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    1. Matern, D; Shehata, BM; Shekhawat, P; Strauss, AW; Bennett, MJ; Rinaldo, P
      Placental floor infarction complicating the pregnancy of a fetus with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency

      MOLECULAR GENETICS AND METABOLISM
    2. Yoon, HR; Strauss, AW; Yoo, HW
      Sudden death in a Korean infant with very long-chain acyl-CoA dehydrogenase deficiency

      JOURNAL OF INHERITED METABOLIC DISEASE
    3. Albers, S; Levy, HL; Irons, M; Strauss, AW; Marsden, D
      Compound heterozygosity in four asymptomatic siblings with medium-chain acyl-CoA dehydrogenase deficiency

      JOURNAL OF INHERITED METABOLIC DISEASE
    4. Wood, JC; Magera, MJ; Rinaldo, P; Seashore, MR; Strauss, AW; Friedman, A
      Diagnosis of very long chain acyl-dehydrogenase deficiency from an infant's newborn screening card

      PEDIATRICS
    5. Ibdah, JA; Zhao, YW; Viola, J; Gibson, B; Bennett, MJ; Strauss, AW
      Molecular prenatal diagnosis in families with fetal mitochondrial trifunctional protein mutations

      JOURNAL OF PEDIATRICS
    6. Ibdah, JA; Paul, H; Zhao, Y; Binford, S; Salleng, K; Cline, M; Matern, D; Bennett, MJ; Rinaldo, P; Strauss, AW
      Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death

      JOURNAL OF CLINICAL INVESTIGATION
    7. Barycki, JJ; O'Brien, LK; Strauss, AW; Banaszak, LJ
      Glutamate 170 of human L-3-hydroxyacyl-CoA dehydrogenase is required for proper orientation of the catalytic histidine and structural integrity of the enzyme

      JOURNAL OF BIOLOGICAL CHEMISTRY
    8. Jones, PM; Moffitt, M; Joseph, D; Harthcock, PA; Boriack, RL; Ibdah, JA; Strauss, AW; Bennett, MJ
      Accumulation of free 3-hydroxy fatty acids in the culture media of fibroblasts from patients deficient in long-chain L-3-hydroxyacyl-CoA dehydrogenase: A useful diagnostic aid

      CLINICAL CHEMISTRY
    9. Zytkovicz, TH; Fitzgerald, EF; Marsden, D; Larson, CA; Shih, VE; Johnson, DM; Strauss, AW; Comeau, AM; Eaton, RB; Grady, GF
      Tandem mass spectrometric analysis for amino, organic, and fatty acid disorders in newborn dried blood spots: A two-year summary from the New Englandnewborn screening program

      CLINICAL CHEMISTRY
    10. Schlattner, U; Eder, M; Dolder, M; Khuchua, ZA; Strauss, AW; Wallimann, T
      Divergent enzyme kinetics and structural properties of the two human mitochondrial creatine kinase isoenzymes

      BIOLOGICAL CHEMISTRY
    11. Bennett, MJ; Rinaldo, P; Strauss, AW
      Inborn errors of mitochondrial fatty acid oxidation

      CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES
    12. Barycki, JJ; O'Brien, LK; Strauss, AW; Banaszak, LJ
      Sequestration of the active site by interdomain shifting - Crystallographic and spectroscopic evidence for distinct conformations of L-3-hydroxyacyl-CoA dehydrogenase

      JOURNAL OF BIOLOGICAL CHEMISTRY
    13. Zhou, YQ; Kelly, DP; Strauss, AW; Sims, H; Zhang, ZF
      Characterization of the human very-long-chain acyl-CoA dehydrogenase gene promoter region: A role for activator protein 2

      MOLECULAR GENETICS AND METABOLISM
    14. Barycki, JJ; O'Brien, LK; Birktoft, JJ; Strauss, AW; Banaszak, LJ
      Pig heart short chain L-3-hydroxyacyl-CoA dehydrogenase revisited: Sequence analysis and crystal structure determination

