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Results: 1-18 |
Results: 18

Authors: KHELEF N BUTON X BEATINI N WANG HX MEINER V CHANG TY FARESE RV MAXFIELD FR TABAS I
Citation: N. Khelef et al., IMMUNOLOCALIZATION OF ACYL-COENZYME A-CHOLESTEROL O-ACYLTRANSFERASE IN MACROPHAGES, The Journal of biological chemistry, 273(18), 1998, pp. 11218-11224

Authors: LOSSOS A MEINER Z BARASH V SOFFER D ABRAMSKY O ARGOV Z MEINER V
Citation: A. Lossos et al., ADULT POLYGLUCOSAN BODY DISEASE CAUSED BY THE TYR329SER MUTATION IN THE GLYCOGEN BRANCHING ENZYME GENE IN ASHKENAZI JEWS, Annals of neurology, 42(6), 1997, pp. 7-7

Authors: LOSSOS A COHEN O MEINER V BLUMENFELD A RECHES A
Citation: A. Lossos et al., INTRAFAMILIAL HETEROGENEITY OF MOVEMENT-DISORDERS - REPORT OF 3 CASESIN ONE FAMILY, Journal of neurology, 244(7), 1997, pp. 426-430

Authors: MEINER V TAM C GUNN MD DONG LM WEISGRABER KH NOVAK S MYERS HM ERICKSON SK FARESE RV
Citation: V. Meiner et al., TISSUE EXPRESSION STUDIES ON THE MOUSE ACYL-COA-CHOLESTEROL ACYLTRANSFERASE GENE (ACACT) - FINDINGS SUPPORTING THE EXISTENCE OF MULTIPLE CHOLESTEROL ESTERIFICATION ENZYMES IN MICE, Journal of lipid research, 38(9), 1997, pp. 1928-1933

Authors: CASES S ZHENG YW NOVAK S MEINER V MYERS H ERICKSON SK FARESE RV
Citation: S. Cases et al., IDENTIFICATION AND CLONING OF 2 NEW MAMMALIAN ACAT GENE FAMILY MEMBERS, Circulation, 96(8), 1997, pp. 1264-1264

Authors: BARDAVID S LERER I SARFATY CK KOHAN ZG MEINER V ZLOTOGORA J ABELIOVICH D
Citation: S. Bardavid et al., LOCALIZATION OF 2 X-LINKED MENTAL-RETARDATION (XLMR) GENES TO XP-MRX37 GENE AT XP22.31-P22.32 AND A PUTATIVE MRX GENE ON XP22.11-P22.2, American journal of medical genetics, 64(1), 1996, pp. 83-88

Authors: GROSS DJ AVISHAI N MEINER V FILON D ZBAR B ABELIOVICH D
Citation: Dj. Gross et al., FAMILIAL PHEOCHROMOCYTOMA ASSOCIATED WITH A NOVEL MUTATION IN THE VONHIPPEL-LINDAU GENE, The Journal of clinical endocrinology and metabolism, 81(1), 1996, pp. 147-149

Authors: MEINER V CASES S MYERS HM RULAND SL SANDE ER FARESE RV
Citation: V. Meiner et al., DISRUPTION OF THE ACAT GENE - EVIDENCE SUGGESTING ALTERNATIVE CHOLESTEROL ESTERIFICATION ENZYME, Circulation, 94(8), 1996, pp. 194-194

Authors: ABELIOVICH D DAGAN J WERNER M LERER I SHAPIRA Y MEINER V
Citation: D. Abeliovich et al., SIMULTANEOUS FORMATION OF INV DUP(15) AND DUP(15Q) IN A GIRL WITH DEVELOPMENTAL DELAY - ORIGIN OF THE ABNORMAL CHROMOSOMES, European journal of human genetics, 3(1), 1995, pp. 49-55

