13 results on '"D. Burford"'
Search Results
2. Deacidification of black cumin seed oil by selective supercritical carbon dioxide extraction
- Author
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Selma Türkay, Mark D. Burford, M. Kemal Sangün, Keith D. Bartle, Ekrem Ekinci, and Anthony A. Clifford
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chemistry.chemical_classification ,Supercritical carbon dioxide ,Chromatography ,General Chemical Engineering ,Organic Chemistry ,Extraction (chemistry) ,Nigella sativa ,Fatty acid ,Supercritical fluid ,chemistry.chemical_compound ,chemistry ,Carbon dioxide ,Methanol ,Selectivity - Abstract
The deacidification of high-acidity oils from Black cumin seeds (Nigella sativa) was investigated with supercritical carbon dioxide at two temperatures (40 and 60°C), pressures (15 and 20 MPa) and polarities (pure CO2 and CO2/10% MeOH). For pure CO2 at a relatively low pressure (15 MPa) and relatively high temperature (60°C), the deacidification of a highacidity (37.7 wt% free fatty acid) oil to a low-acidity (7.8 wt% free fatty acid) oil was achieved. The free fatty acids were quantitatively (90 wt%) extracted from the oil and left the majority (77 wt%) of the valuable neutral oils in the seed to be recovered at a later stage by using a higher extraction pressure. By reducing the extraction temperature to 40°C, increasing the extraction pressure to 20 MPa, or increasing the polarity of the supercritical fluid via the addition of a methanol modifier, the selectivity of the extraction was significantly reduced; the amount of neutral oil that co-extracted with the free fatty acids was increased from 23 to 94 wt%.
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- 1996
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3. The ontogeny of terminal deoxynucleotidyl transferase positive cells in the human fetus
- Author
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M P, Bodger, G, Janossy, F J, Bollum, G D, Burford, and A V, Hoffbrand
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endocrine system ,Immunology ,Antibodies, Monoclonal ,Bone Marrow Cells ,Gestational Age ,Growth ,Thymus Gland ,Cell Biology ,Hematology ,Biochemistry ,stomatognathic diseases ,Phenotype ,Fetal Organ Maturity ,Liver ,Bone Marrow ,DNA Nucleotidylexotransferase ,Pregnancy ,Antigens, Surface ,DNA Nucleotidyltransferases ,Humans ,Female ,Lymphocytes - Abstract
he ontogeny of cells containing the enzyme terminal deoxynucleotidyl transferase (TdT) in human fetal liver, bone marrow, and thymus has been studied using a highly specific antiserum to TdT together with monoclonal antiprecursor cell antibodies in double and triple marker immunofluorescence. TdT+ cells were first observed in fetal liver at 12 wk of gestation and accounted for 55% of the lymphoid-like cells isolated after Ficoll-Hypaque separation. TdT+ cells were first observed in the bone marrow 16 wk after gestation. Like TdT+ cells in normal infant bone marrow, the majority of TdT+ cells in fetal liver and bone marrow expressed both BA-1 and RFB-1 antigens. This suggests that fetal TdT+ cells include progenitors of the B lineage (BA-1+) and perhaps of thymocytes (RFB-1+). Nevertheless, TdT was not observed in fetal thymocytes until after 20 wk of gestation, although thymic blasts and the majority of thymocytes were strongly RFB-1+ from 12 wk of gestation. These results clearly show that fetal thymus is first populated by TdT, RFB-1+, BA-1 cells, but does not exclude the fact that a second “wave” of TdT+ prothymocytes, possibly bone marrow derived, also exists.
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- 1983
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4. Polymerizing equilibria in neurophysin
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M. Ginsburg, G. D. Burford, and P. J. Thomas
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Chromatography ,Aqueous solution ,Polymers ,Swine ,Vasopressins ,Physiology ,Chemistry ,Elution ,Lysine ,Dispersity ,Derivative analysis ,Articles ,Neurophysins ,Ion ,Molecular Weight ,Solutions ,Polymerization ,Chromatography, Gel ,Animals ,Calcium ,Magnesium ,Pituitary Hormones, Posterior ,hormones, hormone substitutes, and hormone antagonists ,Protein Binding ,Lysine vasopressin - Abstract
1. Evidence for the occurrence of a rapidly polymerizing equilibrium system in freshly prepared aqueous solutions of porcine neurophysin has been obtained by frontal and zonal analysis of gel-filtration elution patterns. 2. Elution volumes increased with decreasing protein concentration and derivative analysis of fronts suggested the existence of different polymerizing forms varying in relative proportion with protein concentration. 3. In the presence of lysine vasopressin, the results suggested a shift of the equilibrium in favour of higher polymerizing forms. 4. In the presence of Ca2+ elution patterns became characteristic of a monodisperse system of relatively high molecular weight. The effect of Ca2+ did not survive removal of the ion and was not reproduced by Mg2+. 5. Evidence for a slowly developing polymerization of neurophysin in aqueous solution has been obtained in experiments with solution prepared 24 hr before subjection to gel-filtration. 6. A model is proposed for the description of the binding of lysine vasopressin to porcine neurophysin.
