<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.7//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd">
<ArticleSet>
<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>5</Volume>
				<Issue>3</Issue>
				<PubDate PubStatus="epublish">
					<Year>1994</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>COMPARISON OF SEED PROTEINS
ELECTROPHORESIS OF EIGHT SPECIES
OF THE GENUS SUAEDA (CHENOPODIACEAE)
IN IRAN</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31187</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>Seed proteins of eight species of the genus Suaeda (Chenopodiaceae) were
compared by means of polyacrylamide disc gel electrophoresis. Different
samples of the same species showed not less than 89% similarities, and
geographical separation had no remarkable effect on seed protein patterns of the
same species. Morphological heterogenity, that creates difficulties in
infrageneric classification, was also evident in clustering analysis of protein
bands. S. microsperma, which is morphologically very close to S. acuminata,
was found a great distance away from any other species</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31187_b2934262a65d2f051397cc8390f51dc9.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>5</Volume>
				<Issue>3</Issue>
				<PubDate PubStatus="epublish">
					<Year>1994</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>VARIATIONS OF GLUCOSE 6-PHOSPHATE
DEHYDROGENASE ACTIVITY IN VARIOUS
TISSUES INDUCED BY METABOLIC
ALKALOSIS, ACIDOSIS AND DIABETES</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31188</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>The effects of chronic metabolic acidosis, alkalosis and alloxan-induced
ketoacidosis on G6PD activity of rat kidney, liver and erythrocytes were
studied. Metabolic acidosis significantly increased the activity of kidney
enzyme (55%) but decreased the liver (43%) and erythrocyte (38%) enzyme
activities. Alkalosis did not make a significant change in the kidney or liver
enzyme activity but slightly decreased that of the erythrocyte enzyme. In
alloxan-induced diabetic rats, the rise in G6PD activity of kidney (69%) was
associated with a decline in the enzyme activities of liver (50%) and
erythrocytes (51%). It is suggested that in alloxan-induced diabetes,
ketoacidosis is mainly responsible for the change in G6PD activity of various
tissues and different organs do not respond similarly toward metabolic acidosis
or alkalosis.</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31188_735f505f81a75048db0947fe995b58e9.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>5</Volume>
				<Issue>3</Issue>
				<PubDate PubStatus="epublish">
					<Year>1994</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>EFFECTS OF SOME NOVEL ASCORBIC
ACID-METAL COMPLEXES ON SELECTED
BACTERIAL AND FUNGAL SPECIES</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31189</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>The antimicrobial activity of some novel ascorbic acid-metal complexes
[bisascorbate complexes of copper (II), zinc(II), manganese (11), iron (111),
cobalt(II), lead(II) and cadmium(II)] was investigated. Four standard strains of
bacterial species - Staphylococcus aureus, Escherichia coli, Bacillus subtilis
and Klebsiella pneumonia and four fungal species - Trichophyton sp.
Penicillium sp., Aspergillus flavus and Aspergillus niger were used for the
investigation. The activities of pure ascorbic acid are compared with the
complexes. Generally, percentage inhibition of ascorbic acid on fungal species
was the greatest among all compounds tested. The complexes have little or no
activity on the bacterial species studied. The latter suggests that ascorbic acid
complexation can perhaps be a possible mechanism for the prevention of heavy
metal poisoning in biological systems</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31189_c9d0389bac9d234bd66c88ef7be066d0.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>5</Volume>
				<Issue>3</Issue>
				<PubDate PubStatus="epublish">
					<Year>1994</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>PREPARATION AND MOLECULAR
STRUCTURE OF 2-BENZYLAMINOPYRIDINE COPPER(1) COMPLEX</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31190</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>2-Benzylaminopyridine (HBAP) reacts with NaH in THF and generates the
sodium salt (NaBAP). Further reaction of [Cu(TMEDA) ] [CuCl ] with one
equivalent of this ligand in THF leads to the formation of a dimeric Cu(1)
complex, [Cu (BAP)]  . H 0. The molecular structure has been determined by
using a single-crystal X-ray diffraction method. The yellow compound
crystallizes in the monoclinic space group P2 lc with four molecules per unit
cell. The unit cell dimensions are a = 8.090(4), b = 1 1.220(7), c = 22.412(8)?
with ?=91.3 l(3)?. The final R value is 0.065 for 3859 reflections measured.
Coordination number around each copper is two (nearly linear). The Cu ... Cu
distance is 2.4558(16) ? .</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31190_68c7db132a6299fb17d7ff6bc384a52f.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>5</Volume>
				<Issue>3</Issue>
				<PubDate PubStatus="epublish">
					<Year>1994</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>COMPLEXES OF LEAD (II)*: CRYSTAL
STRUCTURES OF L2Pb (NO,), AND L2Pb(SCN),
L=Z(AMINOMETHYL) PYRIDINE</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31191</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>The reactions of Pb(N0 )   and Pb(SCN)2 with 2-(aminomethy1)pyridine
(C H N  = L) yielded colourless crystals of L Pb(N0 )   ( I ) and L Pb(SCN)  ,
(2), respectively. Their structures were determined by X-ray crystallography.
