AAAAAA

   
Results: 1-25 | 26-50 | 51-67
Results: 1-25/67
MOLECULAR CHARACTERIZATION OF THE CREATINE KINASES AND SOME HISTORICAL PERSPECTIVES
Authors: QIN WN KHUCHUA Z CHENG J BOERO J PAYNE RM STRAUSS AW
Citation: Wn. Qin et al., MOLECULAR CHARACTERIZATION OF THE CREATINE KINASES AND SOME HISTORICAL PERSPECTIVES, Molecular and cellular biochemistry, 184(1-2), 1998, pp. 153-167
MILD TRIFUNCTIONAL PROTEIN-DEFICIENCY IS ASSOCIATED WITH PROGRESSIVE NEUROPATHY AND MYOPATHY AND SUGGESTS A NOVEL GENOTYPE-PHENOTYPE CORRELATION
Authors: IBDAH JA TEIN I DIONISIVICI C BENNETT MJ IJLST L GIBSON B WANDERS RJA STRAUSS AW
Citation: Ja. Ibdah et al., MILD TRIFUNCTIONAL PROTEIN-DEFICIENCY IS ASSOCIATED WITH PROGRESSIVE NEUROPATHY AND MYOPATHY AND SUGGESTS A NOVEL GENOTYPE-PHENOTYPE CORRELATION, The Journal of clinical investigation, 102(6), 1998, pp. 1193-1199
OCTAMER FORMATION AND COUPLING OF CARDIAC SARCOMERIC MITOCHONDRIAL CREATINE-KINASE ARE MEDIATED BY CHARGED N-TERMINAL RESIDUES
Authors: KHUCHUA ZA QIN WN BOERO J CHENG J PAYNE RM SAKS VA STRAUSS AW
Citation: Za. Khuchua et al., OCTAMER FORMATION AND COUPLING OF CARDIAC SARCOMERIC MITOCHONDRIAL CREATINE-KINASE ARE MEDIATED BY CHARGED N-TERMINAL RESIDUES, The Journal of biological chemistry, 273(36), 1998, pp. 22990-22996
A NOVEL ASSOCIATION BETWEEN MICROVESICULAR STEATO-HEPATITIS AND A COMMON MUTATION IN THE BETA-OXIDATION CYCLE
Authors: IBDAH JA BENNETT MJ RINALDO P STRAUSS AW
Citation: Ja. Ibdah et al., A NOVEL ASSOCIATION BETWEEN MICROVESICULAR STEATO-HEPATITIS AND A COMMON MUTATION IN THE BETA-OXIDATION CYCLE, Gastroenterology, 114(4), 1998, pp. 252-252
PHYSIOLOGICAL STRESSORS INDUCING SUDDEN-DEATH IN THE VERY-LONG-CHAIN ACYL-COA DEHYDROGENASE DEFICIENT MICE
Authors: EXIL VJ SIMS H KOVACS A QIN WN BOERO J KHUCHUA Z STRAUSS AW
Citation: Vj. Exil et al., PHYSIOLOGICAL STRESSORS INDUCING SUDDEN-DEATH IN THE VERY-LONG-CHAIN ACYL-COA DEHYDROGENASE DEFICIENT MICE, Circulation, 98(17), 1998, pp. 24-24
REDUCED PENETRANCE, VARIABLE EXPRESSIVITY, AND GENETIC-HETEROGENEITY OF FAMILIAL ATRIAL SEPTAL-DEFECTS
Authors: BENSON DW SHARKEY A FATKIN D LANG P BASSON CT MCDONOUGH B STRAUSS AW SEIDMAN JG SEIDMAN CE
Citation: Dw. Benson et al., REDUCED PENETRANCE, VARIABLE EXPRESSIVITY, AND GENETIC-HETEROGENEITY OF FAMILIAL ATRIAL SEPTAL-DEFECTS, Circulation, 97(20), 1998, pp. 2043-2048
REGULATION OF THE HUMAN LONG-CHAIN ACYL-COA DEHYDROGENASE GENE BY NUCLEAR HORMONE-RECEPTOR TRANSCRIPTION FACTORS
Authors: ZHANG ZF ZHOU YQ MENDELSOHN NJ BAUER GS STRAUSS AW
Citation: Zf. Zhang et al., 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, 1350(1), 1997, pp. 53-64
SHPRINTZEN-GOLDBERG SYNDROME RESULTS FROM MUTATIONS IN FIBRILLIN-I, NOT MONOSOMY 22Q11 - REPLY
Authors: JOHNSON MC WATSON MS DOWTON SB STRAUSS AW
Citation: Mc. Johnson et al., SHPRINTZEN-GOLDBERG SYNDROME RESULTS FROM MUTATIONS IN FIBRILLIN-I, NOT MONOSOMY 22Q11 - REPLY, The Journal of pediatrics, 131(1), 1997, pp. 165-165