      PROTEIN SCIENCE
    15. Strauss, AW; Bennett, MJ; Rinaldo, P; Sims, HF; O'Brien, LK; Zhao, YW; Gibson, B; Ibdah, J
      Inherited long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease and other pregnancy complications

      SEMINARS IN PERINATOLOGY
    16. Ibdah, JA; Dasouki, MJ; Strauss, AW
      Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Variable expressivity of maternal illness during pregnancy and unusual presentation with infantile cholestasis and hypocalcaemia

      JOURNAL OF INHERITED METABOLIC DISEASE
    17. Matern, D; Strauss, AW; Hillman, SL; Mayatepek, E; Millington, DS; Trefz, FK
      Diagnosis of mitochondrial trifunctional protein deficiency in a blood spot from the newborn screening card by tandem mass spectrometry and DNA analysis

      PEDIATRIC RESEARCH
    18. Ibdah, JA; Bennett, MJ; Rinaldo, P; Zhao, YW; Gibson, B; Sims, HF; Strauss, AW
      A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women

      NEW ENGLAND JOURNAL OF MEDICINE
    19. Hahn, SH; Lee, EH; Jung, JW; Hong, CH; Yoon, HR; Rinaldo, P; Sims, H; Gibson, B; Strauss, AW
      Very long chain acyl coenzyme A dehydrogenase deficiency in a 5-month-old Korean boy: Identification of a novel mutation

      JOURNAL OF PEDIATRICS
    20. Qin, WN; Khuchua, Z; Boero, J; Payne, RM; Strauss, AW
      Oxidative myocytes of heart and skeletal muscle express abundant sarcomeric mitochondrial creatine kinase

      HISTOCHEMICAL JOURNAL
    21. Mathur, A; Sims, HF; Gopalakrishnan, D; Gibson, B; Rinaldo, P; Vockley, J; Hug, G; Strauss, AW
      Molecular heterogeneity in very-long-chain acyl-CoA dehydrogenase deficiency causing pediatric cardiomyopathy and sudden death

      CIRCULATION
    22. Barycki, JJ; O'Brien, LK; Bratt, JM; Zhang, RG; Sanishvili, R; Strauss, AW; Banaszak, LJ
      Biochemical characterization and crystal structure determination of human heart short chain L-3-Hydroxyacyl-CoA dehydrogenase provide insights into catalytic mechanism

      BIOCHEMISTRY
    23. QIN WN; KHUCHUA Z; CHENG J; BOERO J; PAYNE RM; STRAUSS AW
      MOLECULAR CHARACTERIZATION OF THE CREATINE KINASES AND SOME HISTORICAL PERSPECTIVES

      Molecular and cellular biochemistry
    24. IBDAH JA; TEIN I; DIONISIVICI C; BENNETT MJ; IJLST L; GIBSON B; WANDERS RJA; STRAUSS AW
      MILD TRIFUNCTIONAL PROTEIN-DEFICIENCY IS ASSOCIATED WITH PROGRESSIVE NEUROPATHY AND MYOPATHY AND SUGGESTS A NOVEL GENOTYPE-PHENOTYPE CORRELATION

      The Journal of clinical investigation
    25. KHUCHUA ZA; QIN WN; BOERO J; CHENG J; PAYNE RM; SAKS VA; STRAUSS AW
      OCTAMER FORMATION AND COUPLING OF CARDIAC SARCOMERIC MITOCHONDRIAL CREATINE-KINASE ARE MEDIATED BY CHARGED N-TERMINAL RESIDUES

      The Journal of biological chemistry
    26. IBDAH JA; BENNETT MJ; RINALDO P; STRAUSS AW
      A NOVEL ASSOCIATION BETWEEN MICROVESICULAR STEATO-HEPATITIS AND A COMMON MUTATION IN THE BETA-OXIDATION CYCLE

