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Results: 1-25 | 26-50 | 51-67
Results: 26-50/67
SARCOMERIC MITOCHONDRIAL CREATINE-KINASE IS COUPLED TO CARDIAC OXIDATIVE-PHOSPHORYLATION THROUGH INNER MEMBRANE-BINDING MEDIATED BY POSITIVELY-CHARGED N-TERMINAL RESIDUES
Authors: KHUCHUA ZA QIN WN CHENG J PAYNE M STRAUSS AW
Citation: Za. Khuchua et al., SARCOMERIC MITOCHONDRIAL CREATINE-KINASE IS COUPLED TO CARDIAC OXIDATIVE-PHOSPHORYLATION THROUGH INNER MEMBRANE-BINDING MEDIATED BY POSITIVELY-CHARGED N-TERMINAL RESIDUES, Circulation, 94(8), 1996, pp. 724-724
THE GENETIC-BASIS OF PEDIATRIC HEART-DISEASE
Authors: JOHNSON MC PAYNE RM GRANT JW STRAUSS AW
Citation: Mc. Johnson et al., THE GENETIC-BASIS OF PEDIATRIC HEART-DISEASE, Annals of medicine, 27(3), 1995, pp. 289-300
MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY IN PENNSYLVANIA - NEONATAL SCREENING SHOWS HIGH-INCIDENCE AND UNEXPECTED MUTATION FREQUENCIES
Authors: ZIADEH R HOFFMAN EP FINEGOLD DN HOOP RC BRACKETT JC STRAUSS AW NAYLOR EW
Citation: R. Ziadeh et al., MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY IN PENNSYLVANIA - NEONATAL SCREENING SHOWS HIGH-INCIDENCE AND UNEXPECTED MUTATION FREQUENCIES, Pediatric research, 37(5), 1995, pp. 675-678
THE MOLECULAR-BASIS OF VERY LONG-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY CAUSING INFANTILE CARDIOMYOPATHY
Authors: POWELL CK SIMS HF AHUJA A STRAUSS AW
Citation: Ck. Powell et al., THE MOLECULAR-BASIS OF VERY LONG-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY CAUSING INFANTILE CARDIOMYOPATHY, Pediatric research, 37(4), 1995, pp. 32-32
MOLECULAR CHARACTERIZATION OF FETAL LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY ASSOCIATED WITH ACUTE FATTY LIVER OF PREGNANCY
Authors: POWELL CK ISAACS JD SIMS HF STRAUSS AW
Citation: Ck. Powell et al., MOLECULAR CHARACTERIZATION OF FETAL LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY ASSOCIATED WITH ACUTE FATTY LIVER OF PREGNANCY, Pediatric research, 37(4), 1995, pp. 151-151
THE MOLECULAR-BASIS OF PEDIATRIC LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY ASSOCIATED WITH MATERNAL ACUTE FATTY LIVER OF PREGNANCY
Authors: SIMS HF BRACKETT JC POWELL CK TREEM WR HALE DE BENNETT MJ GIBSON B SHAPIRO S STRAUSS AW
Citation: Hf. Sims et al., 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, 92(3), 1995, pp. 841-845
MOLECULAR-BASIS OF HUMAN MITOCHONDRIAL VERY-LONG-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY CAUSING CARDIOMYOPATHY AND SUDDEN-DEATH IN CHILDHOOD
Authors: STRAUSS AW POWELL CK HALE DE ANDERSON MM AHUJA A BRACKETT JC SIMS HF
Citation: Aw. Strauss et al., 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, 92(23), 1995, pp. 10496-10500
2 ALPHA-SUBUNIT DONOR SPLICE-SITE MUTATIONS CAUSE HUMAN TRIFUNCTIONALPROTEIN-DEFICIENCY
