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K Bejaoui S Le Bozec B Maton 《European journal of applied physiology and occupational physiology》1987,56(1):97-104
Reflex EMG responses to sudden passive flexion of the elbow were recorded from anconeus and triceps brachii in 5 human volunteers. While the subjects were required not to resist the flexion movement, they were required to maintain an extension torque of 3.5 or 7.0 Nm prior to its onset. Under these isotonic conditions, the latency and amplitude of the reflex activities from anconeus and triceps brachii did not differ significantly, in contrast to the findings of Le Bozec (1986) in actively relaxed subjects. The myotatic/postmyotatic EMG amplitude ratio did not provide a further quantitative way to distinguish between these muscles. The absence of a difference between the reflex activities of a slow (anconeus) and a fast (triceps brachii) muscle is interpreted as resulting from a strong drive of spindle activity on the whole extensor motoneuron pool, which outweights the differences in recruitment due to the differing relative amounts of type I and type II fibres in the two muscles. Differences like those described between finger and calf muscles by other authors are thought to be due to the relative degree of corticalization of these muscles. All short and long latency responses of the muscles increased in magnitude and decreased in latency with increasing background EMG activity as well as with increasing initial length. The position and tonic activity dependency of these responses is explained in terms of alpha-gamma coactivation. 相似文献
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Faten Talmoudi Olfa Kilani Wiem Ayed Nizar Ben Halim Fethi Mellouli Lamia Torjmane Lamia Aissaoui Yosra Ben Youssef Lobna Kammoun Tarek Ben Othmane Mohamed Bejaoui Neila Ben Romdhane Moez Elloumi Sondes Hadiji Sofiene Hentati Imene Chemkhi Nabila Abidli Helmi Guermani Sonia Abdelhak Ahlem Amouri 《Comptes rendus biologies》2013,336(1):29-33
Fanconi anemia (FA) is a recessive chromosomal instability syndrome that is clinically characterized by multiple symptoms. Chromosome breakage hypersensitivity to alkylating agents is the gold standard test for FA diagnosis. In this study, we provide a detailed laboratory protocol for accurate assessment of FA diagnosis based on mitomycin C (MMC) test. Induced chromosomal breakage study was successful in 171 out of 205 aplastic anemia (AA) patients. According to the sensitivity of MMC at 50 ng/ml, 38 patients (22.22%) were diagnosed as affected and 132 patients (77.17%) as unaffected. Somatic mosaicism was suspected in an 11-year-old patient with a FA phenotype. Twenty-six siblings of FA patients were also evaluated and five of them (19.23%) were diagnosed as FA. From this study, a standard protocol for diagnosis of FA was developed. It is routinely used as a diagnostic test of FA in Tunisia. 相似文献
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Awatef Béjaoui Khiari Ibtissem Guériri Radhia Ben Mohammed Boutheina Ben Abdelmoumen Mardassi 《BMC microbiology》2010,10(1):6
Background
In Mycoplasma synoviae, type strain WVU 1853, a single member of the haemaglutinin vlhA gene family has been previously shown to be expressed. Variants of vlhA are expressed from the same unique vlhA promoter by recruiting pseudogene sequences via site-specific recombination events, thus generating antigenic variability. Using a bacterial stock of M. synoviae WVU 1853 that had been colony purified thrice and maintained in our laboratory at low passage level, we previously identified a vlhA gene-related partial coding sequence, referred to as MS2/28.1. The E. coli-expressed product of this partial coding sequence was found to be immunodominant, suggesting that it might be expressed. 相似文献6.