ELEMENTS REGULATING CARDIOMYOCYTE EXPRESSION OF THE HUMAN SARCOMERIC MITOCHONDRIAL CREATINE-KINASE GENE IN TRANSGENIC MICE
Authors: QIN WN KHUCHUA Z KLEIN SC STRAUSS AW
Citation: Wn. Qin et al., ELEMENTS REGULATING CARDIOMYOCYTE EXPRESSION OF THE HUMAN SARCOMERIC MITOCHONDRIAL CREATINE-KINASE GENE IN TRANSGENIC MICE, The Journal of biological chemistry, 272(40), 1997, pp. 25210-25216
CHARACTERIZATION OF HUMAN AND PIG-KIDNEY LONG-CHAIN-ACYL-COA DEHYDROGENASES AND THEIR ROLE IN BETA-OXIDATION
Authors: EDER M KRAUTLE F DONG Y VOCK P KIEWEG V KIM JJP STRAUSS AW GHISLA S
Citation: M. Eder et al., CHARACTERIZATION OF HUMAN AND PIG-KIDNEY LONG-CHAIN-ACYL-COA DEHYDROGENASES AND THEIR ROLE IN BETA-OXIDATION, European journal of biochemistry, 245(3), 1997, pp. 600-607
A FAMILIAL ATRIAL SEPTAL-DEFECT GENE MAPS TO CHROMOSOME 5P - EVIDENCEFOR REDUCED GENE PENETRANCE, VARIABLE EXPRESSIVITY AND GENETIC-HETEROGENEITY
Authors: BENSON DW STRAUSS AW SHARKEY A FATKIN D SCHOTT JJ SANGWATANAROJ S PEASE WE BASSON CT SEIDMAN JG SEIDMAN CE
Citation: Dw. Benson et al., A FAMILIAL ATRIAL SEPTAL-DEFECT GENE MAPS TO CHROMOSOME 5P - EVIDENCEFOR REDUCED GENE PENETRANCE, VARIABLE EXPRESSIVITY AND GENETIC-HETEROGENEITY, Circulation, 96(8), 1997, pp. 76-76
OCTAMER FORMATION OF CARDIAC SARCOMERIC MITOCHONDRIAL CREATINE-KINASEMEDIATED BY CHARGED N-TERMINAL RESIDUES
Authors: KHUCHUA ZA QIN WN BOERO JA STRAUSS AW
Citation: Za. Khuchua et al., OCTAMER FORMATION OF CARDIAC SARCOMERIC MITOCHONDRIAL CREATINE-KINASEMEDIATED BY CHARGED N-TERMINAL RESIDUES, Circulation, 96(8), 1997, pp. 1754-1754
CIS-ACTING ELEMENTS REGULATING EXPRESSION OF THE HUMAN SARCOMERIC MITOCHONDRIAL CREATINE-KINASE GENE IN THE HEART
Authors: QIN WN KHUCHUA ZA BOERO JA CHUGH R STRAUSS AW
Citation: Wn. Qin et al., CIS-ACTING ELEMENTS REGULATING EXPRESSION OF THE HUMAN SARCOMERIC MITOCHONDRIAL CREATINE-KINASE GENE IN THE HEART, Circulation, 96(8), 1997, pp. 2807-2807
MYOCYTE-SPECIFIC EXPRESSION OF THE SARCOMERIC MITOCHONDRIAL CREATINE-KINASE GENE IN HEART AND SKELETAL-MUSCLE
Authors: QIN WN KHUCHUA ZA STRAUSS AW
Citation: Wn. Qin et al., MYOCYTE-SPECIFIC EXPRESSION OF THE SARCOMERIC MITOCHONDRIAL CREATINE-KINASE GENE IN HEART AND SKELETAL-MUSCLE, Circulation, 96(8), 1997, pp. 3774-3774
DEFECTS OF MITOCHONDRIAL PROTEINS AND PEDIATRIC HEART-DISEASE
Authors: STRAUSS AW
Citation: Aw. Strauss, DEFECTS OF MITOCHONDRIAL PROTEINS AND PEDIATRIC HEART-DISEASE, Progress in pediatric cardiology, 6(1), 1996, pp. 83-90
IDENTIFICATION OF A POTENTIAL RIBOSOME-BINDING INTEGRAL MEMBRANE-PROTEIN IN YEAST
Authors: CROWLEY KS STRAUSS AW
Citation: Ks. Crowley et Aw. Strauss, IDENTIFICATION OF A POTENTIAL RIBOSOME-BINDING INTEGRAL MEMBRANE-PROTEIN IN YEAST, The FASEB journal, 10(6), 1996, pp. 2358-2358
THE MOLECULAR-BASIS OF ACUTE FATTY LIVER OF PREGNANCY-ASSOCIATED WITHPEDIATRIC LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY
Authors: IBDAH JA ISAACS J TREEM W BENNETT M STRAUSS AW
