| Year |
Citation |
Score |
| 2010 |
Beutler E, Geet CV, Loo DMWMt, Gelbart T, Crain K, Truksa J, Lee PL. Polymorphisms and mutations of human TMPRSS6 in iron deficiency anemia Blood Cells Molecules and Diseases. 44: 16-21. PMID 19818657 DOI: 10.1016/J.Bcmd.2009.09.001 |
0.334 |
|
| 2009 |
Truksa J, Gelbart T, Peng H, Beutler E, Beutler B, Lee P. Suppression of the hepcidin-encoding gene Hamp permits iron overload in mice lacking both hemojuvelin and matriptase-2/TMPRSS6 British Journal of Haematology. 147: 571-581. PMID 19751239 DOI: 10.1111/J.1365-2141.2009.07873.X |
0.503 |
|
| 2009 |
Lee P, Rice L, McCarthy JJ, Beutler E. Severe iron overload with a novel aminolevulinate synthase mutation and hepatitis C infection. A case report. Blood Cells, Molecules & Diseases. 42: 1-4. PMID 18823803 DOI: 10.1016/J.Bcmd.2008.08.001 |
0.303 |
|
| 2008 |
Du X, She E, Gelbart T, Truksa J, Lee P, Xia Y, Khovananth K, Mudd S, Mann N, Moresco EM, Beutler E, Beutler B. The serine protease TMPRSS6 is required to sense iron deficiency. Science (New York, N.Y.). 320: 1088-92. PMID 18451267 DOI: 10.1126/Science.1157121 |
0.5 |
|
| 2008 |
Beutler E. Glucose-6-phosphate dehydrogenase deficiency: a historical perspective. Blood. 111: 16-24. PMID 18156501 DOI: 10.1182/Blood-2007-04-077412 |
0.328 |
|
| 2008 |
Waalen J, Felitti VJ, Gelbart T, Beutler E. Screening for hemochromatosis by measuring ferritin levels: a more effective approach. Blood. 111: 3373-6. PMID 18025154 DOI: 10.1182/Blood-2007-07-102673 |
0.3 |
|
| 2008 |
Friedman J, Waalen J, Takeda A, Beutler E. Evidence for Increased Red Cell Turnover in Unexplained Anemia in Patients Over 70 Years of Age Blood. 112: 3445-3445. DOI: 10.1182/Blood.V112.11.3445.3445 |
0.31 |
|
| 2007 |
Aslan D, Crain K, Beutler E. A new case of human atransferrinemia with a previously undescribed mutation in the transferrin gene. Acta Haematologica. 118: 244-7. PMID 18097132 DOI: 10.1159/000112726 |
0.318 |
|
| 2007 |
Pereira MM, Gelbart T, Ristoff E, Crain KC, Bergua JM, Lafuente AL, Kalko SG, Mateos EG, Beutler E, Corrons JLV. Chronic non-spherocytic hemolytic anemia associated with severe neurological disease due to γ-glutamylcysteine synthetase deficiency in a patient of Moroccan origin Haematologica. 92. PMID 18024385 DOI: 10.3324/Haematol.11238 |
0.324 |
|
| 2007 |
Beutler E. Iron storage disease: facts, fiction and progress. Blood Cells, Molecules & Diseases. 39: 140-7. PMID 17540589 DOI: 10.1016/J.Bcmd.2007.03.009 |
0.317 |
|
| 2007 |
Beutler E, Lee P, Gelbart T, Du X, Beutler B. The Mask Mutation Identifies TMPRSS6 as an Essential Suppressor of Hepcidin Gene Expression, Required for Normal Uptake of Dietary Iron. Blood. 110: 3-3. DOI: 10.1182/Blood.V110.11.3.3 |
0.516 |
|
| 2006 |
Repiso A, Oliva B, Vives-Corrons JL, Beutler E, Carreras J, Climent F. Red cell glucose phosphate isomerase (GPI): a molecular study of three novel mutations associated with hereditary nonspherocytic hemolytic anemia. Human Mutation. 27: 1159. PMID 17041899 DOI: 10.1002/Humu.9466 |
0.341 |
|
| 2006 |
Flanagan JM, Rhodes M, Wilson M, Beutler E. The identification of a recurrent phosphoglycerate kinase mutation associated with chronic haemolytic anaemia and neurological dysfunction in a family from USA. British Journal of Haematology. 134: 233-7. PMID 16740138 DOI: 10.1111/J.1365-2141.2006.06143.X |
0.3 |
|
| 2006 |
Beutler E. Gaucher disease: multiple lessons from a single gene disorder. Acta Paediatrica (Oslo, Norway : 1992). Supplement. 95: 103-9. PMID 16720474 DOI: 10.1080/08035320600619039 |
0.316 |
|
| 2006 |
Flanagan JM, Beutler E. The genetic basis of human erythrocyte pyridoxal kinase activity variation. Haematologica. 91: 801-4. PMID 16704963 DOI: 10.1182/Blood.V104.11.1579.1579 |
0.315 |
|
| 2006 |
Lee PL, Barton JC, Rao SV, Acton RT, Adler BK, Beutler E. Three kinships with ALAS2 P520L (c. 1559 C --> T) mutation, two in association with severe iron overload, and one with sideroblastic anemia and severe iron overload. Blood Cells, Molecules & Diseases. 36: 292-7. PMID 16446107 DOI: 10.1016/J.Bcmd.2005.12.004 |
0.33 |
|
| 2006 |
Noel N, Flanagan J, Kalko SG, Bajo MJR, Mañú MDM, Fuster JLG, Beutler E, Corrons JLV. Two new phosphoglycerate kinase mutations associated with chronic haemolytic anaemia and neurological dysfunction in two patients from Spain British Journal of Haematology. 132: 523-529. PMID 16412025 DOI: 10.1111/J.1365-2141.2005.05882.X |
0.344 |
|
| 2006 |
Beutler E. Hemochromatosis: genetics and pathophysiology. Annual Review of Medicine. 57: 331-47. PMID 16409153 DOI: 10.1146/Annurev.Med.57.121304.131310 |
0.329 |
|
| 2005 |
Beutler E, Waalen J, Gelbart T. Chronic inflammation does not appear to modify the homozygous hereditary hemochromatosis phenotype. Blood Cells, Molecules & Diseases. 35: 326-7. PMID 16154780 DOI: 10.1016/J.Bcmd.2005.08.003 |
0.304 |
|
| 2005 |
Barton JC, Lee PL, Bertoli LF, Beutler E. Iron overload in an African American woman with SS hemoglobinopathy and a promoter mutation in the X-linked erythroid-specific 5-aminolevulinate synthase (ALAS2) gene. Blood Cells, Molecules & Diseases. 34: 226-8. PMID 15885606 DOI: 10.1016/J.BCMD.2005.01.001 |
0.329 |
|
| 2005 |
Sham RL, Phatak PD, West C, Lee P, Andrews C, Beutler E. Autosomal dominant hereditary hemochromatosis associated with a novel ferroportin mutation and unique clinical features. Blood Cells, Molecules & Diseases. 34: 157-61. PMID 15727899 DOI: 10.1016/J.Bcmd.2004.12.002 |
0.323 |
|
| 2005 |
Lee PL, Barton JC, West C, Crain K, Rao SV, Beutler E. Examination of ALAS2, ABC7, Rag1, and IL6 Genes as Candidate Modifiers of Iron Overload in HFE C282Y Homozygotes with Severe Iron Overload. Blood. 106: 3724-3724. DOI: 10.1182/Blood.V106.11.3724.3724 |
0.331 |
|
| 2005 |
Lee PL, Barton JC, Rao SV, Acton RT, Adler BK, Beutler E. Three Kinships with ALAS2 P520L Mutations, Two in Association with Severe Iron Overload, and One with Sideroblastic Anemia and Severe Iron Overload. Blood. 106: 3723-3723. DOI: 10.1182/Blood.V106.11.3723.3723 |
0.335 |
|
| 2005 |
