Thomas Jefferson University

Saul Surrey

TitleDecision Supp Analyst Shrd Fac
InstitutionThomas Jefferson University
DepartmentResearch Support Services Adm
Address1020 Locust St.
Philadelphia PA 19107
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. 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. Am J Med Genet A. 2014 Sep; 164(9):2294-9. PMID: 24898194.
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    2. 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 Dev. 2014 Jan 15; 23(2):167-79. PMID: 23980595.
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    3. 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 Neurosurg. 2014 Nov; 82(5):684-95. PMID: 23994074.
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    4. 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 Mol Biol. 2013; 1015:127-46. PMID: 23824853.
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    5. 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. 2011; 12:464. PMID: 21943378.
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    6. 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? Eur J Hum Genet. 2010 Feb; 18(2):178-85. PMID: 19809473.
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    7. 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. Arch Biochem Biophys. 2009 Jan 15; 481(2):137-44. PMID: 19022217.
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    8. 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. Clin Chem. 2008 Oct; 54(10):1657-63. PMID: 18703765.
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    9. 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 J Hum Genet. 2008 May; 14(2):55-64. PMID: 20300295.
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    10. Adachi K, Ding M, Surrey S. Role of the beta4Thr-beta73Asp hydrogen bond in HbS polymer and domain formation from multinucleate-containing clusters. Biochemistry. 2008 May 13; 47(19):5441-9. PMID: 18419131.
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    11. Fortina P, Surrey S. Digital mRNA profiling. Nat Biotechnol. 2008 Mar; 26(3):293-4. PMID: 18327237.
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    12. 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. J Cell Mol Med. 2008 Aug; 12(4):1284-302. PMID: 18266966.
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    13. 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. Arch Biochem Biophys. 2007 Jul 01; 463(1):60-7. PMID: 17418086.
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    14. 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 Biotechnol. 2007 Apr; 25(4):145-52. PMID: 17316852.
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    15. 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 Oncol. 2006 Dec; 2(6):705-16. PMID: 17155897.
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    16. 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. Physiol Genomics. 2006 Dec 13; 28(1):114-28. PMID: 16940433.
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    17. 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. J Mol Biol. 2006 Sep 22; 362(3):528-38. PMID: 16926024.
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    18. 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. 2006 Jul 11; 45(27):8358-67. PMID: 16819835.
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    19. 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. Genet Test. 2006; 10(1):8-17. PMID: 16544997.
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    20. 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 Res. 2005 Aug; 15(8):1168-76. PMID: 16077016.
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    21. Fortina P, Kricka LJ, Surrey S, Grodzinski P. Nanobiotechnology: the promise and reality of new approaches to molecular recognition. Trends Biotechnol. 2005 Apr; 23(4):168-73. PMID: 15780707.
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    22. 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. 2005 Mar 30; 334(1):59-73. PMID: 15749123.
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    23. 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. J Mol Cell Cardiol. 2005 Feb; 38(2):345-51. PMID: 15698841.
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    24. 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. 2005 Apr 15; 105(8):3162-8. PMID: 15632207.
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    25. 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. Hum Mutat. 2004 Sep; 24(3):261-71. PMID: 15300853.
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    26. Adachi K, Lakka V, Zhao Y, Surrey S. Ubiquitylation of nascent globin chains in a cell-free system. J Biol Chem. 2004 Oct 01; 279(40):41767-74. PMID: 15297454.
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    27. 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. Physiol Genomics. 2004 Sep 16; 19(1):117-30. PMID: 15252187.
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    28. 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-alpha over-expressing mice demonstrates the development of autoimmune myocarditis. J Mol Cell Cardiol. 2004 Apr; 36(4):515-30. PMID: 15081311.
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    29. 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. Br J Haematol. 2004 Jan; 124(2):240-3. PMID: 14687036.
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    30. 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. Clin Chem. 2003 Oct; 49(10):1675-9. PMID: 14500598.
