LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 10 of total 428

Search options

  1. Article: Les vaccins à ARN anti-COVID-19.

    Galibert, F

    Bulletin de l'Academie nationale de medecine

    2021  Volume 205, Issue 3, Page(s) 199–202

    Title translation Anti-COVID-19 RNA vaccines.
    Language French
    Publishing date 2021-01-09
    Publishing country Netherlands
    Document type Editorial
    ZDB-ID 213227-8
    ISSN 0001-4079
    ISSN 0001-4079
    DOI 10.1016/j.banm.2021.01.001
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: Le séquençage de l’ADN, cinquante ans de prouesses technologiques et d’avancées scientifiques (1re partie).

    Galibert, Francis

    La Revue du praticien

    2021  Volume 71, Issue 1, Page(s) 109–114

    Title translation DNA sequencing: fifty years of technological prowess and scientific advances (part 1).
    MeSH term(s) History, 19th Century ; History, 20th Century ; History, 21st Century ; Humans ; Sequence Analysis, DNA
    Language French
    Publishing date 2021-06-23
    Publishing country France
    Document type Historical Article ; Journal Article
    ZDB-ID 205365-2
    ISSN 2101-017X ; 0035-2640
    ISSN (online) 2101-017X
    ISSN 0035-2640
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: Le séquençage de l’ADN, 50  ans de prouesses technologiques et d’avancées scientifiques (2e partie).

    Galibert, Francis

    La Revue du praticien

    2021  Volume 71, Issue 2, Page(s) 225–230

    Title translation DNA sequencing: fifty years of technological prowess and scientific advances (part 2).
    MeSH term(s) History, 19th Century ; History, 20th Century ; History, 21st Century ; Humans ; Sequence Analysis, DNA
    Language French
    Publishing date 2021-06-23
    Publishing country France
    Document type Historical Article ; Journal Article
    ZDB-ID 205365-2
    ISSN 2101-017X ; 0035-2640
    ISSN (online) 2101-017X
    ISSN 0035-2640
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  4. Article ; Online: Baculovirus VP80 protein and the F-actin cytoskeleton interact and connect the viral replication factory with the nuclear periphery.

    Marek, Martin / Merten, Otto-Wilhelm / Galibert, Lionel / Vlak, Just M / van Oers, Monique M

    Journal of virology

    2011  Volume 85, Issue 11, Page(s) 5350–5362

    Abstract: ... protein is entirely localized in nuclei, adjacent to the virus-triggered F-actin scaffold that forms ...

    Abstract Recently, we showed that the Autographa californica multicapsid nucleopolyhedrovirus (AcMNPV) VP80 protein is essential for the formation of both virion types, budded virus (BV) and occlusion-derived virus (ODV). Deletion of the vp80 gene did not affect assembly of nucleocapsids. However, these nucleocapsids were not able to migrate from the virogenic stroma to the nuclear periphery. In the current paper, we constructed a baculovirus recombinant with enhanced-green fluorescent protein (EGFP)-tagged VP80, allowing visualization of the VP80 distribution pattern during infection. In baculovirus-infected cells, the EGFP-VP80 protein is entirely localized in nuclei, adjacent to the virus-triggered F-actin scaffold that forms a highly organized three-dimensional network connecting the virogenic stroma physically with the nuclear envelope. Interaction between VP80 and host actin was confirmed by coimmunoprecipitation. We further showed that VP80 is associated with the nucleocapsid fraction of both BVs and ODVs, typically at one end of the nucleocapsids. In addition, the presence of sequence motifs with homology to invertebrate paramyosin proteins strongly supports a role for VP80 in the polar transport of nucleocapsids to the periphery of the nucleus on their way to the plasma membrane to form BVs and for assembly in the nuclear periphery to form ODVs for embedding in viral occlusion bodies.
    MeSH term(s) Actins/metabolism ; Animals ; Artificial Gene Fusion ; Capsid Proteins/metabolism ; Cell Line ; Cell Nucleus/chemistry ; Genes, Reporter ; Green Fluorescent Proteins/genetics ; Green Fluorescent Proteins/metabolism ; Host-Pathogen Interactions ; Immunoprecipitation ; Lepidoptera ; Nucleopolyhedroviruses/pathogenicity ; Protein Binding ; Protein Interaction Mapping ; Staining and Labeling/methods
    Chemical Substances Actins ; Capsid Proteins ; enhanced green fluorescent protein ; Green Fluorescent Proteins (147336-22-9) ; Ac-vp80 protein, Autographa californica nucleopolyhedrovirus (148686-07-1)
    Language English
    Publishing date 2011-03-30
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80174-4
    ISSN 1098-5514 ; 0022-538X
    ISSN (online) 1098-5514
    ISSN 0022-538X
    DOI 10.1128/JVI.00035-11
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  5. Article ; Online: Are the Olfactory Receptors Present at the Sperm Membrane Involved in Reproduction?