Authors: MEINER V MARAIS DA RESHEF A BJORKHEM I LEITERSDORF E
Citation: V. Meiner et al., PREMATURE TERMINATION CODON AT THE STEROL 27-HYDROXYLASE GENE CAUSES CEREBROTENDINOUS XANTHOMATOSIS IN AN AFRIKANER FAMILY, Human molecular genetics, 3(1), 1994, pp. 193-194

Authors: LERER I MEINER V PASHUTLAVON I ABELIOVICH D
Citation: I. Lerer et al., MOLECULAR DIAGNOSIS OF PRADER-WILLI-SYNDROME - PARENT-OF-ORIGIN DEPENDENT METHYLATION SITES AND NONISOTOPIC DETECTION OF (CA)(N) DINUCLEOTIDE REPEAT POLYMORPHISMS, American journal of medical genetics, 52(1), 1994, pp. 79-84

Authors: MEINER V MEINER Z RESHEF A BJORKHEM I LEITERSDORF E
Citation: V. Meiner et al., CEREBROTENDINOUS XANTHOMATOSIS - MOLECULAR DIAGNOSIS ENABLES PRESYMPTOMATIC DETECTION OF A TREATABLE DISEASE, Neurology, 44(2), 1994, pp. 288-290

Authors: ARBER N PRAS E COPPERMAN Y SCHAPIRO JM MEINER V LOSSOS IS MILITIANU A HASSIN D PRAS E SHAI A MOSHKOWITZ M SIDI Y
Citation: N. Arber et al., PACEMAKER ENDOCARDITIS - REPORT OF 44 CASES AND REVIEW OF THE LITERATURE, Medicine, 73(6), 1994, pp. 299-305

Authors: RESHEF A MEINER V BERGINER VM LEITERSDORF E
Citation: A. Reshef et al., MOLECULAR-GENETICS OF CEREBROTENDINOUS XANTHOMATOSIS IN JEWS OF NORTH-AFRICAN ORIGIN, Journal of lipid research, 35(3), 1994, pp. 478-483

Authors: LEITERSDORF E MURATTI EN ELIAV O MEINER V EISENBERG S DANN EJ SEHAYEK E PETERS TK STEIN Y
Citation: E. Leitersdorf et al., EFFICACY AND SAFETY OF A COMBINATION FLUVASTATIN-BEZAFIBRATE TREATMENT FOR FAMILIAL HYPERCHOLESTEROLEMIA - COMPARATIVE-ANALYSIS WITH A FLUVASTATIN-CHOLESTYRAMINE COMBINATION, The American journal of medicine, 96(5), 1994, pp. 401-407

Authors: LEITERSDORF E SAFADI R MEINER V RESHEF A BJORKHEM I FRIEDLANDER Y MORKOS S BERGINER VM
Citation: E. Leitersdorf et al., CEREBROTENDINOUS XANTHOMATOSIS IN THE ISRAELI DRUZE - MOLECULAR-GENETICS AND PHENOTYPIC CHARACTERISTICS, American journal of human genetics, 55(5), 1994, pp. 907-915

Authors: LEITERSDORF E EISENBERG S ELIAV O BERKMAN N DANN EJ LANDSBERGER D SEHAYEK E MEINER V PETERS TK MURATTI EN BARD JM FRUCHART JC STEIN Y
Citation: E. Leitersdorf et al., EFFICACY AND SAFETY OF HIGH-DOSE FLUVASTATIN IN PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA, European Journal of Clinical Pharmacology, 45(6), 1993, pp. 513-518

Authors: LEITERSDORF E RESHEF A MEINER V LEVITZKI R SCHWARTZ SP DANN EJ BERKMAN N CALI JJ KLAPHOLZ L BERGINER VM
Citation: E. Leitersdorf et al., FRAMESHIFT AND SPLICE-JUNCTION MUTATIONS IN THE STEROL 27-HYDROXYLASEGENE CAUSE CEREBROTENDINOUS XANTHOMATOSIS IN JEWS OF MOROCCAN ORIGIN, The Journal of clinical investigation, 91(6), 1993, pp. 2488-2496
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