PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 9048549-6 1997 The thermodynamic quantities obtained from the DSC studies in phosphate buffer at pH 7.0 are as follows: t1/2 = 54.7 degrees C (heating rate of 2.34 K min-1), delta H0 = 690 kJ mol-1, and delta Cp = 10.3 kJ mol-1 K-1 which correspondends to a value of delta G0D (20 degrees C) of 53.4 kJ mol-1. Phosphates 62-71 CD59 molecule (CD59 blood group) Homo sapiens 151-156 3075149-4 1988 Phosphate excretion showed an initial fall followed by a more than twofold increase afterwards (6.52 +/- 0.92 vs. 3.14 +/- 0.92 and 15.29 +/- 3.82 mumol/min/1.73 m2, respectively). Phosphates 0-9 CD59 molecule (CD59 blood group) Homo sapiens 153-158 2355823-6 1990 Phosphate loading significantly increased maximal oxygen uptake from 4.77 +/- 0.29 to 5.18 +/- 0.25 l.min-1 and ventilatory anaerobic threshold from 3.74 +/- 0.28 to 4.18 +/- 0.14 l.min-1. Phosphates 0-9 CD59 molecule (CD59 blood group) Homo sapiens 102-107 2355823-6 1990 Phosphate loading significantly increased maximal oxygen uptake from 4.77 +/- 0.29 to 5.18 +/- 0.25 l.min-1 and ventilatory anaerobic threshold from 3.74 +/- 0.28 to 4.18 +/- 0.14 l.min-1. Phosphates 0-9 CD59 molecule (CD59 blood group) Homo sapiens 182-187 2355823-8 1990 However, mean performance run oxygen uptake was significantly lower (3.87 +/- 0.3 to 3.80 +/- 0.3 l.min-1) with phosphate ingestion. Phosphates 112-121 CD59 molecule (CD59 blood group) Homo sapiens 100-105 1722443-7 1991 Infusion of islet amyloid polypeptide (150 pmol min-1 kg-1) caused a fall in serum calcium and phosphate concentrations in five patients with Paget"s disease of the bone. Phosphates 95-104 CD59 molecule (CD59 blood group) Homo sapiens 48-58 2155543-5 1990 The VIP-induced decrease in phosphate uptake was due to decrease in maximal transport (VmaxVIP = 2.78 +/- 0.16 nmol.mg protein-1.3 min-1) and not to a change in the affinity of the transporter for phosphate (KmVIP = 0.11 +/- 0.01 mM phosphate). Phosphates 28-37 CD59 molecule (CD59 blood group) Homo sapiens 131-136 2820729-2 1987 The purification resulted in enzyme with a specific activity in excess of 1,000 nmol phosphate mg-1 min-1 in relatively high yield. Phosphates 85-94 CD59 molecule (CD59 blood group) Homo sapiens 100-105 3543359-6 1986 Spectral data were used to calculate a rate constant of (5.4 +/- 0.3) X 10(-3) min-1 for the intracellular disappearance of 4 at 23 degrees C. The intracellular pH was determined to be 7.1 from the chemical shift of the internal inorganic phosphate signal. Phosphates 239-248 CD59 molecule (CD59 blood group) Homo sapiens 79-84 3105577-2 1987 The initial rate of phosphorylation of these proteins in the presence of EGF was 5.2 and 3.5 nmol of phosphate min-1 (mg of receptor protein)-1, and this was approximately 10- and 6-fold higher than the basal rate, respectively. Phosphates 101-110 CD59 molecule (CD59 blood group) Homo sapiens 111-143 7059981-4 1982 Conversion of 4-hydroxycyclophosphamide to phosphoramide mustard and acrolein was first-order with respect to 4-hydroxycyclophosphamide (k = 0.126 min-1 in 0.5 M phosphate buffer, pH 8, 37 degrees) as well as first-order with respect to phosphate serving as a catalyst. Phosphates 162-171 CD59 molecule (CD59 blood group) Homo sapiens 147-152 7059981-4 1982 Conversion of 4-hydroxycyclophosphamide to phosphoramide mustard and acrolein was first-order with respect to 4-hydroxycyclophosphamide (k = 0.126 min-1 in 0.5 M phosphate buffer, pH 8, 37 degrees) as well as first-order with respect to phosphate serving as a catalyst. Phosphates 237-246 CD59 molecule (CD59 blood group) Homo sapiens 147-152 31812060-4 2020 In the absence of phosphate buffer, the rate constant of 2,4-DCP degradation increased from 9.4 x 10-3 to 2.4 x 10-2 min-1 when pH value was increased from 3.0 to 6.0. Phosphates 18-27 CD59 