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  • 1
    In: Revue Neurologique, Elsevier BV, Vol. 174, No. 3 ( 2018-03), p. 150-156
    Type of Medium: Online Resource
    ISSN: 0035-3787
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2018
    detail.hit.zdb_id: 2036356-4
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  • 2
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2013
    In:  Transactions of the Royal Society of Tropical Medicine and Hygiene Vol. 107, No. 1 ( 2013-01-01), p. 8-14
    In: Transactions of the Royal Society of Tropical Medicine and Hygiene, Oxford University Press (OUP), Vol. 107, No. 1 ( 2013-01-01), p. 8-14
    Type of Medium: Online Resource
    ISSN: 0035-9203 , 1878-3503
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2013
    detail.hit.zdb_id: 2135136-3
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  • 3
    Online Resource
    Online Resource
    Elsevier BV ; 2000
    In:  Experimental Cell Research Vol. 258, No. 2 ( 2000-08), p. 279-287
    In: Experimental Cell Research, Elsevier BV, Vol. 258, No. 2 ( 2000-08), p. 279-287
    Type of Medium: Online Resource
    ISSN: 0014-4827
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2000
    detail.hit.zdb_id: 1466780-0
    SSG: 12
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  • 4
    Online Resource
    Online Resource
    Societe Senegalaise de Cancerologie ; 2022
    In:  African Journal of Oncology Vol. 2, No. 1 Supplement ( 2022-03-01), p. S3-
    In: African Journal of Oncology, Societe Senegalaise de Cancerologie, Vol. 2, No. 1 Supplement ( 2022-03-01), p. S3-
    Abstract: INTRODUCTION: Looking for the mutational landscape on a genomic scale has provided in the last few years unprecedented perspectives for understanding molecular pathogenesis of cancer progression, response to treatment and genetic predisposition. In oral cancers, numerous genomic studies have been devoted to alterations in the TP53 gene and their clinical significance in carcinogenesis. Herein, we screened for genomic variants of TP53 predisposing to oral cancers in Senegalese patients. MATERIALS AND METHODS: Eighty-eight patients with confirmed diagnostic were recruited after informed consent from Stomatology Unit of Aristide le Dantec Hospital. Blood samples were collected from each patient to perform DNA extraction, PCR amplification of all coding exons of TP53 followed by Sanger Sequencing of PCR products. Nucleotidic sequences were analyzed with Genalys software. RESULTS: Mean age at diagnosis was estimated at 51.9 ± 17.98 years with a sex-ratio of 0.76. The majority of patients (64/88) had a negative alcohol-tobacco status. Tumor histology showed that 90% of patients had squamous cell carcinoma localised preferentially on the tongue (22.7%), gum (20.5%) and cheek mucosa (19.3%). Mutation screening of TP53 showed that 52.27% of the patients carried at least one mutation. Eleven genomic variants were identified, seven already reported in mutation databases and four new variants. The most recurrent variants was p.Pro72Arg (rs1042522; Arginine allelic frequency estimated at 31.26%) and a 16 bp deletion in intron 3 (rs59758982; allelic frequency estimated at 26.25%). Linkage disequilibrium (LD) calculation has shown that these two variants are in strong LD but tests of association with controls show that they could not predispose towards oral cancers. CONCLUSION: The results of the present investigation suggest that the two most common variants found in Senegalese patients are not predisposing to oral cancers. Further comprehensive investigations on reported and new variants found in this study should be conducted to highlight their functional impacts and hypothetic oncogenic associated function.
    Type of Medium: Online Resource
    ISSN: 2772-2457
    URL: Issue
    Language: Unknown
    Publisher: Societe Senegalaise de Cancerologie
    Publication Date: 2022
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  • 5
    Online Resource
    Online Resource
    SAGE Publications ; 2003
    In:  Cell Transplantation Vol. 12, No. 1 ( 2003-01), p. 91-100
    In: Cell Transplantation, SAGE Publications, Vol. 12, No. 1 ( 2003-01), p. 91-100
    Abstract: Migration of transplanted myogenic cells occurs during both embryogenesis and regeneration of skeletal muscles and is important for successful myoblast transplantation, but little is known about factors that promote chemotaxis of these cells. Tumor necrosis factor-α (TNF-α) is known to induce chemotactic effect on several cell types. In this study, we investigated its influence on the in vitro and in vivo motility of C2C12 and primary myoblasts. In the in vitro test performed in the blind-well Boyden chambers, we showed that TNF-α (50–400 U/ml) significantly enhanced the ability of myogenic cells to migrate. The dose–response curve for this factor was bell shaped, with maximum activity in the 200 U/ml range. In the in vivo test, intramuscular administration of TNF-α was performed by an Alzet pump connected to a perforated polyethylene microtube inserted in the tibialis anterior (TA) of CD1 mice. In these experiments, myoblasts were injected under the muscle epimysium. The recipient mice were immunosuppressed with FK506. Our results showed that, 5 days after myoblast transplantation, cells migrated further in the muscles infused with TNF-α than in the muscles not exposed to TNF-α. TNF-α not only has a chemotactic activity but may also modify cell migration via its action on matrix metalloproteinase (MMP) expression. The proteolytic activities of the MMPs secreted in the muscles were thus also assessed by gelatin zymography. The results showed an increased of MMP-2 and MMP-9 transcripts in the TNF-α-infused muscles injected with myogenic cells. Myoblast migration during transplantation may be enhanced by overlapping gradients of several effector molecules such as TNF-α, interferon-γ (INF-γ), and interleukins, released at the site of muscle injury. We propose that TNF-α may promote myoblast migration directly through chemotactic activity and indirectly by enhancing MMP activity at the site of muscle injury.
