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2.
Indian J Psychiatry ; 53(1): 9-12, 2011 Jan.
Article in English | MEDLINE | ID: mdl-21431001
3.
Indian J Psychiatry ; 52(2): 110-2, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20838497
6.
Indian J Psychiatry ; 51(3): 171-2, 2009.
Article in English | MEDLINE | ID: mdl-19881043
7.
Indian J Psychiatry ; 51(2): 82-4, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19823624
8.
Indian J Psychiatry ; 51(1): 9-11, 2009 Jan.
Article in English | MEDLINE | ID: mdl-19742188
9.
Indian J Psychiatry ; 51(4): 244-6, 2009.
Article in English | MEDLINE | ID: mdl-20048447
10.
Physiol Mol Biol Plants ; 14(3): 227-34, 2008 Jul.
Article in English | MEDLINE | ID: mdl-23572890

ABSTRACT

The interaction of phosphoenolpyruvate carboxylase (PEPC) with a compatible solute, PEG-6000, was examined using crude leaf extracts as well as the purified protein from leaves of Amaranthus hypochondriacus, a NAD-malic enzyme type C4 plant. The inclusion in the assay medium of PEG-6000 stimulated the activity of purified PEPC by about 2.5-fold over control. The addition of PEG during both extraction and assay, stimulated PEPC activity by almost 5.0 fold in crude extracts. The stimulation by PEG of the dark-form of PEPC (2.4 fold) was more than that of the light-form (1.7 fold). Gel filtration of PEPC in leaf extracts on Sephadex G-200, showed the existence of three different oligomeric forms: tetramer, dimer and monomer. The exclusion of PEG and glycerol during extraction and elution on Sephadex resulted in a marked shift of the enzyme into dimer and/or monomer, with a very small proportion of tetramer but on the contrary, the inclusion of PEG and glycerol resulted in the enzyme maintaining predominantly a tetrameric shape. Thus, the activity and the structural properties of PEPC can be influenced by the presence or absence of compatible solutes (PEG or glycerol), obviously due to changes in the microenvironment of the enzyme.

11.
Indian J Psychiatry ; 50(2): 83-4, 2008 Apr.
Article in English | MEDLINE | ID: mdl-19742214
12.
Indian J Psychiatry ; 50(3): 158-60, 2008 Jul.
Article in English | MEDLINE | ID: mdl-19742232
13.
Indian J Psychiatry ; 50(1): 5-6, 2008 Jan.
Article in English | MEDLINE | ID: mdl-19771298
14.
Indian J Psychiatry ; 50(4): 238-40, 2008 Oct.
Article in English | MEDLINE | ID: mdl-19823606
15.
Indian J Psychiatry ; 49(3): 149, 2007 Jul.
Article in English | MEDLINE | ID: mdl-20661373
16.
Indian J Psychiatry ; 49(3): 150-3, 2007 Jul.
Article in English | MEDLINE | ID: mdl-20661374
17.
Indian J Psychiatry ; 49(4): 227, 2007 Oct.
Article in English | MEDLINE | ID: mdl-20680131
18.
Indian J Psychiatry ; 49(4): 228-30, 2007 Oct.
Article in English | MEDLINE | ID: mdl-20680132
19.
Indian J Psychiatry ; 48(3): 177-80, 2006 Jul.
Article in English | MEDLINE | ID: mdl-20844648
20.
Convuls Ther ; 4(1): 81-83, 1988.
Article in English | MEDLINE | ID: mdl-11940945

ABSTRACT

Thirty-two endogenous depressed patients (RDC) were treated with electroconvulsive therapy. Four patients (12.5%) developed a transient manic reaction; in two cases, this reaction occurred in mid-depression. Mania is not a generally recognized side effect of ECT; we detail the clinical characteristics, but fail to define clinical predictors of vulnerability.

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