<?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>9</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>1998</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>DETERMINATION OF PHYLOGENlETIC ALLIES
IN SOME SPECIES OF CROCUS IN IRAN
THROUGH THE STUDY OF SOLUBLE
PROTEINS, PEROXIDASES AND POLYPHENOL
OXUDASES</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31476</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>The taxonomic affinity of six species of Crocus (C, cancellatus subsp. Damascenus 
C. almehensis, C. gilanicus, C. sativus, C.pallassi subsp. haussknechtii,C. speciosus subsp. speciosus) from Iran were studied usingdifferent electrophoresis techniques.
The similarity index of the species was computed by comparison of protein bands of -
Corm and seed tissues, and the related dendrogms of affinity dies were drawn. The
local populations of C. cancellatus constitute the first cluster of dendrogram and
along with autumnal species form a common cluster. C. almehensis, which in contrast  to other species is vernal, joined them at a farther distance</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31476_78147341bba904f5b3f3c6123055a974.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>9</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>1998</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>APPLICATION OF TWO-DIMENSIONAL
ELECTROPHORESIS AND NIH 3T3 CELL
TRANSFECTION ASSAY IN THE STUDY OF
TUMOR-AS SOCIATED PROTEINS AND
GENOMIC DNA TUMOROGENICITY IN
MALIGNANT HUMAN ESOPHAGEAL
SPECIMENS</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31477</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>Total protein and DNA extracted from histologically diagnosed normal
nonmalignant and esophageal tumor tissues were used for analysis of polypeptides
pattern by two-dimensional gel electrophoresis and DNA transforming activity in
NIH 3T3 cell transfection assay, respectively. In comparison to normal tissues, eight
polypeptides underwent down-regulation or disappeared, while seven polypeptides
were subjected to up-regulation or appeared for the first time in tumor tissues. We
suggest that the first eight polypeptides are necessary for maintenance of normal
phenotype and the other seven polypeptides are involved in the development of
malignant phenotype. However, results obtained from NIH 3T3 cell transfection with
esophageal tumorous DNA showed that such DNAs lack transforming efficiency.
These data may agree with the published reports about the absence of activated
transforming oncogenes such as the ras family in esophageal cancer specimens</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31477_9dfe9454b8b6c1b80bbb33fb12e890af.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>9</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>1998</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>KINETIC DETERMINATION OF ASCORBIC ACID
a WITH SPECTROPHOTOMETRIC DETECTION</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31478</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>A simple and rapid method has been developed for the determination of ascorbic
acid in fruit and pharmaceutical products. The method is based on the measurement
of the reaction rate between ammonium molybdate and ascorbic acid in acidic media.
The reaction was monitored spectrophotometrically at 800 nm by fixed-time and
variable-time methods. The calibration graph was linear in the range of 5 0 ×1 0 -
6.0 ×10  M ascorbic acid when using a fixed-time method. The relative standard
deviation for ten replicate analyses is 2.7% for 5.0 × 10  a scorbic acid. The limit of
detection is 2.0×10 M. T he effect ofvarious species was studied for this determination.</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31478_dee7539590036bbddca5ab8fc0b8357e.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>9</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>1998</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>SPECTROPHOTOMETRIC STUDY OF THE
THERMODYNAMICS AND KINETICS OF
CHARGE-TRANSFER COMPLEXATION OF
DIBENZO- 18-CROWN-6 WITH IODINE IN
CHLOROFORM SOLUTION</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31479</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>The charge-transfer complexation reaction between iodine and dibenzo- 18-crown-
6 (DB18C6) has been studied spectrophotometrically in chloroform solution at
different temperatures. The resulting donor-acceptor complex was formulated as
(DB 18C6…I )I . The spectrophotometric results , as well as the conductivity
measurements, indicated that the gradual release of tiiodide ion from its contact ion
paired form, in the molecular complex, into the solution is the rate determining step
of the reaction. The rate constants at various temperatures and the activation
parameters E , ?H  and AS  were calculated. The enthalpy and entropy of the complex
formation reaction were evaluated from the temperature dependence of the formation
constant. It was found that the resulting charge-transfer complex is both enthalpy and
entropy stabilized.</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31479_4467c5ebcc8206601625e713d31605f9.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>9</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>1998</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>AROMATIZATION OF 1 , CDIHYDROPYRIDINES
