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dc.contributor.authorFortier, Normand Leonarden_US
dc.date.accessioned2019-08-01T16:56:15Z
dc.date.issued1964
dc.date.submitted1964
dc.identifier.otherb14618291
dc.identifier.urihttps://hdl.handle.net/2144/36813
dc.descriptionThesis (Ph.D.)--Boston Universityen_US
dc.descriptionPLEASE NOTE: Boston University Libraries did not receive an Authorization To Manage form for this thesis or dissertation. It is therefore not openly accessible, though it may be available by request. If you are the author or principal advisor of this work and would like to request open access for it, please contact us at open-help@bu.edu. Thank you.en_US
dc.description.abstractThe biochemical pathway for the conversion of pentoses to hexoses is readily demonstrated in erythrocytes because of the abundance of the enzymes transaldolase. The pathway of pentose-phosphate synthesis from nucleosides is of interest because it is a means of providing erythrocytes with hexose- and triosephosphates without the participation of adenosine triphosphate. In contrast to glycolysis, the major metabolic chemical sequence in the erythrocyte, the pentose pathway, can be considered to be an energy conserving one [TRUNCATED]en_US
dc.language.isoen_US
dc.publisherBoston Universityen_US
dc.subjectBiochemistryen_US
dc.titlePentose pathways in erythrocyte ghostsen_US
dc.typeThesis/Dissertationen_US
dc.description.embargo2031-01-01
etd.degree.nameDoctor of Philosophyen_US
etd.degree.leveldoctoralen_US
etd.degree.disciplineBiochemistryen_US
etd.degree.grantorBoston Universityen_US
dc.identifier.barcode11719025754849
dc.identifier.mmsid99187805020001161


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