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EN
Duplication of the inferior vena cava (IVC) is the most common anomaly to affect the vena cava. Variations in the IVC are diagnosed in routine dissection studies, in retroperitoneal surgeries, or in computerised tomography (CT) sections ordered for various reasons. In this paper we present two cases of a double IVC together with the CT findings. The duplication might have occurred during embryological development. Although venous anomalies are rare, they have particular importance with respect to the interruptions that may occur during retroperitoneal and thoracic surgery or in the treatment of thrombo-embolic disease.
EN
In this paper, we introduce the concept of monochromatic kernel-perfect digraph, and we prove the following two results: (1) If D is a digraph without monochromatic directed cycles, then D and each $α_v,v ∈ V(D)$ are monochromatic kernel-perfect digraphs if and only if the composition over D of $(α_v)_{v ∈ V(D)}$ is a monochromatic kernel-perfect digraph. (2) D is a monochromatic kernel-perfect digraph if and only if for any B ⊆ V(D), the duplication of D over B, $D^B$, is a monochromatic kernel-perfect digraph.
EN
The translation of poetry has caused many debates because the translator is seen as a re-creator of the text and his work becomes « poetry en abyme ». Poetry is difficult to translate because of its conciseness and intertextual dynamics. The translator’s work supposes a comparative perspective and an analysis of the text’s peculiarities. Among the translation methods employed, one can identify duplication, i.e., strict and faithful reproduction in the target language, transposition, the creation of an effect similar to the original one, and dialogic analysis. The poetics of translation will be adapted to the features of each poem.
FR
La traduction de la poésie a suscité des débats parce que le traducteur est vu comme re-créateur du texte, comme poète en abyme. La poésie est difficile à traduire à cause de sa concision et de sa dynamique intertextuelle. La démarche traductologique suppose une perspective comparative et une analyse des particularités du texte. En tant que procédés de traduction, on identifie la duplication, qui est la reproduction rigoureuse et fidèle dans la langue cible, la transposition, la création d’un effet comparable à celui original et l’analyse dialogique. La poétique du traduire sera adaptée aux particularités de chaque poème.
EN
Completion of rice genome sequencing has necessitated identification of transcripts encoded by the genome and their corresponding functions. In the present study we have catalogued cytoplasmic ribosomal protein complement of rice genome corresponding to 68 families. Mining TIGR (The Institute for Genomic Research) rice database and unigene sequences available from National Centre for Biotechnology Information (NCBI) produced a non-redundant set of these sequences. This resulted in identification of 209 candidate r-proteins of which 22 have not been reported previously. The number of genes per family ranges from 1 to 8 distributed throughout the genome with maximum occurrence at chromosome 7. Mapping of r-proteins on BAC clones revealed several small clusters of genes. Unigene sequences correspondtng to most of the reported r-proteins were identified indicating these genes are being expressed.
EN
Folds of the meningeal layer of the dura mater, the falx cerebri and tentorium cerebelli, traverse the vertebrate intracranial cavity and thus compartmentalise the brain. The falx cerebelli, another dural fold, is found in the posterior cranial fossa and attaches to the inferior aspect of the tentorium cerebelli and to the internal occipital crest. We present a case of a duplicated falx cerebelli, occipital venous sinus and internal occipital crest that was detected upon routine dissection of a male cadaver. Since haemorrhage of a dural venous sinus can be a fatal complication of posterior cranial fossa surgery, knowledge of venous sinus variations in this region may prevent unpredictable complications during intracranial procedures.
