| Year |
Citation |
Score |
| 2014 |
Londin ER, Adijanto J, Philp N, Novelli A, Vitale E, Perria C, Serra G, Alesi V, Surrey S, Fortina P. Donor splice-site mutation in CUL4B is likely cause of X-linked intellectual disability. American Journal of Medical Genetics. Part A. 164: 2294-9. PMID 24898194 DOI: 10.1002/Ajmg.A.36629 |
0.439 |
|
| 2014 |
Pandey AS, San Antonio JD, Addya S, Surrey S, Fortina P, Van Bockstaele EJ, Veznedaroglu E. Mechanisms of endothelial cell attachment, proliferation, and differentiation on 4 types of platinum-based endovascular coils. World Neurosurgery. 82: 684-95. PMID 23994074 DOI: 10.1016/J.Wneu.2013.08.029 |
0.347 |
|
| 2014 |
Bhatlekar S, Addya S, Salunek M, Orr CR, Surrey S, McKenzie S, Fields JZ, Boman BM. Identification of a developmental gene expression signature, including HOX genes, for the normal human colonic crypt stem cell niche: overexpression of the signature parallels stem cell overpopulation during colon tumorigenesis. Stem Cells and Development. 23: 167-79. PMID 23980595 DOI: 10.1089/Scd.2013.0039 |
0.448 |
|
| 2013 |
Londin E, Yadav P, Surrey S, Kricka LJ, Fortina P. Use of linkage analysis, genome-wide association studies, and next-generation sequencing in the identification of disease-causing mutations. Methods in Molecular Biology (Clifton, N.J.). 1015: 127-46. PMID 23824853 DOI: 10.1007/978-1-62703-435-7_8 |
0.377 |
|
| 2011 |
Londin ER, Keller MA, D'Andrea MR, Delgrosso K, Ertel A, Surrey S, Fortina P. Whole-exome sequencing of DNA from peripheral blood mononuclear cells (PBMC) and EBV-transformed lymphocytes from the same donor. Bmc Genomics. 12: 464. PMID 21943378 DOI: 10.1186/1471-2164-12-464 |
0.369 |
|
| 2011 |
Chetta M, Drmanac A, Santacroce R, Grandone E, Surrey S, Fortina P, Margaglione M. Identification of FVIII gene mutations in patients with hemophilia A using new combinatorial sequencing by hybridization. Indian Journal of Human Genetics. 14: 55-64. PMID 20300295 DOI: 10.4103/0971-6866.44106 |
0.428 |
|
| 2010 |
Bernardini L, Alesi V, Loddo S, Novelli A, Bottillo I, Battaglia A, Digilio MC, Zampino G, Ertel A, Fortina P, Surrey S, Dallapiccola B. High-resolution SNP arrays in mental retardation diagnostics: how much do we gain? European Journal of Human Genetics : Ejhg. 18: 178-85. PMID 19809473 DOI: 10.1038/Ejhg.2009.154 |
0.386 |
|
| 2009 |
Adachi K, Ding M, Asakura T, Surrey S. Relationship between beta4 hydrogen bond and beta6 hydrophobic interactions during aggregate, fiber or crystal formation in oversaturated solutions of hemoglobin A and S. Archives of Biochemistry and Biophysics. 481: 137-44. PMID 19022217 DOI: 10.1016/J.Abb.2008.11.006 |
0.34 |
|
| 2008 |
Battistella S, Damin F, Chiari M, Delgrosso K, Surrey S, Fortina P, Ferrari M, Cremonesi L. Genotyping beta-globin gene mutations on copolymer-coated glass slides with the ligation detection reaction. Clinical Chemistry. 54: 1657-63. PMID 18703765 DOI: 10.1373/Clinchem.2008.107870 |
0.436 |
|
| 2008 |
Adachi K, Ding M, Surrey S. Role of the beta4Thr-beta73Asp hydrogen bond in HbS polymer and domain formation from multinucleate-containing clusters. Biochemistry. 47: 5441-9. PMID 18419131 DOI: 10.1021/Bi800149U |
0.4 |
|
| 2008 |
Fortina P, Surrey S. Digital mRNA profiling. Nature Biotechnology. 26: 293-4. PMID 18327237 DOI: 10.1038/Nbt0308-293 |
0.422 |
|
| 2008 |
Thirunavukkarasu M, Addya S, Juhasz B, Pant R, Zhan L, Surrey S, Maulik G, Menon VP, Maulik N. Heterozygous disruption of Flk-1 receptor leads to myocardial ischaemia reperfusion injury in mice: application of affymetrix gene chip analysis. Journal of Cellular and Molecular Medicine. 12: 1284-302. PMID 18266966 DOI: 10.1111/J.1582-4934.2008.00269.X |
0.384 |
|
| 2008 |
Anni F, Galanello R, Surrey S, Fortina PM, Bowser M, Devoto M. Genome-Wide Association Study for Hb F Determinants in Sardinian Patients with Thalassemia Major and Intermedia. Blood. 112: 1875-1875. DOI: 10.1182/Blood.V112.11.1875.1875 |
0.465 |
|
| 2007 |
Adachi K, Zhao Y, Lakka V, Weiss MJ, Surrey S. Assembly of recently translated full-length and C-terminal truncated human gamma-globin chains with a pool of alpha-globin chains to form Hb F in a cell-free system. Archives of Biochemistry and Biophysics. 463: 60-7. PMID 17418086 DOI: 10.1016/J.Abb.2007.02.030 |
0.383 |
|
| 2007 |
Fortina P, Kricka LJ, Graves DJ, Park J, Hyslop T, Tam F, Halas N, Surrey S, Waldman SA. Applications of nanoparticles to diagnostics and therapeutics in colorectal cancer. Trends in Biotechnology. 25: 145-52. PMID 17316852 DOI: 10.1016/J.Tibtech.2007.02.005 |
0.321 |
|
| 2006 |
Waldman SA, Fortina P, Surrey S, Hyslop T, Kricka LJ, Graves DJ. Opportunities for near-infrared thermal ablation of colorectal metastases by guanylyl cyclase C-targeted gold nanoshells. Future Oncology (London, England). 2: 705-16. PMID 17155897 DOI: 10.2217/14796694.2.6.705 |
0.322 |
|
| 2006 |
Keller MA, Addya S, Vadigepalli R, Banini B, Delgrosso K, Huang H, Surrey S. Transcriptional regulatory network analysis of developing human erythroid progenitors reveals patterns of coregulation and potential transcriptional regulators. Physiological Genomics. 28: 114-28. PMID 16940433 DOI: 10.1152/Physiolgenomics.00055.2006 |
0.735 |
|
| 2006 |
Adachi K, Ding M, Surrey S, Rotter M, Aprelev A, Zakharov M, Weng W, Ferrone FA. The Hb A variant (beta73 Asp-->Leu) disrupts Hb S polymerization by a novel mechanism. Journal of Molecular Biology. 362: 528-38. PMID 16926024 DOI: 10.1016/J.Jmb.2006.07.047 |
0.35 |
|
| 2006 |
Akbar MG, Tamura Y, Ding M, Ding H, Rosenblatt MM, Reddy KS, Surrey S, Adachi K. Inhibition of hemoglobin S polymerization in vitro by a novel 15-mer EF-helix beta73 histidine-containing peptide. Biochemistry. 45: 8358-67. PMID 16819835 DOI: 10.1021/Bi0604734 |
0.391 |
|
| 2006 |
Schirinzi A, Drmanac S, Dallapiccola B, Huang S, Scott K, De Luca A, Swanson D, Drmanac R, Surrey S, Fortina P. Combinatorial sequencing-by-hybridization: analysis of the NF1 gene. Genetic Testing. 10: 8-17. PMID 16544997 DOI: 10.1089/Gte.2006.10.8 |