Waalen J, Beutler E. A New Perspective on the Natural History of Hereditary Hemochromatosis. Blood. 106: 3595-3595. DOI: 10.1182/Blood.V106.11.3595.3595 |
0.326 |
|
| 2004 |
Efferth T, Bachli EB, Schwarzl SM, Goede JS, West C, Smith JC, Beutler E. Glucose-6-phosphate dehydrogenase (G6PD) deficiency-type Zurich: a splice site mutation as an uncommon mechanism producing enzyme deficiency. Blood. 104: 2608. PMID 15466166 DOI: 10.1182/Blood-2004-06-2135 |
0.338 |
|
| 2004 |
Lee PL, Barton JC, Brandhagen D, Beutler E. Hemojuvelin (HJV) mutations in persons of European, African-American and Asian ancestry with adult onset haemochromatosis. British Journal of Haematology. 127: 224-9. PMID 15461631 DOI: 10.1111/J.1365-2141.2004.05165.X |
0.332 |
|
| 2004 |
Beutler E. Iron absorption in carriers of the C282Y hemochromatosis mutation. The American Journal of Clinical Nutrition. 80: 799-800. PMID 15447883 DOI: 10.1093/Ajcn/80.4.799 |
0.302 |
|
| 2004 |
Barton J, West C, Lee P, Beutler E. A previously undescribed frameshift deletion mutation of HFE (c.del277; G93fs) associated with hemochromatosis and iron overload in a C282Y heterozygote. Clinical Genetics. 66: 214-216. PMID 15324319 DOI: 10.1111/J.1399-0004.2004.00285.X |
0.31 |
|
| 2004 |
Beutler E, Beutler L, West C. Mutations in the gene encoding cytosolic beta-glucosidase in Gaucher disease. The Journal of Laboratory and Clinical Medicine. 144: 65-8. PMID 15322500 DOI: 10.1016/J.Lab.2004.03.013 |
0.315 |
|
| 2004 |
Beutler L, Beutler E. Hematologically important mutations: iron storage diseases. Blood Cells, Molecules & Diseases. 33: 40-4. PMID 15223009 DOI: 10.1016/J.Bcmd.2004.03.002 |
0.321 |
|
| 2004 |
Waalen J, Beutler E. No age-related decrease in frequency of heterozygotes for the HFE C282Y haemochromatosis mutation. Journal of Hepatology. 40: 1044; author reply 1. PMID 15158353 DOI: 10.1016/J.Jhep.2004.02.001 |
0.33 |
|
| 2004 |
Hoyer JD, Allen SL, Beutler E, Kubik K, West C, Fairbanks VF. Erythrocytosis Due to Bisphosphoglycerate Mutase Deficiency with Concurrent Glucose-6-Phosphate Dehydrogenase (G-6-PD) Deficiency American Journal of Hematology. 75: 205-208. PMID 15054810 DOI: 10.1002/Ajh.20014 |
0.315 |
|
| 2004 |
Beutler E, West C. The Role of α-Thalassemia and Iron Deficiency in the Difference between Hemoglobin Levels of African-Americans (AA) and Whites. Blood. 104: 3706-3706. DOI: 10.1182/Blood.V104.11.3706.3706 |
0.305 |
|
| 2004 |
Lee PL, Barton JC, Brandhagen DJ, Niyongere S, Bohannon S, Rivers CA, Acton RA, Beutler E. Hemojuvelin Mutations in Whites, Blacks and Asians with Primary Iron Overload and in Control Subjects. Blood. 104: 3198-3198. DOI: 10.1182/Blood.V104.11.3198.3198 |
0.329 |
|
| 2003 |
Barton JC, Acton RT, Rivers CA, Bertoli LF, Gelbart T, West C, Beutler E. Genotypic and phenotypic heterogeneity of African Americans with primary iron overload Blood Cells, Molecules, and Diseases. 31: 310-319. PMID 14636644 DOI: 10.1016/S1079-9796(03)00166-9 |
0.319 |
|
| 2003 |
Beutler E, Barton JC, Felitti VJ, Gelbart T, West C, Lee PL, Waalen J, Vulpe C. Ferroportin 1 (SCL40A1) variant associated with iron overload in African-Americans. Blood Cells, Molecules & Diseases. 31: 305-9. PMID 14636643 DOI: 10.1016/S1079-9796(03)00165-7 |
0.311 |
|
| 2003 |
Beutler E, Hoffbrand AV, Cook JD. Iron deficiency and overload Hematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program. 40-61. PMID 14633776 DOI: 10.1182/Asheducation-2003.1.40 |
0.334 |
|
| 2003 |
McLaren CE, Li KT, Garner CP, Beutler E, Gordeuk VR. Mixture distribution analysis of phenotypic markers reflecting HFE gene mutations. Blood. 102: 4563-6. PMID 12907432 DOI: 10.1182/Blood-2003-04-1278 |
0.306 |
|
| 2003 |
Corrons JL, Garcia E, Tusell JJ, Varughese KI, West C, Beutler E. Red cell adenylate kinase deficiency: molecular study of 3 new mutations (118G>A, 190G>A, and GAC deletion) associated with hereditary nonspherocytic hemolytic anemia. Blood. 102: 353-6. PMID 12649162 DOI: 10.1182/Blood-2002-07-2288 |
0.34 |
|
| 2003 |
Beutler E, Felitti V, Gelbart T, Waalen J. Haematological effects of the C282Y HFE mutation in homozygous and heterozygous states among subjects of northern and southern European ancestry. British Journal of Haematology. 120: 887-93. PMID 12614226 DOI: 10.1046/J.1365-2141.2003.04215.X |
0.341 |
|
| 2003 |
van Wijk R, van Solinge WW, Nerlov C, Beutler E, Gelbart T, Rijksen G, Nielsen FC. Disruption of a novel regulatory element in the erythroid-specific promoter of the human PKLR gene causes severe pyruvate kinase deficiency. Blood. 101: 1596-602. PMID 12393511 DOI: 10.1182/Blood-2002-07-2321 |
0.31 |
|
| 2003 |
Beutler E. Unlocking the mysteries of iron homeostasis and of the anemia of chronic disease: is hepcidin the key? Blood. 102: 775-775. DOI: 10.1182/Blood-2003-05-1594 |
0.314 |
|
| 2002 |
Waalen J, Felitti V, Gelbart T, Ho NJ, Beutler E. Penetrance of hemochromatosis. Blood Cells, Molecules & Diseases. 29: 418-32. PMID 12678056 DOI: 10.1006/Bcmd.2002.0596 |
0.307 |
|
| 2002 |
Lee P, Gelbart T, West C, Halloran C, Beutler E. Seeking candidate mutations that affect iron homeostasis. Blood Cells, Molecules & Diseases. 29: 471-87. PMID 12547238 DOI: 10.1006/Bcmd.2002.0586 |
0.346 |
|
| 2002 |
Barton JC, Rao SV, Pereira NM, Gelbart T, Beutler E, Rivers CA, Acton RT. Juvenile hemochromatosis in the southeastern United States: a report of seven cases in two kinships Blood Cells, Molecules &Amp; Diseases. 29: 104-115. PMID 12482411 DOI: 10.1006/Bcmd.2002.0545 |
0.304 |
|
| 2002 |
Beutler B, Beutler E. Toll-like receptor 4 polymorphisms and atherogenesis. The New England Journal of Medicine. 347: 1978-80; author repl. PMID 12479194 |
0.348 |
|
| 2002 |
Sipe JC, Lee P, Beutler E. Brain iron metabolism and neurodegenerative disorders. Developmental Neuroscience. 24: 188-96. PMID 12401958 DOI: 10.1159/000065701 |
0.303 |
|
| 2002 |
Beutler E, West C. Polymorphisms in the 5' flanking region of the HFE gene: linkage disequilibrium and relationship to iron homeostasis. Blood Cells Molecules and Diseases. 28: 191-195. PMID 12064915 DOI: 10.1006/Bcmd.2002.0509 |
0.313 |
|
| 2002 |