      Gastroenterology
    27. EXIL VJ; SIMS H; KOVACS A; QIN WN; BOERO J; KHUCHUA Z; STRAUSS AW
      PHYSIOLOGICAL STRESSORS INDUCING SUDDEN-DEATH IN THE VERY-LONG-CHAIN ACYL-COA DEHYDROGENASE DEFICIENT MICE

      Circulation
    28. BENSON DW; SHARKEY A; FATKIN D; LANG P; BASSON CT; MCDONOUGH B; STRAUSS AW; SEIDMAN JG; SEIDMAN CE
      REDUCED PENETRANCE, VARIABLE EXPRESSIVITY, AND GENETIC-HETEROGENEITY OF FAMILIAL ATRIAL SEPTAL-DEFECTS

      Circulation
    29. ZHANG ZF; ZHOU YQ; MENDELSOHN NJ; BAUER GS; STRAUSS AW
      REGULATION OF THE HUMAN LONG-CHAIN ACYL-COA DEHYDROGENASE GENE BY NUCLEAR HORMONE-RECEPTOR TRANSCRIPTION FACTORS

      Biochimica et biophysica acta, N. Gene structure and expression
    30. JOHNSON MC; WATSON MS; DOWTON SB; STRAUSS AW
      SHPRINTZEN-GOLDBERG SYNDROME RESULTS FROM MUTATIONS IN FIBRILLIN-I, NOT MONOSOMY 22Q11 - REPLY

      The Journal of pediatrics
    31. QIN WN; KHUCHUA Z; KLEIN SC; STRAUSS AW
      ELEMENTS REGULATING CARDIOMYOCYTE EXPRESSION OF THE HUMAN SARCOMERIC MITOCHONDRIAL CREATINE-KINASE GENE IN TRANSGENIC MICE

      The Journal of biological chemistry
    32. EDER M; KRAUTLE F; DONG Y; VOCK P; KIEWEG V; KIM JJP; STRAUSS AW; GHISLA S
      CHARACTERIZATION OF HUMAN AND PIG-KIDNEY LONG-CHAIN-ACYL-COA DEHYDROGENASES AND THEIR ROLE IN BETA-OXIDATION

      European journal of biochemistry
    33. BENSON DW; STRAUSS AW; SHARKEY A; FATKIN D; SCHOTT JJ; SANGWATANAROJ S; PEASE WE; BASSON CT; SEIDMAN JG; SEIDMAN CE
      A FAMILIAL ATRIAL SEPTAL-DEFECT GENE MAPS TO CHROMOSOME 5P - EVIDENCEFOR REDUCED GENE PENETRANCE, VARIABLE EXPRESSIVITY AND GENETIC-HETEROGENEITY

      Circulation
    34. KHUCHUA ZA; QIN WN; BOERO JA; STRAUSS AW
      OCTAMER FORMATION OF CARDIAC SARCOMERIC MITOCHONDRIAL CREATINE-KINASEMEDIATED BY CHARGED N-TERMINAL RESIDUES

      Circulation
    35. QIN WN; KHUCHUA ZA; BOERO JA; CHUGH R; STRAUSS AW
      CIS-ACTING ELEMENTS REGULATING EXPRESSION OF THE HUMAN SARCOMERIC MITOCHONDRIAL CREATINE-KINASE GENE IN THE HEART

      Circulation
    36. QIN WN; KHUCHUA ZA; STRAUSS AW
      MYOCYTE-SPECIFIC EXPRESSION OF THE SARCOMERIC MITOCHONDRIAL CREATINE-KINASE GENE IN HEART AND SKELETAL-MUSCLE

      Circulation
    37. STRAUSS AW
      DEFECTS OF MITOCHONDRIAL PROTEINS AND PEDIATRIC HEART-DISEASE

      Progress in pediatric cardiology
    38. CROWLEY KS; STRAUSS AW
      IDENTIFICATION OF A POTENTIAL RIBOSOME-BINDING INTEGRAL MEMBRANE-PROTEIN IN YEAST