0.46 |
|
| 2006 |
Banini BA, Addya S, Delgrosso K, Keller MA, Surrey S. 53 EARLY EXPOSURE TO BUTYRATE INCREASES FETAL HEMOGLOBIN DURING ADULT ERYTHROID DEVELOPMENT IN VITRO. Journal of Investigative Medicine. 54: S352.2-S352. DOI: 10.2310/6650.2005.X0015.52 |
0.392 |
|
| 2006 |
Adachi K, Zhao Y, Lakka V, Weiss MJ, Surrey S. Assembly of Recently Translated Human γ-Globin Chains with a Pool of α-Globin Chains To Form Hb F in a Cell-Free System. Blood. 108: 366-366. DOI: 10.1182/Blood.V108.11.366.366 |
0.386 |
|
| 2005 |
Maris JM, Hii G, Gelfand CA, Varde S, White PS, Rappaport E, Surrey S, Fortina P. Region-specific detection of neuroblastoma loss of heterozygosity at multiple loci simultaneously using a SNP-based tag-array platform. Genome Research. 15: 1168-76. PMID 16077016 DOI: 10.1101/Gr.3865305 |
0.426 |
|
| 2005 |
Fortina P, Kricka LJ, Surrey S, Grodzinski P. Nanobiotechnology: the promise and reality of new approaches to molecular recognition. Trends in Biotechnology. 23: 168-73. PMID 15780707 DOI: 10.1016/J.Tibtech.2005.02.007 |
0.323 |
|
| 2005 |
Chen W, Tang Z, Fortina P, Patel P, Addya S, Surrey S, Acheampong EA, Mukhtar M, Pomerantz RJ. Ethanol potentiates HIV-1 gp120-induced apoptosis in human neurons via both the death receptor and NMDA receptor pathways. Virology. 334: 59-73. PMID 15749123 DOI: 10.1016/J.Virol.2005.01.014 |
0.326 |
|
| 2005 |
Addya S, Shiroto K, Turoczi T, Zhan L, Kaga S, Fukuda S, Surrey S, Duan LJ, Fong GH, Yamamoto F, Maulik N. Ischemic preconditioning-mediated cardioprotection is disrupted in heterozygous Flt-1 (VEGFR-1) knockout mice. Journal of Molecular and Cellular Cardiology. 38: 345-51. PMID 15698841 DOI: 10.1016/J.Yjmcc.2004.11.033 |
0.377 |
|
| 2005 |
Keller MA, Martinez J, Baradet TC, Nagaswami C, Chernysh IN, Borowski MK, Surrey S, Weisel JW. Fibrinogen Philadelphia, a hypodysfibrinogenemia characterized by abnormal polymerization and fibrinogen hypercatabolism due to gamma S378P mutation. Blood. 105: 3162-8. PMID 15632207 DOI: 10.1182/Blood-2004-04-1621 |
0.431 |
|
| 2005 |
Keller MA, Addya S, Vadigepalli R, Ponte CM, Banini B, Delgrosso K, Surrey S. Transcriptome Analysis of Human Hematopoietic Progenitor Cells during In Vitro Erythroid Differentiation. Blood. 106: 1750-1750. DOI: 10.1182/Blood.V106.11.1750.1750 |
0.744 |
|
| 2004 |
Cowie S, Drmanac S, Swanson D, Delgrosso K, Huang S, du Sart D, Drmanac R, Surrey S, Fortina P. Identification of APC gene mutations in colorectal cancer using universal microarray-based combinatorial sequencing-by-hybridization. Human Mutation. 24: 261-71. PMID 15300853 DOI: 10.1002/Humu.20078 |
0.456 |
|
| 2004 |
Adachi K, Lakka V, Zhao Y, Surrey S. Ubiquitylation of nascent globin chains in a cell-free system. The Journal of Biological Chemistry. 279: 41767-74. PMID 15297454 DOI: 10.1074/Jbc.M405059200 |
0.374 |
|
| 2004 |
Addya S, Keller MA, Delgrosso K, Ponte CM, Vadigepalli R, Gonye GE, Surrey S. Erythroid-induced commitment of K562 cells results in clusters of differentially expressed genes enriched for specific transcription regulatory elements. Physiological Genomics. 19: 117-30. PMID 15252187 DOI: 10.1152/Physiolgenomics.00028.2004 |
0.442 |
|
| 2004 |
Tang Z, McGowan BS, Huber SA, McTiernan CF, Addya S, Surrey S, Kubota T, Fortina P, Higuchi Y, Diamond MA, Wyre DS, Feldman AM. Gene expression profiling during the transition to failure in TNF-α over-expressing mice demonstrates the development of autoimmune myocarditis Journal of Molecular and Cellular Cardiology. 36: 515-530. PMID 15081311 DOI: 10.1016/J.Yjmcc.2004.01.008 |
0.386 |
|
| 2004 |
Sharan K, Surrey S, Ballas S, Borowski M, Devoto M, Wang KF, Sandler E, Keller M. Association of T-786C eNOS gene polymorphism with increased susceptibility to acute chest syndrome in females with sickle cell disease. British Journal of Haematology. 124: 240-3. PMID 14687036 DOI: 10.1046/J.1365-2141.2003.04762.X |
0.387 |
|
| 2004 |
Keller MA, Borowski MK, Devoto M, Li H, Brown M, Surrey S, Ballas SK. Predictors of Renal Insufficiency in Sickle Cell Disease. Blood. 104: 3747-3747. DOI: 10.1182/Blood.V104.11.3747.3747 |
0.403 |
|
| 2004 |
Akbar MG, Ding M, Surrey S, Adachi K. Inhibition of Hb S Polymerization In Vitro by a Novel EF Helix ß73 His Containing Peptide. Blood. 104: 3569-3569. DOI: 10.1182/Blood.V104.11.3569.3569 |
0.352 |
|
| 2004 |
Sharan K, Surrey S, Ballas SK, Borowski MK, Devoto M, Wang K, Sandler E, Keller MA. Reply to 'Gender-specific disease modification by NOS3' British Journal of Haematology. 126: 161-161. DOI: 10.1111/J.1365-2141.2004.05002.X |
0.376 |
|
| 2003 |
Palmieri O, Toth S, Ferraris A, Andriulli A, Latiano A, Annese V, Dallapiccola B, Vecchi M, Devoto M, Surrey S, Fortina P. CARD15 genotyping in inflammatory bowel disease patients by multiplex pyrosequencing. Clinical Chemistry. 49: 1675-9. PMID 14500598 DOI: 10.1373/49.10.1675 |
0.4 |
|
| 2003 |
Adachi K, Yang Y, Lakka V, Wehrli S, Reddy KS, Surrey S. Significance of beta116 His (G18) at alpha1beta1 contact sites for alphabeta assembly and autoxidation of hemoglobin. Biochemistry. 42: 10252-9. PMID 12939154 DOI: 10.1021/Bi030095S |
0.437 |
|
| 2003 |
Adachi K, Zhao Y, Surrey S. Effects of heme addition on formation of stable human globin chains and hemoglobin subunit assembly in a cell-free system. Archives of Biochemistry and Biophysics. 413: 99-106. PMID 12706346 DOI: 10.1016/S0003-9861(03)00089-4 |
0.426 |
|
| 2003 |
Adachi K, Ding M, Wehrli S, Reddy KS, Surrey S, Horiuchi K. Effects of different beta73 amino acids on formation of 14-stranded fibers of Hb S versus double-stranded crystals of Hb C-Harlem. Biochemistry. 42: 4476-84. PMID 12693943 DOI: 10.1021/Bi026740X |
0.417 |
|
| 2003 |
Kajiyama T, Miyahara Y, Kricka LJ, Wilding P, Graves DJ, Surrey S, Fortina P. Genotyping on a thermal gradient DNA chip. Genome Research. 13: 467-75. PMID 12618377 DOI: 10.1101/Gr.790603 |
0.405 |
|
| 2003 |