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- 1969
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5. Progress in behavior therapy
- Author
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Duncan D. Burford
- Subjects
Psychiatry and Mental health ,Clinical Psychology ,Psychology - Published
- 1969
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- View/download PDF
6. Synthesis of both neurohypophysial hormones in both the paraventricular and supraoptic nuclei of the rat
- Author
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G D, Burford, R E, Dyball, R L, Moss, and B T, Pickering
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Male ,Neurons ,Neurophysins ,Vasopressins ,Hypothalamus ,Oxytocin ,Sulfur Radioisotopes ,Rats ,Animals ,Electrophoresis, Polyacrylamide Gel ,Cysteine ,Supraoptic Nucleus ,Paraventricular Hypothalamic Nucleus ,Research Article - Published
- 1974
7. The number of neurophysins in the rat. Influence of the concentration of Bromophenol Blue, used as a tracking dye, on the resolution of proteins by polyacrylamide-gel electrophoresis
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G. D. Burford and B. T. Pickering
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Male ,Neurophysins ,History ,Chromatography ,Resolution (mass spectrometry) ,Coloring agents ,Bromophenol blue ,Articles ,Bromine ,Computer Science Applications ,Education ,Rats ,Electrophoresis ,chemistry.chemical_compound ,chemistry ,Phenols ,Methods ,Animals ,Electrophoresis, Polyacrylamide Gel ,Sulfonic Acids ,Coloring Agents ,Polyacrylamide gel electrophoresis - Abstract
1. The concentration of Bromophenol Blue used as tracking dye in polyacrylamide-gel electrophoresis affected the resolution of rat neurophysins. 2. A final dye concentration of 1μg/ml in the tris–glycine running buffer was found to give the best results. 3. The presence of two major and one minor neurophysin(s) in the rat was confirmed. 4. The two major proteins were found to re-run as single discrete bands, which had the same mobilities in the absence of dye and different mobilities in its presence.
- Published
- 1972
8. Preferential labelling of 'oxytocin-neurophysin' by injection of (35S)cysteine into the paraventricular nucleus of the rat
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G D, Burford, R E, Dyball, R L, Moss, and B T, Pickering
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Vasopressins ,Protein Biosynthesis ,Sulfur Isotopes ,Hypothalamus ,Animals ,Cysteine ,Oxytocin ,Protein Binding ,Rats - Published
- 1972
9. Arrhythmic and antiarrhythmic effects of sodium, potassium, and calcium salts and of glucose injected into coronary arteries of infarcted and normal hearts
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Djamadina Anwar, Louis A. Toth, Tan Eng Hoey, Dunca D. Burford, Richard A. Liptak, and A. Sidney Harris
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medicine.medical_specialty ,Physiology ,Sodium ,Potassium ,Myocardial Infarction ,chemistry.chemical_element ,Infarction ,Calcium ,chemistry.chemical_compound ,Internal medicine ,medicine ,Sodium lactate ,Humans ,Chemistry ,Arrhythmias, Cardiac ,Heart ,medicine.disease ,Coronary Vessels ,Coronary arteries ,medicine.anatomical_structure ,Endocrinology ,Glucose ,Ventricular fibrillation ,Cardiology ,Lactates ,Salts ,Cardiology and Cardiovascular Medicine ,Antagonism ,Anti-Arrhythmia Agents - Abstract
Substances that have not exhibited properties as excitants of ectopic activity by intracoronary injection into normal hearts often produce rapid ectopic activity and sometimes ventricular fibrillation upon slow injection through the vascular bed of an infarcted area, particularly upon the first one or two injections. Sodium lactate has reduced and stopped ectopic activity for brief periods. Excesses of both potassium and calcium have increased ectopic activity in infarction and produced it in normal hearts. No antagonism between these two ions, with respect to ectopic activity, has been demonstrated.