Beutler E, Gelbart T, Miller W. Severe jaundice in a patient with a previously undescribed glucose-6-phosphate dehydrogenase (G6PD) mutation and Gilbert syndrome. Blood Cells Molecules and Diseases. 28: 104-107. PMID 12064902 DOI: 10.1006/Bcmd.2002.0491 |
0.333 |
|
| 2002 |
Beutler E, Griffin M, Gelbart T, West C. A previously undescribed nonsense mutation of the HFE gene. Clinical Genetics. 61: 40-42. PMID 11903354 DOI: 10.1034/J.1399-0004.2002.610108.X |
0.316 |
|
| 2002 |
Beutler E, Felitti V, Koziol JA, Gelbart T. Clinical haemochromatosis in HFE mutation carriers The Lancet. 360: 413-414. DOI: 10.1016/S0140-6736(02)09584-3 |
0.302 |
|
| 2001 |
Herschel M, Beutler E. Low glucose-6-phosphate dehydrogenase enzyme activity level at the time of hemolysis in a male neonate with the African type of deficiency. Blood Cells Molecules and Diseases. 27: 918-923. PMID 11783956 DOI: 10.1006/Bcmd.2001.0467 |
0.343 |
|
| 2001 |
Peters LL, Lane PW, Andersen SG, Gwynn B, Barker JE, Beutler E. Downeast anemia (dea), a new mouse model of severe nonspherocytic hemolytic anemia caused by hexokinase (HK(1)) deficiency. Blood Cells, Molecules & Diseases. 27: 850-60. PMID 11783948 DOI: 10.1006/Bcmd.2001.0454 |
0.335 |
|
| 2001 |
Lee PL, Gelbart T, West C, Halloran C, Felitti V, Beutler E. A study of genes that may modulate the expression of hereditary hemochromatosis: transferrin receptor-1, ferroportin, ceruloplasmin, ferritin light and heavy chains, iron regulatory proteins (IRP)-1 and -2, and hepcidin. Blood Cells Molecules and Diseases. 27: 783-802. PMID 11783942 DOI: 10.1006/Bcmd.2001.0445 |
0.312 |
|
| 2001 |
Lee PL, Halloran C, Trevino R, Felitti V, Beutler E. Human transferrin G277S mutation: a risk factor for iron deficiency anaemia. British Journal of Haematology. 115: 329-33. PMID 11703331 DOI: 10.1046/J.1365-2141.2001.03096.X |
0.3 |
|
| 2001 |
Beutler E. Discrepancies between genotype and phenotype in hematology: an important frontier. Blood. 98: 2597-2602. PMID 11675327 DOI: 10.1182/Blood.V98.9.2597 |
0.323 |
|
| 2001 |
Kaplan M, Hammerman C, Vreman HJ, Stevenson DK, Beutler E. Acute hemolysis and severe neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase–deficient heterozygotes The Journal of Pediatrics. 139: 137-140. PMID 11445808 DOI: 10.1067/Mpd.2001.115312 |
0.312 |
|
| 2001 |
Beutler E. DNA-based diagnosis of red cell enzymopathies: how we threw out the baby with the bathwater. Blood. 97: 3325-3325. PMID 11369618 DOI: 10.1182/Blood.V97.11.3325 |
0.308 |
|
| 2001 |
Beutler E, West C, Speir JA, Wilson IA, Worley M. The hHFE gene of browsing and grazing rhinoceroses: a possible site of adaptation to a low-iron diet. Blood Cells, Molecules & Diseases. 27: 342-50. PMID 11358396 DOI: 10.1006/Bcmd.2001.0386 |
0.312 |
|
| 2001 |
Lee PL, Halloran C, West C, Beutler E. Mutation analysis of the transferrin receptor-2 gene in patients with iron overload. Blood Cells Molecules and Diseases. 27: 285-289. PMID 11358389 DOI: 10.1006/Bcmd.2001.0381 |
0.332 |
|
| 2001 |
Corrons JV, Alvarez R, Pujades A, Zarza R, Oliva E, Lasheras G, Callis M, Ribes A, Gelbart T, Beutler E. Hereditary non-spherocytic haemolytic anaemia due to red blood cell glutathione synthetase deficiency in four unrelated patients from Spain: clinical and molecular studies. British Journal of Haematology. 112: 475-482. PMID 11167850 DOI: 10.1046/J.1365-2141.2001.02526.X |
0.351 |
|
| 2001 |
Koziol JA, Ho NJ, Felitti VJ, Beutler E. Reference Centiles for Serum Ferritin and Percentage of Transferrin Saturation, with Application to Mutations of the HFE Gene Clinical Chemistry. 47: 1804-1810. DOI: 10.1093/Clinchem/47.10.1804 |
0.308 |
|
| 2001 |
Iancovici-Kidon M, Sthoeger D, Abrahamov A, Volach B, Beutler E, Gelbart T, Barak Y. A New Exon 9 Glucose-6-phosphate Dehydrogenase Mutation (G6PD “Rehovot Blood Cells Molecules and Diseases. 27: 351. DOI: 10.1006/Bcmd.2001.0413 |
0.306 |
|
| 2000 |
Harder H, Eucker J, Zang C, Possinger K, Müller-Höcker J, Beutler E, Petrides PE. Coincidence of Gaucher's disease due to a 1226G/1448C mutation and of an immunoglobulin G lambda multiple myeloma with Bence-Jones proteinuria. Annals of Hematology. 79: 640-643. PMID 11131925 DOI: 10.1007/S002770000202 |
0.31 |
|
| 2000 |
Iancovici-Kidon M, Sthoeger D, Abrahamov A, Volach B, Beutler E, Gelbart T, Barak Y. A new exon 9 glucose-6-phosphate dehydrogenase mutation (G6PD "Rehovot") in a Jewish Ethiopian family with variable phenotypes. Blood Cells Molecules and Diseases. 26: 567-571. PMID 11112389 DOI: 10.1006/Bcmd.2000.0334 |
0.351 |
|
| 2000 |
Beutler E, Felitti V, Gelbart T, Ho N. The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic. Annals of Internal Medicine. 133: 329-37. PMID 10979877 DOI: 10.7326/0003-4819-133-5-200009050-00008 |
0.32 |
|
| 2000 |
Beutler E, Gelbart T. A common intron 3 mutation (IVS3 -48c-->g) leads to misdiagnosis of the c.845G-->A (C282Y) HFE gene mutation. Blood Cells Molecules and Diseases. 26: 229-233. PMID 10950943 DOI: 10.1006/Bcmd.2000.0300 |
0.307 |
|
| 2000 |
Lee PL, Halloran C, Cross AR, Beutler E. NADH-ferric reductase activity associated with dihydropteridine reductase. Biochemical and Biophysical Research Communications. 271: 788-795. PMID 10814540 DOI: 10.1006/Bbrc.2000.2708 |
0.324 |
|
| 2000 |
Efferth T, Osieka R, Beutler E. Molecular characterization of a German variant of glucose-6-phosphate dehydrogenase deficiency (G6PD Aachen). Blood Cells Molecules and Diseases. 26: 101-104. PMID 10772881 DOI: 10.1006/Bcmd.2000.0281 |
0.338 |
|
| 2000 |
Beutler E, Gelbart T, Lee P, Trevino R, Fernandez MA, Fairbanks VF. Molecular characterization of a case of atransferrinemia. Blood. 96: 4071-4074. DOI: 10.1182/Blood.V96.13.4071.H8004071_4071_4074 |
0.313 |
|
| 2000 |
Beutler E, Gelbart T. Estimating the prevalence of pyruvate kinase deficiency from the gene frequency in the general white population Blood. 95: 3585-3588. DOI: 10.1182/Blood.V95.11.3585.011K39_3585_3588 |
0.307 |
|
| 1999 |
Lee PL, Ho NJ, Olson R, Beutler E. The effect of transferrin polymorphisms on iron metabolism. Blood Cells, Molecules & Diseases. 25: 374-9. PMID 10660486 DOI: 10.1006/Bcmd.1999.0267 |