Authors: BRACKETT JC SIMS HF RINALDO P SHAPIRO S POWELL CK BENNETT MJ STRAUSS AW
Citation: Jc. Brackett et al., 2 ALPHA-SUBUNIT DONOR SPLICE-SITE MUTATIONS CAUSE HUMAN TRIFUNCTIONALPROTEIN-DEFICIENCY, The Journal of clinical investigation, 95(5), 1995, pp. 2076-2082
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)
Authors: LEONE TC CRESCI S CARTER ME ZHANG ZF LALA DS STRAUSS AW KELLY DP
Citation: Tc. Leone et al., 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, 270(41), 1995, pp. 24622-24622
THE HUMAN MEDIUM-CHAIN ACYL-COA DEHYDROGENASE GENE PROMOTER CONSISTS OF A COMPLEX ARRANGEMENT OF NUCLEAR RECEPTOR RESPONSE ELEMENTS AND SP1BINDING-SITES
Authors: LEONE TC CRESCI S CARTER ME ZHANG ZF LALA DS STRAUSS AW KELLY DP
Citation: Tc. Leone et al., 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, 270(27), 1995, pp. 16308-16314
GENETIC DISTINCTION BETWEEN AUTOSOMAL-DOMINANT ATRIAL SEPTAL-DEFECTS AND THE HOLT-ORAM SYNDROME
Authors: BRACKETT JC GOODFELLOW PJ STRAUSS AW
Citation: Jc. Brackett et al., GENETIC DISTINCTION BETWEEN AUTOSOMAL-DOMINANT ATRIAL SEPTAL-DEFECTS AND THE HOLT-ORAM SYNDROME, Circulation, 92(8), 1995, pp. 2470-2470
TOWARD A MOLECULAR UNDERSTANDING OF CONGENITAL HEART-DISEASE
Authors: PAYNE RM JOHNSON MC GRANT JW STRAUSS AW
Citation: Rm. Payne et al., TOWARD A MOLECULAR UNDERSTANDING OF CONGENITAL HEART-DISEASE, Circulation, 91(2), 1995, pp. 494-504
RECOMBINANT HUMAN LIVER MEDIUM-CHAIN ACYL-COA DEHYDROGENASE - PURIFICATION, CHARACTERIZATION, AND THE MECHANISM OF INTERACTIONS WITH FUNCTIONALLY DIVERSE C-8-COA MOLECULES
Authors: PETERSON KL SERGIENKO EE WU YH KUMAR NR STRAUSS AW OLESON AE MUHONEN WW SHABB JB SRIVASTAVA DK
Citation: Kl. Peterson et al., RECOMBINANT HUMAN LIVER MEDIUM-CHAIN ACYL-COA DEHYDROGENASE - PURIFICATION, CHARACTERIZATION, AND THE MECHANISM OF INTERACTIONS WITH FUNCTIONALLY DIVERSE C-8-COA MOLECULES, Biochemistry, 34(45), 1995, pp. 14942-14953
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
Authors: WEINBERGER MJ RINALDO P STRAUSS AW BENNETT MJ
Citation: Mj. Weinberger et al., 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, 209(1), 1995, pp. 47-52
ANOMALOUS ORIGIN OF THE RIGHT PULMONARY-ARTERY FROM THE AORTA AND CATCH-22-SYNDROME
Authors: JOHNSON MC WATSON MS STRAUSS AW SPRAY TL
Citation: Mc. Johnson et al., ANOMALOUS ORIGIN OF THE RIGHT PULMONARY-ARTERY FROM THE AORTA AND CATCH-22-SYNDROME, The Annals of thoracic surgery, 60(3), 1995, pp. 681-682
DELETION WITHIN CHROMOSOME-22 IS COMMON IN PATIENTS WITH ABSENT PULMONARY VALVE SYNDROME
Authors: JOHNSON MC STRAUSS AW DOWTON SB SPRAY TL HUDDLESTON CB WOOD MK SLAUGH RA WATSON MS
Citation: Mc. Johnson et al., DELETION WITHIN CHROMOSOME-22 IS COMMON IN PATIENTS WITH ABSENT PULMONARY VALVE SYNDROME, The American journal of cardiology, 76(1), 1995, pp. 66-69
