Elizabeth F. Neufeld - Publications

Affiliations: 
Biological Chemistry University of California, Los Angeles, Los Angeles, CA 
Area:
Human genetic disease (specifically, working on lysosomal storage diseases) and cell organelles, especially lysosomes
Website:
http://www.asbmb.org/uploadedfiles/aboutus/asbmb_history/past_presidents/1990s/1992Neufeld.html

165 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2014 Kan SH, Aoyagi-Scharber M, Le SQ, Vincelette J, Ohmi K, Bullens S, Wendt DJ, Christianson TM, Tiger PM, Brown JR, Lawrence R, Yip BK, Holtzinger J, Bagri A, Crippen-Harmon D, ... ... Neufeld EF, et al. Delivery of an enzyme-IGFII fusion protein to the mouse brain is therapeutic for mucopolysaccharidosis type IIIB. Proceedings of the National Academy of Sciences of the United States of America. 111: 14870-5. PMID 25267636 DOI: 10.1073/pnas.1416660111  1
2013 Neufeld EF. Unexpected observations--a tribute to Christian de Duve (1917-2013). Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 27: 4661-4663. PMID 24298016  1
2011 Ohmi K, Zhao HZ, Neufeld EF. Defects in the medial entorhinal cortex and dentate gyrus in the mouse model of Sanfilippo syndrome type B Plos One. 6. PMID 22096577 DOI: 10.1371/journal.pone.0027461  1
2011 Neufeld EF. From serendipity to therapy Annual Review of Biochemistry. 80: 1-15. PMID 21675915 DOI: 10.1146/annurev.biochem.031209.093756  1
2009 Ohmi K, Kudo LC, Ryazantsev S, Zhao HZ, Karsten SL, Neufeld EF. Sanfilippo syndrome type B, a lysosomal storage disease, is also a tauopathy Proceedings of the National Academy of Sciences of the United States of America. 106: 8332-8337. PMID 19416848 DOI: 10.1073/pnas.0903223106  1
2008 Chen CHB, Dellamaggiore KR, Ouellette CP, Sedano CD, Lizadjohry M, Chernis GA, Gonzales M, Baltasar FE, Fan AL, Myerowitz R, Neufeld EF. Aptamer-based endocytosis of a lysosomal enzyme Proceedings of the National Academy of Sciences of the United States of America. 105: 15908-15913. PMID 18838694 DOI: 10.1073/pnas.0808360105  1
2008 Cathey SS, Kudo M, Tiede S, Raas-Rothschild A, Braulke T, Beck M, Taylor HA, Canfield WM, Leroy JG, Neufeld EF, McKusick VA. Molecular order in mucolipidosis II and III nomenclature. American Journal of Medical Genetics. Part A. 146: 512-3. PMID 18203164 DOI: 10.1002/ajmg.a.32193  1
2007 Ryazantsev S, Yu WH, Zhao HZ, Neufeld EF, Ohmi K. Lysosomal accumulation of SCMAS (subunit c of mitochondrial ATP synthase) in neurons of the mouse model of mucopolysaccharidosis III B Molecular Genetics and Metabolism. 90: 393-401. PMID 17185018 DOI: 10.1016/j.ymgme.2006.11.006  1
2005 Jordan MC, Zheng Y, Ryazantsev S, Rozengurt N, Roos KP, Neufeld EF. Cardiac manifestations in the mouse model of mucopolysaccharidosis I Molecular Genetics and Metabolism. 86: 233-243. PMID 15979918 DOI: 10.1016/j.ymgme.2005.05.003  1
2004 Zheng Y, Ryazantsev S, Ohmi K, Zhao HZ, Rozengurt N, Kohn DB, Neufeld EF. Retrovirally transduced bone marrow has a therapeutic effect on brain in the mouse model of mucopolysaccharidosis IIIB. Molecular Genetics and Metabolism. 82: 286-95. PMID 15308126 DOI: 10.1016/j.ymgme.2004.06.004  1
2003 Zheng Y, Rozengurt N, Ryazantsev S, Kohn DB, Satake N, Neufeld EF. Treatment of the mouse model of mucopolysaccharidosis I with retrovirally transduced bone marrow. Molecular Genetics and Metabolism. 79: 233-44. PMID 12948739 DOI: 10.1016/S1096-7192(03)00116-1  1
2003 Ohmi K, Greenberg DS, Rajavel KS, Ryazantsev S, Li HH, Neufeld EF. Activated microglia in cortex of mouse models of mucopolysaccharidoses I and IIIB. Proceedings of the National Academy of Sciences of the United States of America. 100: 1902-7. PMID 12576554 DOI: 10.1073/pnas.252784899  1
2002 Li HH, Zhao HZ, Neufeld EF, Cai Y, Gómez-Pinilla F. Attenuated plasticity in neurons and astrocytes in the mouse model of Sanfilippo syndrome type B Journal of Neuroscience Research. 69: 30-38. PMID 12111813 DOI: 10.1002/jnr.10278  1
2001 Neufeld EF, d'Azzo A. 14. Biosynthesis of normal and mutant β-hexosaminidases Advances in Genetics. 44: 165-171. PMID 11596981  1
2001 Rajavel KS, Neufeld EF. Nonsense-mediated decay of human HEXA mRNA Molecular and Cellular Biology. 21: 5512-5519. PMID 11463833 DOI: 10.1128/MCB.21.16.5512-5519.2001  1
2001 Kakkis ED, Muenzer J, Tiller GE, Waber L, Belmont J, Passage M, Izykowski B, Phillips J, Doroshow R, Walot I, Hoft R, Neufeld EF, Yu KT, Okazaki S, Lewis D, et al. Enzyme-replacement therapy in mucopolysaccharidosis I New England Journal of Medicine. 344: 182-188. PMID 11172140 DOI: 10.1056/NEJM200101183440304  1