Fortina P, Kricka LJ, Surrey S. DNA Chips and Their Medical Applications The Japan Society of Applied Physics. DOI: 10.7567/Ssdm.2003.F-5-1 |
0.327 |
|
| 2002 |
Santacroce R, Ratti A, Caroli F, Foglieni B, Ferraris A, Cremonesi L, Margaglione M, Seri M, Ravazzolo R, Restagno G, Dallapiccola B, Rappaport E, Pollak ES, Surrey S, Ferrari M, et al. Analysis of clinically relevant single-nucleotide polymorphisms by use of microelectronic array technology. Clinical Chemistry. 48: 2124-30. PMID 12446467 DOI: 10.1093/Clinchem/48.12.2124 |
0.401 |
|
| 2002 |
Ferraris A, Rappaport E, Santacroce R, Pollak E, Krantz I, Toth S, Lysholm F, Margaglione M, Restagno G, Dallapiccola B, Surrey S, Fortina P. Pyrosequencing for detection of mutations in the connexin 26 (GJB2) and mitochondrial 12S RNA (MTRNR1) genes associated with hereditary hearing loss. Human Mutation. 20: 312-20. PMID 12325027 DOI: 10.1002/Humu.10127 |
0.444 |
|
| 2002 |
Heeney MM, Delgrosso K, Robinson R, Johnson CA, Daeschner CW, Campbell TA, Surrey S, Ware RE. Interpretation of fetal hemoglobin only on newborn screening for hemoglobinopathy. Journal of Pediatric Hematology/Oncology. 24: 499-502. PMID 12218602 DOI: 10.1097/00043426-200208000-00019 |
0.382 |
|
| 2002 |
Su HJ, Surrey S, McKenzie SE, Fortina P, Graves DJ. Kinetics of heterogeneous hybridization on indium tin oxide surfaces with and without an applied potential Electrophoresis. 23: 1551-1557. PMID 12116168 DOI: 10.1002/1522-2683(200205)23:10<1551::Aid-Elps1551>3.0.Co;2-9 |
0.375 |
|
| 2002 |
Fortina P, Surrey S, Kricka LJ. Molecular diagnostics: hurdles for clinical implementation. Trends in Molecular Medicine. 8: 264-6. PMID 12067610 DOI: 10.1016/S1471-4914(02)02331-6 |
0.366 |
|
| 2002 |
Graves DJ, Su HJ, Addya S, Surrey S, Fortina P. Four-laser scanning confocal system for microarray analysis Biotechniques. 32: 346-354. PMID 11848412 DOI: 10.2144/02322Rr01 |
0.343 |
|
| 2002 |
Adachi K, Zhao Y, Surrey S. Assembly of human hemoglobin (Hb) beta- and gamma-globin chains expressed in a cell-free system with alpha-globin chains to form Hb A and Hb F. The Journal of Biological Chemistry. 277: 13415-20. PMID 11827978 DOI: 10.1074/Jbc.M200857200 |
0.43 |
|
| 2002 |
Miyahara Y, Kajiyama T, Kricka LJ, Graves DJ, Surrey S, Fortina P. SNP Detection Using Thermal Gradient DNA Chip The Japan Society of Applied Physics. DOI: 10.7567/Ssdm.2002.F-6-3 |
0.361 |
|
| 2000 |
Cassel DL, Subudhi SK, Surrey S, McKenzie SE. GATA and NF-Y participate in transcriptional regulation of FcγRIIA in megakaryocytic cells Blood Cells, Molecules, and Diseases. 26: 587-597. PMID 11112392 DOI: 10.1006/Bcmd.2000.0337 |
0.394 |
|
| 2000 |
Manduchi E, Grant GR, McKenzie SE, Overton GC, Surrey S, Stoeckert CJ. Generation of patterns from gene expression data by assigning confidence to differentially expressed genes Bioinformatics. 16: 685-698. PMID 11099255 DOI: 10.1093/Bioinformatics/16.8.685 |
0.433 |
|
| 2000 |
Fortina P, Delgrosso K, Sakazume T, Santacroce R, Moutereau S, Su HJ, Graves D, McKenzie S, Surrey S. Simple two-color array-based approach for mutation detection. European Journal of Human Genetics : Ejhg. 8: 884-94. PMID 11093279 DOI: 10.1038/Sj.Ejhg.5200558 |
0.445 |
|
| 2000 |
Adachi K, Yamaguchi T, Yang Y, Konitzer PT, Pang J, Reddy KS, Ivanova M, Ferrone F, Surrey S. Expression of functional soluble human α-globin chains of hemoglobin in bacteria Protein Expression and Purification. 20: 37-44. PMID 11035948 DOI: 10.1006/Prep.2000.1277 |
0.265 |
|
| 2000 |
Keller MA, Delgrosso K, Surrey S, Schwartz E. Identification of the nucleotide change (CAC → CGC) responsible for Hb P-Galveston [β117(G19)His → Arg] Hemoglobin. 24: 165-167. PMID 10870891 |
0.524 |
|
| 2000 |
Adachi K, Zhao Y, Yamaguchi T, Surrey S. Assembly of gamma- with alpha-globin chains to form human fetal hemoglobin in vitro and in vivo. The Journal of Biological Chemistry. 275: 12424-9. PMID 10777526 DOI: 10.1074/Jbc.C000137200 |
0.415 |
|
| 2000 |
McKenzie SE, Surrey S, Orr CR, Schmidt LC, Ni H, Grant GR, Manduchi E, Overton GC, Stoeckert CJ. Array-based analysis of gene expression: New candidates for the biological basis of normal and malignant erythroid development Journal of Pediatric Hematology/Oncology. 22: 365. DOI: 10.1097/00043426-200007000-00019 |
0.419 |
|
| 1999 |
McKenzie SE, Taylor SM, Malladi P, Yuhan H, Cassel DL, Chien P, Schwartz E, Schreiber AD, Surrey S, Reilly MP. The role of the human Fc receptor FcγRIIA in the immune clearance of platelets: A transgenic mouse model Journal of Immunology. 162: 4311-4318. PMID 10201963 |
0.254 |
|
| 1998 |
Graves DJ, Su HJ, McKenzie SE, Surrey S, Fortina P. System for preparing microhybridization arrays on glass slides Analytical Chemistry. 70: 5085-5092. PMID 9852790 DOI: 10.1021/Ac980456N |
0.339 |
|
| 1998 |
McKenzie SE, Mansfield E, Rappaport E, Surrey S, Fortina P. Parallel molecular genetic analysis European Journal of Human Genetics. 6: 417-429. PMID 9801865 DOI: 10.1038/Sj.Ejhg.5200218 |
0.431 |
|
| 1998 |
Yamaguchi T, Pang J, Reddy KS, Surrey S, Adachi K. Role of beta112 Cys (G14) in homo- (beta4) and hetero- (alpha2 beta2) tetramer hemoglobin formation. The Journal of Biological Chemistry. 273: 14179-85. PMID 9603919 DOI: 10.1074/Jbc.273.23.14179 |
0.426 |
|
| 1998 |
Cui Z, Reilly MP, Surrey S, Schwartz E, McKenzie SE. -245 bp of 5'-flanking region from the human platelet factor 4 gene is sufficient to drive megakaryocyte-specific expression in vivo Blood. 91: 2326-2333. PMID 9516130 DOI: 10.1182/Blood.V91.7.2326.2326_2326_2333 |
0.634 |
|
| 1998 |
Estivill X, Fortina P, Surrey S, Rabionet R, Melchionda S, D'Agruma L, Mansfield E, Rappaport E, Govea N, Milà M, Zelante L, Gasparini P. Connexin-26 mutations in sporadic and inherited sensorineural deafness. Lancet (London, England). 351: 394-8. PMID 9482292 DOI: 10.1016/S0140-6736(97)11124-2 |
0.428 |
|
| 1998 |