      The FASEB journal
    39. IBDAH JA; ISAACS J; TREEM W; BENNETT M; STRAUSS AW
      THE MOLECULAR-BASIS OF ACUTE FATTY LIVER OF PREGNANCY-ASSOCIATED WITHPEDIATRIC LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY

      Hepatology
    40. STRAUSS AW; JOHNSON MC
      THE GENETIC-BASIS OF PEDIATRIC CARDIOVASCULAR-DISEASE

      Seminars in perinatology
    41. ISAACS JD; SIMS HF; POWELL CK; BENNETT MJ; HALE DE; TREEM WR; STRAUSS AW
      MATERNAL ACUTE FATTY LIVER OF PREGNANCY-ASSOCIATED WITH FETAL TRIFUNCTIONAL PROTEIN-DEFICIENCY - MOLECULAR CHARACTERIZATION OF A NOVEL MATERNAL MUTANT ALLELE

      Pediatric research
    42. MATHUR A; POWELL CK; SIMS HF; ALLA VL; BENNETT M; STRAUSS AW
      MOLECULAR-BASIS OF VERY LONG-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY - SCREENING AND MUTATIONAL ANALYSIS OF 17 PATIENTS

      Pediatric research
    43. ZHANG ZF; ZHOU YQ; STRAUSS AW
      IN-VIVO AND IN-VITRO ANALYSIS OF THE HUMAN LONG-CHAIN ACYL COA DEHYDROGENASE (LCAD) GENE PROMOTER REGION

      Pediatric research
    44. JOHNSON MC; WATSON MS; STRAUSS AW
      CHROMOSOME 22Q11 MONOSOMY AND THE GENETIC-BASIS OF CONGENITAL HEART-DISEASE

      The Journal of pediatrics
    45. BROMBERG BI; MAZZIOTTI MV; CANTER CE; SPRAY TL; STRAUSS AW; FOGLIA RP
      RECOGNITION AND MANAGEMENT OF NONPENETRATING CARDIAC TRAUMA IN CHILDREN

      The Journal of pediatrics
    46. IBDAH JA; ISAACS J; TREEM W; STRAUSS AW
      ACUTE FATTY LIVER OF PREGNANCY AND MATERNAL LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE

      Gastroenterology
    47. MATHUR A; SIMS HF; POWELL CK; STRAUSS AW
      INFANTILE CARDIOMYOPATHY - A COMMON CLINICAL MANIFESTATION OF VERY LONG-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY

      Circulation
    48. KHUCHUA ZA; QIN WN; CHENG J; PAYNE M; STRAUSS AW
      SARCOMERIC MITOCHONDRIAL CREATINE-KINASE IS COUPLED TO CARDIAC OXIDATIVE-PHOSPHORYLATION THROUGH INNER MEMBRANE-BINDING MEDIATED BY POSITIVELY-CHARGED N-TERMINAL RESIDUES

      Circulation
    49. JOHNSON MC; PAYNE RM; GRANT JW; STRAUSS AW
      THE GENETIC-BASIS OF PEDIATRIC HEART-DISEASE

      Annals of medicine
    50. ZIADEH R; HOFFMAN EP; FINEGOLD DN; HOOP RC; BRACKETT JC; STRAUSS AW; NAYLOR EW
      MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY IN PENNSYLVANIA - NEONATAL SCREENING SHOWS HIGH-INCIDENCE AND UNEXPECTED MUTATION FREQUENCIES

      Pediatric research
    51. POWELL CK; SIMS HF; AHUJA A; STRAUSS AW
      THE MOLECULAR-BASIS OF VERY LONG-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY CAUSING INFANTILE CARDIOMYOPATHY

      Pediatric research
    52. POWELL CK; ISAACS JD; SIMS HF; STRAUSS AW
      MOLECULAR CHARACTERIZATION OF FETAL LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY ASSOCIATED WITH ACUTE FATTY LIVER OF PREGNANCY