2000 Yu WH, Zhao KW, Ryazantsev S, Rozengurt N, Neufeld EF. Short-term enzyme replacement in the murine model of sanfilippo syndrome type B Molecular Genetics and Metabolism. 71: 573-580. PMID 11136549 DOI: 10.1006/mgme.2000.3095  1
2000 Zhao KW, Neufeld EF. Purification and characterization of recombinant human α-N-acetylglucosaminidase secreted by Chinese hamster ovary cells Protein Expression and Purification. 19: 202-211. PMID 10833408 DOI: 10.1006/prep.2000.1230  1
2000 Ruth L, Eisenberg D, Neufeld EF. α-L-iduronidase forms semi-crystalline spherulites with amyloid-like properties Acta Crystallographica Section D: Biological Crystallography. 56: 524-528. PMID 10739940 DOI: 10.1107/S090744490000007X  1
1999 Li HH, Yu WH, Rozengurt N, Zhao HZ, Lyons KM, Anagnostaras S, Fanselow MS, Suzuki K, Vanier MT, Neufeld EF. Mouse model of Sanfilippo syndrome type B produced by targeted disruption of the gene encoding alpha-N-acetylglucosaminidase. Proceedings of the National Academy of Sciences of the United States of America. 96: 14505-10. PMID 10588735 DOI: 10.1073/pnas.96.25.14505  1
1998 Schmidtchen A, Greenberg D, Zhao HG, Li HH, Huang Y, Tieu P, Zhao HZ, Cheng S, Zhao Z, Whitley CB, Di Natale P, Neufeld EF. NAGLU mutations underlying Sanfilippo syndrome type B American Journal of Human Genetics. 62: 64-69. PMID 9443878 DOI: 10.1086/301685  1
1997 Zhao KW, Faull KF, Kakkis ED, Neufeld EF. Carbohydrate structures of recombinant human α-L-iduronidase secreted by Chinese hamster ovary cells Journal of Biological Chemistry. 272: 22758-22765. PMID 9278435 DOI: 10.1074/jbc.272.36.22758  1
1996 Kakkis ED, McEntee MF, Schmidtchen A, Neufeld EF, Ward DA, Gompf RE, Kania S, Bedolla C, Chien SL, Shull RM. Long-term and high-dose trials of enzyme replacement therapy in the canine model of mucopolysaccharidosis I. Biochemical and Molecular Medicine. 58: 156-67. PMID 8812735 DOI: 10.1006/bmme.1996.0044  1
1996 Zhao HG, Li HH, Bach G, Schmidtchen A, Neufeld EF. The molecular basis of Sanfilippo syndrome type B Proceedings of the National Academy of Sciences of the United States of America. 93: 6101-6105. PMID 8650226 DOI: 10.1073/pnas.93.12.6101  1
1996 Zhao KW, Stevens RL, Faull KF, Kakkis ED, Neufeld EF. Oligosaccharides of recombinant human α-L-iduronidasc secreted by chinese hamster ovary cells Faseb Journal. 10: A1108.  1
1995 Tieu PT, Bach G, Matynia A, Hwang M, Neufeld EF. Four novel mutations underlying mild or intermediate forms of alpha-L-iduronidase deficiency (MPS IS and MPS IH/S). Human Mutation. 6: 55-9. PMID 7550232 DOI: 10.1002/humu.1380060111  1
1994 Tieu PT, Menon K, Neufeld EF. A mutant stop codon (TAG) in the IDUA gene is used as an acceptor splice site in a patient with Hurler syndrome (MPS IH) Human Mutation. 3: 333-336. PMID 8019572  1
1994 Kakkis ED, Matynia A, Jonas AJ, Neufeld EF. Overexpression of the human lysosomal enzyme alpha-L-iduronidase in Chinese hamster ovary cells. Protein Expression and Purification. 5: 225-32. PMID 7950365 DOI: 10.1006/prep.1994.1035  1
1994 Menon KP, Neufeld EF. Evidence for degradation of mRNA encoding alpha-L-iduronidase in Hurler fibroblasts with premature termination alleles. Cellular and Molecular Biology. 40: 999-1005. PMID 7849567  1
1994 Shull RM, Kakkis ED, McEntee MF, Kania SA, Jonas AJ, Neufeld EF. Enzyme replacement in a canine model of Hurler syndrome. Proceedings of the National Academy of Sciences of the United States of America. 91: 12937-41. PMID 7809150 DOI: 10.1073/pnas.91.26.12937  1
1993 Moskowitz SM, Tieu PT, Neufeld EF. A deletion/insertion mutation in the IDUA gene in a Libyan Jewish patient with Hurler syndrome (mucopolysaccharidosis IH). Human Mutation. 2: 71-3. PMID 8477267 DOI: 10.1002/humu.1380020113  1
1993 Bach G, Moskowitz SM, Tieu PT, Matynia A, Neufeld EF. Molecular analysis of Hurler syndrome in Druze and Muslim Arab patients in Israel: multiple allelic mutations of the IDUA gene in a small geographic area. American Journal of Human Genetics. 53: 330-8. PMID 8328452  1
1993 Moskowitz SM, Tieu PT, Neufeld EF. Mutation in Scheie syndrome (MPS IS): a G-->A transition creates new splice site in intron 5 of one IDUA allele. Human Mutation. 2: 141-4. PMID 8318992 DOI: 10.1002/humu.1380020215  1
1992 Stoltzfus LJ, Sosa-Pineda B, Moskowitz SM, Menon KP, Dlott B, Hooper L, Teplow DB, Shull RM, Neufeld EF. Cloning and characterization of cDNA encoding canine alpha-L-iduronidase. mRNA deficiency in mucopolysaccharidosis I dog. The Journal of Biological Chemistry. 267: 6570-5. PMID 1551868  1
