited in99+99+
Toward a comprehensive characterization of a human cancer cell phosphoproteome.Zhou H., Di Palma S., Preisinger C., Peng M., Polat A.N., Heck A.J., Mohammed S.View abstractCited forPHOSPHORYLATION [LARGE SCALE ANALYSIS] AT THR-104; THR-2073; SER-2123 AND SER-2125, IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS]TissueErythroleukemiaCategoriesPTM / Processing, SequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Proteome Res. 12:260-271 (2013)Cited in99+99+
An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.Bian Y., Song C., Cheng K., Dong M., Wang F., Huang J., Sun D., Wang L., Ye M., Zou H.View abstractCited forPHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-2043, IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS]TissueLiverCategoriesPTM / Processing, SequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Proteomics 96:253-262 (2014)Cited in99+99+Mapped to2
A protease cascade regulates release of the human malaria parasite Plasmodium falciparum from host red blood cells.Thomas J.A., Tan M.S.Y., Bisson C., Borg A., Umrekar T.R., Hackett F., Hale V.L., Vizcay-Barrena G., Fleck R.A.[...], Blackman M.J.View abstractCited forPROTEOLYTIC CLEAVAGE (MICROBIAL INFECTION)CategoriesPTM / ProcessingSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNat. Microbiol. 3:447-455 (2018)Cited in4
Structural insights into the stability and flexibility of unusual erythroid spectrin repeats.Kusunoki H., MacDonald R.I., Mondragon A.View abstractCited forX-RAY CRYSTALLOGRAPHY (2.4 ANGSTROMS) OF 1064-1275CategoriesStructureSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCStructure 12:645-656 (2004)Cited in1
Spectrin mutations in hereditary elliptocytosis and hereditary spherocytosis.Maillet P., Alloisio N., Morle L., Delaunay J.View abstractCited forREVIEW ON VARIANTSCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCHum. Mutat. 8:97-107 (1996)Cited in2
Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association.Tse W.T., Lecomte M.-C., Costa F.F., Garbarz M., Feo C., Boivin P., Dhermy D., Forget B.G.View abstractCited forVARIANT EL3 PRO-2053CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Clin. Invest. 86:909-916 (1990)Cited in1
Spectrin Cagliari: an Ala-->Gly substitution in helix 1 of beta spectrin repeat 17 that severely disrupts the structure and self-association of the erythrocyte spectrin heterodimer.Sahr K.E., Coetzer T.L., Moy L.S., Derick L.H., Chishti A.H., Jarolim P., Lorenzo F., del Giudice E.M., Iolascon A.[...], Palek J.View abstractCited forVARIANT EL3 CAGLIARI GLY-2018CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Biol. Chem. 268:22656-22662 (1993)Cited in2
Beta spectrin Kissimmee: a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1.Becker P.S., Tse W.T., Lux S.E., Forget B.G.View abstractCited forINVOLVEMENT IN SPH2, VARIANT SPH2 ARG-202CategoriesSequences, Disease & VariantsSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Clin. Invest. 92:612-616 (1993)Cited in1
Identification of three novel spectrin alpha I/74 mutations in hereditary elliptocytosis: further support for a triple-stranded folding unit model of the spectrin heterodimer contact site.Parquet N., Devaux I., Boulanger L., Galand C., Boivin P., Lecomte M.-C., Dhermy D., Garbarz M.View abstractCited forVARIANTS EL3 VAL-2023 AND ARG-2024CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCBlood 84:303-308 (1994)Cited in2
Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene.Gallagher P.G., Weed S.A., Tse W.T., Benoit L., Morrow J.S., Marchesi S.L., Mohandas N., Forget B.G.View abstractCited forVARIANT EL3 PROVIDENCE PRO-2019CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Clin. Invest. 95:1174-1182 (1995)Cited in1
Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia.Gallagher P.G., Petruzzi M.J., Weed S.A., Zhang Z., Marchesi S.L., Mohandas N., Morrow J.S., Forget B.G.View abstractCited forVARIANT EL3 ARG-2025CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Clin. Invest. 99:267-277 (1997)Cited in1
Receptor-induced polymerization of coatomer.Reinhard C., Harter C., Bremser M., Brugger B., Sohn K., Helms J.B., Wieland F.T.View abstractAnnotationPathwayCategoriesFunctionSourceReactome: R-HSA-391565PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 96:1224-1228 (1999)Cited in1Mapped to46