0.31 |
|
| 1999 |
Roos D, Zwieten Rv, Wijnen JT, Gómez-Gallego F, Boer Md, Stevens D, Pronk-Admiraal CJ, Rijk Td, Noorden CJFv, Weening RS, Vulliamy TJ, Ploem JE, Mason PJ, Bautista JM, Khan PM, ... Beutler E, et al. Molecular Basis and Enzymatic Properties of Glucose 6-Phosphate Dehydrogenase Volendam, Leading to Chronic Nonspherocytic Anemia, Granulocyte Dysfunction, and Increased Susceptibility to Infections Blood. 94: 2955-2962. DOI: 10.1182/Blood.V94.9.2955.421K22_2955_2962 |
0.356 |
|
| 1999 |
Beutler E, Gelbart T, Kondo T, Matsunaga AT. The Molecular Basis of a Case of γ-Glutamylcysteine Synthetase Deficiency Blood. 94: 2890-2894. DOI: 10.1182/Blood.V94.8.2890.420K16_2890_2894 |
0.328 |
|
| 1999 |
Felitti VJ, Beutler E. New Developments in Hereditary Hemochromatosis The American Journal of the Medical Sciences. 318: 257-268. DOI: 10.1016/S0002-9629(15)40629-9 |
0.323 |
|
| 1998 |
Petrides PE, leCoutre P, Müller-Höcker J, Magin E, Harzer K, Demina A, Beutler E. Coincidence of Gaucher's Disease Due to a Private Mutation and Ph* Positive Chronic Myeloid Leukemia American Journal of Hematology. 59: 87-90. PMID 9723584 DOI: 10.1002/(Sici)1096-8652(199809)59:1<87::Aid-Ajh17>3.0.Co;2-Z |
0.315 |
|
| 1998 |
Lee PL, Gelbart T, West C, Halloran C, Beutler E. The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms. Blood Cells Molecules and Diseases. 24: 199-215. PMID 9642100 DOI: 10.1006/Bcmd.1998.0186 |
0.314 |
|
| 1998 |
Vlachos A, Westwood B, Lipton JM, Beutler E. G6PD Mount Sinai: A new severe hemolytic variant characterized by dual mutations at nucleotides 376G and 1159T (N126D) Human Mutation. 11: S154-S155. PMID 9452072 DOI: 10.1002/Humu.1380110151 |
0.317 |
|
| 1998 |
Demina A, Varughese KI, Barbot J, Forman L, Beutler E. Six previously undescribed pyruvate kinase mutations causing enzyme deficiency. Blood. 92: 647-652. DOI: 10.1182/Blood.V92.2.647.414K13_647_652 |
0.307 |
|
| 1997 |
Beutler E, West C, Britton HA, Harris J, Forman L. Glucosephosphate Isomerase (GPI) Deficiency Mutations Associated with Hereditary Nonspherocytic Hemolytic Anemia (HNSHA) Blood Cells Molecules and Diseases. 23: 402-409. PMID 9446754 DOI: 10.1006/Bcmd.1997.0157 |
0.307 |
|
| 1997 |
Beutler E. Gaucher Disease Phenotypes Outflanked Genome Research. 7: 950-951. PMID 9331364 DOI: 10.1101/Gr.7.10.950 |
0.326 |
|
| 1997 |
Zimmerman SA, Ware RE, Forman L, Westwood B, Beutler E. Glucose-6-phosphate dehydrogenase Durham: A de novo mutation associated with chronic hemolytic anemia Journal of Pediatrics. 131: 284-287. PMID 9290617 DOI: 10.1016/S0022-3476(97)70167-7 |
0.342 |
|
| 1997 |
Coutre Pl, Demina A, Beutler E, Beck M, Petrides PE. Molecular analysis of Gaucher disease: distribution of eight mutations and the complete gene deletion in 27 patients from Germany. Human Genetics. 99: 816-821. PMID 9187679 DOI: 10.1007/S004390050454 |
0.31 |
|
| 1996 |
Beutler E. G6PD: Population genetics and clinical manifestations Blood Reviews. 10: 45-52. PMID 8861278 DOI: 10.1016/S0268-960X(96)90019-3 |
0.35 |
|
| 1996 |
Beutler E, Vulliamy T, Luzzatto L. Hematologically important mutations: glucose-6-phosphate dehydrogenase. Blood Cells Molecules and Diseases. 22: 302-313. PMID 8807085 DOI: 10.1006/Bcmd.1996.0008 |
0.308 |
|
| 1996 |
Beutler E, Baronciani L. Mutations in pyruvate kinase Human Mutation. 7: 1-6. PMID 8664896 DOI: 10.1002/(Sici)1098-1004(1996)7:1<1::Aid-Humu1>3.0.Co;2-H |
0.318 |
|
| 1995 |
Yoshida A, Twele TW, Davé V, Beutler E. Molecular abnormality of a phosphoglycerate kinase variant (PGK-Alabama). Blood Cells Molecules and Diseases. 21: 179-181. PMID 8673469 DOI: 10.1006/Bcmd.1995.0020 |
0.324 |
|
| 1995 |
Beutler E, Westwood B, Melemed A, Borgo PD, Margolis D. Three New Exon 10 Glucose-6-Phosphate Dehydrogenase Mutations Blood Cells Molecules and Diseases. 21: 64-72. PMID 7655862 DOI: 10.1006/Bcmd.1995.0010 |
0.334 |
|
| 1995 |
Xu W, Westwood B, Bartsocas CS, Malcorra-Azpiazu JJ, Indrak K, Beutler E. Glucose-6 phosphate dehydrogenase mutations and haplotypes in various ethnic groups. Blood. 85: 257-263. DOI: 10.1182/Blood.V85.1.257.Bloodjournal851257 |
0.322 |
|
| 1994 |
Beutler E, Gelbart T. Two new Gaucher disease mutations. Human Genetics. 93: 209-210. PMID 8112750 DOI: 10.1007/Bf00210614 |
0.305 |
|
| 1994 |
Beutler E, Demina A, Gelbart T. Glucocerebrosidase mutations in Gaucher disease. Molecular Medicine. 1: 82-92. DOI: 10.1007/Bf03403534 |
0.303 |
|
| 1993 |
Beutler E. Gaucher disease as a paradigm of current issues regarding single gene mutations of humans Proceedings of the National Academy of Sciences of the United States of America. 90: 5384-5390. PMID 8516282 DOI: 10.1073/Pnas.90.12.5384 |
0.322 |
|
| 1993 |
Baronciani L, Tricta F, Beutler E. G6PD "campinas: " A deficient enzyme with a mutation at the far 3′ end of the gene Human Mutation. 2: 77-78. PMID 8477268 DOI: 10.1002/Humu.1380020115 |
0.333 |
|
| 1993 |
Beutler E. Study of glucose‐6‐phosphate dehydrogenase: History and molecular biology American Journal of Hematology. 42: 53-58. PMID 8416297 DOI: 10.1002/Ajh.2830420111 |
0.342 |
|
| 1993 |
Ninfali P, Baronciani L, Ruzzo A, Fortini C, Amadori E, Dall'ara G, Magnani M, Beutler E. Molecular analysis of G6PD variants in northern Italy: a study on the population from the Ferrara district. Human Genetics. 92: 139-142. PMID 8370579 DOI: 10.1007/Bf00219681 |
0.326 |
|
| 1993 |
Vulliamy T, Beutler E, Luzzatto L. Variants of glucose-6-phosphate dehydrogenase are due to missense mutations spread throughout the coding region of the gene. Human Mutation. 2: 159-167. PMID 8364584 DOI: 10.1002/Humu.1380020302 |
0.325 |
|
| 1993 |
Hsia YE, Miyakawa F, Baltazar J, Ching NSP, Yuen J, Westwood B, Beutler E. Frequency of glucose-6-phosphate dehydrogenase (G6PD) mutations in Chinese, Filipinos, and Laotians from Hawaii. Human Genetics. 92: 470-476. PMID 8244337 DOI: 10.1007/Bf00216453 |
0.318 |
|
| 1993 |
Shalev O, Shalev RS, Forman L, Beutler E. GPI Mount Scopus--a variant of glucosephosphate isomerase deficiency. Annals of Hematology. 67: 197-200. PMID 8218542 DOI: 10.1007/Bf01695868 |
0.321 |
|
| 1992 |
