Please enable Javascript

Labmeeting uses lots of Javascript - basically you can't use the site without it. So please enable Javascript in your browser. If your browser does not support Javascript, we recommend Firefox.

Papers authored by Rappaport EF

Collect these papers and discover other ones on Labmeeting. Learn more.

Cross-platform expression microarray performance in a mouse model of mitochondrial disease therapy.

+ cite this

+ View Abstract

Zhang Z, Gasser DL, Rappaport EF, and Falk MJ

Molecular genetics and metabolism 99(3):309-18, 2010 Mar - Who cited this? | PubMed ID: 19944634 | Fulltext

CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics.

+ cite this

+ View Abstract

Gai X, Perin JC, Murphy K, O'Hara R, D'arcy M, Wenocur A, Xie HM, Rappaport EF, Shaikh TH, and White PS

BMC bioinformatics 11(1):74, 2010 - Who cited this? | PubMed ID: 20132550 | Fulltext

High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications.

+ cite this

+ View Abstract

Shaikh TH, Gai X, Perin JC, Glessner JT, Xie H, Murphy K, O'Hara R, Casalunovo T, Conlin LK, D'Arcy M, Frackelton EC, Geiger EA, Haldeman-Englert C, Imielinski M, Kim CE, Medne L,

(show remaining authors)

Genome research 19(9):1682-90, 2009 Sep - Who cited this? | PubMed ID: 19592680 | Fulltext

Cyclical expression of the Notch/Wnt regulator Nrarp requires modulation by Dll3 in somitogenesis.

+ cite this

+ View Abstract

Sewell W, Sparrow DB, Smith AJ, Gonzalez DM, Rappaport EF, Dunwoodie SL, and Kusumi K

Developmental biology 329(2):400-9, 2009 May 15 - Who cited this? | PubMed ID: 19268448 | Fulltext

Proline affects brain function in 22q11DS children with the low activity COMT 158 allele.

+ cite this

+ View Abstract

Vorstman JA, Turetsky BI, Sijmens-Morcus ME, de Sain MG, Dorland B, Sprong M, Rappaport EF, Beemer FA, Emanuel BS, Kahn RS, van Engeland H, and Kemner C

Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 34(3):739-46, 2009 Feb - Who cited this? | PubMed ID: 18769474 | Fulltext

Chromosome 6p22 locus associated with clinically aggressive neuroblastoma.

+ cite this

+ View Abstract

Maris JM, Mosse YP, Bradfield JP, Hou C, Monni S, Scott RH, Asgharzadeh S, Attiyeh EF, Diskin SJ, Laudenslager M, Winter C, Cole KA, Glessner JT, Kim C, Frackelton EC, Casalunovo T,

(show remaining authors)

The New England journal of medicine 358(24):2585, 2008 Jun 12 - Who cited this? | PubMed ID: 18463370 | Fulltext

Dll3 and Notch1 genetic interactions model axial segmental and craniofacial malformations of human birth defects.

+ cite this

Loomes KM, Stevens SA, O'Brien ML, Gonzalez DM, Ryan MJ, Segalov M, Dormans NJ, Mimoto MS, Gibson JD, Sewell W, Schaffer AA, Nah HD, Rappaport EF, Pratt SC, Dunwoodie SL, and Kusumi K

Developmental dynamics : an official publication of the American Association of Anatomists 237(6):1754, 2008 Jun - Who cited this? | PubMed ID: 18488996 | Fulltext

De novo identification of MIZ-1 (ZBTB17) encoding a MYC-interacting zinc-finger protein as a new favorable neuroblastoma gene.

+ cite this

+ View Abstract

Ikegaki N, Gotoh T, Kung B, Riceberg JS, Kim DY, Zhao H, Rappaport EF, Hicks SL, Seeger RC, and Tang XX

Clinical cancer research : an official journal of the American Association for Cancer Research 13(20):6001-9, 2007 Oct 15 - Who cited this? | PubMed ID: 17947461 | Fulltext

Dll3 and Notch1 genetic interactions model axial segmental and craniofacial malformations of human birth defects.

+ cite this

+ View Abstract

Loomes KM, Stevens SA, O'Brien ML, Gonzalez DM, Ryan MJ, Segalov M, Dormans NJ, Mimoto MS, Gibson JD, Sewell W, Schaffer AA, Nah HD, Rappaport EF, Pratt SC, Dunwoodie SL, and Kusumi K

Developmental dynamics : an official publication of the American Association of Anatomists 236(10):2943-51, 2007 Oct - Who cited this? | PubMed ID: 17849441 | Fulltext

A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.