Flihi Jihène Rhimi Awatef Yangui Islem Messaoud Chokri Ben ElHadj Ali Imen 《Molecular biology reports》2022,49(7):6215-6224
Molecular Biology Reports - In Tunisia, Kermes oak (Quercus coccifera L.) populations are severely destroyed due to deforestation. Nowadays, no preservation programs are attempted, yet, to conserve... 相似文献
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Allouch A Di Primio C Alpi E Lusic M Arosio D Giacca M Cereseto A 《Cell host & microbe》2011,9(6):484-495
The integration of viral cDNA into the host genome is a critical step in the life cycle of HIV-1. This step is catalyzed by integrase (IN), a viral enzyme that is positively regulated by acetylation via the cellular histone acetyl transferase (HAT) p300. To investigate the relevance of IN acetylation, we searched for cellular proteins that selectively bind acetylated IN and identified KAP1, a protein belonging to the TRIM family of antiviral proteins. KAP1 binds acetylated IN and induces its deacetylation through the formation of a protein complex which includes the deacetylase HDAC1. Modulation of intracellular KAP1 levels in different cell types including T cells, the primary HIV-1 target, revealed that KAP1 curtails viral infectivity by selectively affecting HIV-1 integration. This study identifies KAP1 as a cellular factor restricting HIV-1 infection and underscores the relevance of IN acetylation as a crucial step in the viral infectious cycle. 相似文献
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Marwa Chaouali Mouna Ben Azaiez Aymen Tezeghdenti Awatef Lagha Basma Yacoubi-Oueslati Ezzeddine Ghazouani Hatem Ben Abdallah Radhia Kochkar 《Biochemical genetics》2018,56(6):650-662
Autoimmune hepatitis (AIH) is a chronic hepatitis of unknown etiology and several proinflammatory cytokines are implicated in its pathogenesis. The association of TNF-α gene polymorphism with AIH onset is not fully elucidated especially in the Tunisian population. The aim of this study was to determine the association of TNF-α (-308 G?>?A) polymorphism with AIH susceptibility and with TNF-α expression or clinical manifestations of AIH. A total of 50 AIH patients and 150 controls were included. Evaluation of TNF-α polymorphism was performed by ARMS PCR method. A significantly higher frequence of the AA genotype was found in AIH patients compared to controls (34 vs. 8%, p?=?0.00002, OR 5.88). The frequency of the A-allele was significantly higher in patients with AIH compared to controls (55 vs. 37.3%, p?=?0.002, OR 2.05). The G-allele was significantly more frequent in healthy controls compared to AIH patients [43 vs. 61.3%, p?=?0.001, OR 0.47 (0.3–0.75)]. There was a positive correlation between the A/A genotype and a higher serum expression of TNF-α. The TNF*A allele confer susceptibility to AIH in the Tunisian patients and is associated with increased production of TNF-α. Anti-TNF antibodies could be an alternative to the use of corticotherapy and may avoid the exacerbated immune response in AIH. 相似文献
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Sameh Bejaoui Francesco Sciuto Narjess Karoui-Yaakoub Nebiha Bel Haj Ali 《Annales de Paléontologie》2018,104(1):71-80
This article concerns the study of the ostracods of the Upper Pliocene-Lower Pleistocene sedimentary deposits cropping out along the south-eastern coast of the Cape Bon Peninsula (Tunisia, Hammamet region, Sidi Khelas section). Fourteen samples were taken along a thirty-two-meters thick sedimentary silico-clastic series. Seventy species of ostracods belonging to twenty-four genera were found. The autochthonous association, which originally lived in an environment located in the infralittoral and upper circalittoral stages of the benthic marine domain, is cyclically affected by inputs from the more superficial environments due to the presence of relatively well-developed lagoon and/or estuary environments in the surrounding coastal areas. Within the ostracod association, the presence of Bythocythere turgida – a true “northern guest” – is particularly significant. This species indicates that these sediments were deposited during the cold phases of the Early Pleistocene. Among the ostracods found, those belonging to the families Trachyleberididae, Hemicytheridae and Bythocytheridae, which are dominant and include particularly significant species from the environmental and paleoclimatic point of view, are systematically recorded and commented on. Some species that are probably new have been described and photographed, but are currently left in open nomenclature because of how few specimens have been found. 相似文献