      Pediatric research
    53. SIMS HF; BRACKETT JC; POWELL CK; TREEM WR; HALE DE; BENNETT MJ; GIBSON B; SHAPIRO S; STRAUSS AW
      THE MOLECULAR-BASIS OF PEDIATRIC LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY ASSOCIATED WITH MATERNAL ACUTE FATTY LIVER OF PREGNANCY

      Proceedings of the National Academy of Sciences of the United Statesof America
    54. STRAUSS AW; POWELL CK; HALE DE; ANDERSON MM; AHUJA A; BRACKETT JC; SIMS HF
      MOLECULAR-BASIS OF HUMAN MITOCHONDRIAL VERY-LONG-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY CAUSING CARDIOMYOPATHY AND SUDDEN-DEATH IN CHILDHOOD

      Proceedings of the National Academy of Sciences of the United Statesof America
    55. BRACKETT JC; SIMS HF; RINALDO P; SHAPIRO S; POWELL CK; BENNETT MJ; STRAUSS AW
      2 ALPHA-SUBUNIT DONOR SPLICE-SITE MUTATIONS CAUSE HUMAN TRIFUNCTIONALPROTEIN-DEFICIENCY

      The Journal of clinical investigation
    56. LEONE TC; CRESCI S; CARTER ME; ZHANG ZF; LALA DS; STRAUSS AW; KELLY DP
      THE HUMAN MEDIUM-CHAIN ACYL-COA DEHYDROGENASE GENE PROMOTER CONSISTS OF A COMPLEX ARRANGEMENT OF NUCLEAR RECEPTOR RESPONSE ELEMENTS AND SP1BINDING-SITES (VOL 270, PG 16308, 1995)

      The Journal of biological chemistry
    57. LEONE TC; CRESCI S; CARTER ME; ZHANG ZF; LALA DS; STRAUSS AW; KELLY DP
      THE HUMAN MEDIUM-CHAIN ACYL-COA DEHYDROGENASE GENE PROMOTER CONSISTS OF A COMPLEX ARRANGEMENT OF NUCLEAR RECEPTOR RESPONSE ELEMENTS AND SP1BINDING-SITES

      The Journal of biological chemistry
    58. BRACKETT JC; GOODFELLOW PJ; STRAUSS AW
      GENETIC DISTINCTION BETWEEN AUTOSOMAL-DOMINANT ATRIAL SEPTAL-DEFECTS AND THE HOLT-ORAM SYNDROME

      Circulation
    59. PAYNE RM; JOHNSON MC; GRANT JW; STRAUSS AW
      TOWARD A MOLECULAR UNDERSTANDING OF CONGENITAL HEART-DISEASE

      Circulation
    60. PETERSON KL; SERGIENKO EE; WU YH; KUMAR NR; STRAUSS AW; OLESON AE; MUHONEN WW; SHABB JB; SRIVASTAVA DK
      RECOMBINANT HUMAN LIVER MEDIUM-CHAIN ACYL-COA DEHYDROGENASE - PURIFICATION, CHARACTERIZATION, AND THE MECHANISM OF INTERACTIONS WITH FUNCTIONALLY DIVERSE C-8-COA MOLECULES

      Biochemistry
    61. WEINBERGER MJ; RINALDO P; STRAUSS AW; BENNETT MJ
      INTACT ALPHA-SUBUNIT IS REQUIRED FOR MEMBRANE-BINDING OF HUMAN MITOCHONDRIAL TRIFUNCTIONAL BETA-OXIDATION PROTEIN, BUT IS NOT NECESSARY FORCONFERRING 3-KETOACYL-COA THIOLASE ACTIVITY TO THE BETA-SUBUNIT

      Biochemical and biophysical research communications
    62. JOHNSON MC; WATSON MS; STRAUSS AW; SPRAY TL
      ANOMALOUS ORIGIN OF THE RIGHT PULMONARY-ARTERY FROM THE AORTA AND CATCH-22-SYNDROME