Beutler E. Gaucher disease: new molecular approaches to diagnosis and treatment. Science. 256: 794-799. PMID 1589760 DOI: 10.1126/Science.1589760 |
0.324 |
|
| 1992 |
Beutler E. The molecular biology of G6PD variants and other red cell enzyme defects. Annual Review of Medicine. 43: 47-59. PMID 1580603 DOI: 10.1146/Annurev.Me.43.020192.000403 |
0.347 |
|
| 1992 |
Beutler E, West C, Gelbart T. Polymorphisms in the human glucocerebrosidase gene. Genomics. 12: 795-800. PMID 1572652 DOI: 10.1016/0888-7543(92)90311-F |
0.311 |
|
| 1992 |
Beutler E, Westwood B, Prchal J, Vaca G, Bartsocas C, Baronciani L. New glucose-6-phosphate dehydrogenase mutations from various ethnic groups Blood. 80: 255-256. DOI: 10.1182/Blood.V80.1.255.Bloodjournal801255 |
0.325 |
|
| 1992 |
Beutler E, Gelbart T, Kuhl W, Zimran A, West C. Mutations in Jewish patients with Gaucher disease Blood. 79: 1662-1666. DOI: 10.1182/Blood.V79.7.1662.Bloodjournal7971662 |
0.307 |
|
| 1992 |
Maeda M, Bawle E, Kulkarni R, Beutler E, Yoshida A. Molecular abnormalities of a phosphoglycerate kinase variant generated by spontaneous mutation Blood. 79: 2759-2762. DOI: 10.1182/Blood.V79.10.2759.2759 |
0.348 |
|
| 1991 |
Beutler E, Kuhl W, Ramirez E, Lisker R. Some Mexican glucose-6-phosphate dehydrogenase variants revisited. Human Genetics. 86: 371-374. PMID 1999339 DOI: 10.1007/Bf00201837 |
0.346 |
|
| 1991 |
Beutler E. Glucose-6-phosphate dehydrogenase deficiency. The New England Journal of Medicine. 324: 169-174. PMID 1984194 DOI: 10.1056/Nejm199101173240306 |
0.344 |
|
| 1991 |
Beutler E, Gelbart T, Kuhl W, Sorge J, West C. Identification of the second common Jewish Gaucher disease mutation makes possible population-based screening for the heterozygous state Proceedings of the National Academy of Sciences of the United States of America. 88: 10544-10547. PMID 1961718 DOI: 10.1073/Pnas.88.23.10544 |
0.313 |
|
| 1991 |
Beutler E, Kuhl W, Sáenz GFR, Rodríguez RW. Mutation analysis of glucose-6-phosphate dehydrogenase (G6PD) variants in Costa Rica Human Genetics. 87: 462-464. PMID 1879833 DOI: 10.1007/Bf00197169 |
0.323 |
|
| 1991 |
Beutler E, Westwood B, Kuhl W. Definition of the mutations of G6PD Wayne, G6PD Viangchan, G6PD Jammu, and G6PD 'LeJeune'. Acta Haematologica. 86: 179-182. PMID 1805484 DOI: 10.1159/000204830 |
0.319 |
|
| 1991 |
Glew RH, Gopalan V, Hubbell CA, Beutler E, Geil JD, Lee RE. A case of nonneurologic Gaucher's disease that biochemically resembles the neurologic types. Journal of Neuropathology and Experimental Neurology. 50: 108-17. PMID 1672707 DOI: 10.1097/00005072-199103000-00002 |
0.322 |
|
| 1991 |
Beutler E, Kay A, Saven A, Garver P, Thurston D, Dawson A, Rosenbloom B. Enzyme replacement therapy for Gaucher disease. Blood. 78: 1183-1189. DOI: 10.1182/Blood.V78.5.1183.Bloodjournal7851183 |
0.309 |
|
| 1990 |
Beutler E, Gelbart T, Kuhl W. Human red cell glucose-6-phosphate dehydrogenase: All active enzyme has sequence predicted by the X chromosome-encoded cDNA Cell. 62: 7-9. PMID 2364435 DOI: 10.1016/0092-8674(90)90231-3 |
0.3 |
|
| 1990 |
Zimran A, Kuhl WC, Beutler E. Detection of the 1226 (Jewish) mutation for Gaucher's disease by color PCR : a means for studying the gene frequency of the disorder American Journal of Clinical Pathology. 93: 788-791. PMID 2346136 DOI: 10.1093/Ajcp/93.6.788 |
0.308 |
|
| 1990 |
Zimran A, Forman L, Suzuki T, Dale GL, Beutler E. In vivo aging of red cell enzymes: Study of biotinylated red blood cells in rabbits American Journal of Hematology. 33: 249-254. PMID 2316508 DOI: 10.1002/Ajh.2830330407 |
0.323 |
|
| 1990 |
Beutler E, Gelbart T. Gaucher disease associated with a unique Kphl restriction site: identification of the amino‐acid substitution Annals of Human Genetics. 54: 149-153. PMID 1974409 DOI: 10.1111/J.1469-1809.1990.Tb00371.X |
0.318 |
|
| 1990 |
Beutler E, Moroose R, Kramer L, Gelbart T, Forman L. Gamma-glutamylcysteine synthetase deficiency and hemolytic anemia. Blood. 75: 271-273. DOI: 10.1182/Blood.V75.1.271.Bloodjournal751271 |
0.326 |
|
| 1989 |
Hirono A, Kuhl W, Gelbart T, Forman L, Fairbanks VF, Beutler E. Identification of the binding domain for NADP+ of human glucose-6-phosphate dehydrogenase by sequence analysis of mutants. Proceedings of the National Academy of Sciences of the United States of America. 86: 10015-10017. PMID 2602358 DOI: 10.1073/Pnas.86.24.10015 |
0.302 |
|
| 1989 |
Zimran A, Gross E, West C, Sorge J, Kubitz M, Beutler E. Prediction of severity of Gaucher's disease by identification of mutations at DNA level. The Lancet. 334: 349-352. PMID 2569551 DOI: 10.1016/S0140-6736(89)90536-9 |
0.303 |
|
| 1989 |
Miwa S, Luzzatto L, Rosa R, Paglia DE, Schröter W, Flora A, Fujii H, Board PG, Beutler E. Recommended methods for an additional red cell enzyme (pyrimidine 5′-nucleotidase) assay and the determination of red cell adenosine-5′-triphosphate, 2,3-diphosphoglycerate and reduced glutathione Clinical and Laboratory Haematology. 11: 131-138. PMID 2548802 DOI: 10.1111/J.1365-2257.1989.Tb00195.X |
0.314 |
|
| 1989 |
Beutler E, Gelbart T, Han J, Koziol JA, Beutler B. Evolution of the genome and the genetic code: Selection at the dinucleotide level by methylation and polyribonucleotide cleavage Proceedings of the National Academy of Sciences of the United States of America. 86: 192-196. PMID 2463621 DOI: 10.1073/Pnas.86.1.192 |
0.441 |
|
| 1989 |
Beutler E, Kuhl W, Vives-Corrons J, Prchal J. Molecular heterogeneity of glucose-6-phosphate dehydrogenase A-. Blood. 74: 2550-2555. DOI: 10.1182/Blood.V74.7.2550.Bloodjournal7472550 |
0.359 |
|
| 1988 |
Hirono A, Forman L, Beutler E. Enzymatic diagnosis in non-spherocytic hemolytic anemia. Medicine. 67: 110. PMID 3352512 DOI: 10.1097/00005792-198803000-00004 |
0.361 |
|
| 1988 |
Beutler E, Yoshida A. Genetic variation of glucose-6-phosphate dehydrogenase: a catalog and future prospects. Medicine. 67: 311-334. PMID 3045479 DOI: 10.1097/00005792-198809000-00003 |
0.327 |
|
| 1988 |
Zimran A, Torem S, Beutler E. The in vivo ageing of red cell enzymes: direct evidence of biphasic decay from polycythaemic rabbits with reticulocytosis British Journal of Haematology. 69: 67-70. PMID 2838067 DOI: 10.1111/J.1365-2141.1988.Tb07604.X |