Norris CF, Pricop L, Millard SS, Taylor SM, Surrey S, Schwartz E, Salmon JE, McKenzie SE. A naturally occurring mutation in Fc gamma RIIA: a Q to K127 change confers unique IgG binding properties to the R131 allelic form of the receptor. Blood. 91: 656-62. PMID 9427722 |
0.549 |
|
| 1998 |
Mansfield ES, Vainer M, Harris DW, Gasparini P, Estivill X, Surrey S, Fortina P. Rapid sizing of polymorphic microsatellite markers by capillary array electrophoresis. Journal of Chromatography. A. 781: 295-305. PMID 9368392 DOI: 10.1016/S0021-9673(97)00542-6 |
0.437 |
|
| 1998 |
Zelante L, Gasparini P, Estivill X, Melchionda S, D'Agruma L, Govea N, Milá M, Monica MD, Lutfi J, Shohat M, Mansfield E, Delgrosso K, Rappaport E, Surrey S, Fortina P. Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans. Human Molecular Genetics. 6: 1605-9. PMID 9285800 DOI: 10.1093/Hmg/6.9.1605 |
0.481 |
|
| 1998 |
McKenzie SE, Taylor SM, Reilly MP, Surrey S, Schwartz E. Immune-mediated Thrombocytopenia is More Severe in Human FcγRIIa Transgenic Mice than in Wild-type Mice • 782 Pediatric Research. 43: 136-136. DOI: 10.1203/00006450-199804001-00803 |
0.563 |
|
| 1998 |
Adachi K, Yamaguchi T, Pang J, Surrey S. Effects of Increased Anionic Charge in the β-Globin Chain on Assembly of Hemoglobin In Vitro Blood. 91: 1438-1445. DOI: 10.1182/Blood.V91.4.1438 |
0.354 |
|
| 1998 |
Norris CF, Pricop L, Millard SS, Taylor SM, Surrey S, Schwartz E, Salmon JE, McKenzie SE. A Naturally Occurring Mutation in FcγRIIA: A Q to K127 Change Confers Unique IgG Binding Properties to the R131 Allelic Form of the Receptor Blood. 91: 656-662. DOI: 10.1182/Blood.V91.2.656 |
0.581 |
|
| 1998 |
Chan V, McKenzie SE, Surrey S, Fortina P, Graves DJ. Effect of hydrophobicity and electrostatics on adsorption and surface diffusion of DNA oligonucleotides at liquid/solid interfaces Journal of Colloid and Interface Science. 203: 197-207. DOI: 10.1006/Jcis.1998.5495 |
0.33 |
|
| 1997 |
Reddy LR, Reddy KS, Surrey S, Adachi K. Role of beta87 Thr in the beta6 Val acceptor site during deoxy Hb S polymerization. Biochemistry. 36: 15992-8. PMID 9398334 DOI: 10.1021/Bi9717439 |
0.412 |
|
| 1997 |
Tamary H, Surrey S, Augustine J, Shalmon L, Schwartz E, Rappaport EF. Molecular analysis of a compound heterozygote for hypoprothrombinemia and dysprothrombinemia (-G 7248/7249 and ARG 340 TRP). Blood Coagulation & Fibrinolysis : An International Journal in Haemostasis and Thrombosis. 8: 337-43. PMID 9351523 DOI: 10.1097/00001721-199709000-00003 |
0.603 |
|
| 1997 |
Camaschella C, Kattamis AC, Petroni D, Roetto A, Sivera P, Sbaiz L, Cohen A, Ohene-Frempong K, Trifillis P, Surrey S, Fortina P. Different hematological phenotypes caused by the interaction of triplicated alpha-globin genes and heterozygous beta-thalassemia. American Journal of Hematology. 55: 83-8. PMID 9209003 DOI: 10.1002/(Sici)1096-8652(199706)55:2<83::Aid-Ajh6>3.0.Co;2-Z |
0.481 |
|
| 1997 |
Tamary H, Klinger G, Shalmon L, Attias D, Fortina P, Kobayashi M, Surrey S, Zaizov R. alpha-thalassemia caused by a 16 bp deletion in the 3' untranslated region of the alpha 2-globin gene including the first nucleotide of the poly A signal sequence. Hemoglobin. 21: 121-30. PMID 9101281 DOI: 10.3109/03630269708997516 |
0.45 |
|
| 1997 |
Kattamis AC, Kelly KM, Ohene-Frempong K, Reilly MP, Keller M, Cubeddu R, Adachi K, Surrey S, Fortina P. Hb Osler [beta 145(HC2)Tyr-->Asp] results from posttranslational modification. Hemoglobin. 21: 109-20. PMID 9101280 DOI: 10.3109/03630269708997515 |
0.474 |
|
| 1997 |
Adachi K, Konitzer P, Pang J, Reddy KS, Surrey S. Amino Acids Responsible for Decreased 2, 3-Biphosphosphoglycerate Binding to Fetal Hemoglobin Blood. 90: 2916-2920. DOI: 10.1182/Blood.V90.8.2916 |
0.344 |
|
| 1997 |
McKenzie SE, Subudhi SK, Cassel DL, Malladi P, Surrey S, Schwartz E. #644 c-kit gene promoter region polymorphism in a family with congenital hypoplastic anemia Journal of Pediatric Hematology/Oncology. 19: 383. DOI: 10.1097/00043426-199707000-00092 |
0.621 |
|
| 1997 |
Fortina P, Cheng J, Shoffner MA, Surrey S, Hitchcock WM, Kricka LJ, Wilding P. Diagnosis of Duchenne/Becker muscular dystrophy and quantitative identification of carrier status by use of entangled solution capillary electrophoresis Clinical Chemistry. 43: 745-751. DOI: 10.1093/Clinchem/43.5.745 |
0.359 |
|
| 1997 |
Gasparini P, Estivill X, Volpini V, Totaro A, Castellvi-Bel S, Govea N, Mila M, Monica MD, Ventruto V, Benedetto MD, Stanziale P, Zelante L, Mansfield ES, Sandkuijl L, Surrey S, et al. Linkage of DFNB1 to non-syndromic neurosensory autosomal-recessive deafness in Mediterranean families. European Journal of Human Genetics. 5: 83-88. DOI: 10.1007/Bf03405882 |
0.404 |
|
| 1996 |
Cheng J, Fortina P, Surrey S, Kricka L, Wilding P. Microchip-based Devices for Molecular Diagnosis of Genetic Diseases. Molecular Diagnosis. 1: 183-200. PMID 10462559 DOI: 10.1016/S1084-8592(96)70004-8 |
0.358 |
|
| 1996 |
Trifillis P, Adachi K, Yamaguchi T, Schwartz E, Surrey S. Expression studies of delta-globin gene alleles associated with reduced hemoglobin A2 levels in Greek Cypriots. The Journal of Biological Chemistry. 271: 26931-8. PMID 8900178 DOI: 10.1074/Jbc.271.43.26931 |
0.618 |
|
| 1996 |
Yamaguchi T, Pang J, Reddy KS, Witkowska HE, Surrey S, Adachi K. Expression of soluble human beta-globin chains in bacteria and assembly in vitro with alpha-globin chains. The Journal of Biological Chemistry. 271: 26677-83. PMID 8900144 DOI: 10.1074/jbc.271.43.26677 |
0.343 |
|
| 1996 |
Kattamis AC, Camaschella C, Sivera P, Surrey S, Fortina P. Human alpha-thalassemia syndromes: detection of molecular defects. American Journal of Hematology. 53: 81-91. PMID 8892732 DOI: 10.1002/(Sici)1096-8652(199610)53:2<81::Aid-Ajh5>3.0.Co;2-# |
0.376 |
|
| 1996 |
Camaschella C, Roetto A, Gasparini P, Piperno A, Fortina P, Surrey S, Rappaport E. Allelic association of microsatellites of 6p in Italian hemochromatosis patients. Human Genetics. 97: 476-81. PMID 8834246 DOI: 10.1007/Bf02267070 |
0.424 |
|
| 1996 |