      The Annals of thoracic surgery
    63. JOHNSON MC; STRAUSS AW; DOWTON SB; SPRAY TL; HUDDLESTON CB; WOOD MK; SLAUGH RA; WATSON MS
      DELETION WITHIN CHROMOSOME-22 IS COMMON IN PATIENTS WITH ABSENT PULMONARY VALVE SYNDROME

      The American journal of cardiology
    64. OSHEA DL; GAST MJ; MURDOCK GL; PAYNE RM; STRAUSS AW
      EXPRESSION OF ENGINEERED HUMAN 17-BETA-ESTRADIOL DEHYDROGENASE IN A PROKARYOTIC SYSTEM

      Journal of the Society for Gynecologic Investigation
    65. JOHNSON MC; STRAUSS AW
      THE JURY IS STILL OUT REGARDING BALLOON THERAPY FOR NATIVE AORTIC COARCTATION

      Journal of the American College of Cardiology
    66. PAYNE RM; STRAUSS AW
      EXPRESSION OF THE MITOCHONDRIAL CREATINE-KINASE GENES

      Molecular and cellular biochemistry
    67. PAYNE RM; STRAUSS AW
      DEVELOPMENTAL EXPRESSION OF SARCOMERIC AND UBIQUITOUS MITOCHONDRIAL CREATINE-KINASE IS TISSUE-SPECIFIC

      Biochimica et biophysica acta, N. Gene structure and expression
    68. HALE DE; STRAUSS AW; CAIRA T; KELLY DP
      REGULATION OF FATTY-ACID OXIDATION ENZYME EXPRESSION BY ENERGY SUBSTRATE

      Pediatric research
    69. ZHANG ZF; ZHOU YQ; KELLY DP; STRAUSS AW
      STRUCTURAL ORGANIZATION AND REGULATORY ELEMENT ANALYSIS OF THE HUMAN LONG-CHAIN ACYL-COA DEHYDROGENASE GENE

      Pediatric research
    70. KELLY DP; STRAUSS AW
      MECHANISMS OF DISEASE - INHERITED CARDIOMYOPATHIES

      The New England journal of medicine
    71. BRACKETT JC; SIMS HF; STEINER RD; NUNGE M; ZIMMERMAN EM; DEMARTINVILLE B; RINALDO P; SLAUGH R; STRAUSS AW
      A NOVEL MUTATION IN MEDIUM-CHAIN ACYL-COA DEHYDROGENASE CAUSES SUDDENNEONATAL DEATH

      The Journal of clinical investigation
    72. BRACKETT JC; SIMS HF; STEINER R; RINALDO P; SLAUGH R; STRAUSS AW
      A RARE MUTATION IN THE MEDIUM-CHAIN ACYL-COENZYME-A DEHYDROGENASE CAUSES SUDDEN NEONATAL DEATH

      Clinical research
    73. BRACKETT JC; SIMS HF; POWELL CK; RINALDO P; STRAUSS AW
      MOLECULAR CHARACTERIZATION OF LONG-CHAIN 3-HYDROXYACYL-COENZYME-A DEHYDROGENASE-DEFICIENCY

      Circulation
    74. BRACKETT JC; SIMS HF; POWELL CK; RINALDO P; STRAUSS AW
      MOLECULAR CHARACTERIZATION OF LONG-CHAIN 3-HYDROXYACYL-COENZYME-A DEHYDROGENASE-DEFICIENCY

      Circulation
    75. QIN WN; KLEIN SC; STRAUSS AW
      ELEMENTS REGULATING CARDIAC-SPECIFIC EXPRESSION OF THE HUMAN SARCOMERIC MITOCHONDRIAL CREATINE-KINASE GENE IN TRANSGENIC MICE

      Circulation
    76. QIN WN; KLEIN SC; STRAUSS AW
      ELEMENTS REGULATING CARDIAC-SPECIFIC EXPRESSION OF THE HUMAN SARCOMERIC MITOCHONDRIAL CREATINE-KINASE GENE IN TRANSGENIC MICE

      Circulation
    77. POWELL CK; SIMS HF; BRACKETT JC; STRAUSS AW
      COMPLETE CHARACTERIZATION OF THE HUMAN CARDIAC LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE CDNA AND GENE

