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  • 1
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    Skin tumor-promoting activity of benzoyl peroxide, a widely used free radical-generating compound (1981)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1981-08-28
    Description: Benzoyl peroxide, a widely used free radical-generating compound, promoted both papillomas and carcinomas when it was topically applied to mice after 7,12-dimethylbenz[a]anthracene initiation. Benzoyl peroxide was inactive on the skin as a complete carcinogen or as a tumor initiator. A single topical application of benzoyl peroxide produced a marked epidermal hyperplasia and induced a large number of dark basal keratinocytes, effects similar to those produced by the potent tumor promoter 12-O-tetradecanoyl phorbol-13-acetate. Benzoyl peroxide, like other known tumor promoters, also inhibited metabolic cooperation (intercellular communication) in Chinese hamster cells. In view of these results caution should be recommended in the use of this and other free radical-generating compounds.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Slaga, T J -- Klein-Szanto, A J -- Triplett, L L -- Yotti, L P -- Trosko, K E -- CA 21104/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1981 Aug 28;213(4511):1023-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6791284" target="_blank"〉PubMed〈/a〉
    Keywords: 9,10-Dimethyl-1,2-benzanthracene ; Animals ; *Benzoyl Peroxide ; *Cocarcinogenesis ; Free Radicals ; Mice ; Neoplasms, Experimental ; *Peroxides ; Skin Neoplasms/*chemically induced ; Tetradecanoylphorbol Acetate
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Published by American Association for the Advancement of Science (AAAS)
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  • 2
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    Saliva as a chemical cue in the development of social behavior (1981)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1981-03-06
    Description: Throughout development, Mongolian gerbils engage in conspicuous naso-oral investigations of their social partners' mouth areas. The behavioral contribution of saliva-related stimuli in regulating oral-directed responses was studied during several important phases of the gerbil's social life. Weanlings were preferentially attracted to their mother's saliva, subadults at puberty preferred saliva of littermates to that of nonlittermates, and sexually experienced males preferred the saliva of estrous females to that of nonestrous females. The use of saliva as a discriminative cue during various developmental periods suggests that oral chemostimuli have a perennial role in regulating social interchanges.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Block, M L -- Volpe, L C -- Hayes, M J -- R03MH 27346/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1981 Mar 6;211(4486):1062-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7466378" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Suckling/physiology ; Behavior, Animal/*physiology ; Female ; Gerbillinae/*physiology ; Male ; Maternal Behavior ; Saliva/*physiology ; *Social Behavior
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Published by American Association for the Advancement of Science (AAAS)
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  • 3
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    Genetically determined deficiency of the third component of complement in the dog (1981)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1981-06-05
    Description: A genetically determined deficiency of the third component of complement (C3) has been identified in a colony of Brittany spaniels. Immunochemical methods show no detectable C3 in the serum of the affected dogs, and there is no evidence of an inhibitor of C3 in the serum. The C3 deficiency appears to be transmitted as an autosomal recessive trait.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Winkelstein, J A -- Cork, L C -- Griffin, D E -- Griffin, J W -- Adams, R J -- Price, D L -- AI-11637/AI/NIAID NIH HHS/ -- NS-10580/NS/NINDS NIH HHS/ -- RR-00130/RR/NCRR NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1981 Jun 5;212(4499):1169-70.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7233211" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Complement C3/deficiency/*genetics ; Dog Diseases/genetics ; Dogs ; Female ; Genes, Recessive ; Heterozygote Detection ; Homozygote ; Male ; Muscular Atrophy/genetics/veterinary ; Pedigree
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 4
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    Male vole urine changes luteinizing hormone-releasing hormone and norepinephrine in female olfactory bulb (1981)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1981-05-01