1992 Muenzer J, Neufeld EF, Constantopoulos G, Caruso RC, Kaiser-Kupfer MI, Pikus A, Danoff J, Berry RR, McDonald HD, Thompson JN, Rodén L, Zasloff MA. Attempted enzyme replacement using human amnion membane implantations in mucopolysaccharidoses Journal of Inherited Metabolic Disease. 15: 25-37. PMID 1533888 DOI: 10.1007/BF01800340  1
1992 Menon KP, Tieu PT, Neufeld EF. Architecture of the canine IDUA gene and mutation underlying canine mucopolysaccharidosis I Genomics. 14: 763-768. PMID 1339393 DOI: 10.1016/S0888-7543(05)80182-X  1
1991 Neufeld EF. Lysosomal storage diseases Annual Review of Biochemistry. 60: 257-280. PMID 1883197  1
1991 Paw BH, Wood LC, Neufeld EF. A third mutation at the CpG dinucleotide of codon 504 and a silent mutation at codon 506 of the HEX A gene American Journal of Human Genetics. 48: 1139-1146. PMID 1827944  1
1990 Wood LC, Neufeld EF. A cystic fibrosis phenotype in cells cultured from sweat gland secretory coil: Altered kinetics of 36Cl efflux Journal of Biological Chemistry. 265: 12796-12800. PMID 2376576  1
1990 Paw BH, Tieu PT, Kaback MM, Lim J, Neufeld EF. Frequency of three Hex A mutant alleles among Jewish and non-Jewish carriers identified in a Tay-Sachs screening program American Journal of Human Genetics. 47: 698-705. PMID 2220809  1
1990 Dlott B, D'Azzo A, Quon DVK, Neufeld EF. Two mutations produce intron insertion in mRNA and elongated β-subunit of human β-hexosaminidase Journal of Biological Chemistry. 265: 17921-17927. PMID 2170400  1
1990 Paw BH, Moskowitz SM, Uhrhammer N, Wright N, Kaback MM, Neufeld EF. Juvenile GM2 gangliosidosis caused by substitution of histidine for arginine at position 499 or 504 of the alpha-subunit of beta-hexosaminidase. The Journal of Biological Chemistry. 265: 9452-7. PMID 2140574  1
1989 Lau MMH, Neufeld EF. A frameshift mutation in a patient with Tay-Sachs disease causes premature termination and defective intracellular transport of the α-subunit of β-hexosaminidase Journal of Biological Chemistry. 264: 21376-21380. PMID 2531748  1
1989 Neufeld EF. Natural history and inherited disorders of a lysosomal enzyme, β-hexosaminidase Journal of Biological Chemistry. 264: 10927-10930. PMID 2525553  1
1989 Paw BH, Kaback MM, Neufeld EF. Molecular basis of adult-onset and chronic G(M2) gangliosidoses in patients of Ashkenazi Jewish origin: substitution of serine for glycine at position 269 of the α-subunit of β-hexosaminidase Proceedings of the National Academy of Sciences of the United States of America. 86: 2413-2417. PMID 2522660  1
1989 Quon DVK, Proia RL, Fowler AV, Bleibaum J, Neufeld EF. Proteolytic processing of the β-subunit of the lysosomal enzyme, β-hexosaminidase, in normal human fibroblasts Journal of Biological Chemistry. 264: 3380-3384. PMID 2521634  1
1988 Little LE, Lau MMH, Quon DVK, Fowler AV, Neufeld EF. Proteolytic processing of the α-chain of the lysosomal enzyme, β-hexosaminidase, in normal human fibroblasts Journal of Biological Chemistry. 263: 4288-4292. PMID 2964446  1
1988 Paw BH, Neufeld EF. Normal transcription of the β-hexosaminidase α-chain gene in the Ashkenazi Tay-Sachs mutation Journal of Biological Chemistry. 263: 3012-3015. PMID 2449434  1
1987 Zokaeem G, Bayleran J, Kaplan P, Hechtman P, Neufeld EF. A shortened β-hexosaminidase α-chain in an Italian patient with infantile Tay-Sachs disease American Journal of Human Genetics. 40: 537-547. PMID 2954459  1
1986 Grebner EE, Mansfield DA, Raghavan SS, Kolodny EH, d'Azzo A, Neufeld EF, Jackson LG. Two abnormalities of hexosaminidase A in clinically normal individuals. American Journal of Human Genetics. 38: 505-14. PMID 2939713  1
1985 Constantopoulos G, Shull RM, Hastings N, Neufeld EF. Neurochemical characterization of canine alpha-L-iduronidase deficiency disease (model of human mucopolysaccharidosis I). Journal of Neurochemistry. 45: 1213-7. PMID 3928817 DOI: 10.1111/j.1471-4159.1985.tb05544.x  1
1985 Myerowitz R, Piekarz R, Neufeld EF, Shows TB, Suzuki K. Human β-hexosaminidase α chain: Coding sequence and homology with the β chain Proceedings of the National Academy of Sciences of the United States of America. 82: 7830-7834. PMID 2933746 DOI: 10.1073/pnas.82.23.7830  1
1984 Shull RM, Helman RG, Spellacy E, Constantopoulos G, Munger RJ, Neufeld EF. Morphologic and biochemical studies of canine mucopolysaccharidosis I. The American Journal of Pathology. 114: 487-95. PMID 6320652  1