Reddy LR, Reddy KS, Surrey S, Adachi K. Role of hydrophobic amino acids at beta85 and beta88 in stabilizing F helix conformation of hemoglobin S. The Journal of Biological Chemistry. 271: 24564-8. PMID 8798719 DOI: 10.1074/Jbc.271.40.24564 |
0.368 |
|
| 1996 |
Adachi K, Pang J, Reddy LR, Bradley LE, Chen Q, Trifillis P, Schwartz E, Surrey S. Polymerization of three hemoglobin A2 variants containing Val6 and inhibition of hemoglobin S polymerization by hemoglobin A2. The Journal of Biological Chemistry. 271: 24557-63. PMID 8798718 DOI: 10.1074/Jbc.271.40.24557 |
0.561 |
|
| 1996 |
Kiss C, Surrey S, Schreiber AD, Schwartz E, McKenzie SE. Human c-kit ligand (stem cell factor) induces platelet Fc receptor expression in megakaryoblastic cells Experimental Hematology. 24: 1232-1237. PMID 8765499 |
0.321 |
|
| 1996 |
Norris CF, Surrey S, Bunin GR, Schwartz E, Buchanan GR, McKenzie SE. Relationship between Fc receptor IIA polymorphism and infection in children with sickle cell disease. The Journal of Pediatrics. 128: 813-9. PMID 8648541 DOI: 10.1016/S0022-3476(96)70334-7 |
0.572 |
|
| 1996 |
Adachi K, Pang J, Konitzer P, Surrey S. Polymerization of recombinant hemoglobin F gamma E6V and hemoglobin F gamma E6V, gamma Q87T alone, and in mixtures with hemoglobin S Blood. 87: 1617-1624. DOI: 10.1182/Blood.V87.4.1617.Bloodjournal8741617 |
0.377 |
|
| 1996 |
McKenzic SE, Surrey S, Schwartz E. #502 Models of human platelet gene expression in vivo Journal of Pediatric Hematology/Oncology. 18: 426. DOI: 10.1097/00043426-199611000-00025 |
0.316 |
|
| 1995 |
Sartore M, Grasso M, Piccolo G, Fasani R, Bergamaschi R, Malaspina A, Ceroni M, Kobayashi M, Semeraro A, Arbustini E, Surrey S, Fortina P. Leber′s Hereditary Optic Neuropathy (LHON)-Related Mitochondrial DNA Sequence Changes in Italian Patients Presenting with Sporadic Bilateral Optic Neuritis Biochemical and Molecular Medicine. 56: 45-51. PMID 8593537 DOI: 10.1006/Bmme.1995.1055 |
0.389 |
|
| 1995 |
Kobayashi M, Kaplan BS, Bellah RD, Sartore M, Rappaport E, Steele MW, Mansfield E, Gasparini P, Surrey S, Fortina P. Infundibulopelvic stenosis, multicystic kidney, and calyectasis in a kindred: clinical observations and genetic analysis. American Journal of Medical Genetics. 59: 218-24. PMID 8588589 DOI: 10.1002/Ajmg.1320590219 |
0.378 |
|
| 1995 |
Ramachandran B, Surrey S, Schwartz E. Megakaryocyte-specific positive regulatory sequence 5' to the human PF4 gene. Experimental Hematology. 23: 49-57. PMID 7995371 |
0.387 |
|
| 1995 |
Keller MA, McKenzie SE, Cassel DL, Rappaport EF, Schwartz E, Surrey S. Lineage-specific alternative splicing of the human Fc gamma RIIA transmembrane exon requires sequences near the 3' splice site. Gene Expression. 4: 217-25. PMID 7787414 |
0.386 |
|
| 1995 |
Parrella T, Surrey S, Iolascon A, Sartore M, Heidenreich R, Diamond G, Ponzone A, Guardamagna O, Burlina AB, Cerone R. Maple syrup urine disease (MSUD): screening for known mutations in Italian patients. Journal of Inherited Metabolic Disease. 17: 652-60. PMID 7707687 DOI: 10.1007/Bf00712006 |
0.493 |
|
| 1995 |
Adachi K, Reddy LR, Reddy KS, Surrey S. Mutational analysis of phenylalanine beta 85 in the valine beta 6 acceptor pocket during hemoglobin S polymerization. Protein Science : a Publication of the Protein Society. 4: 1272-8. PMID 7670370 DOI: 10.1002/Pro.5560040703 |
0.415 |
|
| 1995 |
Adachi K, Sabnekar P, Adachi M, Reddy LR, Pang J, Reddy KS, Surrey S. Polymerization of recombinant Hb S-Kempsey (deoxy-R state) and Hb S-Kansas (oxy-T state). The Journal of Biological Chemistry. 270: 26857-62. PMID 7592928 DOI: 10.1074/Jbc.270.45.26857 |
0.342 |
|
| 1995 |
Kobayashi M, Rappaport E, Blasband A, Semeraro A, Sartore M, Surrey S, Fortina P. Fluorescence-based DNA minisequence analysis for detection of known single-base changes in genomic DNA. Molecular and Cellular Probes. 9: 175-82. PMID 7477010 DOI: 10.1006/Mcpr.1995.0027 |
0.452 |
|
| 1995 |
Mansfield ES, Worley JM, McKenzie SE, Surrey S, Rappaport E, Fortina P. Nucleic acid detection using non-radioactive labelling methods Molecular and Cellular Probes. 9: 145-156. PMID 7477006 DOI: 10.1006/Mcpr.1995.0023 |
0.376 |
|
| 1994 |
Reilly AF, Norris CF, Surrey S, Bruchak FJ, Rappaport EF, Schwartz E, McKenzie SE. Genetic diversity in human Fc receptor II for immunoglobulin G: Fcgamma receptor IIA ligand-binding polymorphism Clinical and Diagnostic Laboratory Immunology. 1: 640-644. PMID 8556514 |
0.527 |
|
| 1994 |
Tamary H, Surrey S, Kirschmann H, Shalmon L, Zaizov R, Schwartz E, Rappaport EF. Systematic use of automated fluorescence-based sequence analysis of amplified genomic DNA for rapid detection of point mutations. American Journal of Hematology. 46: 127-33. PMID 8172179 DOI: 10.1002/Ajh.2830460213 |
0.64 |
|
| 1994 |
Iolascon A, Parrella T, Perrotta S, Guardamagna O, Coates PM, Sartore M, Surrey S, Fortina P. Rapid detection of medium chain acyl-CoA dehydrogenase gene mutations by non-radioactive, single strand conformation polymorphism minigels. Journal of Medical Genetics. 31: 551-4. PMID 7966191 DOI: 10.1136/Jmg.31.7.551 |
0.468 |
|
| 1994 |
Reilly AF, Surrey S, Rappaport EF, Schwartz E, McKenzie SE. Variation in human FCGR2C gene copy number Immunogenetics. 40: 456. PMID 7959956 DOI: 10.1007/Bf00177829 |
0.62 |
|
| 1994 |
Mansfield ES, Robertson JM, Lebo RV, Lucero MY, Mayrand PE, Rappaport E, Parrella T, Sartore M, Surrey S, Fortina P. Duchenne/Becker muscular dystrophy carrier detection using quantitative PCR and fluorescence-based strategies. American Journal of Medical Genetics. 48: 200-8. PMID 7510932 DOI: 10.1002/Ajmg.1320480406 |
0.435 |
|
| 1994 |
Adachi K, Lai C, Konitzer P, Donahee M, Campbell A, Surrey S. Crystallization of recombinant hemoglobins with basic amino acid substitutions (Lys and Arg) at the beta 6 position Blood. 84: 1309-1313. DOI: 10.1182/blood.v84.4.1309.bloodjournal8441309 |
0.325 |
|
| 1994 |
Adachi K, Lai C, Konitzer P, Donahee M, Campbell A, Surrey S. Crystallization of recombinant hemoglobins with basic amino acid substitutions (Lys and Arg) at the beta 6 position Blood. 84: 1309-1313. DOI: 10.1182/Blood.V84.4.1309.1309 |