    Description: Female prairie voles (Microtus ochrogaster) exposed to a single drop of male urine on the upper lip showed changes in concentrations of luteinizing hormone-releasing hormone (LHRH) and norepinephrine in olfactory bulb tissue; no such changes occurred in dopamine concentration. The changes were measured in the posterior but not the anterior olfactory bulb tissue of females within 1 hour after they were exposed to urine. These females also showed rapid increases in serum concentrations of luteinizing hormone. Females exposed to water on the upper lip showed none of these changes. These results suggest that in this species LHRH and norepinephrine in the olfactory bulb may mediate luteinizing hormone release in response to external (pheromonal) chemical cues.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dluzen, D E -- Ramirez, V D -- Carter, C S -- Getz, L L -- HDO9328/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 1981 May 1;212(4494):573-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7010608" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arvicolinae/*physiology ; Estrus ; Female ; Gonadotropin-Releasing Hormone/*metabolism ; Humans ; Luteinizing Hormone/blood ; Male ; Norepinephrine/*metabolism ; Olfactory Bulb/*metabolism ; Pheromones/*urine ; Pregnancy ; Reproduction ; Rodentia/*physiology ; Stress, Psychological/physiopathology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Published by American Association for the Advancement of Science (AAAS)
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  • 5
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    Inherited primary hypothyroidism in mice (1981)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1981-04-03
    Description: A new autosomal recessive mutation that causes hypothyroidism has been identified in mice. The gene, herein named hypothyroid (hyt), has been mapped on chromosome 12 approximately 30 units from the centromere. The mutants are characterized by retarded growth, infertility, mild anemia, elevated serum cholesterol, very low to undetectable serum thyroxine, and elevated serum thyroid-stimulating hormone. Thyroid glands are in the normal location but are reduced in size and hypoplastic. Mutant mice respond to thyroid hormone therapy by improved growth and fertility. These findings suggest that the hyt mutant gene results in primary hypothyroidism unresponsive to thyroid-stimulating hormone.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Beamer, W J -- Eicher, E M -- Maltais, L J -- Southard, J L -- AM-17947/AM/NIADDK NIH HHS/ -- NS-09378/NS/NINDS NIH HHS/ -- RR-01138/RR/NCRR NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1981 Apr 3;212(4490):61-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7209519" target="_blank"〉PubMed〈/a〉
    Keywords: Anemia/etiology ; Animals ; Cholesterol/blood ; Chromosome Mapping ; Crosses, Genetic ; Female ; Genes, Recessive ; Humans ; Hypothyroidism/blood/*genetics/veterinary ; Male ; Mice ; Mice, Mutant Strains/*genetics ; Rodent Diseases/genetics ; Thyroid Gland/pathology ; Thyrotropin/metabolism
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 6
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    Fetal female rats are masculinized by male littermates located caudally in the uterus (1981)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1981-07-10
    Description: Female rats are masculinized in utero by male littermates sharing the same uterine horn. Increased anogenital distances in neonatal females and mounting behavior in adult females are related to the presence of males on the caudal side of the females in the uterine horn. Contrary to current beliefs, interamniotic diffusion may not be responsible for the exchange of masculinizing agents among fetuses. Since uterine blood flow in the rat is from the direction of the cervix toward the ovary, masculinizing hormones secreted by fetal males may be carried via the uterine vasculature to female littermates located further downstream.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Meisel, R L -- Ward, I L -- HD-04688/HD/NICHD NIH HHS/ -- K2-MH00049/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1981 Jul 10;213(4504):239-42.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7244634" target="_blank"〉PubMed〈/a〉
    Keywords: Androgens/*physiology ; Animals ; Castration ; Estradiol/pharmacology ; Female ; Fetus/*physiology ; Male ; Posture ; Pregnancy ; Progesterone/pharmacology ; Rats ; *Sex Characteristics/drug effects ; Sexual Behavior, Animal/drug effects ; Uterus/physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 7
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    Thyrotropin-releasing hormone effects in the central nervous system: dependence on arousal state (1981)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1981-11-06
    Description: Thyrotropin-releasing hormone was microinjected into the dorsal hippocampus of ground squirrels (Citellus lateralis) when they were at different levels of arousal, as assessed by electrophysiological and behavioral criteria. When administered to the awake animal, thyrotropin-releasing hormone produced dose-dependent decreases in body temperature accompanied by behavioral quieting and reductions in metabolic rate and electromyographic activity. The magnitude of these effects was greater when the peptide was microinjected during a period of behavioral activation. In contrast, administration of the peptide during slow wave sleep produced increased thermogenesis, an increase in electromyographic activity, and an increase in the amount of electroencephalographic desynchronization.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stanton, T L -- Bechman, A L -- Winokur, A -- New York, N.Y. -- Science. 1981 Nov 6;214(4521):678-81.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6794147" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arousal/*drug effects ; Body Temperature Regulation/*drug effects ; Dose-Response Relationship, Drug ; Female ; Hippocampus/*drug effects ; Male ; Sciuridae/*physiology ; Thyrotropin-Releasing Hormone/*pharmacology ; Wakefulness/drug effects