+ cite this

+ View Abstract

Hakonarson H, Grant SF, Bradfield JP, Marchand L, Kim CE, Glessner JT, Grabs R, Casalunovo T, Taback SP, Frackelton EC, Lawson ML, Robinson LJ, Skraban R, Lu Y, Chiavacci RM, Stanley CA,

(show remaining authors)

Nature 448(7153):591-4, 2007 Aug 2 - Who cited this? | PubMed ID: 17632545 | Fulltext

Identification of oscillatory genes in somitogenesis from functional genomic analysis of a human mesenchymal stem cell model.

+ cite this

+ View Abstract

William DA, Saitta B, Gibson JD, Traas J, Markov V, Gonzalez DM, Sewell W, Anderson DM, Pratt SC, Rappaport EF, and Kusumi K

Developmental biology 305(1):172-86, 2007 May 1 - Who cited this? | PubMed ID: 17362910 | Fulltext

Identification of cord blood-derived mesenchymal stem/stromal cell populations with distinct growth kinetics, differentiation potentials, and gene expression profiles.

+ cite this

+ View Abstract

Markov V, Kusumi K, Tadesse MG, William DA, Hall DM, Lounev V, Carlton A, Leonard J, Cohen RI, Rappaport EF, and Saitta B

Stem cells and development 16(1):53-73, 2007 Feb - Who cited this? | PubMed ID: 17348805 | Fulltext

MLPA: a rapid, reliable, and sensitive method for detection and analysis of abnormalities of 22q.

+ cite this

+ View Abstract

Vorstman JA, Jalali GR, Rappaport EF, Hacker AM, Scott C, and Emanuel BS

Human mutation 27(8):814-21, 2006 Aug - Who cited this? | PubMed ID: 16791841 | Fulltext

Differential gene expression in mouse sclera during ocular development.

+ cite this

+ View Abstract

Zhou J, Rappaport EF, Tobias JW, and Young TL

Investigative ophthalmology & visual science 47(5):1794, 2006 May - Who cited this? | PubMed ID: 16638983 | Fulltext

Norrie disease gene sequence variants in an ethnically diverse population with retinopathy of prematurity.

+ cite this

+ View Abstract

Hutcheson KA, Paluru PC, Bernstein SL, Koh J, Rappaport EF, Leach RA, and Young TL

Molecular vision 11:501, 2005 Jul 14 - Who cited this? | PubMed ID: 16052165 | Fulltext

Identification of a novel locus on 2q for autosomal dominant high-grade myopia.

+ cite this

+ View Abstract

Paluru PC, Nallasamy S, Devoto M, Rappaport EF, and Young TL

Investigative ophthalmology & visual science 46(7):2300-7, 2005 Jul - Who cited this? | PubMed ID: 15980214 | Fulltext

Genomic structure and organization of the high grade Myopia-2 locus (MYP2) critical region: mutation screening of 9 positional candidate genes.

+ cite this

+ View Abstract

Scavello GS, Paluru PC, Zhou J, White PS, Rappaport EF, and Young TL

Molecular vision 11:97, 2005 Feb 2 - Who cited this? | PubMed ID: 15723005 | Fulltext

Microarray analysis of gene expression in human donor sclera.

+ cite this

+ View Abstract

Young TL, Scavello GS, Paluru PC, Choi JD, Rappaport EF, and Rada JA

Molecular vision 10:163, 2004 Mar 22 - Who cited this? | PubMed ID: 15041956 | Fulltext

Reciprocal DNA topoisomerase II cleavage events at 5'-TATTA-3' sequences in MLL and AF-9 create homologous single-stranded overhangs that anneal to form der(11) and der(9) genomic breakpoint junctions in treatment-related AML without further processing.

+ cite this

+ View Abstract

Whitmarsh RJ, Saginario C, Zhuo Y, Hilgenfeld E, Rappaport EF, Megonigal MD, Carroll M, Liu M, Osheroff N, Cheung NK, Slater DJ, Ried T, Knutsen T, Blair IA, and Felix CA

Oncogene 22(52):8448-59, 2003 Nov 20 - Who cited this? | PubMed ID: 14627986 | Fulltext

Expression profiles of acute lymphoblastic and myeloblastic leukemias with ALL-1 rearrangements.