    Galibert, Francis / Azzouzi, Naoual

    International journal of molecular sciences

    2023  Volume 24, Issue 14

    Abstract: Olfactory receptors (ORs), key components in ensuring the detection of myriad odorants, are expressed not only on the surface of olfactory neurons but also in many other tissues. In the case of ORs expressed at the sperm membrane, in vitro experiments ... ...

    Abstract Olfactory receptors (ORs), key components in ensuring the detection of myriad odorants, are expressed not only on the surface of olfactory neurons but also in many other tissues. In the case of ORs expressed at the sperm membrane, in vitro experiments with human and mouse spermatozoids have shown that they move toward the regions with the highest concentration of bourgeonal and lyral, respectively. However, to date, no in vivo experiment has shown any biological function of these ORs. To demonstrate a possible role in vivo of ORs in sperm chemotaxis, we overloaded the vaginal space of female mice from the prolific Swiss CD1 strain with lyral to induce competition with the supposed natural ligand and to prevent its detection. As shown, the mice that received lyral had much fewer newborns than the control mice treated with PBS, showing that lyral has a strong negative impact on procreation. This indicates that the ORs at the sperm surface are biologically active and make an important contribution to reproduction. Control experiments performed with hexanal, which does not alter sperm movement in vitro, indicate that the inhibition of reproduction observed was specific to lyral. In addition, we show that males are attracted to the smell of lyral, which acts as a pheromone, and prefer to copulate with mice marked on their back with lyral rather than with those that have not been marked. These results suggest an explanation for some cases of human infertility, which could result from an absence of recognition between the natural ligand and the ORs, either due to a mutation or a lack of expression from one of the two partners, allowing for the development of a diagnostic tests. These results might also lead to the development of a novel contraception strategy based on the use of vaginal tablets delivering an odorant or a drug that competes with the natural ligand.
    MeSH term(s) Infant, Newborn ; Humans ; Male ; Mice ; Female ; Animals ; Receptors, Odorant/metabolism ; Ligands ; Semen/metabolism ; Spermatozoa/metabolism ; Odorants ; Reproduction ; Olfactory Receptor Neurons/metabolism
    Chemical Substances hydroxyisohexyl 3-cyclohexene carboxaldehyde (QUE43B9Z2Q) ; Receptors, Odorant ; Ligands
    Language English
    Publishing date 2023-07-10
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms241411277
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  6. Article ; Online: Baculovirus VP80 Protein and the F-Actin Cytoskeleton Interact and Connect the Viral Replication Factory with the Nuclear Periphery

    Marek, M. / Merten, O.W. / Galibert, L. / Vlak, J.M. / van Oers, M.M.

    Journal of Virology

    2011  Volume 85, Issue 11

    Abstract: ... protein is entirely localized in nuclei, adjacent to the virus-triggered F-actin scaffold that forms ...

    Abstract Recently, we showed that the Autographa californica multicapsid nucleopolyhedrovirus (AcMNPV) VP80 protein is essential for the formation of both virion types, budded virus (BV) and occlusion-derived virus (ODV). Deletion of the vp80 gene did not affect assembly of nucleocapsids. However, these nucleocapsids were not able to migrate from the virogenic stroma to the nuclear periphery. In the current paper, we constructed a baculovirus recombinant with enhanced-green fluorescent protein (EGFP)-tagged VP80, allowing visualization of the VP80 distribution pattern during infection. In baculovirus-infected cells, the EGFP-VP80 protein is entirely localized in nuclei, adjacent to the virus-triggered F-actin scaffold that forms a highly organized three-dimensional network connecting the virogenic stroma physically with the nuclear envelope. Interaction between VP80 and host actin was confirmed by coimmunoprecipitation. We further showed that VP80 is associated with the nucleocapsid fraction of both BVs and ODVs, typically at one end of the nucleocapsids. In addition, the presence of sequence motifs with homology to invertebrate paramyosin proteins strongly supports a role for VP80 in the polar transport of nucleocapsids to the periphery of the nucleus on their way to the plasma membrane to form BVs and for assembly in the nuclear periphery to form ODVs for embedding in viral occlusion bodies
    Keywords autographa-californica nucleopolyhedrovirus ; dna-replication ; efficient egress ; mammalian-cells ; multicapsid nucleopolyhedrovirus ; multiple sequence alignment ; new-generation ; occlusion-derived virus ; orgyia-pseudotsugata ; polyhedrosis-virus
    Subject code 570
    Language English
    Publishing country nl
    Document type Article ; Online
    ZDB-ID 80174-4
    ISSN 1098-5514 ; 0022-538X
    ISSN (online) 1098-5514
    ISSN 0022-538X
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  7. Article: Systematic sequencing of the human HLA-A/HLA-F region: establishment of a cosmid contig and identification of a new gene cluster within 37 kb of sequence.