0.419 |
|
| 1993 |
Rappaport EF, Cassel DL, Walterhouse DO, McKenzie SE, Surrey S, Keller MA, Schreiber AD, Schwartz E. A soluble form of the human Fc receptor Fc gamma RIIA: cloning, transcript analysis and detection. Experimental Hematology. 21: 689-96. PMID 8513871 |
0.329 |
|
| 1993 |
Cassel DL, Keller MA, Surrey S, Schwartz E, Schreiber AD, Rappaport EF, McKenzie SE. Differential expression of Fc gamma RIIA, Fc gamma RIIB and Fc gamma RIIC in hematopoietic cells: analysis of transcripts. Molecular Immunology. 30: 451-60. PMID 8464427 DOI: 10.1016/0161-5890(93)90113-P |
0.615 |
|
| 1993 |
Adachi K, Kim JY, Konitzer P, Asakura T, Saviola B, Surrey S. Effects of beta 6 amino acid hydrophobicity on stability and solubility of hemoglobin tetramers. Febs Letters. 315: 47-50. PMID 8416810 DOI: 10.1016/0014-5793(93)81130-R |
0.413 |
|
| 1993 |
Trifillis P, Kyrri A, Kalogirou E, Kokkofitou A, Ioannou P, Schwartz E, Surrey S. Analysis of delta-globin gene mutations in Greek cypriots. Blood. 82: 1647-51. PMID 8364213 DOI: 10.1182/Blood.V82.5.1647.1647 |
0.647 |
|
| 1993 |
Mansfield ES, Blasband A, Kronick MN, Wrabetz L, Kaplan P, Rappaport E, Sartore M, Parrella T, Surrey S, Fortina P. Fluorescent approaches to diagnosis of Lesch-Nyhan syndrome and quantitative analysis of carrier status. Molecular and Cellular Probes. 7: 311-24. PMID 8232348 DOI: 10.1006/Mcpr.1993.1045 |
0.461 |
|
| 1993 |
Adachi K, Surrey S, Tamary H, Kim J, Eck HS, Rappaport E, Ohene-Frempong K. Hb Shelby [beta 131(H9)Gln-->Lys] in association with Hb S [beta 6(A3)Glu-->Val]: characterization, stability, and effects on Hb S polymerization. Hemoglobin. 17: 329-43. PMID 8226094 DOI: 10.3109/03630269308997486 |
0.403 |
|
| 1993 |
Keller MA, Cassel DL, Rappaport EF, McKenzie SE, Schwartz E, Surrey S. Fluorescence-based RT PCR analysis: determination of the ratio of soluble to membrane-bound forms of Fc gamma RIIA transcripts in hematopoietic cell lines. Pcr Methods and Applications. 3: 32-8. PMID 8220183 DOI: 10.1101/Gr.3.1.32 |
0.618 |
|
| 1993 |
Adachi K, Konitzer P, Lai CH, Kim J, Surrey S. Oxygen binding and other physical properties of human hemoglobin made in yeast. Protein Engineering. 5: 807-10. PMID 1287662 DOI: 10.1093/Protein/5.8.807 |
0.386 |
|
| 1992 |
Adachi K, Rappaport E, Eck HS, Konitzer P, Kim J, Surrey S. Polymerization and solubility of recombinant hemoglobins alpha 2 beta 2 (6Val) (Hb S) and alpha 2 beta 2(6Leu) (Hb Leu). Hemoglobin. 15: 417-30. PMID 1802884 DOI: 10.3109/03630269108998861 |
0.43 |
|
| 1992 |
Fortina P, Dotti G, Conant R, Monokian G, Parrella T, Hitchcock W, Rappaport E, Schwartz E, Surrey S. Detection of the most common mutations causing beta-thalassemia in Mediterraneans using a multiplex amplification refractory mutation system (MARMS). Pcr Methods and Applications. 2: 163-6. PMID 1477672 DOI: 10.1101/Gr.2.2.163 |
0.651 |
|
| 1992 |
Fortina P, Conant R, Parrella T, Rappaport E, Scanlin T, Schwartz E, Robertson JM, Surrey S. Fluorescence-based, multiplex allele-specific PCR (MASPCR) detection of the delta F508 deletion in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Molecular and Cellular Probes. 6: 353-6. PMID 1382222 DOI: 10.1016/0890-8508(92)90013-N |
0.628 |
|
| 1992 |
McKenzie SE, Keller MA, Cassel DL, Schreiber AD, Schwartz E, Surrey S, Rappaport EF. Characterization of the 5'-flanking transcriptional regulatory region of the human Fc gamma receptor gene, Fc gamma RIIA. Molecular Immunology. 29: 1165-74. PMID 1382218 DOI: 10.1016/0161-5890(92)90052-Y |
0.661 |
|
| 1992 |
Fortina P, Conant R, Monokian G, Dotti G, Parrella T, Hitchcock W, Kant J, Scanlin T, Rappaport E, Schwartz E, Surrey S. Non-radioactive detection of the most common mutations in the cystic fibrosis transmembrane conductance regulator gene by multiplex allele-specific polymerase chain reaction Human Genetics. 90: 375-378. PMID 1282898 DOI: 10.1007/Bf00220462 |
0.625 |
|
| 1991 |
Trifillis P, Ioannou P, Schwartz E, Surrey S. Identification of four novel delta-globin gene mutations in Greek Cypriots using polymerase chain reaction and automated fluorescence-based DNA sequence analysis. Blood. 78: 3298-305. PMID 1742490 DOI: 10.1182/Blood.V78.12.3298.Bloodjournal78123298 |
0.655 |
|
| 1991 |
Ballas SK, Talacki CA, Adachi K, Schwartz E, Surrey S, Rappaport E. The Xmn I site (-158, C----T) 5' to the G gamma gene: correlation with the Senegalese haplotype and G gamma globin expression. Hemoglobin. 15: 393-405. PMID 1724976 DOI: 10.3109/03630269108998859 |
0.632 |
|
| 1991 |
Fortina P, Delgrosso K, Werner E, Haines K, Rappaport E, Schwartz E, Surrey S. A greater than 200 kb deletion removing the entire beta-like globin gene cluster in a family of Irish descent. Hemoglobin. 15: 23-41. PMID 1717405 DOI: 10.3109/03630269109072482 |
0.645 |
|
| 1990 |
Heidenreich R, Eisman R, Surrey S, Delgrosso K, Bennett JS, Schwartz E, Poncz M. Organization of the gene for platelet glycoprotein IIb. Biochemistry. 29: 1232-44. PMID 2322558 DOI: 10.1021/Bi00457A020 |
0.642 |
|
| 1990 |
Talacki CA, Rappaport E, Schwartz E, Surrey S, Ballas SK. Beta-globin gene cluster haplotypes in Hb C heterozygotes. Hemoglobin. 14: 229-40. PMID 2228698 DOI: 10.3109/03630269009002261 |
0.63 |
|
| 1990 |
Park KS, Rifat S, Eck H, Adachi K, Surrey S, Poncz M. Biologic and biochemic properties of recombinant platelet factor 4 demonstrate identity with the native protein. Blood. 75: 1290-5. PMID 2178704 |
0.277 |
|
| 1990 |
Ramachandran B, Rappaport EF, Surrey S, Poncz M, Schwartz E. Polymerase chain reaction (PCR) for detection of PstI polymorphism in the human PF4 gene. Nucleic Acids Research. 18: 5919. PMID 1977142 DOI: 10.1093/Nar/18.19.5919 |
0.625 |
|
| 1990 |
Eisman R, Surrey S, Ramachandran B, Schwartz E, Poncz M. Structural and functional comparison of the genes for human platelet factor 4 and PF4alt. Blood. 76: 336-44. PMID 1695112 DOI: 10.1182/Blood.V76.2.336.336 |
