Hasil Pencarian - Isabelle Meunier

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  1. 1
    Genome Editing as a Treatment for the Most Prevalent Causative Genes of Autosomal Dominant Retinitis Pigmentosa

    Genome Editing as a Treatment for the Most Prevalent Causative Genes of Autosomal Dominant Retinitis Pigmentosa oleh Michalitsa Diakatou, Gaël Manes, Beatrice Bocquet, Isabelle Meunier, Vasiliki Kalatzis

    Diterbitkan 2019-05-01
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  2. 2
    Allele-Specific Knockout by CRISPR/Cas to Treat Autosomal Dominant Retinitis Pigmentosa Caused by the G56R Mutation in NR2E3

    Allele-Specific Knockout by CRISPR/Cas to Treat Autosomal Dominant Retinitis Pigmentosa Caused by the G56R Mutation in NR2E3 oleh Michalitsa Diakatou, Gregor Dubois, Nejla Erkilic, Carla Sanjurjo-Soriano, Isabelle Meunier, Vasiliki Kalatzis

    Diterbitkan 2021-03-01
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  3. 3
    Quantification of the early pupillary dilation kinetic to assess rod and cone activity

    Quantification of the early pupillary dilation kinetic to assess rod and cone activity oleh Corinne Kostic, Sylvain V. Crippa, Lorette Leon, Christian Hamel, Isabelle Meunier, Aki Kawasaki

    Diterbitkan 2021-05-01
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  4. 4
    Infection with a Mouse-Adapted Strain of the 2009 Pandemic Virus Causes a Highly Severe Disease Associated with an Impaired T Cell Response.

    Infection with a Mouse-Adapted Strain of the 2009 Pandemic Virus Causes a Highly Severe Disease Associated with an Impaired T Cell Response. oleh Isabelle Meunier, Olivier Morisseau, Émilie Garneau, Isabelle Marois, Alexandre Cloutier, Martin V Richter

    Diterbitkan 2015-01-01
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  5. 5
    Cultivo in vitro de ápices caulinares de abacaxizeiro para limpeza clonal em relação à fusariose Shoot tip in vitro culture of pineapple for fusarium elimination

    Cultivo in vitro de ápices caulinares de abacaxizeiro para limpeza clonal em relação à fusariose Shoot tip in vitro culture of pineapple for fusarium elimination oleh Cynthia Cavalcanti Albuquerque, Terezinha Rangel Camara, Maria Menezes, Lilia Willadino, Isabelle Meunier, Cláudia Ulisses

    Diterbitkan 2000-06-01
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  6. 6
    Inhibition of influenza virus replication by targeting broad host cell pathways.

    Inhibition of influenza virus replication by targeting broad host cell pathways. oleh Isabelle Marois, Alexandre Cloutier, Isabelle Meunier, Hana M Weingartl, André M Cantin, Martin V Richter

    Diterbitkan 2014-01-01
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  7. 7
    Efeitos do estádio de desenvolvimento da antera e da radiação gama na formação de calos derivados de anteras de tomate

    Efeitos do estádio de desenvolvimento da antera e da radiação gama na formação de calos derivados de anteras de tomate oleh Ana Christina R. Brasileiro, Lilia Willadino, Marcelo Guerra, Waldeciro Colaço, Isabelle Meunier, Terezinha R. Camara

    Diterbitkan 1999-10-01
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  8. 8
    Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosis

    Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosis oleh Nejla Erkilic, Carla Sanjurjo-Soriano, Gaël Manes, Gregor Dubois, Christian P. Hamel, Isabelle Meunier, Vasiliki Kalatzis

    Diterbitkan 2019-07-01
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  9. 9
    Generation of a human iPSC line, INMi005-A, from a patient with non-syndromic USH2A-associated retinitis pigmentosa

    Generation of a human iPSC line, INMi005-A, from a patient with non-syndromic USH2A-associated retinitis pigmentosa oleh Carla Sanjurjo-Soriano, Nejla Erkilic, Christel Vache, Gregor Dubois, Anne-Françoise Roux, Isabelle Meunier, Vasiliki Kalatzis

    Diterbitkan 2022-04-01
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  10. 10
    Generation of a human iPSC line, INMi002-A, carrying the most prevalent USH2A variant associated with Usher syndrome type 2

    Generation of a human iPSC line, INMi002-A, carrying the most prevalent USH2A variant associated with Usher syndrome type 2 oleh Carla Sanjurjo-Soriano, Nejla Erkilic, Gaël Manes, Gregor Dubois, Christian P. Hamel, Isabelle Meunier, Vasiliki Kalatzis

    Diterbitkan 2018-12-01
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  11. 11
    Seleção in vitro de gemas de bananeira 'Nanicão' tolerantes à salinidade

    Seleção in vitro de gemas de bananeira 'Nanicão' tolerantes à salinidade oleh Cláudia Ulisses, Terezinha Rangel Camara, Lilia Willadino, Isabelle Meunier, Paulo Sérgio Gomes da Rocha, Cynthia Albuquerque