    Lepourcelet, M / Andrieux, N / Giffon, T / Pichon, L / Hampe, A / Galibert, F / Mosser, J

    Genomics

    1996  Volume 37, Issue 3, Page(s) 316–326

    Abstract: ... of the HLA-A/HLA-F region with a view to defining its contents in genes and pseudogenes ...

    Abstract The class I region of the human histocompatibility complex is characterized by a high density of genes and pseudogenes and a complex structural organization. To elucidate the complete structure of the HLA-A/HLA-F region with a view to defining its contents in genes and pseudogenes, we developed a strategy of systematic sequencing. This report describes the establishment of a cosmid contig spanning most of the region and the analysis of a 37-kb sequence from one of the cosmids. Four new genes, organized with the HCG-V gene in a clustered structure, have been identified. Two of these contain a zinc finger motif characteristic of DNA-binding proteins. The former, a member of the C3HC4 protein family, is highly expressed in prostate and contains a B30-2-like sequence identified in several genes mapped within the class I region. The latter, which is ubiquitously expressed, is the human equivalent of the yeast polymerase IA12.2 subunit and of the murine tctex6 gene. Of the two other genes, one remains an anonymous gene with no particular feature, while the fourth, specifically expressed in testis, is the human equivalent of the murine tctex4 gene. This cluster, located in a region corresponding to a syntenic unit between mouse and human, appears to be highly conserved.
    MeSH term(s) Amino Acid Sequence ; Animals ; Base Sequence ; Chromosome Walking ; Chromosomes, Human, Pair 6/genetics ; Cosmids/genetics ; DNA-Binding Proteins/genetics ; Dyneins ; Evolution, Molecular ; Genes ; Genes, MHC Class I ; HLA Antigens/genetics ; HLA-A Antigens/genetics ; Hemochromatosis/genetics ; Histocompatibility Antigens Class I/genetics ; Humans ; Intracellular Signaling Peptides and Proteins ; Male ; Mice ; Microtubule-Associated Proteins ; Molecular Sequence Data ; Nuclear Proteins/genetics ; Sequence Alignment ; Sequence Homology ; Species Specificity ; Testis/metabolism ; Zinc Fingers/genetics ; t-Complex Genome Region
    Chemical Substances DNA-Binding Proteins ; HLA Antigens ; HLA-A Antigens ; HLA-F antigens ; Histocompatibility Antigens Class I ; Intracellular Signaling Peptides and Proteins ; Microtubule-Associated Proteins ; Nuclear Proteins ; PPP1R11 protein, human ; Tcte3 protein, mouse ; Dyneins (EC 3.6.4.2)
    Language English
    Publishing date 1996-11-01
    Publishing country United States
    Document type Comparative Study ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 356334-0
    ISSN 1089-8646 ; 0888-7543
    ISSN (online) 1089-8646
    ISSN 0888-7543
    DOI 10.1006/geno.1996.0566
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  8. Article: Nucleotide sequence of the EcoRI-F fragment of adenovirus 2 genome.

    Galibert, F / Hérissé, J / Courtois, G

    Gene

    1979  Volume 6, Issue 1, Page(s) 1–22

    Abstract: ... 2 EcoRI-F fragment was determined. Information contained in that nucleotide sequence, which is 1743 ... by the EcoRI-F fragment. A method to rapidly determine the cleavage site of restriction endonucleases is also ...

    Abstract Using the DNA sequence method of Maxam and Gilbert the entire nucleotide sequence of the adenovirus 2 EcoRI-F fragment was determined. Information contained in that nucleotide sequence, which is 1743 base pairs long, is interpreted with respect to the mapping and processing of the three mRNAs partly encoded by the EcoRI-F fragment. A method to rapidly determine the cleavage site of restriction endonucleases is also reported.
    MeSH term(s) Adenoviridae/genetics ; Base Sequence ; Chromosome Mapping ; DNA Restriction Enzymes/metabolism ; DNA, Viral/analysis ; Electrophoresis, Polyacrylamide Gel ; Genes ; RNA, Messenger/genetics
    Chemical Substances DNA, Viral ; RNA, Messenger ; DNA Restriction Enzymes (EC 3.1.21.-)
    Language English
    Publishing date 1979-05
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 391792-7
    ISSN 1879-0038 ; 0378-1119
    ISSN (online) 1879-0038
    ISSN 0378-1119
    DOI 10.1016/0378-1119(79)90081-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  9. Article ; Online: Dog olfactory receptor gene expression profiling using samples derived from nasal epithelium brushing.