7
Content available Biogeneza centrioli
63%
Kosmos
|
2018
|
tom 67
|
nr 1
163-170
PL
Centriole są mikrotubularnymi strukturami wchodzącymi w skład centrosomu, występującymi u zwierząt. Struktury te pełnią istotne funkcje zarówno podczas interfazy i mitozy komórek proliferujących, jak i w zróżnicowanych komórkach, włączając nabłonki orzęsione. Liczba centrioli w komórce jest ściśle kontrolowana, gdyż ich nadmiar lub niedobór prowadzi do zaburzeń podziału komórkowego lub funkcjonowania komórek. Centriole powstają w procesie zwanym biogenezą lub duplikacją. W komórkach proliferujących centriole są powielane jeden raz, podczas gdy w komórkach nabłonków orzęsionych dochodzi do namnożenia większej ich liczby, co związane jest z odmiennym mechanizmem powielania tych organelli. W procesie tzw. "klasycznej" duplikacji, zwanej też "centriolarną", która ma miejsce w komórkach dzielących się, dochodzi do wytworzenia dwóch nowych centrioli. Z kolei podczas tzw. duplikacji "deuterosomalnej", w różnicujących komórkach nabłonków orzęsionych wytwarzanych jest nawet kilkaset centrioli.
EN
Centrioles are microtubule-based organelles that in animal cells are a part of the centrosome. These structures play an important role during both interphase and mitosis in proliferating cells, as well as in differentiated cells, including ciliation of epithelial cells. The number of centrioles is strictly regulated as their excess or reduction leads to abnormalities in cell division or cell functions. Centrioles are formed in a process called biogenesis or duplication. In proliferating cells, centrioles are duplicated only once in each cell cycle, while in epithelial cells before ciliation, numerous centrioles are assembled, suggesting different mechanisms of duplication. During the so-called "classic" or "centriolar" duplication, in proliferating cells two new centrioles are formed before mitosis. By contrast, during differentiating into ciliated epithelial cells even few hundreds of new centrioles are assembled (so-called "deuterosomal" biogenesis).
EN
We report on a 13-month-old girl showing dysmorphic features and a delay in psychomotor development. She was diagnosed with a balanced de novo translocation 46,X,t(X; 13)(p 11,2; p 13) and non-random inactivation of the X chromosome. FISH analysis, employing the X chromosome centromere and XIST-region-specific probes, showed that the XIST locus was not involved in the translocation. Selective inactivation of paternal X, which was involved in translocation, was revealed by the HUMARA assay. The pattern of methylation of 5 genes located within Xp, which are normally silenced on an inactive X chromosome, corresponded to an active (unmethylated) X chromosome. These results revealed that in our proband the X chromosome involved in translocation (Xt) was preferentially inactivated. However, genes located on the translocated Xp did not include XIST. This resulted in functional Xp disomy, which most probably accounts for the abnormal phenotype in our patient.
EN
Chaetognaths constitute a small marine phylum of approximately 120 species. Two classes of both 18S and 28S rRNA gene sequences have been evidenced in this phylum, even though significant intraindividual variation in the sequences of rRNA genes is unusual in animal genomes. These observations led to the hypothesis that this unusual genetic characteristic could play one or more physiological role(s). Using in situ hybridization on the frontal sections of the chaetognath Spadella cephaloptera, we found that the 18S Class I genes are expressed in the whole body, with a strong expression throughout the gut epithelium, whereas the expression of the 18S Class II genes is restricted to the oocytes. Our results could suggest that the paralog products of the 18S Class I genes are probably the “housekeeping” 18S rRNAs, whereas those of class II would only be essential in specific tissues. These results provide support for the idea that each type of 18S paralog is important for specific cellular functions and is under the control of selective factors.
EN
Screening of male gametophytie mutants from the Versailles collection of T-DNA transformants allowed us to isolate and characterize two novel genes: KINKY POLLEN (KIP) and POKY POLLEN TUBE (POK), which are required for correct tip growth in Arabidopsis thaliana. As KIP and POK are expressed in all plant tissues, though to a higher level in pollen and roots, their roles may not be restricted to tip growth only, but might extend to more general elongation mechanisms. Both genes are duplicated in the Arabidopsis genome. Specific roles for each duplicate, indicated by mutant phenotypes, will be discussed. Moreover, KIP and POK proteins have putative orthologs in all eukaryotes investigated, suggesting that they may be crucial proteins required for correct polar growth in all eukaryotic species.
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