+ cite this

+ View Abstract

Rozovskaia T, Ravid-Amir O, Tillib S, Getz G, Feinstein E, Agrawal H, Nagler A, Rappaport EF, Issaeva I, Matsuo Y, Kees UR, Lapidot T, Lo Coco F, Foa R, Mazo A, Nakamura T,

(show remaining authors)

Proceedings of the National Academy of Sciences of the United States of America 100(13):7853-8, 2003 Jun 24 - Who cited this? | PubMed ID: 12782787 | Fulltext

MLL-SEPTIN6 fusion recurs in novel translocation of chromosomes 3, X, and 11 in infant acute myelomonocytic leukaemia and in t(X;11) in infant acute myeloid leukaemia, and MLL genomic breakpoint in complex MLL-SEPTIN6 rearrangement is a DNA topoisomerase II cleavage site.

+ cite this

+ View Abstract

Slater DJ, Hilgenfeld E, Rappaport EF, Shah N, Meek RG, Williams WR, Lovett BD, Osheroff N, Autar RS, Ried T, and Felix CA

Oncogene 21(30):4706-14, 2002 Jul 11 - Who cited this? | PubMed ID: 12096348 | Fulltext

Panhandle and reverse-panhandle PCR enable cloning of der(11) and der(other) genomic breakpoint junctions of MLL translocations and identify complex translocation of MLL, AF-4, and CDK6.

+ cite this

+ View Abstract

Raffini LJ, Slater DJ, Rappaport EF, Lo Nigro L, Cheung NK, Biegel JA, Nowell PC, Lange BJ, and Felix CA

Proceedings of the National Academy of Sciences of the United States of America 99(7):4568-73, 2002 Apr 2 - Who cited this? | PubMed ID: 11930009 | Fulltext

Near-precise interchromosomal recombination and functional DNA topoisomerase II cleavage sites at MLL and AF-4 genomic breakpoints in treatment-related acute lymphoblastic leukemia with t(4;11) translocation.

+ cite this

+ View Abstract

Lovett BD, Lo Nigro L, Rappaport EF, Blair IA, Osheroff N, Zheng N, Megonigal MD, Williams WR, Nowell PC, and Felix CA

Proceedings of the National Academy of Sciences of the United States of America 98(17):9802-7, 2001 Aug 14 - Who cited this? | PubMed ID: 11493704 | Fulltext

Etoposide metabolites enhance DNA topoisomerase II cleavage near leukemia-associated MLL translocation breakpoints.

+ cite this

+ View Abstract

Lovett BD, Strumberg D, Blair IA, Pang S, Burden DA, Megonigal MD, Rappaport EF, Rebbeck TR, Osheroff N, Pommier YG, and Felix CA

Biochemistry 40(5):1159-70, 2001 Feb 6 - Who cited this? | PubMed ID: 11170441 | Fulltext

t(3;11) translocation in treatment-related acute myeloid leukemia fuses MLL with the GMPS (GUANOSINE 5' MONOPHOSPHATE SYNTHETASE) gene.

+ cite this

+ View Abstract

Pegram LD, Megonigal MD, Lange BJ, Nowell PC, Rowley JD, Rappaport EF, and Felix CA

Blood 96(13):4360-2, 2000 Dec 15 - Who cited this? | PubMed ID: 11110714 | Fulltext

Panhandle PCR for cDNA: a rapid method for isolation of MLL fusion transcripts involving unknown partner genes.

+ cite this

+ View Abstract

Megonigal MD, Rappaport EF, Wilson RB, Jones DH, Whitlock JA, Ortega JA, Slater DJ, Nowell PC, and Felix CA

Proceedings of the National Academy of Sciences of the United States of America 97(17):9597-602, 2000 Aug 15 - Who cited this? | PubMed ID: 10920186 | Fulltext

Detection of leukemia-associated MLL-GAS7 translocation early during chemotherapy with DNA topoisomerase II inhibitors.

+ cite this

+ View Abstract

Megonigal MD, Cheung NK, Rappaport EF, Nowell PC, Wilson RB, Jones DH, Addya K, Leonard DG, Kushner BH, Williams TM, Lange BJ, and Felix CA

Proceedings of the National Academy of Sciences of the United States of America 97(6):2814-9, 2000 Mar 14 - Who cited this? | PubMed ID: 10706619 | Fulltext

Duplicated regions of AF-4 intron 4 at t(4;11) translocation breakpoints.