      Circulation
    78. POWELL CK; SIMS HF; BRACKETT JC; STRAUSS AW
      COMPLETE CHARACTERIZATION OF THE HUMAN CARDIAC LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE CDNA AND GENE

      Circulation
    79. CHENG JM; PAYNE RM; STRAUSS AW
      3'-UNTRANSLATED REGIONS OF B-CREATINE KINASE AND UBIQUITOUS MITOCHONDRIAL CREATINE-KINASE BIND PROTEINS IN A TISSUE-SPECIFIC MANNER

      Circulation
    80. CHENG JM; PAYNE RM; STRAUSS AW
      3'-UNTRANSLATED REGIONS OF B-CREATINE KINASE AND UBIQUITOUS MITOCHONDRIAL CREATINE-KINASE BIND PROTEINS IN A TISSUE-SPECIFIC MANNER

      Circulation
    81. DJORDJEVIC S; DONG Y; PASCHKE R; FRERMAN FE; STRAUSS AW; KIM JJP
      IDENTIFICATION OF THE CATALYTIC BASE IN LONG-CHAIN ACYL-COA DEHYDROGENASE

      Biochemistry
    82. WHELAN AJ; STRAUSS AW; HALE DE; MENDELSOHN NJ; KELLY DP
      EXPRESSION AND CHARACTERIZATION OF HUMAN MUTANT (GLUTAMIC ACID(304)) MEDIUM-CHAIN ACYL-COENZYME-A DEHYDROGENASE IN MAMMALIAN-CELLS

      Pediatric research
    83. MOLLER JH; ALLEN HD; CLARK EB; DAJANI AS; GOLDEN A; HAYMAN LL; LAUER RM; MARMER EL; MCANULTY JH; OPARIL S; STRAUSS AW; TAUBERT KA; WAGNER A
      REPORT OF THE TASK-FORCE-ON-CHILDREN-AND-YOUTH

      Circulation
    84. CARTER ME; CAIRA T; ZHANG Z; STRAUSS AW; KELLY DP
      THE MEDIUM-CHAIN ACYL-COA DEHYDROGENASE GENE PROMOTER HAS A MODULAR STRUCTURE AND INTERACTS WITH MULTIPLE TRANSCRIPTION FACTORS

      Circulation
    85. BRACKETT JC; SIMS HF; MANAHAN CL; DEMARTINVILLE B; STRAUSS AW
      A NOVEL MUTATION IN MEDIUM-CHAIN ACYL-COENZYME-A DEHYDROGENASE CAUSESSUDDEN NEONATAL DEATH

      Circulation
    86. HAINLINE BE; KAHLENBECK DJ; GRANT J; STRAUSS AW
      TISSUE-SPECIFIC AND DEVELOPMENTAL EXPRESSION OF RAT LONG-AND MEDIUM-CHAIN ACYL-COA DEHYDROGENASES

      Biochimica et biophysica acta
    87. PAYNE RM; FRIEDMAN DL; GRANT JW; PERRYMAN MB; STRAUSS AW
      CREATINE-KINASE ISOENZYMES ARE HIGHLY REGULATED DURING PREGNANCY IN RAT UTERUS AND PLACENTA

      The American journal of physiology
    88. ZHANG ZF; KOLVRAA S; ZHOU YQ; KELLY DP; GREGERSEN N; STRAUSS AW
      3 RFLPS DEFINING A HAPLOTYPE ASSOCIATED WITH THE COMMON MUTATION IN HUMAN MEDIUM-CHAIN ACYL-COA DEHYDROGENASE (MCAD) DEFICIENCY OCCUR IN ALU REPEATS

      American journal of human genetics
    89. JOHNSON MC; STRAUSS AW; CANTER CE; SPRAY TL
      BALLOON DILATION OF AORTIC COARCTATION - REPLY

      The American heart journal


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Documento generato il 10/08/20 alle ore 07:51:21