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    31. 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. 2003 Sep 02; 42(34):10252-9. PMID: 12939154.
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    32. 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. Arch Biochem Biophys. 2003 May 01; 413(1):99-106. PMID: 12706346.
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    33. 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. 2003 Apr 22; 42(15):4476-84. PMID: 12693943.
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    34. Kajiyama T, Miyahara Y, Kricka LJ, Wilding P, Graves DJ, Surrey S, Fortina P. Genotyping on a thermal gradient DNA chip. Genome Res. 2003 Mar; 13(3):467-75. PMID: 12618377.
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    35. 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, Fortina P. Analysis of clinically relevant single-nucleotide polymorphisms by use of microelectronic array technology. Clin Chem. 2002 Dec; 48(12):2124-30. PMID: 12446467.
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    36. 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. Hum Mutat. 2002 Oct; 20(4):312-20. PMID: 12325027.
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    37. 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. J Pediatr Hematol Oncol. 2002 Aug-Sep; 24(6):499-502. PMID: 12218602.
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    38. Fortina P, Surrey S, Kricka LJ. Molecular diagnostics: hurdles for clinical implementation. Trends Mol Med. 2002 Jun; 8(6):264-6. PMID: 12067610.
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    39. 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. 2002 May; 23(10):1551-7. PMID: 12116168.
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    40. 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. J Biol Chem. 2002 Apr 19; 277(16):13415-20. PMID: 11827978.
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    41. Graves DJ, Su HJ, Addya S, Surrey S, Fortina P. Four-laser scanning confocal system for microarray analysis. Biotechniques. 2002 Feb; 32(2):346-8, 350, 352, 354. PMID: 11848412.
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    42. Cassel DL, Subudhi SK, Surrey S, McKenzie SE. GATA and NF-Y participate in transcriptional regulation of FcgammaRIIA in megakaryocytic cells. Blood Cells Mol Dis. 2000 Dec; 26(6):587-97. PMID: 11112392.
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    43. 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. Eur J Hum Genet. 2000 Nov; 8(11):884-94. PMID: 11093279.
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    44. Adachi K, Yamaguchi T, Yang Y, Konitzer PT, Pang J, Reddy KS, Ivanova M, Ferrone F, Surrey S. Expression of functional soluble human alpha-globin chains of hemoglobin in bacteria. Protein Expr Purif. 2000 Oct; 20(1):37-44. PMID: 11035948.
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    45. 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. 2000 Aug; 16(8):685-98. PMID: 11099255.
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    46. Delgrosso K, Surrey S, Schwartz E. Identification of the nucleotide change (CAC-->CGC) responsible for Hb P-Galveston [BETA117(G19)His-->Arg]. Hemoglobin. 2000 May; 24(2):165-7. PMID: 10870891.
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    47. 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. J Biol Chem. 2000 Apr 28; 275(17):12424-9. PMID: 10777526.
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    48. 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 Fc gamma RIIA in the immune clearance of platelets: a transgenic mouse model. J Immunol. 1999 Apr 01; 162(7):4311-8. PMID: 10201963.
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    49. Graves DJ, Su HJ, McKenzie SE, Surrey S, Fortina P. System for preparing microhybridization arrays on glass slides. Anal Chem. 1998 Dec 01; 70(23):5085-92. PMID: 9852790.
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    50. McKenzie SE, Mansfield E, Rappaport E, Surrey S, Fortina P. Parallel molecular genetic analysis. Eur J Hum Genet. 1998 Sep-Oct; 6(5):417-29. PMID: 9801865.
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    51. 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. J Biol Chem. 1998 Jun 05; 273(23):14179-85. PMID: 9603919.
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    52. 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. 1998 Apr 01; 91(7):2326-33. PMID: 9516130.
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    53. Adachi K, Yamaguchi T, Pang J, Surrey S. Effects of increased anionic charge in the beta-globin chain on assembly of hemoglobin in vitro. Blood. 1998 Feb 15; 91(4):1438-45. PMID: 9454775.