+ cite this

+ View Abstract

Felix CA, Hosler MR, Slater DJ, Megonigal MD, Lovett BD, Williams TM, Nowell PC, Spinner NB, Owens NL, Hoxie J, Croce CM, Lange BJ, and Rappaport EF

Molecular diagnosis : a journal devoted to the understanding of human disease through the clinical application of molecular biology 4(4):269-83, 1999 Dec - Who cited this? | PubMed ID: 10671636 | Fulltext

t(11;22)(q23;q11.2) In acute myeloid leukemia of infant twins fuses MLL with hCDCrel, a cell division cycle gene in the genomic region of deletion in DiGeorge and velocardiofacial syndromes.

+ cite this

+ View Abstract

Megonigal MD, Rappaport EF, Jones DH, Williams TM, Lovett BD, Kelly KM, Lerou PH, Moulton T, Budarf ML, and Felix CA

Proceedings of the National Academy of Sciences of the United States of America 95(11):6413, 1998 May 26 - Who cited this? | PubMed ID: 9600980 | Fulltext

Potential role for wild-type p53 in leukemias with MLL gene translocations.

+ cite this

+ View Abstract

Megonigal MD, Rappaport EF, Nowell PC, Lange BJ, and Felix CA

Oncogene 16(10):1351-6, 1998 Mar 12 - Who cited this? | PubMed ID: 9546437 | Fulltext

Panhandle polymerase chain reaction amplifies MLL genomic translocation breakpoint involving unknown partner gene.

+ cite this

+ View Abstract

Felix CA, Kim CS, Megonigal MD, Slater DJ, Jones DH, Spinner NB, Stump T, Hosler MR, Nowell PC, Lange BJ, and Rappaport EF

Blood 90(12):4679-86, 1997 Dec 15 - Who cited this? | PubMed ID: 9389682 | Fulltext

Panhandle PCR strategy to amplify MLL genomic breakpoints in treatment-related leukemias.

+ cite this

+ View Abstract

Megonigal MD, Rappaport EF, Jones DH, Kim CS, Nowell PC, Lange BJ, and Felix CA

Proceedings of the National Academy of Sciences of the United States of America 94(21):11583-8, 1997 Oct 14 - Who cited this? | PubMed ID: 9326653 | Fulltext

Molecular analysis of a compound heterozygote for hypoprothrombinemia and dysprothrombinemia (-G 7248/7249 and ARG 340 TRP).

+ cite this

+ View Abstract

Tamary H, Surrey S, Augustine J, Shalmon L, Schwartz E, and Rappaport EF

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 8(6):337-43, 1997 Sep - Who cited this? | PubMed ID: 9351523 | Fulltext

Lineage-specific alternative splicing of the human Fc gamma RIIA transmembrane exon requires sequences near the 3' splice site.

+ cite this

+ View Abstract

Keller MA, McKenzie SE, Cassel DL, Rappaport EF, Schwartz E, and Surrey S

Gene expression 4(4-5):217-25, 1995 - Who cited this? | PubMed ID: 7787414 | Fulltext

Genetic diversity in human Fc receptor II for immunoglobulin G: Fc gamma receptor IIA ligand-binding polymorphism.

+ cite this

+ View Abstract

Reilly AF, Norris CF, Surrey S, Bruchak FJ, Rappaport EF, Schwartz E, and McKenzie SE

Clinical and diagnostic laboratory immunology 1(6):640-4, 1994 Nov - Who cited this? | PubMed ID: 8556514 | Fulltext

Systematic use of automated fluorescence-based sequence analysis of amplified genomic DNA for rapid detection of point mutations.

+ cite this

+ View Abstract

Tamary H, Surrey S, Kirschmann H, Shalmon L, Zaizov R, Schwartz E, and Rappaport EF

American journal of hematology 46(2):127-33, 1994 Jun - Who cited this? | PubMed ID: 8172179 | Fulltext

Variation in human FCGR2C gene copy number.

+ cite this

Reilly AF, Surrey S, Rappaport EF, Schwartz E, and McKenzie SE

Immunogenetics 40(6):456, 1994 - Who cited this? | PubMed ID: 7959956 | Fulltext

Fluorescence-based RT PCR analysis: determination of the ratio of soluble to membrane-bound forms of Fc gamma RIIA transcripts in hematopoietic cell lines.

+ cite this

+ View Abstract

Keller MA, Cassel DL, Rappaport EF, McKenzie SE, Schwartz E, and Surrey S

PCR methods and applications 3(1):32-8, 1993 Aug - Who cited this? | PubMed ID: 8220183 | Fulltext

A soluble form of the human Fc receptor Fc gamma RIIA: cloning, transcript analysis and detection.

