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Results: 1-7 |
Results: 7
C-13 AND H-1 NUCLEAR-MAGNETIC-RESONANCE STUDY OF GLYCOGEN FUTILE CYCLING IN STRAINS OF THE GENUS FIBROBACTER
Authors: MATHERON C DELORT AM GAUDET G FORANO E LIPTAJ T
Citation: C. Matheron et al., C-13 AND H-1 NUCLEAR-MAGNETIC-RESONANCE STUDY OF GLYCOGEN FUTILE CYCLING IN STRAINS OF THE GENUS FIBROBACTER, Applied and environmental microbiology, 64(1), 1998, pp. 74-81
REINVESTIGATION OF GLUCOSE-METABOLISM IN FIBROBACTER-SUCCINOGENES, USING NMR-SPECTROSCOPY AND ENZYMATIC ASSAYS - EVIDENCE FOR PENTOSE PHOSPHATES PHOSPHOKETOLASE AND PYRUVATE FORMATE LYASE ACTIVITIES
Authors: MATHERON C DELORT AM GAUDET G FORANO E
Citation: C. Matheron et al., REINVESTIGATION OF GLUCOSE-METABOLISM IN FIBROBACTER-SUCCINOGENES, USING NMR-SPECTROSCOPY AND ENZYMATIC ASSAYS - EVIDENCE FOR PENTOSE PHOSPHATES PHOSPHOKETOLASE AND PYRUVATE FORMATE LYASE ACTIVITIES, Biochimica et biophysica acta. Molecular cell research, 1355(1), 1997, pp. 50-60
MOLECULAR-BASIS FOR PROTEIN-S HEREDITARY-DEFICIENCY - GENETIC-DEFECTSOBSERVED IN 118 PATIENTS WITH TYPE-I AND TYPE IIA DEFICIENCIES
Authors: BORGEL D DUCHEMIN J ALHENCGELAS M MATHERON C AIACH M GANDRILLE S
Citation: D. Borgel et al., MOLECULAR-BASIS FOR PROTEIN-S HEREDITARY-DEFICIENCY - GENETIC-DEFECTSOBSERVED IN 118 PATIENTS WITH TYPE-I AND TYPE IIA DEFICIENCIES, The Journal of laboratory and clinical medicine, 128(2), 1996, pp. 218-227
SIMULTANEOUS BUT DIFFERENTIAL METABOLISM OF GLUCOSE AND CELLOBIOSE INFIBROBACTER-SUCCINOGENES CELLS, STUDIED BY IN-VIVO C-13-NMR
Authors: MATHERON C DELORT AM GAUDET G FORANO E
Citation: C. Matheron et al., SIMULTANEOUS BUT DIFFERENTIAL METABOLISM OF GLUCOSE AND CELLOBIOSE INFIBROBACTER-SUCCINOGENES CELLS, STUDIED BY IN-VIVO C-13-NMR, Canadian journal of microbiology, 42(11), 1996, pp. 1091-1099
MOLECULAR DEFECTS RESPONSIBLE FOR TYPE-I AND TYPE IIA PROTEIN-S (PS) DEFICIENCIES IN A PANEL OF 120 FRENCH FAMILIES
Authors: BORGEL D DUCHEMIN J MATHERON C AIACH M GANDRILLE S
Citation: D. Borgel et al., MOLECULAR DEFECTS RESPONSIBLE FOR TYPE-I AND TYPE IIA PROTEIN-S (PS) DEFICIENCIES IN A PANEL OF 120 FRENCH FAMILIES, Thrombosis and haemostasis, 73(6), 1995, pp. 1256-1256
THE SER 460 TO PRO SUBSTITUTION OF THE PROTEIN-S-ALPHA (PROS1) GENE IS A FREQUENT MUTATION ASSOCIATED WITH FREE PROTEIN-S (TYPE-IIA) DEFICIENCY
Authors: DUCHEMIN J GANDRILLE S BORGEL D FEURGARD P ALHENCGELAS M MATHERON C DREYFUS M DUPUY E JUHANVAGUE I AIACH M
Citation: J. Duchemin et al., THE SER 460 TO PRO SUBSTITUTION OF THE PROTEIN-S-ALPHA (PROS1) GENE IS A FREQUENT MUTATION ASSOCIATED WITH FREE PROTEIN-S (TYPE-IIA) DEFICIENCY, Blood, 86(9), 1995, pp. 3436-3443
IDENTIFICATION OF 15 DIFFERENT CANDIDATE CAUSAL POINT MUTATIONS AND 3POLYMORPHISMS IN 19 PATIENTS WITH PROTEIN-S DEFICIENCY USING A SCANNING METHOD FOR THE ANALYSIS OF THE PROTEIN-S ACTIVE GENE
Authors: GANDRILLE S BORGEL D ESCHWEGEGUFFLET V AILLAUD M DREYFUS M MATHERON C GAUSSEM P ABGRALL JF JUDE B SIE P TOULON P AIACH M
Citation: S. Gandrille et al., IDENTIFICATION OF 15 DIFFERENT CANDIDATE CAUSAL POINT MUTATIONS AND 3POLYMORPHISMS IN 19 PATIENTS WITH PROTEIN-S DEFICIENCY USING A SCANNING METHOD FOR THE ANALYSIS OF THE PROTEIN-S ACTIVE GENE, Blood, 85(1), 1995, pp. 130-138
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