1984 d'Azzo A, Proia RL, Kolodny EH, Kaback MM, Neufeld EF. Faulty association of alpha- and beta-subunits in some forms of beta-hexosaminidase A deficiency. The Journal of Biological Chemistry. 259: 11070-4. PMID 6236221  1
1984 Proia RL, d'Azzo A, Neufeld EF. Associaton of α- and β-subunits during the biosynthesis of β-hexosaminidase in cultured human fibroblasts Journal of Biological Chemistry. 259: 3350-3354. PMID 6230359  1
1983 Neufeld EF. The William Allan Memorial Award address: cell mixing and its sequelae. American Journal of Human Genetics. 35: 1081-1085. PMID 6417999  1
1983 Spellacy E, Shull RM, Constantopoulos G, Neufeld EF. A canine model of human alpha-L-iduronidase deficiency. Proceedings of the National Academy of Sciences of the United States of America. 80: 6091-5. PMID 6412235  1
1983 Sahagian GG, Neufeld EF. Biosynthesis and turnover of the mannose 6-phosphate receptor in cultured Chinese hamster ovary cells Journal of Biological Chemistry. 258: 7121-7128. PMID 6304079  1
1983 Bach G, Neufeld EF. Synthesis and maturation of cross-reactive glycoprotein in fibroblasts deficient in arylsulfatase a activity Biochemical and Biophysical Research Communications. 112: 198-205. PMID 6132606 DOI: 10.1016/0006-291X(83)91816-8  1
1982 Neufeld EF, Robbins AR. Pleiotropic mutations of lysosomal function in human patients and in Chinese hamster ovary cells. Progress in Clinical and Biological Research. 103: 177-185. PMID 7163219  1
1982 Thomas GH, Raghavan S, Kolodny EH, Frisch A, Neufeld EF, O'Brien JS, Reynolds LW, Miller CS, Shapiro J, Kazazian HH, Heller RH. Nonuniform deficiency of hexosaminidase A in tissues and fluids of two unrelated individuals. Pediatric Research. 16: 232-7. PMID 7063277  1
1982 Proia RL, Neufeld EF. Synthesis of β-hexosaminidase in cell-free translation and in intact fibroblasts: An insoluble precursor α chain in a rare form of Tay-Sachs disease Proceedings of the National Academy of Sciences of the United States of America. 79: 6360-6364. PMID 6959123  1
1982 Wasteson A, Neufeld EF. [51] Iduronate sulfatase from human plasma Methods in Enzymology. 83: 573-578. PMID 6954344 DOI: 10.1016/0076-6879(82)83053-X  1
1982 Brown FR, Hall CW, Neufeld EF, Munoz LL, Braine H, Andrzejewski S, Camargo EE, Mark SA, Richard JM, Moser HW. Administration of iduronate sulfatase by plasma exchange to patients with the Hunter syndrome: a clinical study. American Journal of Medical Genetics. 13: 309-18. PMID 6817638 DOI: 10.1002/ajmg.1320130314  1
1982 Owada M, Neufeld EF. Is there a mechanism for introducing acid hydrolases into liver lysosomes that is independent of mannose 6-phosphate recognition? evidence from I-cell disease Biochemical and Biophysical Research Communications. 105: 814-820. PMID 6807313 DOI: 10.1016/0006-291X(82)91042-7  1
1982 Robey PG, Neufeld EF. Defective phosphorylation and processing of β-hexosaminidase by intact cultured fibroblasts from patients with mucolipidosis III Archives of Biochemistry and Biophysics. 213: 251-257. PMID 6460470 DOI: 10.1016/0003-9861(82)90459-3  1
1982 Shull RM, Munger RJ, Spellacy E, Hall CW, Constantopoulos G, Neufeld EF. Canine alpha-L-iduronidase deficiency. A model of mucopolysaccharidosis I. The American Journal of Pathology. 109: 244-8. PMID 6215865  1
1981 Myerowitz R, Neufeld EF. Maturation of α-L-iduronidase in cultured human fibroblasts Journal of Biological Chemistry. 256: 3044-3048. PMID 7204389  1
1981 Frisch A, Neufeld EF. Limited proteolysis of the beta-hexosaminidase precursor in a cell-free system. Journal of Biological Chemistry. 256: 8242-8246. PMID 6455422  1
1981 Willingham MC, Pastan IH, Sahagian GG, Jourdian GW, Neufeld EF. Morphologic study of the internalization of a lysosomal enzyme by the mannose 6-phosphate receptor in cultured Chinese hamster ovary cells Proceedings of the National Academy of Sciences of the United States of America. 78: 6967-6971. PMID 6273898  1
1981 Neufeld EF. The uptake of enzymes into lysosomes: An overview Birth Defects: Original Article Series. 17: 77-84.  1
1980 Neufeld EF. The uptake of enzymes into lysosomes: an overview. Birth Defects Original Article Series. 16: 77-84. PMID 7448363  1
1980 Karson EM, Neufeld EF, Sando GN. p-isothiocyanatophenyl 6-phospho-α-D-mannopyranoside coupled to albumin. A model compound recognized by the fibroblast lysosomal enzyme uptake system. 2. Biological properties Biochemistry. 19: 3856-3860. PMID 7407073  1
1980 Hasilik A, Neufeld EF. Biosynthesis of lysosomal enzymes in fibroblasts. Phosphorylation of mannose residues Journal of Biological Chemistry. 255: 4946-4950. PMID 6989822  1