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- 1958
10. A model for the passage of the nurohypophysial hormones and their related proteins through the rat neurohypophysis
- Author
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C. W. Jones, Peter Clifford, G. D. Burford, and B. T. Pickering
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History ,medicine.medical_specialty ,Vasopressin ,Vasopressins ,Hypothalamus ,Exponential regression ,Sulfur Radioisotopes ,Models, Biological ,Education ,Reaction rate constant ,Pituitary Gland, Posterior ,Internal medicine ,medicine ,Animals ,Cysteine ,Neurophysins ,Chemistry ,Computers ,Cellular Interactions and Control Processes ,Proteins ,Computer Science Applications ,Rats ,Endocrinology ,Biophysics ,Mathematics ,Hormone - Abstract
The change in the radioactivity of vasopressin–neurophysin in the rat neurohypophysis after an intracisternal injection of [35S]cysteine was fitted to several mathematical models. The data fitted best a model in which there is a linear input of radioactive protein into one pool of the neurohypophysis, from which it is either released by an exponential process or transferred to a second pool from which it is released by a second exponential process with a rate constant much lower than the first. This model is compatible with the existence of a ‘readily releasable’ pool first postulated by Sachs et al. (1967). Data for the change in radioactivity of vasopressin also gave a good fit in this model. Calculation of the rate constants suggested that the first pool represented about 2% of the total hormone.
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- 1973
11. Tentative identification of a vasopressin-neurophysin and an oxytocin-neurophysin in the rat
- Author
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G. D. Burford, C. W. Jones, and B. T. Pickering
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History ,Pituitary gland ,Vasopressin ,medicine.medical_specialty ,Heterozygote ,Swine ,Vasopressins ,Neurophysins ,Biology ,Oxytocin ,Education ,chemistry.chemical_compound ,Pituitary Gland, Posterior ,Internal medicine ,Sulfur Isotopes ,medicine ,Animals ,Cysteine ,Cysteine metabolism ,Dehydration ,Homozygote ,Proteins ,Articles ,medicine.disease ,Electrophoresis, Disc ,Computer Science Applications ,Rats ,medicine.anatomical_structure ,Endocrinology ,Biochemistry ,chemistry ,Protein Biosynthesis ,Diabetes insipidus ,hormones, hormone substitutes, and hormone antagonists ,Diabetes Insipidus ,Hormone ,medicine.drug ,Protein Binding - Abstract
1. Rat neurohypophysial extracts have been examined by polyacrylamide-gel electrophoresis. 2. Three of the proteins were tentatively identified as neurophysins by their acidic nature and their disappearance after dehydration of the animals. 3. These proteins were radioactive 24h after intracisternal injection of [35S]cysteine. 4. Two of the proteins were present in much greater quantities than the third, and these two were present in the gland in the same ratio as the hormones vasopressin and oxytocin. 5. One of these proteins was absent from glands of rats homozygous for diabetes insipidus but present in heterozygous animals. 6. It is suggested that these two proteins are the vasopressin–neurophysin and oxytocin–neurophysin of the rat.
