Cmos Cells
Mostrando 13-24 de 48 artigos, teses e dissertações.
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13. Quaternary digital to analog converter / Conversor digital quaternario para analogico
In this work is presented the multiple value logic as option to substitute or to be used as interface with the binary logic. The multiple value logic differs of the classic binary logic to the fact that its digits are beyond zeros and ones. Using the multiple logic value obtains communication in between blocks or with the external world to one chip with less
Publicado em: 2005
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14. "Implementação monolitica de uma rede neural para assistencia em equalização adapatativa de sinais"
The design and test of a Kohonen neural network VLSI ASIC for adaptive signal equalization purposes is presented. The ASIC is used in the decision stage of a DFE (Decision Feedback Equalizer) and QAM (Quadrature Amplitude Modulation) with 16 symbols was considered. A comparative study of this adaptive equalizer and conventional types was done. The ASIC was f
Publicado em: 1999
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15. PROJETO DE CÉLULAS CMOS ANALÓGICAS DE BAIXO CONSUMO A PARTIR DE TRANSISTORES OPERANDO EM INVERSÃO FRACA / DESIGN OF LOW POWER ANALOG CMOS CELLS FROM TRANSISTORS BIAS IN WEAK INVERSION
A indústria eletrônica tem apresentado uma demanda crescente pela fabricação de aparelhos onde o baixo consumo de energia é uma das características mais importantes. Como exemplo, temos os telefones celulares, os computadores pessoais portáteis e os implantes biomédicos. Este trabalho investiga o projeto e o layout de células analógicas de consumo
Publicado em: 1996
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16. Distinct developmental patterns of c-mos protooncogene expression in female and male mouse germ cells.
The protooncogene c-mos is expressed in murine reproductive tissues, producing transcripts of 1.7 and 1.4 kilobases in testis and ovary, respectively. In situ hybridization analysis of c-mos expression in histological sections of mouse ovaries revealed that oocytes are the predominant if not exclusive source of c-mos transcripts. c-mos transcripts accumulate
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17. Identification of a negative regulatory element that inhibits c-mos transcription in somatic cells.
We have used transient expression assays to identify a cis-acting region in the 5' flanking sequence of murine c-mos which, when deleted, allows expression from the c-mos promoter in NIH 3T3 cells. This negative regulatory sequence, located 400 to 500 nucleotides upstream of the c-mos ATG, also inhibited expression from a heterologous promoter. In addition t
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18. Expression of c-mos RNA in germ cells of male and female mice.
We have investigated the cell types in mouse testis and ovary in which the c-mos protooncogene is normally transcribed. Blot hybridization analysis of electrophoretically fractionated RNAs from testes of mice with defects in germ-cell development and from prepubertal and adult mice indicated that c-mos was transcribed during male germ-cell development. Analy
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19. Identification of a candidate c-mos repressor that restricts transcription of germ cell-specific genes.
The c-mos proto-oncogene is specifically expressed in female and male germ cells. Previous studies identified a negative regulatory element (NRE) upstream of the c-mos promoter that suppresses c-mos transcription in transfected NIH 3T3 cells. In this study, we used gel shift assays to detect proteins in nuclear extracts of NIH 3T3 cells that bind to the c-mo
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20. Microinjection of antisense c-mos oligonucleotides prevents meiosis II in the maturing mouse egg.
Injection of antisense oligonucleotides was used to investigate the function of c-mos in murine oocytes. Oocytes injected with antisense c-mos oligonucleotides completed the first meiotic division but failed to initiate meiosis II. Instead, loss of c-mos function led to chromosome decondensation, reformation of a nucleus after meiosis I, and cleavage to two
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21. Cellular Moloney murine sarcoma (c-mos) sequences are hypermethylated and transcriptionally silent in normal and transformed rodent cells.
Moloney murine sarcoma virus carries an oncogenic sequence (v-mos) which is homologous to a single copy gene (c-mos) present in the normal cells of several vertebrate species. Because of the possible significance of c-mos sequences in normal development and malignant transformation induced by physical or chemical agents, we have examined the state of integra
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22. Evidence for the involvement of the proto-oncogene c-mos in mammalian meiotic maturation and possibly very early embryogenesis.
The c-mos proto-oncogene exists as a maternal mRNA in mammalian oocytes, in that it has been shown to accumulate in mouse oocytes during the growth phase and to be present at high levels in fully grown oocytes. The function of c-mos during the subsequent development of the oocytes and embryos was examined by determining the fate of the oocyte c-mos mRNAs by
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23. Chicken homolog of the mos proto-oncogene.
We compared the sequence and properties of the chicken mos homolog with the previously characterized mouse and human c-mos genes. Sequence analysis revealed one major open reading frame of 1,047 base pairs encoding a protein of 349 amino acids. Both the nucleotide sequence and the deduced amino acid sequence showed 62% overall homology to mouse and human c-m
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24. Mouse c-mos oncogene activation is prevented by upstream sequences.
Although the molecularly cloned mouse c-mos oncogene locus can be efficiently activated by insertion of a retroviral long terminal repeat (LTR) 5' to its coding region, only low-frequency transformation occurs with the LTR element inserted 3' to this region. Analysis of several of the latter transformed cell lines suggested that loss of 2 kilobases (kb) of n