diphosphate


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diphosphate

[dī′fäs‚fāt]
(chemistry)
A salt that has two phosphate groups.
McGraw-Hill Dictionary of Scientific & Technical Terms, 6E, Copyright © 2003 by The McGraw-Hill Companies, Inc.
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Optical aggregation using adenosine diphosphate (ADP).
External Quality Assurance of Platelet Function Assays: Results of the College of American Pathologists Proficiency Testing Program
A prominent decrease in concentration of hepatic uridine diphosphate (UDP) glucuronic acid may be caused due to the absence of thyroid hormones, which is considerably low in infants as a result of the decrease in UDPG dehydrogenase activity.
THYROID HORMONE LEVELS IN NEONATAL HYPERBILIRUBINEMIA
Consensus and future directions on the definition of high on-treatment platelet reactivity to adenosine diphosphate. J Am Coll Cardiol 2010;56:919-33.
A Multicenter, Randomized, Double-Blind, and Placebo-Controlled Study of the Effects of Tongxinluo Capsules in Acute Coronary Syndrome Patients with High On-Treatment Platelet Reactivity
IPP isomerase (IDI) catalyzes the isomerization of IPP to DMAPP and condensation of two IPP molecules to form GPP (geranyl diphosphate).
Plant Sources, Extraction Methods, and Uses of Squalene
[8], the sticky platelet syndrome is defined as a qualitative alteration of the platelet function and of autosomal dominant inheritance, characterized by platelet hyperaggregation in vitro with low concentrations of adenosine diphosphate (ADE) and/or epinephrine (EPI) but with normal aggregation in response to collagen, arachidonic acid, ristocetin, and thrombin [9].
Sticky Platelet Syndrome: An Unrecognized Cause of Acute Thrombosis and Graft Loss
ADP, adenosine diphosphate; PT, prothrombin time; PTT, partial thromboplastin time.
Epistaxis as a Common Presenting Symptom of Glanzmann's Thrombasthenia, a Rare Qualitative Platelet Disorder: Illustrative Case Examples
Whitington et al., "Genetic predisposition to the metabolism of irinotecan (CPT-11): role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN-38) in human liver microsomes," The Journal of Clinical Investigation, vol.
Life-Threatening Irinotecan-Induced Toxicity in an Adult Patient with Alveolar Rhabdomyosarcoma: The Role of a UGT1A1 Polymorphism
In humans, there are 10 genes belonging to the NM23 gene family, of which the two most abundantly expressed are NM23-H1 and NM23-H2 that encode the A and B subunits of nucleoside diphosphate kinase, respectively [9].
Meta-Analysis of the Relationship between NM23 Expression to Gastric Cancer Risk and Clinical Features
This involved the decoration of AR with Ti[O.sub.2] nanoparticles (Ti[O.sub.2]NPs) of an average particle size of 21 nm in presence of maleate diphosphate as flame retardant (FR).
Nanoparticles Decorated on Resin Particles and Their Flame Retardancy Behavior for Polymer Composites
It irreversibly inhibits the receptor of adenosine diphosphate (ADP), called P2Y12, expressed on the surface of platelets.
Does i-T744C P2Y12 Polymorphism Modulate Clopidogrel Response among Moroccan Acute Coronary Syndromes Patients?
AbbVie was granted Orphan Drug Designation by the FDA for veliparib, an oral poly (adenosine diphosphate [ADP]ribose) polymerase (PARP) inhibitor, being studied in combination with chemotherapy or radiation for the treatment of advanced squamous non-small cell lung cancer (NSCLC).
AbbVie was granted Orphan Drug Designation by the FDA for veliparib
The US Food and Drug Administration has granted Orphan Drug Designation to United States-based AbbVie's veliparib, an oral poly (adenosine diphosphate [ADP]-ribose) polymerase (PARP) inhibitor, it was reported yesterday.
US Food and Drug Administration grants Orphan Drug Designation to AbbVie's veliparib

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