0.671 |
|
| 1990 |
Month SR, Wood RW, Trifillis PT, Orchowski PJ, Sharon B, Ballas SK, Surrey S, Schwartz E. Analysis of 5' flanking regions of the gamma globin genes from major African haplotype backgrounds associated with sickle cell disease. The Journal of Clinical Investigation. 85: 364-70. PMID 1688883 DOI: 10.1172/Jci114447 |
0.632 |
|
| 1990 |
Gumucio DL, Lockwood WK, Weber JL, Saulino AM, Delgrosso K, Surrey S, Schwartz E, Goodman M, Collins FS. The -175T → C mutation increases promoter strength in erythroid cells: Correlation with evolutionary conservation of binding sites for two trans-acting factors Blood. 75: 756-761. PMID 1688723 DOI: 10.1182/Blood.V75.3.756.Bloodjournal753756 |
0.375 |
|
| 1990 |
Eisman R, Surrey S, Ramachandran B, Schwartz E, Poncz M. Structural and functional comparison of the genes for human platelet factor 4 and PF4alt Blood. 76: 336-344. DOI: 10.1182/blood.v76.2.336.bloodjournal762336 |
0.638 |
|
| 1990 |
Park K, Rifat S, Eck H, Adachi K, Surrey S, Poncz M. Biologic and biochemic properties of recombinant platelet factor 4 demonstrate identity with the native protein Blood. 75: 1290-1295. DOI: 10.1182/Blood.V75.6.1290.1290 |
0.378 |
|
| 1990 |
Gumucio D, Lockwood W, Weber J, Saulino A, Delgrosso K, Surrey S, Schwartz E, Goodman M, Collins F. The -175T----C mutation increases promoter strength in erythroid cells: correlation with evolutionary conservation of binding sites for two trans-acting factors Blood. 75: 756-761. DOI: 10.1182/blood.v75.3.756.756 |
0.606 |
|
| 1990 |
FORTINA P, DELGROSSO K, HAINES K, RAPPAPORT E, WERNER E, SCHWARTZ E, SURREY S. Mapping of Deletional Forms of ?- and ???-Thalassemia Annals of the New York Academy of Sciences. 612: 480-484. DOI: 10.1111/J.1749-6632.1990.Tb24337.X |
0.557 |
|
| 1989 |
Fortina P, Delgrosso K, Rappaport E, Werner E, Ballas S, Schwartz E, Surrey S. Large deletions encompassing the entire alpha- and beta-like globin gene clusters in humans. Progress in Clinical and Biological Research. 316: 151-9. PMID 2575754 |
0.382 |
|
| 1989 |
TALACKI CA, LARNER J, SCHWARTZ E, SURREY S, RAPPAPORT EF, BALLAS SK. The Effect of Alpha Thalassemia on the Clinical Course of Hemoglobin SC Disease Annals of the New York Academy of Sciences. 565: 365-366. DOI: 10.1111/J.1749-6632.1989.Tb24189.X |
0.573 |
|
| 1989 |
BALLAS SK, LARNER J, SMITH ED, SURREY S, SCHWARTZ E, RAPPAPORT EF. Rheological Properties of SickleErythrocytes in the Steady State Predict the Frequency and Severity of the Sickle Cell Painful Crisis Annals of the New York Academy of Sciences. 565: 363-364. DOI: 10.1111/J.1749-6632.1989.Tb24188.X |
0.54 |
|
| 1988 |
Ballas SK, Larner J, Smith ED, Surrey S, Schwartz E, Rappaport EF. Rheologic predictors of the severity of the painful sickle cell crisis. Blood. 72: 1216-23. PMID 3167204 DOI: 10.1182/Blood.V72.4.1216.Bloodjournal7241216 |
0.389 |
|
| 1988 |
Fortina P, Delgrosso K, Rappaport E, Poncz M, Ballas SK, Schwartz E, Surrey S. A large deletion encompassing the entire alpha-like globin gene cluster in a family of northern European extraction. Nucleic Acids Research. 16: 11223-35. PMID 2905048 DOI: 10.1093/Nar/16.23.11223 |
0.634 |
|
| 1988 |
Sharon B, Poncz M, Surrey S, Schwartz E. Non-random association of the Rsa I polymorphic site 5' to the beta-globin gene with major sickle cell haplotypes. Hemoglobin. 12: 115-24. PMID 2898459 DOI: 10.3109/03630268808998018 |
0.652 |
|
| 1988 |
Bayever E, Haines K, Duprey S, Rappaport E, Douglas SD, Surrey S. Protection of uninfected human bone marrow cells in long-term culture from G418 toxicity after retroviral-mediated transfer of the NEOr gene. Experimental Cell Research. 179: 168-80. PMID 2844566 DOI: 10.1016/0014-4827(88)90356-4 |
0.411 |
|
| 1988 |
Schwartz E, Cohen A, Surrey S. Overview of the beta thalassemias: genetic and clinical aspects. Hemoglobin. 12: 551-64. PMID 2463234 DOI: 10.3109/03630268808991644 |
0.648 |
|
| 1988 |
Surrey S, Delgrosso K, Malladi P, Schwartz E. A single-base change at position -175 in the 5'-flanking region of the G gamma-globin gene from a black with G gamma-beta+ HPFH. Blood. 71: 807-10. PMID 2449926 DOI: 10.1182/Blood.V71.3.807.807 |
0.655 |
|
| 1987 |
Poncz M, Sutton M, Delgrosso K, Schwartz E, Surrey S. DNA methylation in hereditary persistence of fetal hemoglobin (HPFH-2). Nucleic Acids Research. 15: 5169-79. PMID 3601670 DOI: 10.1093/Nar/15.13.5169 |
0.667 |
|
| 1987 |
Fisher EA, Carroll RD, Cortner JA, Surrey S. Transcriptional activity of the genes for apoproteins A-I and E in neonatal rat liver Atherosclerosis. 68: 249-253. PMID 3122771 DOI: 10.1016/0021-9150(87)90204-8 |
0.376 |
|
| 1987 |
Poncz M, Surrey S, LaRocco P, Weiss MJ, Rappaport EF, Conway TM, Schwartz E. Cloning and characterization of platelet factor 4 cDNA derived from a human erythroleukemic cell line. Blood. 69: 219-23. PMID 3098319 |
0.587 |
|
| 1987 |
Ballas SK, Larner J, Smith ED, Surrey S, Schwartz E, Rappaport EF. The xerocytosis of Hb SC disease. Blood. 69: 124-30. PMID 2947642 DOI: 10.1182/Blood.V69.1.124.Bloodjournal691124 |
0.595 |
|
| 1987 |
Guzzo C, Weiner M, Rappaport E, Larocco P, Surrey S, Poncz M, Schwartz E. An Eco R1 polymorphism of a human platelet factor 4 (PF4) gene Nucleic Acids Research. 15: 380. PMID 2881257 DOI: 10.1093/Nar/15.1.380 |
0.608 |
|
| 1987 |
Schwartz E, Month S, Delgrosso K, Rappaport E, Orchowski P, Malladi P, Surrey S. DNA sequence changes in the 5'-flanking region of G gamma-globin genes in a black with beta S and a non-deletional form of G gamma-beta+ HPFH. Progress in Clinical and Biological Research. 251: 363-71. PMID 2448806 |
0.381 |
|
| 1987 |
Poncz M, Eisman R, Heidenreich R, Silver SM, Vilaire G, Surrey S, Schwartz E, Bennett JS. Structure of the platelet membrane glycoprotein IIb. Homology to the alpha subunits of the vitronectin and fibronectin membrane receptors. The Journal of Biological Chemistry. 262: 8476-82. PMID 2439501 |
0.329 |
|
| 1987 |