    Type of Medium: Online Resource
    ISSN: 0963-6897 , 1555-3892
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2003
    detail.hit.zdb_id: 2020466-8
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  • 6
    Online Resource
    Online Resource
    Elsevier BV ; 2017
    In:  JMV-Journal de Médecine Vasculaire Vol. 42, No. 6 ( 2017-12), p. 333-337
    In: JMV-Journal de Médecine Vasculaire, Elsevier BV, Vol. 42, No. 6 ( 2017-12), p. 333-337
    Type of Medium: Online Resource
    ISSN: 2542-4513
    Language: French
    Publisher: Elsevier BV
    Publication Date: 2017
    detail.hit.zdb_id: 2899719-0
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  • 7
    Online Resource
    Online Resource
    SAGE Publications ; 2000
    In:  Cell Transplantation Vol. 9, No. 4 ( 2000-07), p. 539-549
    In: Cell Transplantation, SAGE Publications, Vol. 9, No. 4 ( 2000-07), p. 539-549
    Abstract: The effect of pretreatments of host muscles with metalloproteinases (MMPs) or with notexin on the migration of transplanted myoblasts was investigated. Transgenic TnILacZ mice in which the β-galactosidase gene is under the control of a quail fast skeletal troponin I gene promoter were used as donors. A polyethylene microtube with four perforations was inserted in the tibialis anterior (TA) of CD1 mice. Both pretreatment substances and cells were slowly injected through that microtube. Muscles were pretreated 2 days before myoblast injection either with a mixture of collagenase, matrilysin, and notexin or with only collagenase and matrilysin or only notexin. As control for our experiments, TnILacZ and C2C12 myoblasts were also injected in TA muscles not pretreated. Comparison of short and long-term myoblast radial migration was performed using a dye (PKH26) and X-gal staining, respectively. The recipient mice were immunosuppressed with FK506. Two days after myoblast transplantation, the cell movement in muscles pretreated with collagenase, matrilysin, and notexin was slightly greater than in muscles pretreated only with collagenase and matrilysin but was about twice that observed in muscles treated with notexin alone. Almost no radial migration of TnILacZ myoblasts was observed in untreated muscles. The C2C12 myoblasts showed a four-to fivefold higher migration capacity than TnILacZ myoblasts. At 15 days after TnILacZ myoblast transplantation, the farthest positive β-gal muscle fibers show a two- to threefold extension of the initial migration observed at 2 days, demonstrating the ability of myoblasts to continue the migration following all pretreatments and even in the untreated muscles. In addition, more muscle fibers expressed the β-gal reporter gene in muscles pretreated only with MMPs. Our results clearly demonstrate that muscle pretreatments with MMPs increase myoblast migration and fusion with host muscle fibers after transplantation and that the C2C12 cell line producing MMPs has a higher migratory capacity.