Crystal data: 1, monoclinic, P2 /c, a = 9.263 (4) ?, b = 7.783 (2) ?, c = 6.692
(3) ?, ? = 101.26 (2)?, Z = 2, Mo K?, 1540 observed (I &gt; 2.5 ?(I) data (22 ? C),
R = 0.038; 2, monoclinic P2 /c, a = 10.010 (3) ?, b = 8.212 (10) ?. c = 11.010
(5) ?, ?= 94.26 (5) ?, Z = 2, Mo K? 1856 observed (I &gt; 2.5 ? ( I )) data (22 ?  C), R
= 0.040</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31191_f9827b6430547fd3f2c94fabf299fb97.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>5</Volume>
				<Issue>3</Issue>
				<PubDate PubStatus="epublish">
					<Year>1994</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>SYNTHESIS OF SOME IMIDAZO [ I , 2-b] [l , 2,4]
TRIAZINE AND N-ALKYLATED IMIDAZO
[l , 2-b] [1 , 2,4]-TRIAZINES</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31192</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>A number of 3-amino-1, 2, 4-triazin-5 (2H)- ones(1) were synthesized and
condensed with a-haloketones to give 2,6-disubstituted imidazo [1, 2-b] [1, 2,
4]-triazin-3 (4H)-ones (2). These compounds were reacted further with a -
haloketones to yield N-alkylated products (3).</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31192_f230c4cd39d680d4cde59248861bdf9d.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>5</Volume>
				<Issue>3</Issue>
				<PubDate PubStatus="epublish">
					<Year>1994</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>SYNTHESIS OF (k) - 6,8-DIHYDROXY-3-
ISOPROPYL-7-METHYLISOCHROMAN</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31193</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>The title isochroman ( 8 ) was synthesized as a suitable substrate for
acetoxylation studies leading to an intermediate of type (4), expected to afford,
on condensation with diketen, the fungal metabolite &quot;rotiorin&quot; type linear
product (1). Cyclocondensation of alcohol (6), obtained by the reduction of
ketone (5) with paraform in the presence of anhydrous aluminum chloride
afforded the dimethoxyisochroman (7). Demethylation of (7) using boron
tribromide in dichloromethane furnished the title isochroman (8).</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31193_d7524e44b42e52a688f6b5cc14bb3006.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>5</Volume>
				<Issue>3</Issue>
				<PubDate PubStatus="epublish">
					<Year>1994</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>KINETIC SPECTROPHOTOMETRIC
DETERMINATION OF MERCURY IN
DIFFERENT MATERIALS BASED ON ITS
INHIBITORY EFFECT ON THE BRILLIANT
GREEN-SULFITE REACTION</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31194</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>A new kinetic method for the determination of Hg(II) based on its inhibitory
effect on the Brilliant green-sulfite reaction at pH 6.5 is proposed. The reaction
is followed spectrophotometrically at 615 nm by measuring the change in
absorbance at the fixed time of 3.5 min after the initiation of the reaction. Both
the influence of the reaction variables and the interference of many ions have
been studied. Under the selected experimental conditions, Hg(II) was
determined in the range 5.0 - 1300 ng.ml . The method was applied to the
determination of mercury in cleaning solutions for contact lenses and in
industrial waste water</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31194_b6622e4ef1a8d811316fe50fd2975faf.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>5</Volume>
				<Issue>3</Issue>
				<PubDate PubStatus="epublish">
					<Year>1994</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>ON THE LIFTS OF SEMI-RIEMANNIAN
METRICS</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31195</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>In this paper, we extend Sasaki metric for tangent bundle of a Riemannian
manifold and Sasaki-Mok metric for the frame bundle of a Riemannian
manifold [I] to the case of a semi-Riemannian vector bundle over a semi-
Riemannian manifold. In fact, if E is a semi-Riemannian vector bundle over a
semi-Riemannian manifold M, then by using an arbitrary (linear) connection on
E, we can make E, as a manifold, into a semi-Riemannian manifold. When the
metric of the vector bundle E is parallel with respect to the chosen connection,
we compute the Levi-Civita connection of E, its geodesics, and its curvature
tensors. We also show that the sphere and pseudo-sphere bundles of E are nondegenerate
submanifolds of E, and we shall compute their second fundamental
forms. We shall also prove some results on the metric of E</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31195_16a153a27394122922a55fb102f602e3.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>5</Volume>
				<Issue>3</Issue>
				<PubDate PubStatus="epublish">
					<Year>1994</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>ROTATIONAL ASSIGNMENT OF NEW BANDS
IN THE NO , EXCITATION SPECTRUM IN THE
SPECTRAL RANGE OF 15600 cm  TO 15633 cm</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31196</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>Sub-Doppler excitation spectroscopy in a collimated cold supersonic beam
of 5% NO  seeded in argon has been performed with a spectral resolution down
to 10 MHz for four vibronic bands within the perturbed  B  ?X  A  system of
NO . The rotational temperature of about 15 K achieved by adiabatic cooling
allows the separation of closely lying vibronic bands which overlap in absorption
spectra taken at room temperature and which therefore could not be iden$-
fied from the broad band excitation measurements</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31196_6a6a73c9c5eecb746b0ab4c888939818.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