Poncz M, Surrey S, LaRocco P, Weiss M, Rappaport E, Conway T, Schwartz E. Cloning and characterization of platelet factor 4 cDNA derived from a human erythroleukemic cell line Blood. 69: 219-223. DOI: 10.1182/Blood.V69.1.219.219 |
0.623 |
|
| 1986 |
Schwartz E, Surrey S. Molecular biologic diagnosis of the hemoglobinopathies. Hospital Practice (Office Ed.). 21: 163-78. PMID 3091617 |
0.198 |
|
| 1985 |
Surrey S, Delgrosso K, Malladi P, Schwartz E. Functional analysis of a beta-globin gene containing a TATA box mutation from a Kurdish Jew with beta thalassemia. The Journal of Biological Chemistry. 260: 6507-10. PMID 2987224 |
0.438 |
|
| 1984 |
Liebhaber SA, Rappaport EF, Cash FE, Ballas SK, Schwartz E, Surrey S. Hemoglobin I mutation encoded at both alpha-globin loci on the same chromosome: concerted evolution in the human genome. Science (New York, N.Y.). 226: 1449-51. PMID 6505702 DOI: 10.1126/Science.6505702 |
0.607 |
|
| 1984 |
Semenza GL, Malladi P, Surrey S, Delgrosso K, Poncz M, Schwartz E. Detection of a novel DNA polymorphism in the beta-globin gene cluster. The Journal of Biological Chemistry. 259: 6045-8. PMID 6327661 |
0.655 |
|
| 1984 |
Rappaport EF, Schwartz E, Poncz M, Surrey S. Frequent occurrence of a zeta-globin-region deletion in American blacks accounts for a previously-described restriction site polymorphism. Biochemical and Biophysical Research Communications. 125: 817-23. PMID 6097249 DOI: 10.1016/0006-291X(84)90612-0 |
0.647 |
|
| 1984 |
Semenza GL, Delgrosso K, Poncz M, Malladi P, Schwartz E, Surrey S. The silent carrier allele: beta thalassemia without a mutation in the beta-globin gene or its immediate flanking regions. Cell. 39: 123-8. PMID 6091904 DOI: 10.1016/0092-8674(84)90197-1 |
0.753 |
|
| 1984 |
Semenza GL, Delgrosso K, Surrey S, Malladi P, Schwartz E, Ponca M. THE SILENT CARRIER ALLELE: β-THALASSEMIA WITHOUT A MUTATION IN THE β-GLOBIN GENE REGION Pediatric Research. 18: 248A-248A. DOI: 10.1203/00006450-198404001-00931 |
0.737 |
|
| 1984 |
Semenza GL, Malladi P, Poncz M, Delgrosso K, Schwartz E, Surrey S. DETECTION OF A NOVEL DNA POLYMORPHISM IN THE β-GLOBIN CLUSTER AND EVIDENCE FOR SITE-SPECIFIC RECOMBINATION Pediatric Research. 18: 225A-225A. DOI: 10.1203/00006450-198404001-00794 |
0.738 |
|
| 1983 |
Poncz M, Schwartz E, Ballantine M, Surrey S. Nucleotide sequence analysis of the delta beta-globin gene region in humans. The Journal of Biological Chemistry. 258: 11599-609. PMID 6311816 |
0.429 |
|
| 1982 |
Poncz M, Ballantine M, Solowiejczyk D, Barak I, Schwartz E, Surrey S. beta-Thalassemia in a Kurdish Jew. Single base changes in the T-A-T-A box. The Journal of Biological Chemistry. 257: 5994-6. PMID 7076659 |
0.397 |
|
| 1982 |
Poncz M, Solowiejczyk D, Harpel B, Mory Y, Schwartz E, Surrey S. Construction of human gene libraries from small amounts of peripheral blood: analysis of beta-like globin genes. Hemoglobin. 6: 27-36. PMID 7068433 DOI: 10.3109/03630268208996930 |
0.648 |
|
| 1982 |
Poncz M, Solowiejczyk D, Ballantine M, Schwartz E, Surrey S. "Nonrandom" DNA sequence analysis in bacteriophage M13 by the dideoxy chain-termination method. Proceedings of the National Academy of Sciences of the United States of America. 79: 4298-302. PMID 6956859 DOI: 10.1073/Pnas.79.14.4298 |
0.604 |
|
| 1982 |
Balsley JF, Rappaport E, Schwartz E, Surrey S. The gamma-delta-beta-globin gene region in G gamma-beta +-hereditary persistence of fetal hemoglobin. Blood. 59: 828-31. PMID 6174163 DOI: 10.1182/Blood.V59.4.828.828 |
0.648 |
|
| 1980 |
Ohene-Frempong K, Rappaport E, Atwater J, Schwartz E, Surrey S. Alpha-gene deletions in black newborn infants with Hb Bart's. Blood. 56: 931-3. PMID 7426755 DOI: 10.1182/Blood.V56.5.931.Bloodjournal565931 |
0.62 |
|
| 1980 |
Surrey S, Ohene-Frempong K, Rappaport E, Atwater J, Schwartz E. Linkage of alpha G-Philadelphia to alpha-thalassemia in African-Americans . Proceedings of the National Academy of Sciences of the United States of America. 77: 4885-9. PMID 6933536 DOI: 10.1073/Pnas.77.8.4885 |
0.613 |
|
| 1980 |
Surrey S, Ohene-Frempong K, Rappaport E, Atwater J, Schwartz E. alpha Thalassemia and the expression of hemoglobin G-Philadelphia. Annals of the New York Academy of Sciences. 344: 62-72. PMID 6930883 DOI: 10.1111/J.1749-6632.1980.Tb33649.X |
0.615 |
|
| 1979 |
Surrey S, Ginzburg I, Nemer M. Ribosomal RNA synthesis in pre- and post-gastrula-stage sea urchin embryos. Developmental Biology. 71: 83-99. PMID 467793 DOI: 10.1016/0012-1606(79)90084-8 |
0.186 |
|
| 1979 |
Nemer M, Surrey S, Ginzburg I, Echols MM. The 5′ terminal capping of heterogeneous nuclear RNA at different embryonic stages of the sea urchin Nucleic Acids Research. 6: 2307-2326. PMID 461190 DOI: 10.1093/Nar/6.6.2307 |
0.344 |
|
| 1979 |
Nemer M, Ginzburg I, Surrey S, Litwin S. Rates of synthesis and turnover of 5′ cap structures of hnRNA and mRNA and their changes during sea urchin development Developmental Genetics. 1: 151-165. DOI: 10.1002/dvg.1020010204 |
0.216 |
|
| 1978 |
Surrey S, Chambers JS, Muni D, Schwartz E. Restriction endonuclease analysis of human globin genes in cellular DNA. Biochemical and Biophysical Research Communications. 83: 1125-31. PMID 708430 DOI: 10.1016/0006-291X(78)91512-7 |
0.644 |
|
| 1977 |
Nemer M, Surrey S. mRNAs containing and lacking poly (A) function as separate and distinct classes during embryonic development. Progress in Nucleic Acid Research and Molecular Biology. 19: 119-22. PMID 1032908 DOI: 10.1016/S0079-6603(08)60913-7 |
0.248 |
|
| 1977 |
Surrey S, Nemer M. Methylated blocked 5' terminal sequences of sea urchin embryo messenger RNA classes containing and lacking poly(A). Cell. 9: 589-95. PMID 1009578 DOI: 10.1016/0092-8674(76)90041-6 |
0.257 |
|
| 1977 |
Travaglini EC, Dube DK, Surrey S, Loeb LA. Template recognition and chain elongation in DNA synthesis in vitro. Journal of Molecular Biology. 106: 605-21. PMID 185394 DOI: 10.1016/0022-2836(76)90254-0 |
0.283 |
|
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