    Diterbitkan 2000-12-01
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  12. 12
    Generation of an iPSC line, INMi001-A, carrying the two most common USH2A mutations from a compound heterozygote with non-syndromic retinitis pigmentosa

    Generation of an iPSC line, INMi001-A, carrying the two most common USH2A mutations from a compound heterozygote with non-syndromic retinitis pigmentosa oleh Carla Sanjurjo-Soriano, Nejla Erkilic, Gaël Manes, Gregor Dubois, Christian P. Hamel, Isabelle Meunier, Vasiliki Kalatzis

    Diterbitkan 2018-12-01
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  13. 13
    Generation of a human iPSC line, INMi003-A, with a missense mutation in CRX associated with autosomal dominant cone-rod dystrophy

    Generation of a human iPSC line, INMi003-A, with a missense mutation in CRX associated with autosomal dominant cone-rod dystrophy oleh Nejla Erkilic, Carla Sanjurjo-Soriano, Michalitsa Diakatou, Gaël Manes, Gregor Dubois, Christian P. Hamel, Isabelle Meunier, Vasiliki Kalatzis

    Diterbitkan 2019-07-01
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  14. 14
    Type I IFN triggers RIG-I/TLR3/NLRP3-dependent inflammasome activation in influenza A virus infected cells.

    Type I IFN triggers RIG-I/TLR3/NLRP3-dependent inflammasome activation in influenza A virus infected cells. oleh Julien Pothlichet, Isabelle Meunier, Beckley K Davis, Jenny P-Y Ting, Emil Skamene, Veronika von Messling, Silvia M Vidal

    Diterbitkan 2013-01-01
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  15. 15
    Genome Editing in Patient iPSCs Corrects the Most Prevalent USH2A Mutations and Reveals Intriguing Mutant mRNA Expression Profiles

    Genome Editing in Patient iPSCs Corrects the Most Prevalent USH2A Mutations and Reveals Intriguing Mutant mRNA Expression Profiles oleh Carla Sanjurjo-Soriano, Nejla Erkilic, David Baux, Daria Mamaeva, Christian P. Hamel, Isabelle Meunier, Anne-Françoise Roux, Vasiliki Kalatzis

    Diterbitkan 2020-06-01
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  16. 16
    <i>Casitas B-lineage lymphoma</i> Gene Mutation Ocular Phenotype

    <i>Casitas B-lineage lymphoma</i> Gene Mutation Ocular Phenotype oleh Christine Fardeau, Munirah Alafaleq, Marie-Adélaïde Ferchaud, Miguel Hié, Caroline Besnard, Sonia Meynier, Frédéric Rieux-Laucat, Damien Roos-Weil, Fleur Cohen, Isabelle Meunier

    Diterbitkan 2022-07-01
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  17. 17
    RIPK3 interacts with MAVS to regulate type I IFN-mediated immunity to Influenza A virus infection.

    RIPK3 interacts with MAVS to regulate type I IFN-mediated immunity to Influenza A virus infection. oleh Jeffrey Downey, Erwan Pernet, François Coulombe, Benoit Allard, Isabelle Meunier, Joanna Jaworska, Salman Qureshi, Donald C Vinh, James G Martin, Philippe Joubert, Maziar Divangahi

    Diterbitkan 2017-04-01
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  18. 18
    Novel and Recurrent Copy Number Variants in <i>ABCA4</i>-Associated Retinopathy

    Novel and Recurrent Copy Number Variants in <i>ABCA4</i>-Associated Retinopathy oleh Zelia Corradi, Claire-Marie Dhaenens, Olivier Grunewald, Ipek Selen Kocabaş, Isabelle Meunier, Sandro Banfi, Marianthi Karali, Frans P. M. Cremers, Rebekkah J. Hitti-Malin

    Diterbitkan 2024-05-01
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  19. 19
    Characterization of SSBP1-related optic atrophy and foveopathy

    Characterization of SSBP1-related optic atrophy and foveopathy oleh Isabelle Meunier, Béatrice Bocquet, Sabine Defoort-Dhellemmes, Vasily Smirnov, Carl Arndt, Marie Christine Picot, Hélène Dollfus, Majida Charif, Isabelle Audo, Hélèna Huguet, Xavier Zanlonghi, Guy Lenaers

    Diterbitkan 2021-09-01
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  20. 20
    Hereditary spastic paraplegia and prominent sensorial involvement: think MAG mutations!

    Hereditary spastic paraplegia and prominent sensorial involvement: think MAG mutations! oleh Agathe Roubertie, Majida Charif, Pierre Meyer, Gael Manes, Isabelle Meunier, Guillaume Taieb, Raul Junta Morales, Agnès Guichet, Cecile Delettre, Emmanuelle Sarzi, Nicolas Leboucq, François Rivier, Guy Lenaers

    Diterbitkan 2019-08-01
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