0.318 |
|
| 1988 |
Beutler E, Forman L, West C, Gelbart T. Mechanism of improved maintenance of 2,3-diphosphoglycerate in stored blood by the xanthone compound 2-(2-hydroxyethoxy)-6-(1-H-tetrazole-5-yl)xanthen-9-one (BW A440C)☆☆☆ Biochemical Pharmacology. 37: 1057-1060. PMID 2833271 DOI: 10.1016/0006-2952(88)90510-2 |
0.3 |
|
| 1988 |
Beutler E, Dunning D, Dabe I, Forman L. Erythrocyte glutathione S-transferase deficiency and hemolytic anemia Blood. 72: 73-77. DOI: 10.1182/Blood.V72.1.73.Bloodjournal72173 |
0.35 |
|
| 1988 |
Beutler E. The Common Anemias Jama. 259: 2433-2437. DOI: 10.1001/Jama.1988.03720160053030 |
0.34 |
|
| 1987 |
Beutler E, Forman L, Rios-Larrain E. Elevated pyruvate kinase activity in patients with hemolytic anemia due to red cell pyruvate kinase "deficiency". The American Journal of Medicine. 83: 899-904. PMID 3674096 DOI: 10.1016/0002-9343(87)90648-6 |
0.316 |
|
| 1987 |
Ravindranath Y, Beutler E. Two new variants of glucose-6-phosphate dehydrogenase associated with hereditary non-spherocytic hemolytic anemia: G6PD Wayne and G6PD Huron. American Journal of Hematology. 24: 357-363. PMID 3565372 DOI: 10.1002/Ajh.2830240405 |
0.334 |
|
| 1987 |
Beutler E, Forman L, West C. Effect of oxalate and malonate on red cell metabolism Blood. 70: 1389-1393. DOI: 10.1182/Blood.V70.5.1389.1389 |
0.313 |
|
| 1986 |
Beutler E, Kuhl W, Gelbart T. Blood cell phosphogluconolactonase: assay and properties. British Journal of Haematology. 62: 577-586. PMID 3954969 DOI: 10.1111/J.1365-2141.1986.Tb02970.X |
0.33 |
|
| 1985 |
Lisker R, Pérez-Briceño R, Beutler E. A new glucose-6-phosphate dehydrogenase variant, Gd(-) Tepic, characterized by moderate enzyme deficiency and mild episodes of hemolytic anemia. Human Genetics. 69: 19-21. PMID 3967887 DOI: 10.1007/Bf00295523 |
0.331 |
|
| 1985 |
Beutler E, Kuhl W, Gelbart T. 6-Phosphogluconolactonase deficiency, a hereditary erythrocyte enzyme deficiency: possible interaction with glucose-6-phosphate dehydrogenase deficiency Proceedings of the National Academy of Sciences of the United States of America. 82: 3876-3878. PMID 3858849 DOI: 10.1073/Pnas.82.11.3876 |
0.345 |
|
| 1984 |
Weimer TA, Schüler L, Beutler E, Salzano FM. Gd (+) Laguna, a new rare glucose-6-phosphate dehydrogenase variant from Brazil. Human Genetics. 65: 402-404. PMID 6693129 DOI: 10.1007/Bf00291568 |
0.356 |
|
| 1983 |
Johnson CS, Tegos C, Beutler E. Thalassemia minor: Routine erythrocyte measurements and differentiation from iron deficiency American Journal of Clinical Pathology. 80: 31-36. PMID 6858962 DOI: 10.1093/Ajcp/80.1.31 |
0.31 |
|
| 1983 |
Beutler E. Selectivity of proteases as a basis for tissue distribution of enzymes in hereditary deficiencies. Proceedings of the National Academy of Sciences of the United States of America. 80: 3767-3768. PMID 6344088 DOI: 10.1073/Pnas.80.12.3767 |
0.317 |
|
| 1983 |
Beutler E, Carson D, Dannawi H, Forman L, Kuhl W, West C, Westwood B. Metabolic compensation for profound erythrocyte adenylate kinase deficiency. A hereditary enzyme defect without hemolytic anemia. Journal of Clinical Investigation. 72: 648-655. PMID 6308059 DOI: 10.1172/Jci111014 |
0.34 |
|
| 1981 |
Beutler E. Enzyme replacement therapy Trends in Biochemical Sciences. 6: 95-97. DOI: 10.1016/0968-0004(81)90035-9 |
0.306 |
|
| 1980 |
Beutler E. G-6-PD as a genetic marker. Hemoglobin. 4: 761-767. PMID 7440221 DOI: 10.3109/03630268008997744 |
0.314 |
|
| 1979 |
Dale GL, Kuhl W, Beutler E. Incorporation of glucocerebrosidase into Gaucher's disease monocytes in vitro Proceedings of the National Academy of Sciences of the United States of America. 76: 473-475. PMID 284362 DOI: 10.1073/Pnas.76.1.473 |
0.305 |
|
| 1979 |
Beutler E. Red Cell Enzyme Defects as Nondiseases and as Diseases Blood. 54: 1-7. DOI: 10.1182/Blood.V54.1.1.Bloodjournal5411 |
0.312 |
|
| 1977 |
Skala H, Dreyfus JC, Vives-Corrons JL, Matsumoto F, Beutler E. Triose phosphate isomerase deficiency. Biochemical Medicine. 18: 226-234. PMID 907660 DOI: 10.1016/0006-2944(77)90094-1 |
0.34 |
|
| 1977 |
Beutler E, Dale GL, Guinto E, Kuhl W. Enzyme replacement therapy in Gaucher's disease: Preliminary clinical trial of a new enzyme preparation Proceedings of the National Academy of Sciences of the United States of America. 74: 4620-4623. PMID 200923 DOI: 10.1073/Pnas.74.10.4620 |
0.32 |
|
| 1976 |
Lieberman J, Beutler E. Elevation of serum angiotensin-converting enzyme in Gaucher's disease. The New England Journal of Medicine. 294: 1442-1444. PMID 179000 DOI: 10.1056/Nejm197606242942609 |
0.307 |
|
| 1976 |
Beutler E. Glutathione Deficiency, Pyroglutamic Acidemia and Amino Acid Transport The New England Journal of Medicine. 295: 441-443. PMID 6911 DOI: 10.1056/Nejm197608192950809 |
0.35 |
|
| 1976 |
Srivastava S, Awasthi Y, Miller S, Yoshida A, Beutler E. Studies on gamma-glutamyl transpeptidase in human and rabbit erythrocytes Blood. 47: 645-650. DOI: 10.1182/Blood.V47.4.645.Bloodjournal474645 |
0.619 |
|
| 1976 |
Srivastava S, Awasthi Y, Miller S, Yoshida A, Beutler E. Studies on gamma-glutamyl transpeptidase in human and rabbit erythrocytes Blood. 47: 645-650. DOI: 10.1182/blood.V47.4.645.bloodjournal474645 |
0.584 |
|
| 1975 |
Beutler E, Beutler B, Matsumoto F. Glutathione peroxidase activity of inorganic selenium and seleno-DL-cysteine. Cellular and Molecular Life Sciences. 31: 769-770. PMID 1140308 DOI: 10.1007/Bf01938453 |
0.486 |
|
| 1975 |
Prchal J, Srivastava S, Beutler E. Active transport of GSSG from reconstituted erythrocyte ghosts Blood. 46: 111-117. DOI: 10.1182/Blood.V46.1.111.111 |
0.467 |
|
| 1975 |
Beutler E. Genetic disorders of human red blood cells. Jama. 233: 1184-1188. DOI: 10.1001/Jama.1975.03260110042019 |
0.354 |
|
| 1974 |
Beutler E, Sigalove WH, Muir WA, Matsumoto F, West C. Glucosephosphate-isomerase (GPI) deficiency: GPI elyria. Annals of Internal Medicine. 80: 730-732. PMID 4832160 DOI: 10.7326/0003-4819-80-6-730 |
0.302 |
|
| 1974 |