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    54. Estivill X, Fortina P, Surrey S, Rabionet R, Melchionda S, D'Agruma L, Mansfield E, Rappaport E, Govea N, Mil? M, Zelante L, Gasparini P. Connexin-26 mutations in sporadic and inherited sensorineural deafness. Lancet. 1998 Feb 07; 351(9100):394-8. PMID: 9482292.
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    55. 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. 1998 Jan 15; 91(2):656-62. PMID: 9427722.
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    56. Reddy LR, Reddy KS, Surrey S, Adachi K. Role of beta87 Thr in the beta6 Val acceptor site during deoxy Hb S polymerization. Biochemistry. 1997 Dec 16; 36(50):15992-8. PMID: 9398334.
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    57. Adachi K, Konitzer P, Pang J, Reddy KS, Surrey S. Amino acids responsible for decreased 2,3-biphosphoglycerate binding to fetal hemoglobin. Blood. 1997 Oct 15; 90(8):2916-20. PMID: 9376571.
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    58. Mansfield ES, Vainer M, Harris DW, Gasparini P, Estivill X, Surrey S, Fortina P. Rapid sizing of polymorphic microsatellite markers by capillary array electrophoresis. J Chromatogr A. 1997 Sep 26; 781(1-2):295-305. PMID: 9368392.
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    59. Zelante L, Gasparini P, Estivill X, Melchionda S, D'Agruma L, Govea N, Mil? 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. Hum Mol Genet. 1997 Sep; 6(9):1605-9. PMID: 9285800.
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    60. 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 Coagul Fibrinolysis. 1997 Sep; 8(6):337-43. PMID: 9351523.
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    61. 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. Am J Hematol. 1997 Jun; 55(2):83-8. PMID: 9209003.
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    62. 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. Clin Chem. 1997 May; 43(5):745-51. PMID: 9166226.
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    63. 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. 1997 Mar; 21(2):109-20. PMID: 9101280.
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    64. Gasparini P, Estivill X, Volpini V, Totaro A, Castellvi-Bel S, Govea N, Mila M, Della Monica M, Ventruto V, De Benedetto M, Stanziale P, Zelante L, Mansfield ES, Sandkuijl L, Surrey S, Fortina P. Linkage of DFNB1 to non-syndromic neurosensory autosomal-recessive deafness in Mediterranean families. Eur J Hum Genet. 1997 Mar-Apr; 5(2):83-8. PMID: 9195157.
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    65. 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. 1997 Mar; 21(2):121-30. PMID: 9101281.
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    66. 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. J Biol Chem. 1996 Oct 25; 271(43):26677-83. PMID: 8900144.
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    67. 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. J Biol Chem. 1996 Oct 25; 271(43):26931-8. PMID: 8900178.
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    68. 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. J Biol Chem. 1996 Oct 04; 271(40):24564-8. PMID: 8798719.
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    69. 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. J Biol Chem. 1996 Oct 04; 271(40):24557-63. PMID: 8798718.
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    70. Kattamis AC, Camaschella C, Sivera P, Surrey S, Fortina P. Human alpha-thalassemia syndromes: detection of molecular defects. Am J Hematol. 1996 Oct; 53(2):81-91. PMID: 8892732.
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    71. 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. Exp Hematol. 1996 Aug; 24(10):1232-7. PMID: 8765499.
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    72. 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. J Pediatr. 1996 Jun; 128(6):813-9. PMID: 8648541.
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    73. Camaschella C, Roetto A, Gasparini P, Piperno A, Fortina P, Surrey S, Rappaport E. Allelic association of microsatellites of 6p in Italian hemochromatosis patients. Hum Genet. 1996 Apr; 97(4):476-81. PMID: 8834246.
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    74. 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. 1996 Feb 15; 87(4):1617-24. PMID: 8608256.
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    75. 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). J Biol Chem. 1995 Nov 10; 270(45):26857-62. PMID: 7592928.