1980 Hasilik A, Neufeld EF. Biosynthesis of lysosomal enzymes in fibroblasts. Synthesis as precursors of higher molecular weight Journal of Biological Chemistry. 255: 4937-4945. PMID 6989821  1
1979 Frisch A, Neufeld EF. A rapid and sensitive assay for neuraminidase: Application to cultured flbroblasts Analytical Biochemistry. 95: 222-227. PMID 495958 DOI: 10.1016/0003-2697(79)90209-4  1
1979 Rome LH, Julian Garvin A, Allietta MM, Neufeld EF. Two species of lysosomal organelles in cultured human fibroblasts Cell. 17: 143-153. PMID 455458 DOI: 10.1016/0092-8674(79)90302-7  1
1979 Sando GN, Titus-Dillon P, Hall CW, Neufeld EF. Inhibition of receptor-mediated uptake of a lysosomal enzyme into fibroblasts by chloroquine, procaine and ammonia Experimental Cell Research. 119: 359-364. PMID 428466 DOI: 10.1016/0014-4827(79)90364-1  1
1979 Rome LH, Weissmann B, Neufeld EF. Direct demonstration of binding of a lysosomal enzyme, α-L-iduronidase, to receptors on cultured fibroblasts Proceedings of the National Academy of Sciences of the United States of America. 76: 2331-2334. PMID 287076  1
1979 Nwokoro N, Neufeld EF. Detection of hunter heterozygotes by enzymatic analysis of hair roots American Journal of Human Genetics. 31: 42-49. PMID 107796  1
1978 Rome LH, Garvin AJ, Neufeld EF. Human kidney α-l-Iduronidase: Purification and characterization Archives of Biochemistry and Biophysics. 189: 344-353. PMID 30407 DOI: 10.1016/0003-9861(78)90221-7  1
1978 Hall CW, Liebaers I, Di Natale P, Neufeld EF. Enzymic diagnosis of the genetic mucopolysaccharide storage disorders. Methods in Enzymology. 50: 439-456. PMID 26836  1
1978 Neufeld EF, Sando GN, Garvin AJ, Rome LH. The transport of lysosomal enzymes Progress in Clinical and Biological Research. 35-41.  1
1977 Sando GN, Neufeld EF. Recognition and receptor-mediated uptake of a lysosomal enzyme, α-l-iduronidase, by cultured human fibroblasts Cell. 12: 619-627. PMID 922886 DOI: 10.1016/0092-8674(77)90262-8  1
1977 Neufeld EF, Sando GN, Garvin AJ, Rome LH. The transport of lysosomal enzymes. Journal of Supramolecular Structure. 6: 95-101. PMID 895139 DOI: 10.1002/jss.400060108  1
1977 Neufeld EF, Liebaers I, Epstein CJ, Yatziv S, Milunsky A, Migeon BR. The Hunter syndrome in females: is there an autosomal recessive form of iduronate sulfatase deficiency? American Journal of Human Genetics. 29: 455-61. PMID 409284  1
1977 Migeon BR, Sprenkle JA, Liebaers I, Scott JF, Neufeld EF. X-linked Hunter syndrome: the heterozygous phenotype in cell culture American Journal of Human Genetics. 29: 448-454. PMID 409283  1
1977 Di Natale P, Leder IG, Neufeld EF. A radioactive substrate and assay for α-l-iduronidase Clinica Chimica Acta. 77: 211-218. PMID 406106 DOI: 10.1016/0009-8981(77)90224-8  1
1977 Liebaers I, Natale PD, Neufeld EF. Iduronate sulfatase in amniotic fluid: An aid in the prenatal diagnosis of the Hunter syndrome The Journal of Pediatrics. 90: 423-425. PMID 402458 DOI: 10.1016/S0022-3476(77)80707-5  1
1977 Neufeld EF. The enzymology of inherited mucopolysaccharide storage disorders Trends in Biochemical Sciences. 2: 25-26. DOI: 10.1016/0968-0004(77)90250-X  1
1976 Liebaers I, Neufeld EF. Iduronate sulfatase activity in serum, lymphocytes, and fibroblasts—simplified diagnosis of the hunter syndrome Pediatric Research. 10: 733-736. PMID 821034  1
1976 Neufeld EF, Liebaers I, Lim TW. Iduronate sulfatase determination for the diagnosis of the Hunter syndrome and the detection of the carrier state. Advances in Experimental Medicine and Biology. 68: 253-260. PMID 820168  1
1976 Stevenson RE, Howell RR, McKusick V, Suskind R, Hanson JW, Elliott DE, Neufeld EF. The iduronidase deficient mucopolysaccharidoses: clinical and roentgenographic features Pediatrics. 57: 111-122. PMID 813180  1
1976 Epstein CJ, Yatziv S, Neufeld E, Liebaers I. Genetic counselling for Hunter syndrome. Lancet. 2: 737-8. PMID 61412 DOI: 10.1016/S0140-6736(76)90027-1  1
1976 Shapiro LJ, Hall CW, Leder IG, Neufeld EF. The relationship of α-l-iduronidase and Hurler corrective factor Archives of Biochemistry and Biophysics. 172: 156-161. PMID 3136 DOI: 10.1016/0003-9861(76)90061-8  1
1976 Neufeld EF. Contributions of cell culture to studies of lysosomal enzymes | FIFTH INTERNATIONAL CONGRESS OF HUMAN GENETICS Excerpta Med.,Amsterdam,I.C.S.. No.31.  1
1975 Neufeld EF, Lim TW, Shapiro LJ. Inherited disorders of lysosomal metabolism. Annual Review of Biochemistry. 44: 357-376. PMID 806251  1