Beutler E, Johnson C, Powars D, West C. Prevalence of Glucose-6-Phosphate Dehydrogenase Deficiency in Sickle-Cell Disease The New England Journal of Medicine. 290: 826-828. PMID 4817837 DOI: 10.1056/Nejm197404112901504 |
0.336 |
|
| 1974 |
Beutler E, West C, Beutler B. Electrophoretic polymorphism of glutathione peroxidase Annals of Human Genetics. 38: 163-169. PMID 4467780 DOI: 10.1111/J.1469-1809.1974.Tb01947.X |
0.516 |
|
| 1974 |
Srivastava SK, Awasthi YC, Beutler E. Useful agents for the study of glutathione metabolism in erythrocytes: organic hydroperoxides Biochemical Journal. 139: 289-295. PMID 4447610 DOI: 10.1042/Bj1390289 |
0.634 |
|
| 1974 |
Beutler E, Matsumoto F, Guinto E. The effect of 2,3-DPG on red cell enzymes Cellular and Molecular Life Sciences. 30: 190-192. PMID 4273561 DOI: 10.1007/Bf01927728 |
0.3 |
|
| 1973 |
Wood LA, Beutler E. The effect of ascorbate on the maintenance of 2,3-diphosphoglycerate (2,3-DPG) in stored red cells. British Journal of Haematology. 25: 611-18. PMID 4753226 DOI: 10.1111/J.1365-2141.1973.Tb01774.X |
0.305 |
|
| 1973 |
Srivastava SK, Beutler E. A new fluorometric method for the determination of pyridoxal 5'-phosphate. Biochimica Et Biophysica Acta. 304: 765-773. PMID 4726857 DOI: 10.1016/0304-4165(73)90223-7 |
0.486 |
|
| 1973 |
Ben-Bassat I, Beutler E. Inhibition by ATP of Erythrocyte Glucose-6-Phosphate Dehydrogenase Variants Experimental Biology and Medicine. 142: 410-411. PMID 4689372 DOI: 10.3181/00379727-142-37034 |
0.308 |
|
| 1973 |
Blume K, Paniker NV, Beutler E. Enzymes of glutathione synthesis in patients with myeloproliferative disorders Clinica Chimica Acta. 45: 281-285. PMID 4513517 DOI: 10.1016/0009-8981(73)90439-7 |
0.323 |
|
| 1973 |
Srivastava SK, Beutler E. Cleavage of lens protein-GSH mixed disulfide by glutathione reductase Experimental Eye Research. 17: 33-42. PMID 4148072 DOI: 10.1016/0014-4835(73)90165-6 |
0.481 |
|
| 1973 |
Srivastava S, Beutler E. Hexosaminidase-A and Hexosamini-dase-B: Studies in Tay-Sachs' and Sandhoff's Disease Nature. 241: 463-463. PMID 4122341 DOI: 10.1038/241463A0 |
0.491 |
|
| 1973 |
Beutler E, Guinto E. Dihydroxyacetone Metabolism by Human Erythrocytes: Demonstration of Triokinase Activity and Its Characterization Blood. 41: 559-568. DOI: 10.1182/Blood.V41.4.559.559 |
0.309 |
|
| 1972 |
Srivastava SK, Loon CV, Beutler E. Characterization of a previously unidentified hemoglobin fraction. Biochimica Et Biophysica Acta. 278: 617-621. PMID 5085674 DOI: 10.1016/0005-2795(72)90026-8 |
0.507 |
|
| 1972 |
Srivastava SK, Beutler E. Galactose cataract in riboflavin deficient rats Biochemical Medicine. 6: 372-379. PMID 5048996 DOI: 10.1016/0006-2944(72)90023-3 |
0.49 |
|
| 1972 |
Srivastava SK, Blume KG, Loon CV, Beutler E. Purification and kinetic properties of galactokinase from human placenta Archives of Biochemistry and Biophysics. 150: 191-198. PMID 5028074 DOI: 10.1016/0003-9861(72)90026-4 |
0.514 |
|
| 1972 |
Beutler E, Paniker NV, West CJ. Pyridoxine administration in sickle cell disease: An unsuccessful attempt to influence the properties of sickle hemoglobin Biochemical Medicine. 6: 139-143. PMID 5027148 DOI: 10.1016/0006-2944(72)90031-2 |
0.312 |
|
| 1972 |
Srivastava SK, Villacorte D, Beutler E. Correlation between adenylate metabolizing enzymes and adenine nucleotide levels of erythrocytes during blood storage in various media. Transfusion. 12: 190-7. PMID 5026172 DOI: 10.1111/j.1537-2995.1972.tb00008.x |
0.457 |
|
| 1972 |
Srivastava SK, Beutler E. Antibody against purified human hexosaminidase B cross-reacting with human hexosaminidase A Biochemical and Biophysical Research Communications. 47: 753-759. PMID 4623705 DOI: 10.1016/0006-291X(72)90556-6 |
0.479 |
|
| 1972 |
Beutler E. Disorders due to enzyme defects in the red blood cell. Advances in Metabolic Disorders. 60: 131-160. PMID 4354659 DOI: 10.1016/B978-0-12-027306-5.50010-3 |
0.301 |
|
| 1972 |
Srivastava SK, Beutler E. The effect of normal red cell constituents on the activities of red cell enzymes. Archives of Biochemistry and Biophysics. 148: 249-255. PMID 4258115 DOI: 10.1016/0003-9861(72)90138-5 |
0.535 |
|
| 1972 |
Srivastava S, Blume KG, Beutler E, Yoshida A. Immunological difference between glucose-6-P dehydrogenase and hexose-6-P dehydrogenase from human liver. Nature. 238: 240-241. PMID 4116676 DOI: 10.1038/Newbio238240A0 |
0.524 |
|
| 1972 |
Blume KG, Hryniuk W, Powars D, Trinidad F, West C, Beutler E. Characterization of two new variants of glucose-phosphate-isomerase deficiency with hereditary nonspherocytic hemolytic anemia. Journal of Laboratory and Clinical Medicine. 79: 942-949. DOI: 10.5555/Uri:Pii:0022214372900650 |
0.316 |
|
| 1971 |
Siegel NH, Beutler E. Hemolytic anemia caused by G-6-PD Carswell, a new variant. Annals of Internal Medicine. 75: 437-439. PMID 5568155 DOI: 10.7326/0003-4819-75-3-437 |
0.318 |
|
| 1971 |
Srivastava SK, Beutler E. Purification and kinetic studies of adenine phosphoribosyltransferase from human erythrocytes. Archives of Biochemistry and Biophysics. 142: 426-434. PMID 4323725 DOI: 10.1016/0003-9861(71)90506-6 |
0.51 |
|
| 1971 |
Beutler E, Paniker NV, Trinidad F. The assay of red cell galactokinase Biochemical Medicine. 5: 325-332. DOI: 10.1016/0006-2944(71)90036-6 |
0.346 |
|
| 1971 |
Srivastava SK, Beutler E. Effect of l-dopa administration on rabbit lens and erythrocytes Biochemical Medicine. 5: 317-324. DOI: 10.1016/0006-2944(71)90035-4 |
0.461 |
|
| 1970 |
Paniker NV, Srivastava S, Beutler E. Glutathione metabolism of the red cells. Effect of glutathione reductase deficiency on the stimulation of hexose monophosphate shunt under oxidative stress. Biochimica Et Biophysica Acta. 215: 456-460. PMID 5507367 DOI: 10.1016/0304-4165(70)90096-6 |
0.529 |
|
| 1970 |
Srivastava SK, Beutler E. Glutathione metabolism of the erythrocyte. The enzymic cleavage of glutathione-haemoglobin preparations by glutathione reductase. Biochemical Journal. 119: 353-357. PMID 5500299 DOI: 10.1042/Bj1190353 |
0.488 |
|
| 1970 |
Beutler E, Srivastava SK. Relationship between glutathione reductase activity and drug-induced haemolytic anaemia. Nature. 226: 759-760. PMID 5443254 DOI: 10.1038/226759A0 |