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 8
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    Physical dependence on morphine fails to develop during the hibernating state (1981)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1981-06-26
    Description: Physical dependence on morphine occurs in a typical fashion during the active state of the mammalian hibernator Citellus lateralis, but does not occur when morphine exposure is confined to the hibernating state. Morphine exposure during hibernation can produce stereotyped behavior, thus demonstrating partial responsiveness of the central nervous system to opioids during this natural state.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Beckman, A L -- Llados-Eckman, C -- Stanton, T L -- Adler, M W -- DA-02254/DA/NIDA NIH HHS/ -- New York, N.Y. -- Science. 1981 Jun 26;212(4502):1527-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7233241" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Blood-Brain Barrier ; Female ; Hibernation/*drug effects ; Humans ; Male ; Morphine/*pharmacology ; Naloxone/pharmacology ; Sciuridae ; Substance-Related Disorders
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 9
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    Breast imaging in coronal planes with simultaneous pulse echo and transmission ultrasound (1981)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1981-12-04
    Description: Clear delineation of breast architecture was achieved with compound pulse echo ultrasound imaging in which the images were acquired in the coronal planes used for quantitative transmission ultrasonic computed tomography. Since most connective tissue planes in the breast radiate toward the nipple, compound scans from the sides of the breast record normal interfaces more consistently and reveal greater symmetries in normal portions of relatively full breasts than do conventional scans in sagittal or transverse planes. Simultaneous acquisition of the pulse echo images and images representing the local ultrasound attenuation coefficient and speed of ultrasound suggested complementary role for reflection and through-transmission images in breast cancer detection. The high quality of pulse echo images in coronal planes provides the potential for more complete pulse echo diagnosis and the basis for spatial correlation of lesions viewed in pulse echo and ultrasonic computed tomograms. These observations may permit routine ultrasonic computed tomography of the breast in the clinical setting.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Carson, P L -- Meyer, C R -- Scherzinger, A L -- Oughton, T V -- R01 CA 25323/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1981 Dec 4;214(4525):1141-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7302585" target="_blank"〉PubMed〈/a〉
    Keywords: Breast/*anatomy & histology ; Breast Neoplasms/*diagnosis ; Female ; Humans ; *Ultrasonography
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 10
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    GABA analogues activate channels of different duration on cultured mouse spinal neurons (1981)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1981-04-17
    Description: Voltage-clamp recordings from mouse spinal neurons grown in culture were used to study the membrane current fluctuations induced by 12 substances structurally similar to gamma-aminobutyric acid (GABA). Fluctuation analysis provided estimates of the electrical properties of the elementary events underlying these responses. Estimates of the mean conductance of channels activated by all of the substances except glycine did not differ significantly from that estimated for GABA, whereas mean durations of agonist-activated channels all differed significantly from that found for GABA. The results indicate that all of the substances tested except glycine activate channels of similar conductance but of different durations.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Barker, J L -- Mathers, D A -- New York, N.Y. -- Science. 1981 Apr 17;212(4492):358-61.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6259733" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Membrane/drug effects ; Ion Channels/*drug effects ; Membrane Potentials/drug effects ; Mice ; Neurons/drug effects ; Receptors, Cell Surface/metabolism ; Receptors, GABA-A ; Spinal Nerves/*drug effects ; Structure-Activity Relationship ; Time Factors ; gamma-Aminobutyric Acid/*analogs & derivatives/pharmacology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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