1975 Shapiro LJ, Hickman S, Hall CW, Neufeld EF. Biochemical studies in mucolipidoses II and III Birth Defects: Original Article Series. 11: 301-305. PMID 127631  1
1975 Leisti J, Rimoin DL, Kaback MM, Hollister DW, Den Tandt W, Neufeld E, Matalon R, Philippart M. PHENOTYPIC VARIATION IN ALPHA-L-IDURONIDASE DEFICIENCY The Lancet. 305: 1344. PMID 49545 DOI: 10.1016/S0140-6736(75)92351-X  1
1974 Hickman S, Shapiro LJ, Neufeld EF. A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblasts. Biochemical and Biophysical Research Communications. 57: 55-61. PMID 4364008 DOI: 10.1016/S0006-291X(74)80356-6  1
1974 Lim TW, Leder IG, Bach G, Neufeld EF. An assay for iduronate sulfatase (Hunter corrective factor). Carbohydrate Research. 37: 103-9. PMID 4214613 DOI: 10.1016/S0008-6215(00)87067-6  1
1973 Bach G, Eisenberg F, Cantz M, Neufeld EF. The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase. Proceedings of the National Academy of Sciences of the United States of America. 70: 2134-8. PMID 4269173  1
1973 Hall CW, Cantz M, Neufeld EF. A -glucuronidase deficiency mucopolysaccharidosis: studies in cultured fibroblasts. Archives of Biochemistry and Biophysics. 155: 32-8. PMID 4268215 DOI: 10.1016/S0003-9861(73)80006-2  1
1973 Hall CW, Neufeld EF. Alpha-L-iduronidase activity in cultured skin fibroblasts and amniotic fluid cells. Archives of Biochemistry and Biophysics. 158: 817-21. PMID 4205743 DOI: 10.1016/0003-9861(73)90577-8  1
1973 Bach G, Cantz M, Hall CW, Neufeld EF. Genetic errors of mucopolysaccharide degradation Biochemical Society Transactions. 1: 231-234.  1
1972 Cantz M, Chrambach A, Bach G, Neufeld EF. The Hunter corrective factor. Purification and preliminary characterization Journal of Biological Chemistry. 247: 5456-5462. PMID 4626721  1
1972 Hickman S, Neufeld EF. A hypothesis for I-cell disease: Defective hydrolases that do not enter lysosomes Biochemical and Biophysical Research Communications. 49: 992-999. PMID 4345092 DOI: 10.1016/0006-291X(72)90310-5  1
1972 McKusick VA, Howell RR, Hussels IE, Neufeld EF, Stevenson RE. Allelism, non-allelism and genetic compounds among the mucopolysaccharidoses: corrective factors in nosology, genetics and therapy Transactions of the Association of American Physicians. 85: 151-171. PMID 4267098  1
1972 Lie SO, McKusick VA, Neufeld EF. Simulation of genetic mucopolysaccharidoses in normal human fibroblasts by alteration of pH of the medium Proceedings of the National Academy of Sciences of the United States of America. 69: 2361-2363. PMID 4262638  1
1972 Bach G, Friedman R, Weissmann B, Neufeld EF. The defect in the Hurler and Scheie syndromes: deficiency of -L-iduronidase Proceedings of the National Academy of Sciences of the United States of America. 69: 2048-2051. PMID 4262258  1
1972 Kresse H, Neufeld EF. The Sanfilippo A corrective factor. Purification and mode of action Journal of Biological Chemistry. 247: 2164-2170. PMID 4259567  1
1972 Barton RW, Neufeld EF. A distinct biochemical deficit in the maroteaux-lamy syndrome (mucopolysaccharidosis VI) The Journal of Pediatrics. 80: 114-116. PMID 4259536 DOI: 10.1016/S0022-3476(72)80467-0  1
1972 Cantz M, Kresse H, Barton RW, Neufeld EF. [121] Corrective factors for inborn errors of mucopolysaccharide metabolism Methods in Enzymology. 28: 884-897. DOI: 10.1016/0076-6879(72)28127-7  1
1972 Neufeld EF, Sweeley CC, Rogers S, Friedmann T, Roblin R. Gene therapy for human genetic disease? Science. 178: 648-649.  1
1971 Barton RW, Neufeld EF. The Hurler corrective factor. Purification and some properties Journal of Biological Chemistry. 246: 7773-7779. PMID 4257494  1
1971 Neufeld EF, Cantz MJ. Corrective factors for inborn errors of mucopolysaccharide metabolism Annals of the New York Academy of Sciences. 179: 580-587. PMID 4255108  1
1971 Kresse H, Wiesmann U, Cantz M, Hall CW, Neufeld EF. Biochemical heterogeneity of the sanfilippo syndrome: Preliminary characterization of two deficient factors Biochemical and Biophysical Research Communications. 42: 892-898. PMID 4252428 DOI: 10.1016/0006-291X(71)90514-6  1
1970 Cantz M, Chrambach A, Neufeld EF. Characterization of the factor deficient in the Hunter syndrome by polyacrylamide gel electrophoresis Biochemical and Biophysical Research Communications. 39: 936-942. PMID 4987382 DOI: 10.1016/0006-291X(70)90414-6  1
1970 Wiesmann U, Neufeld EF. Metabolism of sulfated mucopolysaccharide in cultured fibroblasts from cystic fibrosis patients The Journal of Pediatrics. 77: 685-690. PMID 4247822 DOI: 10.1016/S0022-3476(70)80215-3  1