WITH OXYGEN OR AIR USING MANGANESE
AND COBALT SALTS OF p-AMINOBENZOIC
ACID SUPPORTED ON SILICA GEL AS
OXIDIZING CATALYSTS</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31480</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>Hantzsch 1,4-dihydropyridines are oxidized to the corresponding pyridine
derivatives using oxygen or air and a mixture of the manganese and cobalt salts of parninobenzoic
acid supported on silica gel as the catalysts. Reactions are clean and the
catalysts can be recovered easily and reused repeatedly.</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31480_87688e644bd630526fedd4f22613cef9.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>9</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>1998</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>REACTIONS OF DIHYDROPYRIDINES
WITH BENZYNE</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31481</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>Reactions  of 1 ,Zdihydropyridines (la-c) and 1,4-dihydropyridines  (2a-c) in the
presence of benzyne (3) under thermal conditions, and in the case of (2c) under
photochemical conditions, have been investigated. Benzyne acts as an oxidizing
agent to convert dihydropyridine (la) and (2a) to the corresponding pyridine (4) or
adds as a dienophile to (lb-c).</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31481_5a897c4ac62db0e169de0b47ae9c2842.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>9</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>1998</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>PHY SICO-CHEMICAL CHARACTERISTICS OF
MINERALIZING FLUIDS AT THE KAMARMEHDI
MINE, TABAS REGION, IRAN</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31482</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>The data obtained from field and geothermometric studies and also the REE
composition of fluorites associated with lead mineralization at the Kamar-Mehdi
mine are compatible with a structurally controlled, fissure filling, epigenetic,
hydrothermal origin. Homogenization and last ice melting temperatures for primary
fluid inclusions trapped in fluorite crystals indicate that the mineralization of fluorite
and the associated (cogenetic ?) lead has taken place over a temperature range of 1 15-
125OC. The mineralizing fluids were dilute and do not show any apparent change in
temperature and salinity with depth. Salinities of inclusion fluids range from 0.7 to
3.7 equivalent wt.% NaCl, and Na/Ca atomic ratio of inclusion leachates is low with
all leachates containing appreciable amounts of K and Mg. The daughter minerals are
mostly Ca, K, Al, Si, C1 phases</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31482_a65f1a3b683798dfd16d5850525c7b8e.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>9</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>1998</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>CHEBYSHEV SUBALGEBRAS OF
JB-ALGEBRAS</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31483</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>In this note, we characterize Chebyshev subalgebras of unital JB-algebras. We
exhibit that if B is Chebyshev subalgebra of a unital JB-algebra A, then either B is a
trivial subalgebra of A or A= H   R .l, where H is a Hilbert space</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31483_d04853731ce0790af8fbd9de5c37c8c1.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>9</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>1998</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>SOME POINTS ON CASIMIR FORCES</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31484</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>Casimir forces of massive ferrnionic Dirac fields are calculated for parallel plates
geometry in spatial space with dimension d and imposing bag model boundary
conditions. It is shown that in the range of ma&gt;&gt;l where m is mass of fields quanta
and a is the separation distance of the plates, it is equal to massive bosonic fields
Casimir force for each degree of freedom. We argue this equality exists for any
massive anyonic field in two-dimensional spatial space. Also the ratio of massless
ferrnionic field Casimir force to its bosonic correspondent in d-dimensional spatial
spaceis (1- )</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31484_bbd230052c26e38339105b7d1af05990.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>9</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>1998</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>EEDF MEASUREMENTS AND EXCITATION
PROCESSES IN THE VICINITY OF A HELIUM
DISCHARGE CONSTRICTION</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31485</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		<Abstract>Axial distributions of plasma and floating potentials, electron number density and
the electron energy distribution function (EEDF) have been measured in the double
layer (DL) region of an He discharge constriction. Excitation processes in the
constriction region are studied. Using a linearization method for the nonstationary
balance equations and choosing appropriate discharge conditions, the step excitation
rate by electron impact for the 2 S   3 D  transition in He is determined</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31485_3ff5ad8918b875387908967a23b9a8d4.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