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    76. 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. Am J Med Genet. 1995 Nov 06; 59(2):218-24. PMID: 8588589.
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    77. 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 Sci. 1995 Jul; 4(7):1272-8. PMID: 7670370.
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    78. 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. Mol Cell Probes. 1995 Jun; 9(3):175-82. PMID: 7477010.
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    79. Mansfield ES, Worley JM, McKenzie SE, Surrey S, Rappaport E, Fortina P. Nucleic acid detection using non-radioactive labelling methods. Mol Cell Probes. 1995 Jun; 9(3):145-56. PMID: 7477006.
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    80. 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 Expr. 1995; 4(4-5):217-25. PMID: 7787414.
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    81. Ramachandran B, Surrey S, Schwartz E. Megakaryocyte-specific positive regulatory sequence 5' to the human PF4 gene. Exp Hematol. 1995 Jan; 23(1):49-57. PMID: 7995371.
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    82. Adachi K, Reddy LR, Surrey S. Role of hydrophobicity of phenylalanine beta 85 and leucine beta 88 in the acceptor pocket for valine beta 6 during hemoglobin S polymerization. J Biol Chem. 1994 Dec 16; 269(50):31563-6. PMID: 7989324.
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    83. Reilly AF, Norris CF, Surrey S, Bruchak FJ, Rappaport EF, Schwartz E, McKenzie SE. Genetic diversity in human Fc receptor II for immunoglobulin G: Fc gamma receptor IIA ligand-binding polymorphism. Clin Diagn Lab Immunol. 1994 Nov; 1(6):640-4. PMID: 8556514.
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    84. Yamashiro DJ, Adachi M, Konitzer P, Surrey S, Adachi K. Polymerization and instability of a recombinant hemoglobin containing valine beta 7. J Biol Chem. 1994 Sep 30; 269(39):23996-9. PMID: 7929049.
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    85. Adachi K, Lai CH, 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. 1994 Aug 15; 84(4):1309-13. PMID: 8049445.
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    86. Adachi K, Konitzer P, Paulraj CG, Surrey S. Role of Leu-beta 88 in the hydrophobic acceptor pocket for Val-beta 6 during hemoglobin S polymerization. J Biol Chem. 1994 Jul 01; 269(26):17477-80. PMID: 8021253.
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    87. 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. J Med Genet. 1994 Jul; 31(7):551-4. PMID: 7966191.
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    88. 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. Am J Hematol. 1994 Jun; 46(2):127-33. PMID: 8172179.
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    89. West TB, Ohene-Frempong K, Stoeckert CJ, Surrey S. Erythroid progenitors in the peripheral blood of children with sickle cell disease. Am J Pediatr Hematol Oncol. 1994 May; 16(2):116-9. PMID: 7513134.
      Citations:    
    90. Adachi K, Konitzer P, Surrey S. Role of gamma 87 Gln in the inhibition of hemoglobin S polymerization by hemoglobin F. J Biol Chem. 1994 Apr 01; 269(13):9562-7. PMID: 7511590.
      Citations:    
    91. Parrella T, Surrey S, Iolascon A, Sartore M, Heidenreich R, Diamond G, Ponzone A, Guardamagna O, Burlina AB, Cerone R, et al. Maple syrup urine disease (MSUD): screening for known mutations in Italian patients. J Inherit Metab Dis. 1994; 17(6):652-60. PMID: 7707687.
      Citations:    
    92. Reilly AF, Surrey S, Rappaport EF, Schwartz E, McKenzie SE. Variation in human FCGR2C gene copy number. Immunogenetics. 1994; 40(6):456. PMID: 7959956.
      Citations:    
    93. 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. Am J Med Genet. 1993 Dec 15; 48(4):200-8. PMID: 7510932.
      Citations:    
    94. Adachi K, Konitzer P, Kim J, Welch N, Surrey S. Effects of beta 6 aromatic amino acids on polymerization and solubility of recombinant hemoglobins made in yeast. J Biol Chem. 1993 Oct 15; 268(29):21650-6. PMID: 8408017.