    Azzouzi, Naoual / Guillory, Anne-Sophie / Chaudieu, Gilles / Galibert, Francis

    Canine medicine and genetics

    2022  Volume 9, Issue 1, Page(s) 7

    Abstract: Dogs have an exquisite sense of olfaction. In many instances this ability has been utilized by humans for a wide range of important situations including detecting explosives and illegal drugs. It is accepted that some breeds have better senses of smell ... ...

    Abstract Dogs have an exquisite sense of olfaction. In many instances this ability has been utilized by humans for a wide range of important situations including detecting explosives and illegal drugs. It is accepted that some breeds have better senses of smell than others. Dogs can detect many volatile compounds at extremely low concentrations in air. To achieve such high levels of detection, the canine olfactory system is both complex and highly developed requiring a high density of olfactory receptors capable of detecting volatiles. Consequently the dog genome encodes a large number of olfactory receptor (OR) genes. However, it remains unclear as to what extent are all of these OR genes expressed on the cell surface. To facilitate such studies, a nasal brushing method was developed to recover dog nasal epithelial cell samples from which total RNA could be extracted and used to prepare high quality cDNA libraries. After capture by hybridization with an extensive set of oligonucleotides, the level of expression of each transcript was measured following next generation sequencing (NGS). The reproducibility of this sampling approach was checked by analyzing replicate samples from the same animal (up to 6 per each naris). The quality of the hybridization capture was also checked by analyzing two DNA libraries; this offered an advantage over RNA libraries by having an equal presence for each gene. Finally, we compared this brushing method performed on living dogs to a nasal epithelium biopsy approach applied to two euthanized terminally ill dogs, following consent from their owners.Comparison the expression levels of each transcript indicate that the ratios of expression between the highest and the least expressed OR in each sample are greater than 10,000 (paralog variation). Furthermore, it was clear that a number of OR genes are not expressed.The method developed and described here will allow researchers to further address whether variations observed in the OR transcriptome relate to dog 'life experiences' and whether any differences observed between samples are dog-specific or breed-specific.
    Language English
    Publishing date 2022-05-20
    Publishing country England
    Document type Journal Article
    ISSN 2662-9380
    ISSN (online) 2662-9380
    DOI 10.1186/s40575-022-00116-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  10. Article: Mapping the DNA fragments produced by cleavage of EcoRI F fragment of adenovirus 2 with HaeIII, HpaII and AluI.

    Hérissé, J / Courtois, G / Galibert, F

    Gene

    1978  Volume 4, Issue 4, Page(s) 279–294

    Abstract: Hydrolysis of the EcoRI F fragment of the adenovirus 2 genome with HaeIII, HpaII and AluI ... other enzymes. Position of the KpnI, HindIII, MboI and SmaI sites within the EcoRI F fragment were also ...

    Abstract Hydrolysis of the EcoRI F fragment of the adenovirus 2 genome with HaeIII, HpaII and AluI restriction enzymes gives respectively 9, 11, and 11 fragments, the size of which ranges from 20 bp for the smallest HpaII k fragment to 585 for the largest AluI A fragment. The order of fragments was mainly deduced from partial hydrolysis analyses. The relative order of all restriction sites and the distance in nucleotides between them were obtained through secondary analyses of each restriction fragment by the two other enzymes. Position of the KpnI, HindIII, MboI and SmaI sites within the EcoRI F fragment were also reevaluated.
    MeSH term(s) Adenoviridae/enzymology ; Adenoviridae/genetics ; Base Sequence ; Chromosome Mapping ; DNA Restriction Enzymes/genetics ; DNA, Viral/genetics ; Electrophoresis, Polyacrylamide Gel ; Genes, Viral ; Hydrolysis ; Transcription Factors ; Transcription, Genetic
    Chemical Substances DNA, Viral ; Transcription Factors ; DNA Restriction Enzymes (EC 3.1.21.-)
    Language English
    Publishing date 1978-12
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 391792-7
    ISSN 1879-0038 ; 0378-1119
    ISSN (online) 1879-0038
    ISSN 0378-1119
    DOI 10.1016/0378-1119(78)90046-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top