Citation: Ja. Ibdah et al., THE MOLECULAR-BASIS OF ACUTE FATTY LIVER OF PREGNANCY-ASSOCIATED WITHPEDIATRIC LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY, Hepatology, 24(4), 1996, pp. 300-300
THE GENETIC-BASIS OF PEDIATRIC CARDIOVASCULAR-DISEASE
Authors: STRAUSS AW JOHNSON MC
Citation: Aw. Strauss et Mc. Johnson, THE GENETIC-BASIS OF PEDIATRIC CARDIOVASCULAR-DISEASE, Seminars in perinatology, 20(6), 1996, pp. 564-576
MATERNAL ACUTE FATTY LIVER OF PREGNANCY-ASSOCIATED WITH FETAL TRIFUNCTIONAL PROTEIN-DEFICIENCY - MOLECULAR CHARACTERIZATION OF A NOVEL MATERNAL MUTANT ALLELE
Authors: ISAACS JD SIMS HF POWELL CK BENNETT MJ HALE DE TREEM WR STRAUSS AW
Citation: Jd. Isaacs et al., MATERNAL ACUTE FATTY LIVER OF PREGNANCY-ASSOCIATED WITH FETAL TRIFUNCTIONAL PROTEIN-DEFICIENCY - MOLECULAR CHARACTERIZATION OF A NOVEL MATERNAL MUTANT ALLELE, Pediatric research, 40(3), 1996, pp. 393-398
MOLECULAR-BASIS OF VERY LONG-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY - SCREENING AND MUTATIONAL ANALYSIS OF 17 PATIENTS
Authors: MATHUR A POWELL CK SIMS HF ALLA VL BENNETT M STRAUSS AW
Citation: A. Mathur et al., MOLECULAR-BASIS OF VERY LONG-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY - SCREENING AND MUTATIONAL ANALYSIS OF 17 PATIENTS, Pediatric research, 39(4), 1996, pp. 866-866
IN-VIVO AND IN-VITRO ANALYSIS OF THE HUMAN LONG-CHAIN ACYL COA DEHYDROGENASE (LCAD) GENE PROMOTER REGION
Authors: ZHANG ZF ZHOU YQ STRAUSS AW
Citation: Zf. Zhang et al., IN-VIVO AND IN-VITRO ANALYSIS OF THE HUMAN LONG-CHAIN ACYL COA DEHYDROGENASE (LCAD) GENE PROMOTER REGION, Pediatric research, 39(4), 1996, pp. 889-889
CHROMOSOME 22Q11 MONOSOMY AND THE GENETIC-BASIS OF CONGENITAL HEART-DISEASE
Authors: JOHNSON MC WATSON MS STRAUSS AW
Citation: Mc. Johnson et al., CHROMOSOME 22Q11 MONOSOMY AND THE GENETIC-BASIS OF CONGENITAL HEART-DISEASE, The Journal of pediatrics, 129(1), 1996, pp. 1-3
RECOGNITION AND MANAGEMENT OF NONPENETRATING CARDIAC TRAUMA IN CHILDREN
Authors: BROMBERG BI MAZZIOTTI MV CANTER CE SPRAY TL STRAUSS AW FOGLIA RP
Citation: Bi. Bromberg et al., RECOGNITION AND MANAGEMENT OF NONPENETRATING CARDIAC TRAUMA IN CHILDREN, The Journal of pediatrics, 128(4), 1996, pp. 536-541
ACUTE FATTY LIVER OF PREGNANCY AND MATERNAL LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE
Authors: IBDAH JA ISAACS J TREEM W STRAUSS AW
Citation: Ja. Ibdah et al., ACUTE FATTY LIVER OF PREGNANCY AND MATERNAL LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE, Gastroenterology, 110(4), 1996, pp. 1215-1215
INFANTILE CARDIOMYOPATHY - A COMMON CLINICAL MANIFESTATION OF VERY LONG-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY
Authors: MATHUR A SIMS HF POWELL CK STRAUSS AW
Citation: A. Mathur et al., INFANTILE CARDIOMYOPATHY - A COMMON CLINICAL MANIFESTATION OF VERY LONG-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY, Circulation, 94(8), 1996, pp. 315-315
Risultati: 1-25 | 26-50 | 51-67