      Citations:    
    95. Trifillis P, Kyrri A, Kalogirou E, Kokkofitou A, Ioannou P, Schwartz E, Surrey S. Analysis of delta-globin gene mutations in Greek cypriots. Blood. 1993 Sep 01; 82(5):1647-51. PMID: 8364213.
      Citations:    
    96. 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. Mol Cell Probes. 1993 Aug; 7(4):311-24. PMID: 8232348.
      Citations:    
    97. 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 Appl. 1993 Aug; 3(1):32-8. PMID: 8220183.
      Citations:    
    98. 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. 1993 Aug; 17(4):329-43. PMID: 8226094.
      Citations:    
    99. 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. Exp Hematol. 1993 May; 21(5):689-96. PMID: 8513871.
      Citations:    
    100. 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. Mol Immunol. 1993 Apr; 30(5):451-60. PMID: 8464427.
      Citations:    
    101. 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 Lett. 1993 Jan 02; 315(1):47-50. PMID: 8416810.
      Citations:    
    102. Adachi K, Konitzer P, Lai CH, Kim J, Surrey S. Oxygen binding and other physical properties of human hemoglobin made in yeast. Protein Eng. 1992 Dec; 5(8):807-10. PMID: 1287662.
      Citations:    
    103. 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 Appl. 1992 Nov; 2(2):163-6. PMID: 1477672.
      Citations:    
    104. 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. Mol Immunol. 1992 Oct; 29(10):1165-74. PMID: 1382218.
      Citations:    
    105. 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. Mol Cell Probes. 1992 Aug; 6(4):353-6. PMID: 1382222.
      Citations:    
    106. 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. 1991 Dec 15; 78(12):3298-305. PMID: 1742490.
      Citations:    
    107. 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. 1991; 15(5):393-405. PMID: 1724976.
      Citations:    
    108. 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. 1991; 15(5):417-30. PMID: 1802884.
      Citations:    
    109. 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. 1991; 15(1-2):23-41. PMID: 1717405.
      Citations:    
    110. 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 Res. 1990 Oct 11; 18(19):5919. PMID: 1977142.
      Citations:    
    111. 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. 1990 Jul 15; 76(2):336-44. PMID: 1695112.
      Citations:    
    112. 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. 1990 Mar 15; 75(6):1290-5. PMID: 2178704.
      Citations:    
    113. Heidenreich R, Eisman R, Surrey S, Delgrosso K, Bennett JS, Schwartz E, Poncz M. Organization of the gene for platelet glycoprotein IIb. Biochemistry. 1990 Feb 06; 29(5):1232-44. PMID: 2322558.
      Citations:    
    114. 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. 1990 Feb 01; 75(3):756-61. PMID: 1688723.
      Citations:    
    115. 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. J Clin Invest. 1990 Feb; 85(2):364-70. PMID: 1688883.
      Citations:    
    116. Talacki CA, Rappaport E, Schwartz E, Surrey S, Ballas SK. Beta-globin gene cluster haplotypes in Hb C heterozygotes. Hemoglobin. 1990; 14(3):229-40. PMID: 2228698.
      Citations:    
    117. 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. Prog Clin Biol Res. 1989; 316B:151-9. PMID: 2575754.
      Citations:    
    118. 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 Res. 1988 Dec 09; 16(23):11223-35. PMID: 2905048.
      Citations:    
    119. 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. Exp Cell Res. 1988 Nov; 179(1):168-80. PMID: 2844566.
      Citations:    
    120. Ballas SK, Larner J, Smith ED, Surrey S, Schwartz E, Rappaport EF. Rheologic predictors of the severity of the painful sickle cell crisis. Blood. 1988 Oct; 72(4):1216-23. PMID: 3167204.