    Type of Medium: Online Resource
    ISSN: 0963-6897 , 1555-3892
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2000
    detail.hit.zdb_id: 2020466-8
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  • 8
    Online Resource
    Online Resource
    Elsevier BV ; 2014
    In:  Journal of Virological Methods Vol. 204 ( 2014-08), p. 38-43
    In: Journal of Virological Methods, Elsevier BV, Vol. 204 ( 2014-08), p. 38-43
    Type of Medium: Online Resource
    ISSN: 0166-0934
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2014
    detail.hit.zdb_id: 2007929-1
    SSG: 12
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  • 9
    In: Biochemistry and Cell Biology, Canadian Science Publishing, Vol. 81, No. 2 ( 2003-04-01), p. 81-90
    Abstract: Myoblast transplantation (MT) is a potential therapeutic approach for several muscular dystrophies. A major limiting factor is that only a low percentage of the transplanted myoblasts survives the procedure. Recent advances regarding how and when the myoblasts die indicate that events preceding actual tissue implantation and during the first days after the transplantation are crucial. Myoseverin, a recently identified tri-substituted purine, was shown to induce in vitro the fission of multinucleated myotubes and affect the expression of a variety of growth factors, and immunomodulation, extracellular matrix-remodeling, and stress response genes. Since the effects of myoseverin are consistent with the activation of pathways involved in wound healing and tissue regeneration, we have investigated whether pretreatment and co-injection of myoblasts with Tubulyzine ® (microtubule lysing triazine), an optimized myoseverin-like molecule recently identified from a triazine library, could reduce myoblast cell death following their transplantation and consequently improves the success of myoblast transplantation. In vitro, using annexin-V labeling, we showed that Tubulyzine (5 µM) prevents normal myoblasts from apoptosis induced by staurosporine (1 µM). In vivo, the pretreatment and co-injection of immortal and normal myoblasts with Tubulyzine reduced significantly cell death (assessed by the radio-labeled thymidine of donor DNA) and increased survival of myoblasts transplanted in Tibialis anterior (TA) muscles of mdx mice, thus giving rise to more hybrid myofibers compared to transplanted untreated cells. Our results suggest that Tubulyzine can be used as an in vivo survival factor to improve the myoblast-mediated gene transfer approach.Key words: myoblast survival, mdx mouse, myoblast transplantation, microtubule-binding molecule, cell death.
    Type of Medium: Online Resource
    ISSN: 0829-8211 , 1208-6002
    Language: English
    Publisher: Canadian Science Publishing
    Publication Date: 2003
    SSG: 12
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  • 10
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 378, No. 6615 ( 2022-10-07)
    Abstract: Investment in Africa over the past year with regard to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) sequencing has led to a massive increase in the number of sequences, which, to date, exceeds 100,000 sequences generated to track the pandemic on the continent. These sequences have profoundly affected how public health officials in Africa have navigated the COVID-19 pandemic. RATIONALE We demonstrate how the first 100,000 SARS-CoV-2 sequences from Africa have helped monitor the epidemic on the continent, how genomic surveillance expanded over the course of the pandemic, and how we adapted our sequencing methods to deal with an evolving virus. Finally, we also examine how viral lineages have spread across the continent in a phylogeographic framework to gain insights into the underlying temporal and spatial transmission dynamics for several variants of concern (VOCs). RESULTS Our results indicate that the number of countries in Africa that can sequence the virus within their own borders is growing and that this is coupled with a shorter turnaround time from the time of sampling to sequence submission. Ongoing evolution necessitated the continual updating of primer sets, and, as a result, eight primer sets were designed in tandem with viral evolution and used to ensure effective sequencing of the virus. The pandemic unfolded through multiple waves of infection that were each driven by distinct genetic lineages, with B.1-like ancestral strains associated with the first pandemic wave of infections in 2020. Successive waves on the continent were fueled by different VOCs, with Alpha and Beta cocirculating in distinct spatial patterns during the second wave and Delta and Omicron affecting the whole continent during the third and fourth waves, respectively. Phylogeographic reconstruction points toward distinct differences in viral importation and exportation patterns associated with the Alpha, Beta, Delta, and Omicron variants and subvariants, when considering both Africa versus the rest of the world and viral dissemination within the continent. Our epidemiological and phylogenetic inferences therefore underscore the heterogeneous nature of the pandemic on the continent and highlight key insights and challenges, for instance, recognizing the limitations of low testing proportions. We also highlight the early warning capacity that genomic surveillance in Africa has had for the rest of the world with the detection of new lineages and variants, the most recent being the characterization of various Omicron subvariants. CONCLUSION Sustained investment for diagnostics and genomic surveillance in Africa is needed as the virus continues to evolve. This is important not only to help combat SARS-CoV-2 on the continent but also because it can be used as a platform to help address the many emerging and reemerging infectious disease threats in Africa. In particular, capacity building for local sequencing within countries or within the continent should be prioritized because this is generally associated with shorter turnaround times, providing the most benefit to local public health authorities tasked with pandemic response and mitigation and allowing for the fastest reaction to localized outbreaks. These investments are crucial for pandemic preparedness and response and will serve the health of the continent well into the 21st century. Expanse of SARS-CoV-2 sequencing capacity in Africa. ( A ) African countries (shaded in gray) and institutions (red circles) with on-site sequencing facilities that are capable of producing SARS-CoV-2 whole genomes locally. ( B ) The number of SARS-CoV-2 genomes produced per country and the proportion of those genomes that were produced locally, regionally within Africa, or abroad. ( C ) Decreased turnaround time of sequencing output in Africa to an almost real-time release of genomic data.
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
    RVK:
    RVK:
    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 2022
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    detail.hit.zdb_id: 2066996-3
    detail.hit.zdb_id: 2060783-0
    SSG: 11
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