1970 Neufeld EF, Fratantoni JC. Inborn errors of mucopolysaccharide metabolism Science. 169: 141-146. PMID 4246678  1
1970 Wiesmann U, Neufeld EF. Scheie and hurler syndromes: Apparent identity of the biochemical defect Science. 169: 72-74. PMID 4246082  1
1969 Grebner EE, Neufeld EF. Stimulation of a protein glycosylation reaction by lysozyme Bba - General Subjects. 192: 347-349. PMID 4984117  1
1969 Fratantoni JC, Hall CW, Neufeld EF. The defect in Hurler and Hunter syndromes. II. Deficiency of specific factors involved in mucopolysaccharide degradation Proceedings of the National Academy of Sciences of the United States of America. 64: 360-366. PMID 4244031  1
1969 Ginsburg V, Neufeld EF. Complex heterosaccharides of animals. Annual Review of Biochemistry. 38: 371-88. PMID 4240949 DOI: 10.1146/annurev.bi.38.070169.002103  1
1969 Fratantoni JC, Neufeld EF, Uhlendorf BW, Jacobson CB. Intrauterine diagnosis of the hurler and hunter syndromes New England Journal of Medicine. 280: 686-688. PMID 4179670  1
1968 Fratantoni JC, Hall CW, Neufeld EF. Hurler and Hunter syndromes: Mutual correction of the defect in cultured fibroblasts Science. 162: 570-572. PMID 4236721  1
1968 Fratantoni JC, Hall CW, Neufeld EF. The defect in Hurler's and Hunter's syndromes: faulty degradation of mucopolysaccharide Proceedings of the National Academy of Sciences of the United States of America. 60: 699-706. PMID 4236091  1
1967 Goudsmit EM, Neufeld EF. Formation of GDP-L-galactose from GDP-D-mannose Biochemical and Biophysical Research Communications. 26: 730-735. PMID 6030986  1
1966 Grebner EE, Hall CW, Neufeld EF. Glycosylation of serine residues by a uridine diphosphate-xylose: Protein xylosyltransferase from mouse mastocytoma Archives of Biochemistry and Biophysics. 116: 391-398. PMID 5961844  1
1966 O'Brien PJ, Canady MR, Hall CW, Neufeld EF. Transfer of N-acetylneuraminic acid to incomplete glycoproteins associated with microsomes Bba - General Subjects. 117: 331-341. PMID 5961299  1
1966 Goudsmit EM, Neufeld EF. Isolation of GDP-L-galactose from the albumen gland of Helix pomatia Bba - General Subjects. 121: 192-195. PMID 5956942  1
1966 Grebner EE, Hall CW, Neufeld EF. Incorporation of D-xylose-C14 into glycoprotein by particles from hen oviduct Biochemical and Biophysical Research Communications. 22: 672-677. PMID 5944767  1
1966 Neufeld EF. [46] UDP-d-galacturonic acid 4-epimerase from radish roots Methods in Enzymology. 8: 276-277. DOI: 10.1016/0076-6879(66)08050-9  1
1965 Neufeld EF, Hall CW. Inhibition of UDP-D-glucose dehydrogenase by UDP-D-xylose: A possible regulatory mechanism Biochemical and Biophysical Research Communications. 19: 456-461. PMID 14338992  1
1965 NEUFELD EF, GINSBURG V. CARBOHYDRATE METABOLISM. Annual Review of Biochemistry. 34: 297-312. PMID 14321172 DOI: 10.1146/annurev.bi.34.070165.001501  1
1964 O'Brien PJ, Neufeld EF. A rapid procedure for the preparation of small quantities of uridine diphosphate-N-[14C]acetylhexosamine Bba - Specialized Section On Mucoproteins and Mucopolysaccharides. 83: 352-354. PMID 14236711  1
1964 KORNFELD S, KORNFELD R, NEUFELD EF, O'BRIEN PJ. THE FEEDBACK CONTROL OF SUGAR NUCLEOTIDE BIOSYNTHESIS IN LIVER Proceedings of the National Academy of Sciences of the United States Of. 52: 371-379. PMID 14206604  1
1964 Neufeld EF, Hall CW. Formation of galactolipids by chloroplasts Biochemical and Biophysical Research Communications. 14: 503-508. PMID 5836548  1
1963 Neufeld EF, Hassid WZ. Biosynthesis of Saccharides from Glycopyranosyl Esters of Nucleotides ("Sugar Nucleotides") Advances in Carbohydrate Chemistry. 18: 309-356. PMID 14272320 DOI: 10.1016/S0096-5332(08)60246-5  1
1963 Frydman RB, Neufeld EF, Hassid WZ. Thymidine diphosphate d-galactose pyrophosphorylase of Phaseolus aureus Bba - Biochimica Et Biophysica Acta. 77: 332-334. PMID 14090450  1
1963 Frydman RB, Neufeld EF. Synthesis of galactosylinositol by extracts from peas Biochemical and Biophysical Research Communications. 12: 121-125. PMID 13960000  1
1963 Feingold DS, Neufeld EF, Hassid WZ. [108] Preparation of UDP-d-xylose and UDP-l-arabinose Methods in Enzymology. 6: 782-787. DOI: 10.1016/0076-6879(63)06248-0  1
1962 Neufeld EF. Formation and epimerization of dTDP-D-galactose catalyzed by plant enzymes Biochemical and Biophysical Research Communications. 7: 461-466. PMID 14479163  1
1962 Felenbok B, Neufeld EF. Hydrolysis of glycopyranosyl phosphates of the β-d (or α-l) configuration by a plant phosphatase Archives of Biochemistry and Biophysics. 97: 116-121. PMID 13892166  1