- Published
- 1971
12. The DNA sequence of the human X chromosome.
- Author
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Ross MT, Grafham DV, Coffey AJ, Scherer S, McLay K, Muzny D, Platzer M, Howell GR, Burrows C, Bird CP, Frankish A, Lovell FL, Howe KL, Ashurst JL, Fulton RS, Sudbrak R, Wen G, Jones MC, Hurles ME, Andrews TD, Scott CE, Searle S, Ramser J, Whittaker A, Deadman R, Carter NP, Hunt SE, Chen R, Cree A, Gunaratne P, Havlak P, Hodgson A, Metzker ML, Richards S, Scott G, Steffen D, Sodergren E, Wheeler DA, Worley KC, Ainscough R, Ambrose KD, Ansari-Lari MA, Aradhya S, Ashwell RI, Babbage AK, Bagguley CL, Ballabio A, Banerjee R, Barker GE, Barlow KF, Barrett IP, Bates KN, Beare DM, Beasley H, Beasley O, Beck A, Bethel G, Blechschmidt K, Brady N, Bray-Allen S, Bridgeman AM, Brown AJ, Brown MJ, Bonnin D, Bruford EA, Buhay C, Burch P, Burford D, Burgess J, Burrill W, Burton J, Bye JM, Carder C, Carrel L, Chako J, Chapman JC, Chavez D, Chen E, Chen G, Chen Y, Chen Z, Chinault C, Ciccodicola A, Clark SY, Clarke G, Clee CM, Clegg S, Clerc-Blankenburg K, Clifford K, Cobley V, Cole CG, Conquer JS, Corby N, Connor RE, David R, Davies J, Davis C, Davis J, Delgado O, Deshazo D, Dhami P, Ding Y, Dinh H, Dodsworth S, Draper H, Dugan-Rocha S, Dunham A, Dunn M, Durbin KJ, Dutta I, Eades T, Ellwood M, Emery-Cohen A, Errington H, Evans KL, Faulkner L, Francis F, Frankland J, Fraser AE, Galgoczy P, Gilbert J, Gill R, Glöckner G, Gregory SG, Gribble S, Griffiths C, Grocock R, Gu Y, Gwilliam R, Hamilton C, Hart EA, Hawes A, Heath PD, Heitmann K, Hennig S, Hernandez J, Hinzmann B, Ho S, Hoffs M, Howden PJ, Huckle EJ, Hume J, Hunt PJ, Hunt AR, Isherwood J, Jacob L, Johnson D, Jones S, de Jong PJ, Joseph SS, Keenan S, Kelly S, Kershaw JK, Khan Z, Kioschis P, Klages S, Knights AJ, Kosiura A, Kovar-Smith C, Laird GK, Langford C, Lawlor S, Leversha M, Lewis L, Liu W, Lloyd C, Lloyd DM, Loulseged H, Loveland JE, Lovell JD, Lozado R, Lu J, Lyne R, Ma J, Maheshwari M, Matthews LH, McDowall J, McLaren S, McMurray A, Meidl P, Meitinger T, Milne S, Miner G, Mistry SL, Morgan M, Morris S, Müller I, Mullikin JC, Nguyen N, Nordsiek G, Nyakatura G, O'Dell CN, Okwuonu G, Palmer S, Pandian R, Parker D, Parrish J, Pasternak S, Patel D, Pearce AV, Pearson DM, Pelan SE, Perez L, Porter KM, Ramsey Y, Reichwald K, Rhodes S, Ridler KA, Schlessinger D, Schueler MG, Sehra HK, Shaw-Smith C, Shen H, Sheridan EM, Shownkeen R, Skuce CD, Smith ML, Sotheran EC, Steingruber HE, Steward CA, Storey R, Swann RM, Swarbreck D, Tabor PE, Taudien S, Taylor T, Teague B, Thomas K, Thorpe A, Timms K, Tracey A, Trevanion S, Tromans AC, d'Urso M, Verduzco D, Villasana D, Waldron L, Wall M, Wang Q, Warren J, Warry GL, Wei X, West A, Whitehead SL, Whiteley MN, Wilkinson JE, Willey DL, Williams G, Williams L, Williamson A, Williamson H, Wilming L, Woodmansey RL, Wray PW, Yen J, Zhang J, Zhou J, Zoghbi H, Zorilla S, Buck D, Reinhardt R, Poustka A, Rosenthal A, Lehrach H, Meindl A, Minx PJ, Hillier LW, Willard HF, Wilson RK, Waterston RH, Rice CM, Vaudin M, Coulson A, Nelson DL, Weinstock G, Sulston JE, Durbin R, Hubbard T, Gibbs RA, Beck S, Rogers J, and Bentley DR
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- Animals, Antigens, Neoplasm genetics, Centromere genetics, Chromosomes, Human, Y genetics, Contig Mapping, Crossing Over, Genetic genetics, Dosage Compensation, Genetic, Female, Genetic Linkage genetics, Genetics, Medical, Humans, Male, Polymorphism, Single Nucleotide genetics, RNA genetics, Repetitive Sequences, Nucleic Acid genetics, Sequence Homology, Nucleic Acid, Testis metabolism, Chromosomes, Human, X genetics, Evolution, Molecular, Genomics, Sequence Analysis, DNA
- Abstract
The human X chromosome has a unique biology that was shaped by its evolution as the sex chromosome shared by males and females. We have determined 99.3% of the euchromatic sequence of the X chromosome. Our analysis illustrates the autosomal origin of the mammalian sex chromosomes, the stepwise process that led to the progressive loss of recombination between X and Y, and the extent of subsequent degradation of the Y chromosome. LINE1 repeat elements cover one-third of the X chromosome, with a distribution that is consistent with their proposed role as way stations in the process of X-chromosome inactivation. We found 1,098 genes in the sequence, of which 99 encode proteins expressed in testis and in various tumour types. A disproportionately high number of mendelian diseases are documented for the X chromosome. Of this number, 168 have been explained by mutations in 113 X-linked genes, which in many cases were characterized with the aid of the DNA sequence.