0.493 |
|
| 1970 |
Beutler E, Srivastava SK, West C. The reversibility of N-ethylmaleimide (NEM) alkylation of red cell glutathione. Biochemical and Biophysical Research Communications. 38: 341-347. PMID 5418706 DOI: 10.1016/0006-291X(70)90718-7 |
0.473 |
|
| 1970 |
Srivastava S, Beutler E. Increased susceptibility of riboflavin deficient rats to galactose cataract. Cellular and Molecular Life Sciences. 26: 250-250. PMID 5417478 DOI: 10.1007/Bf01900074 |
0.483 |
|
| 1970 |
Mandula B, Srivastava SK, Beutler E. Hexose-6-phosphate dehydrogenase: Distribution in rat tissues and effect of diet, age and steroids Archives of Biochemistry and Biophysics. 141: 155-161. PMID 4394694 DOI: 10.1016/0003-9861(70)90118-9 |
0.509 |
|
| 1970 |
Mandula B, Beutler E. Synthesis of riboflavin nucleotides by mature human erythrocytes. Blood. 36: 491-499. DOI: 10.1182/Blood.V36.4.491.491 |
0.322 |
|
| 1969 |
Beutler E, Teeple L. Mannose metabolism in the human erythrocyte. The Journal of Clinical Investigation. 48: 461-6. PMID 5773084 DOI: 10.1172/Jci106003 |
0.343 |
|
| 1969 |
Srivastava SK, Beutler E. The transport of oxidized glutathione from the erythrocytes of various species in the prescence of chromate Biochemical Journal. 114: 833-837. PMID 5387975 DOI: 10.1042/Bj1140833 |
0.513 |
|
| 1969 |
Srivastava SK, Beutler E. Cataract produced by tyrosinase and tyrosine systems in rabbitens in vitro. Biochemical Journal. 112: 421-425. PMID 4979383 DOI: 10.1042/Bj1120421 |
0.49 |
|
| 1968 |
Srivastava SK, Beutler E. Accurate measurement of oxidized glutathione content of human, rabbit, and rat red blood cells and tissues. Analytical Biochemistry. 25: 70-76. PMID 5750729 DOI: 10.1016/0003-2697(68)90082-1 |
0.485 |
|
| 1968 |
Srivastava SK, Beutler E. Permeability of Normal and Cataractous Rabbit Lenses to Glutathione Experimental Biology and Medicine. 127: 512-514. PMID 5645039 DOI: 10.3181/00379727-127-32727 |
0.477 |
|
| 1968 |
Beutler E, Mathai CK, Smith JE. Biochemical variants of glucose-6-phosphate dehydrogenase giving rise to congenital nonspherocytic hemolytic disease. Blood. 31: 131-150. DOI: 10.1182/Blood.V31.2.131.131 |
0.337 |
|
| 1967 |
Kaplan J, Beutler E. Electrophoresis of red cell NADH- and NADPH-diaphorases in normal subjects and patients with congenital methemoglobinemia☆ Biochemical and Biophysical Research Communications. 29: 605-610. PMID 16496543 DOI: 10.1016/0006-291X(67)90529-3 |
0.344 |
|
| 1967 |
Srivastava SK, Beutler E. Permeability of normal and glucose-6-phosphate dehydrogenase deficient erythrocytes to glutathione Biochemical and Biophysical Research Communications. 28: 659-664. PMID 6053190 DOI: 10.1016/0006-291X(67)90365-8 |
0.527 |
|
| 1966 |
Beutler E, Baluda MC. Improved method for measuring galactose-1-phosphate uridyl transferase activity of erythrocytes☆ Clinica Chimica Acta. 13: 369-379. PMID 5943827 DOI: 10.1016/0009-8981(66)90217-8 |
0.313 |
|
| 1966 |
Mathai CK, Beutler E. Electrophoretic Variation of Galactose-1-Phosphate Uridyltransferase Science. 154: 1179-1180. PMID 5921375 DOI: 10.1126/Science.154.3753.1179 |
0.305 |
|
| 1966 |
Ohno S, Payne HW, Morrison M, Beutler E. Hexose-6-phosphate dehydrogenase found in human liver. Science. 153: 1015-1016. PMID 5917551 DOI: 10.1126/Science.153.3739.1015 |
0.311 |
|
| 1965 |
Beutler E, Collins Z. Hybridization of Glucose-6-Phosphate Dehydrogenase from Rat and Human Erythrocytes. Science. 150: 1306-1307. PMID 17751855 DOI: 10.1126/Science.150.3701.1306 |
0.309 |
|
| 1964 |
Beutler E, Baluda M. The Separation Of Glucose-6-Phosphate-Dehydrogenase-Deficient Erythrocytes From The Blood Of Heterozygotes For Glucose-6-Phosphate-Dehydrogenase Deficiency. The Lancet. 283: 189-192. PMID 14074498 DOI: 10.1016/S0140-6736(64)92286-X |
0.311 |
|
| 1963 |
Beutler E, Yeh MKY. Erythrocyte glutathione reductase. Blood. 21: 573-585. DOI: 10.1182/Blood.V21.5.573.573 |
0.309 |
|
| 1962 |
Fairbanks VF, Beutler E. A Simple Method for Detection of Erythrocyte Glucose-6-Phosphate Dehydrogenase Deficiency (G-6-PD Spot Test) Blood. 20: 591-601. DOI: 10.1182/Blood.V20.5.591.591 |
0.304 |
|
| 1960 |
Beutler E, Blaisdell RK. Iron Enzymes in Iron Deficiency. V. Succinic Dehydrogenase in Rat Liver, Kidney and Heart Blood. 15: 30-35. DOI: 10.1182/Blood.V15.1.30.30 |
0.317 |
|
| 1960 |
Beutler E. Iron enzymes in iorn deficiency Annals of Hematology. 6: 130-133. DOI: 10.1007/Bf01630017 |
0.316 |
|
| 1959 |
Beutler E. Iron enzymes in iron deficiency. VI. Aconitase activity and citrate metabolism. Journal of Clinical Investigation. 38: 1605-1616. PMID 13800266 DOI: 10.1172/Jci103939 |
0.309 |
|
| 1959 |
Beutler E. Iron Enzymes in Iron Deficiency. IV. Cytochrome Oxidase in Rat Kidney and Heart Acta Haematologica. 21: 371-377. PMID 13800265 DOI: 10.1159/000205714 |
0.301 |
|
| 1959 |
Beutler E, Yeh MKY, Necheles T. Incidence of the erythrocytic defect associated with drug-sensitivity among oriental subjects. Nature. 183: 684-685. PMID 13632834 DOI: 10.1038/183684B0 |
0.314 |
|
| 1959 |
Beutler E. The red cell indices in the diagnosis of iron-deficiency anemia. Annals of Internal Medicine. 50: 313-322. PMID 13627703 DOI: 10.7326/0003-4819-50-2-313 |
0.301 |
|
| 1959 |
Beutler E. The Hemolytic Effect of Primaquine and Related Compounds: a Review Blood. 14: 103-139. DOI: 10.1182/Blood.V14.2.103.103 |
0.32 |
|
| 1958 |
Beutler E, Blaisdell RK. Iron enzymes in iron deficiency. II. Catalase in human erythrocytes. Journal of Clinical Investigation. 37: 833-835. PMID 13549596 DOI: 10.1172/Jci103672 |
0.306 |
|
| 1957 |
Beutler E. Iron enzymes in iron deficiency. I. Cytochrome c. The American Journal of the Medical Sciences. 234: 517-527. PMID 13487564 DOI: 10.1097/00000441-195711000-00003 |
0.302 |
|
| 1954 |
BEUTLER E, ROBSON MJ, JACOBSON LO. Prolongation of the lag phase of irradiated Escherichia coli. Proceedings of the Society For Experimental Biology and Medicine. Society For Experimental Biology and Medicine (New York, N.Y.). 85: 682-5. PMID 13167179 DOI: 10.3181/00379727-85-20992 |
0.557 |
|
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