1961 NEUFELD EF, FEINGOLD DS, ILVES SM, KESSLER G, HASSID WZ. Phosphorylation of D-galacturonic acid by extracts from germinating seeds of Phaseolus aureus. The Journal of Biological Chemistry. 236: 3102-5. PMID 14479161  1
1961 Barber GA, Neufeld EF. Rhamnosyl transfer from TDP-L-rhamnose catalyzed by a plant enzyme Biochemical and Biophysical Research Communications. 6: 44-48. PMID 13864832  1
1961 KESSLER G, NEUFELD EF, FEINGOLD DS, HASSID WZ. Metabolism of D-glucuronic acid and D-galacturonic acid by Phaseolus aureus seedlings. The Journal of Biological Chemistry. 236: 308-312. PMID 13752745  1
1961 Neufeld EF, Feingold DS. Isolation of uridine diphosphate-galacturonic acid from seedlings of Phaseolus aureus Bba - General Subjects. 53: 589-590.  1
1960 NEUFELD EF, FEINGOLD DS, HASSID WZ. Phosphorylation of D-galactose and L-arabinose by extracts from Phaseolus aureus seedlings. The Journal of Biological Chemistry. 235: 906-909. PMID 14426659  1
1960 FEINGOLD DS, NEUFELD EF, HASSID WZ. The 4-epimerization and decarboxylation of uridine diphosphate D-glucuronic acid by extracts from Phaseolus aureus seedlings. The Journal of Biological Chemistry. 235: 910-3. PMID 13821949  1
1959 Hassid WZ, Neufeld EF, Feingold DS. SUGAR NUCLEOTIDES IN THE INTERCONVERSION OF CARBOHYDRATES IN HIGHER PLANTS. Proceedings of the National Academy of Sciences of the United States of America. 45: 905-15. PMID 16590482  1
1959 Neufeld EF, Feingold DS, Hassid WZ. Enzymic phosphorylation of d-glucuronic acid by extracts from seedlings of Phaseolus aureus Archives of Biochemistry and Biophysics. 83: 96-100. PMID 13661996  1
1959 FEINGOLD DS, NEUFELD EF, HASSID WZ. Xylosyl transfer catalyzed by an asparagus extract. The Journal of Biological Chemistry. 234: 488-489. PMID 13641246  1
1958 Feingold DS, Neufeld EF, Hassid WZ. Enzymic synthesis of uridine diphosphate glucuronic acid and uridine diphosphate galacturonic acid with extracts from Phaseolus aureus seedlings Archives of Biochemistry and Biophysics. 78: 401-406. PMID 13618023  1
1958 FEINGOLD DS, NEUFELD EF, HASSID WZ. Synthesis of a beta-1, 3-linked glucan by extracts of Phaseolus aureus seedlings. The Journal of Biological Chemistry. 233: 783-788. PMID 13587492  1
1958 Neufeld EF, Feingold DS, Hassid WZ. Enzymatic conversion of uridine diphosphate D-glucuronic acid to uridine diphosphate galacturonic acid, uridine diphosphate xylose, and uridine diphosphate arabinose [12] Journal of the American Chemical Society. 80: 4430-4431.  1
1957 Neufeld EF, Ginsburg V, Putman EW, Fanshier D, Hassid WZ. Formation and interconversion of sugar nucleotides by plant extracts Archives of Biochemistry and Biophysics. 69: 602-616. PMID 13445231  1
1956 Ginsburg V, Neufeld EF, Hassid WZ. ENZYMATIC SYNTHESIS OF URIDINE DIPHOSPHATE XYLOSE AND URIDINE DIPHOSPHATE ARABINOSE. Proceedings of the National Academy of Sciences of the United States of America. 42: 333-5. PMID 16578456  1
1955 Neufeld EF, Hassid WZ. Hydrolysis of amylose by β-amylase and Z-enzyme Archives of Biochemistry and Biophysics. 59: 405-419. PMID 13275959  1
1955 NEUFELD EF, KAPLAN NO, COLOWICK SP. Effect of adenine nucleotides on reactions involving triphosphopyridine nucleotide. Biochimica Et Biophysica Acta. 17: 525-35. PMID 13250000  1
1953 KAPLAN NO, COLOWICK SP, NEUFELD EF, CIOTTI MM. Pyridine nucleotide transhydrogenase. IV. Effect of adenylic acid a on the bacterial transhydrogenases. The Journal of Biological Chemistry. 205: 17-29. PMID 13117880  1
1953 KAPLAN NO, COLOWICK SP, NEUFELD EF. Pyridine nucleotide transhydrogenase. III. Animal tissue transhydrogenases. The Journal of Biological Chemistry. 205: 1-15. PMID 13117879  1
1952 KAPLAN NO, COLOWICK SP, NEUFELD EF. Pyridine nucleotide transhydrogenase. II. Direct evidence for and mechanism of the transhydrogenase reaction. The Journal of Biological Chemistry. 195: 107-19. PMID 14938358  1
1952 COLOWICK SP, KAPLAN NO, NEUFELD EF, CIOTTI MM. Pyridine nucleotide transhydrogenase. I. Indirect evidence for the reaction and purification of the enzyme. The Journal of Biological Chemistry. 195: 95-105. PMID 14938357  1
1951 RUSSELL ES, NEUFELD EF, HIGGINS CT. Comparison of normal blood picture of young adults from 18 inbred strains of mice Proceedings of the Society For Experimental Biology and Medicine. Society For Experimental Biology and Medicine (New York, N.Y.). 78: 761-766. PMID 14912022 DOI: 10.3181/00379727-78-19210  1
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