+ cite this

+ View Abstract

Rappaport EF, Cassel DL, Walterhouse DO, McKenzie SE, Surrey S, Keller MA, Schreiber AD, and Schwartz E

Experimental hematology 21(5):689-96, 1993 May - Who cited this? | PubMed ID: 8513871 | Fulltext

Differential expression of Fc gamma RIIA, Fc gamma RIIB and Fc gamma RIIC in hematopoietic cells: analysis of transcripts.

+ cite this

+ View Abstract

Cassel DL, Keller MA, Surrey S, Schwartz E, Schreiber AD, Rappaport EF, and McKenzie SE

Molecular immunology 30(5):451-60, 1993 Apr - Who cited this? | PubMed ID: 8464427 | Fulltext

Characterization of the 5'-flanking transcriptional regulatory region of the human Fc gamma receptor gene, Fc gamma RIIA.

+ cite this

+ View Abstract

McKenzie SE, Keller MA, Cassel DL, Schreiber AD, Schwartz E, Surrey S, and Rappaport EF

Molecular immunology 29(10):1165-74, 1992 Oct - Who cited this? | PubMed ID: 1382218 | Fulltext

Polymerase chain reaction (PCR) for detection of PstI polymorphism in the human PF4 gene.

+ cite this

Ramachandran B, Rappaport EF, Surrey S, Poncz M, and Schwartz E

Nucleic acids research 18(19):5919, 1990 Oct 11 - Who cited this? | PubMed ID: 1977142 | Fulltext

Modulation of human mononuclear phagocyte Fc gamma RII mRNA and protein.

+ cite this

+ View Abstract

Comber PG, Rossman MD, Rappaport EF, Chien P, Hogarth PM, and Schreiber AD

Cellular immunology 124(2):292-307, 1989 Dec - Who cited this? | PubMed ID: 2531041 | Fulltext

Rheologic predictors of the severity of the painful sickle cell crisis.

+ cite this

+ View Abstract

Ballas SK, Larner J, Smith ED, Surrey S, Schwartz E, and Rappaport EF

Blood 72(4):1216-23, 1988 Oct - Who cited this? | PubMed ID: 3167204 | Fulltext

A Taq 1 polymorphism for the human platelet glycoprotein IIIa gene (GP3A).

+ cite this

Burk C, Ingram C, Weiner M, Rappaport EF, Schwartz E, and Poncz M

Nucleic acids research 16(14B):7216, 1988 Jul 25 - Who cited this? | PubMed ID: 2900503 | Fulltext

The xerocytosis of Hb SC disease.

+ cite this

+ View Abstract

Ballas SK, Larner J, Smith ED, Surrey S, Schwartz E, and Rappaport EF

Blood 69(1):124-30, 1987 Jan - Who cited this? | PubMed ID: 2947642 | Fulltext

Cloning and characterization of platelet factor 4 cDNA derived from a human erythroleukemic cell line.

+ cite this

+ View Abstract

Poncz M, Surrey S, LaRocco P, Weiss MJ, Rappaport EF, Conway TM, and Schwartz E

Blood 69(1):219-23, 1987 Jan - Who cited this? | PubMed ID: 3098319 | Fulltext

Hemoglobin I mutation encoded at both alpha-globin loci on the same chromosome: concerted evolution in the human genome.

+ cite this

+ View Abstract

Liebhaber SA, Rappaport EF, Cash FE, Ballas SK, Schwartz E, and Surrey S

Science (New York, N.Y.) 226(4681):1449-51, 1984 Dec 21 - Who cited this? | PubMed ID: 6505702 | Fulltext

Frequent occurrence of a zeta-globin-region deletion in American blacks accounts for a previously-described restriction site polymorphism.

+ cite this

+ View Abstract

Rappaport EF, Schwartz E, Poncz M, and Surrey S

Biochemical and biophysical research communications 125(2):817-23, 1984 Dec 14 - Who cited this? | PubMed ID: 6097249 | Fulltext

Search Google Scholar for Rappaport EF

Join Labmeeting

Organize and search your PDF collection
Collect papers
Search millions of papers
Keep up to date with paper alerts
Read your papers from anywhere
Recommend papers to colleagues
Manage your lab

Labmeeting is a web service for researchers. Sign up with your academic email address.

Individuals or corporations not affiliated with an academic institution can request a trial subscription.