- Published
- 2005
- Full Text
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13. DNA sequence and analysis of human chromosome 9.
- Author
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Humphray SJ, Oliver K, Hunt AR, Plumb RW, Loveland JE, Howe KL, Andrews TD, Searle S, Hunt SE, Scott CE, Jones MC, Ainscough R, Almeida JP, Ambrose KD, Ashwell RI, Babbage AK, Babbage S, Bagguley CL, Bailey J, Banerjee R, Barker DJ, Barlow KF, Bates K, Beasley H, Beasley O, Bird CP, Bray-Allen S, Brown AJ, Brown JY, Burford D, Burrill W, Burton J, Carder C, Carter NP, Chapman JC, Chen Y, Clarke G, Clark SY, Clee CM, Clegg S, Collier RE, Corby N, Crosier M, Cummings AT, Davies J, Dhami P, Dunn M, Dutta I, Dyer LW, Earthrowl ME, Faulkner L, Fleming CJ, Frankish A, Frankland JA, French L, Fricker DG, Garner P, Garnett J, Ghori J, Gilbert JG, Glison C, Grafham DV, Gribble S, Griffiths C, Griffiths-Jones S, Grocock R, Guy J, Hall RE, Hammond S, Harley JL, Harrison ES, Hart EA, Heath PD, Henderson CD, Hopkins BL, Howard PJ, Howden PJ, Huckle E, Johnson C, Johnson D, Joy AA, Kay M, Keenan S, Kershaw JK, Kimberley AM, King A, Knights A, Laird GK, Langford C, Lawlor S, Leongamornlert DA, Leversha M, Lloyd C, Lloyd DM, Lovell J, Martin S, Mashreghi-Mohammadi M, Matthews L, McLaren S, McLay KE, McMurray A, Milne S, Nickerson T, Nisbett J, Nordsiek G, Pearce AV, Peck AI, Porter KM, Pandian R, Pelan S, Phillimore B, Povey S, Ramsey Y, Rand V, Scharfe M, Sehra HK, Shownkeen R, Sims SK, Skuce CD, Smith M, Steward CA, Swarbreck D, Sycamore N, Tester J, Thorpe A, Tracey A, Tromans A, Thomas DW, Wall M, Wallis JM, West AP, Whitehead SL, Willey DL, Williams SA, Wilming L, Wray PW, Young L, Ashurst JL, Coulson A, Blöcker H, Durbin R, Sulston JE, Hubbard T, Jackson MJ, Bentley DR, Beck S, Rogers J, and Dunham I
- Subjects
- Base Composition, Euchromatin genetics, Evolution, Molecular, Female, Gene Duplication, Genes, Duplicate genetics, Genetic Variation genetics, Genetics, Medical, Genomics, Heterochromatin genetics, Humans, Male, Neoplasms genetics, Neurodegenerative Diseases genetics, Pseudogenes genetics, Sequence Analysis, DNA, Sex Determination Processes, Chromosomes, Human, Pair 9 genetics, Genes, Physical Chromosome Mapping
- Abstract
Chromosome 9 is highly structurally polymorphic. It contains the largest autosomal block of heterochromatin, which is heteromorphic in 6-8% of humans, whereas pericentric inversions occur in more than 1% of the population. The finished euchromatic sequence of chromosome 9 comprises 109,044,351 base pairs and represents >99.6% of the region. Analysis of the sequence reveals many intra- and interchromosomal duplications, including segmental duplications adjacent to both the centromere and the large heterochromatic block. We have annotated 1,149 genes, including genes implicated in male-to-female sex reversal, cancer and neurodegenerative disease, and 426 pseudogenes. The chromosome contains the largest interferon gene cluster in the human genome. There is also a region of exceptionally high gene and G + C content including genes paralogous to those in the major histocompatibility complex. We have also detected recently duplicated genes that exhibit different rates of sequence divergence, presumably reflecting natural selection.
- Published
- 2004
- Full Text
- View/download PDF
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