      Citations:    
    121. Adachi K, Kim J, Ballas S, Surrey S, Asakura T. Facilitation of Hb S polymerization by the substitution of Glu for Gln at beta 121. J Biol Chem. 1988 Apr 25; 263(12):5607-10. PMID: 2895770.
      Citations:    
    122. 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. 1988 Mar; 71(3):807-10. PMID: 2449926.
      Citations:    
    123. 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. 1988; 12(2):115-24. PMID: 2898459.
      Citations:    
    124. Poncz M, Henthorn P, Stoeckert C, Surrey S. Globin gene expression in hereditary persistence of fetal haemoglobin and (delta beta) (0)-thalassaemia. Oxf Surv Eukaryot Genes. 1988; 5:163-203. PMID: 2472152.
      Citations:    
    125. Schwartz E, Cohen A, Surrey S. Overview of the beta thalassemias: genetic and clinical aspects. Hemoglobin. 1988; 12(5-6):551-64. PMID: 2463234.
      Citations:    
    126. Fisher EA, Carroll RD, Cortner JA, Surrey S. Transcriptional activity of the genes for apoproteins A-I and E in neonatal rat liver. Atherosclerosis. 1987 Dec; 68(3):249-53. PMID: 3122771.
      Citations:    
    127. Poncz M, Sutton M, Delgrosso K, Schwartz E, Surrey S. DNA methylation in hereditary persistence of fetal hemoglobin (HPFH-2). Nucleic Acids Res. 1987 Jul 10; 15(13):5169-79. PMID: 3601670.
      Citations:    
    128. 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 Res. 1987 Jan 12; 15(1):380. PMID: 2881257.
      Citations:    
    129. 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. 1987 Jan; 69(1):219-23. PMID: 3098319.
      Citations:    
    130. Ballas SK, Larner J, Smith ED, Surrey S, Schwartz E, Rappaport EF. The xerocytosis of Hb SC disease. Blood. 1987 Jan; 69(1):124-30. PMID: 2947642.
      Citations:    
    131. 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. Prog Clin Biol Res. 1987; 251:363-71. PMID: 2448806.
      Citations:    
    132. 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. J Biol Chem. 1985 Jun 10; 260(11):6507-10. PMID: 2987224.
      Citations:    
    133. 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. 1984 Dec 21; 226(4681):1449-51. PMID: 6505702.
      Citations:    
    134. 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. Biochem Biophys Res Commun. 1984 Dec 14; 125(2):817-23. PMID: 6097249.
      Citations:    
    135. 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. 1984 Nov; 39(1):123-8. PMID: 6091904.
      Citations:    
    136. Semenza GL, Malladi P, Surrey S, Delgrosso K, Poncz M, Schwartz E. Detection of a novel DNA polymorphism in the beta-globin gene cluster. J Biol Chem. 1984 May 25; 259(10):6045-8. PMID: 6327661.
      Citations:    
    137. 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. 1982 Apr; 59(4):828-31. PMID: 6174163.
      Citations:    
    138. Ohene-Frempong K, Rappaport E, Atwater J, Schwartz E, Surrey S. Alpha-gene deletions in black newborn infants with Hb Bart's. Blood. 1980 Nov; 56(5):931-3. PMID: 7426755.
      Citations:    
    139. Surrey S, Ohene-Frempong K, Rappaport E, Atwater J, Schwartz E. Linkage of alpha G-Philadelphia to alpha-thalassemia in African-Americans . Proc Natl Acad Sci U S A. 1980 Aug; 77(8):4885-9. PMID: 6933536.
      Citations:    
    140. Surrey S, Ohene-Frempong K, Rappaport E, Atwater J, Schwartz E. alpha Thalassemia and the expression of hemoglobin G-Philadelphia. Ann N Y Acad Sci. 1980; 344:62-72. PMID: 6930883.
      Citations:    
    141. Rovera G, Aden D, Surrey S. Allylisopropylacetamide restricts expression of beta minor globin gene in Friend cells. Nature. 1978 Mar 09; 272(5649):172-5. PMID: 272488.
      Citations:    
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