EXPRESSION OF ENGINEERED HUMAN 17-BETA-ESTRADIOL DEHYDROGENASE IN A PROKARYOTIC SYSTEM
Authors: OSHEA DL GAST MJ MURDOCK GL PAYNE RM STRAUSS AW
Citation: Dl. Oshea et al., EXPRESSION OF ENGINEERED HUMAN 17-BETA-ESTRADIOL DEHYDROGENASE IN A PROKARYOTIC SYSTEM, Journal of the Society for Gynecologic Investigation, 1(2), 1994, pp. 143-149
THE JURY IS STILL OUT REGARDING BALLOON THERAPY FOR NATIVE AORTIC COARCTATION
Authors: JOHNSON MC STRAUSS AW
Citation: Mc. Johnson et Aw. Strauss, THE JURY IS STILL OUT REGARDING BALLOON THERAPY FOR NATIVE AORTIC COARCTATION, Journal of the American College of Cardiology, 24(6), 1994, pp. 1589-1589
EXPRESSION OF THE MITOCHONDRIAL CREATINE-KINASE GENES
Authors: PAYNE RM STRAUSS AW
Citation: Rm. Payne et Aw. Strauss, EXPRESSION OF THE MITOCHONDRIAL CREATINE-KINASE GENES, Molecular and cellular biochemistry, 133, 1994, pp. 235-243
DEVELOPMENTAL EXPRESSION OF SARCOMERIC AND UBIQUITOUS MITOCHONDRIAL CREATINE-KINASE IS TISSUE-SPECIFIC
Authors: PAYNE RM STRAUSS AW
Citation: Rm. Payne et Aw. Strauss, DEVELOPMENTAL EXPRESSION OF SARCOMERIC AND UBIQUITOUS MITOCHONDRIAL CREATINE-KINASE IS TISSUE-SPECIFIC, Biochimica et biophysica acta, N. Gene structure and expression, 1219(1), 1994, pp. 33-38
REGULATION OF FATTY-ACID OXIDATION ENZYME EXPRESSION BY ENERGY SUBSTRATE
Authors: HALE DE STRAUSS AW CAIRA T KELLY DP
Citation: De. Hale et al., REGULATION OF FATTY-ACID OXIDATION ENZYME EXPRESSION BY ENERGY SUBSTRATE, Pediatric research, 35(4), 1994, pp. 10000203-10000203
STRUCTURAL ORGANIZATION AND REGULATORY ELEMENT ANALYSIS OF THE HUMAN LONG-CHAIN ACYL-COA DEHYDROGENASE GENE
Authors: ZHANG ZF ZHOU YQ KELLY DP STRAUSS AW
Citation: Zf. Zhang et al., STRUCTURAL ORGANIZATION AND REGULATORY ELEMENT ANALYSIS OF THE HUMAN LONG-CHAIN ACYL-COA DEHYDROGENASE GENE, Pediatric research, 35(4), 1994, pp. 10000209-10000209
MECHANISMS OF DISEASE - INHERITED CARDIOMYOPATHIES
Authors: KELLY DP STRAUSS AW
Citation: Dp. Kelly et Aw. Strauss, MECHANISMS OF DISEASE - INHERITED CARDIOMYOPATHIES, The New England journal of medicine, 330(13), 1994, pp. 913-919
A NOVEL MUTATION IN MEDIUM-CHAIN ACYL-COA DEHYDROGENASE CAUSES SUDDENNEONATAL DEATH
Authors: BRACKETT JC SIMS HF STEINER RD NUNGE M ZIMMERMAN EM DEMARTINVILLE B RINALDO P SLAUGH R STRAUSS AW
Citation: Jc. Brackett et al., A NOVEL MUTATION IN MEDIUM-CHAIN ACYL-COA DEHYDROGENASE CAUSES SUDDENNEONATAL DEATH, The Journal of clinical investigation, 94(4), 1994, pp. 1477-1483
A RARE MUTATION IN THE MEDIUM-CHAIN ACYL-COENZYME-A DEHYDROGENASE CAUSES SUDDEN NEONATAL DEATH
Authors: BRACKETT JC SIMS HF STEINER R RINALDO P SLAUGH R STRAUSS AW
Citation: Jc. Brackett et al., A RARE MUTATION IN THE MEDIUM-CHAIN ACYL-COENZYME-A DEHYDROGENASE CAUSES SUDDEN NEONATAL DEATH, Clinical research, 42(2), 1994, pp. 10000200-10000200
Risultati: 1-25 | 26-50 | 51-67