molecule (CD59 blood group) Homo sapiens 117-122 722557-10 1978 The rate constants were in 0.2 mM-phosphate 1.29 X 10(-3) min-1, in 0.2 mM 1.95 X 10(-3) min-1, and in 2 mM 3.21 X 10(-3) min-1 at 37 degrees C. After changing the external solution the efflux reached a new level with a time constant of about 9 min. Phosphates 34-43 CD59 molecule (CD59 blood group) Homo sapiens 58-63 7441528-4 1980 The resting rate constant of phosphate efflux was 2.61 X 10(-3) min-1: electrical stimulation (10 sec-1, 3 min) produced an extra fractional loss of 6.75 X 10(-6) impulse-1. Phosphates 29-38 CD59 molecule (CD59 blood group) Homo sapiens 64-69 7441530-3 1980 In solutions with 2 mM-phosphate and 1 mM-K the rate constant of the resting efflux was 2.7 x 10(-3) min(-1); stimulation caused an extra fractional loss of 2.8 x 10(-6) impulse(-1).3. Phosphates 23-32 CD59 molecule (CD59 blood group) Homo sapiens 101-107 7441530-4 1980 Lowering the phosphate concentration decreased the resting and the stimulated efflux; with 0.2 mM-phosphate the corresponding values were 1.9 x 10(-3) min(-1) and 1.8 x 10(-6) impulse(-1), respectively.4. Phosphates 13-22 CD59 molecule (CD59 blood group) Homo sapiens 151-157 7441530-4 1980 Lowering the phosphate concentration decreased the resting and the stimulated efflux; with 0.2 mM-phosphate the corresponding values were 1.9 x 10(-3) min(-1) and 1.8 x 10(-6) impulse(-1), respectively.4. Phosphates 98-107 CD59 molecule (CD59 blood group) Homo sapiens 151-157 23763855-3 2013 The consequences of abnormal phosphate homeostasis are evident at estimated glomerular filtration rates <70 mL/min/1.73 m(2), long before serum phosphate levels increase. Phosphates 29-38 CD59 molecule (CD59 blood group) Homo sapiens 114-119 27739456-4 2016 By using surface complexation kinetic models (SCKMs) to describe phosphate adsorption to PF-HFO, the adsorption rate constant (0.0386-0.205 mM-1 min-1 for SCKM-1 and 0.0680-0.274 mM-1 min-1 for SCKM-2) decreased with increasing pH while the protonation reaction rate constant in SCKM-2 (0.0776-0.0947 mM-1 min-1) increased over the pH range 6.0-8.0. Phosphates 65-74 CD59 molecule (CD59 blood group) Homo sapiens 145-150 27739456-4 2016 By using surface complexation kinetic models (SCKMs) to describe phosphate adsorption to PF-HFO, the adsorption rate constant (0.0386-0.205 mM-1 min-1 for SCKM-1 and 0.0680-0.274 mM-1 min-1 for SCKM-2) decreased with increasing pH while the protonation reaction rate constant in SCKM-2 (0.0776-0.0947 mM-1 min-1) increased over the pH range 6.0-8.0. Phosphates 65-74 CD59 molecule (CD59 blood group) Homo sapiens 184-189 27739456-4 2016 By using surface complexation kinetic models (SCKMs) to describe phosphate adsorption to PF-HFO, the adsorption rate constant (0.0386-0.205 mM-1 min-1 for SCKM-1 and 0.0680-0.274 mM-1 min-1 for SCKM-2) decreased with increasing pH while the protonation reaction rate constant in SCKM-2 (0.0776-0.0947 mM-1 min-1) increased over the pH range 6.0-8.0. Phosphates 65-74 CD59 molecule (CD59 blood group) Homo sapiens 184-189 31774275-7 2020 Under an adverse condition (pH 9.0), the mass transfer was ~2.5 times higher than that in the pore-free one (0.10 min-1 vs. 0.04 min-1), ensuring the possibility of diffusing phosphate in further contact with these active sites. Phosphates 175-184 CD59 molecule (CD59 blood group) Homo sapiens 114-119 31774275-7 2020 Under an adverse condition (pH 9.0), the mass transfer was ~2.5 times higher than that in the pore-free one (0.10 min-1 vs. 0.04 min-1), ensuring the possibility of diffusing phosphate in further contact with these active sites. Phosphates 175-184 CD59 molecule (CD59 blood group) Homo sapiens 129-134 18827360-6 2008 min(-1) in 0.1 M hydrochloric acid (HCl) and pH 6.8 phosphate buffer. Phosphates 52-61 CD59 molecule (CD59 blood group) Homo sapiens 0-6