Hasil Pencarian - Paul Laissue

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  1. 1
    The forkhead-box family of transcription factors: key molecular players in colorectal cancer pathogenesis

    The forkhead-box family of transcription factors: key molecular players in colorectal cancer pathogenesis oleh Paul Laissue

    Diterbitkan 2019-01-01
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  2. 2
    Agammaglobulinemia ligada A X Y onicodistrofia: dos nuevas mutaciones en el gen BTK y exclusión de mutaciones en el gen SOX9

    Agammaglobulinemia ligada A X Y onicodistrofia: dos nuevas mutaciones en el gen BTK y exclusión de mutaciones en el gen SOX9 oleh Carolina Rivera Nieto, Taryn Castro, Carlos Olmos, Carlos M. Restrepo, Paul Laissue

    Diterbitkan 2010-11-01
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  3. 3
    Ausencia de mutaciones en HPGD en una familia colombiana afectada por osteoartropatía hipertrófica primaria sugiere un nuevo locus de la enfermedad

    Ausencia de mutaciones en HPGD en una familia colombiana afectada por osteoartropatía hipertrófica primaria sugiere un nuevo locus de la enfermedad oleh Carolina Rivera Nieto, Carlos M. Restrepo, Chae Bong Whang, David Bonthron, Paul Laissue

    Diterbitkan 2010-11-01
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  4. 4
    Exome sequencing is an efficient tool for variant late-infantile neuronal ceroid lipofuscinosis molecular diagnosis.

    Exome sequencing is an efficient tool for variant late-infantile neuronal ceroid lipofuscinosis molecular diagnosis. oleh Liliana Catherine Patiño, Rajani Battu, Oscar Ortega-Recalde, Jeyabalan Nallathambi, Venkata Ramana Anandula, Umashankar Renukaradhya, Paul Laissue

    Diterbitkan 2014-01-01
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  5. 5
    Refined mapping of a quantitative trait locus on chromosome 1 responsible for mouse embryonic death.

    Refined mapping of a quantitative trait locus on chromosome 1 responsible for mouse embryonic death. oleh Magalie Vatin, Gaetan Burgio, Gilles Renault, Paul Laissue, Virginie Firlej, Françoise Mondon, Xavier Montagutelli, Daniel Vaiman, Catherine Serres, Ahmed Ziyyat

    Diterbitkan 2012-01-01
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  6. 6
    Possible Genetic Determinants of Response to Phenytoin in a Group of Colombian Patients With Epilepsy

    Possible Genetic Determinants of Response to Phenytoin in a Group of Colombian Patients With Epilepsy oleh Carlos Alberto Calderon-Ospina, Carlos Alberto Calderon-Ospina, Jubby Marcela Galvez, Jubby Marcela Galvez, Claudia López-Cabra, Natalia Morales, Carlos Martín Restrepo, Jesús Rodríguez, Jesús Rodríguez, Jesús Rodríguez, Fabio Ancízar Aristizábal-Gutiérrez, Alberto Velez-van-Meerbeke, Paul Laissue, Paul Laissue, Dora Janeth Fonseca-Mendoza

    Diterbitkan 2020-05-01
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  7. 7
    A first description of the Colombian national registry for rare diseases

    A first description of the Colombian national registry for rare diseases oleh Heidi Eliana Mateus, Ana María Pérez, Martha Lucía Mesa, Germán Escobar, Jubby Marcela Gálvez, José Ivo Montaño, Martha Lucía Ospina, Paul Laissue

    Diterbitkan 2017-10-01
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  8. 8
    Novel genes and mutations in patients affected by recurrent pregnancy loss.

    Novel genes and mutations in patients affected by recurrent pregnancy loss. oleh Paula Quintero-Ronderos, Eric Mercier, Michiko Fukuda, Ronald González, Carlos Fernando Suárez, Manuel Alfonso Patarroyo, Daniel Vaiman, Jean-Christophe Gris, Paul Laissue

    Diterbitkan 2017-01-01
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  9. 9
    THBD sequence variants potentially related to recurrent pregnancy loss

    THBD sequence variants potentially related to recurrent pregnancy loss oleh Paula Quintero-Ronderos, Eric Mercier, Jean-Christophe Gris, Clara Esteban-Perez, Harold Moreno-Ortiz, Dora Janeth Fonseca, Elkin Lucena, Daniel Vaiman, Paul Laissue

    Diterbitkan 2017-12-01
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  10. 10
    Linking genotype to trophoblast phenotype in preeclampsia and HELLP syndrome associated with STOX1 genetic variants

    Linking genotype to trophoblast phenotype in preeclampsia and HELLP syndrome associated with STOX1 genetic variants oleh Lorenzo Costa, Luis Bermudez-Guzman, Ikram Benouda, Paul Laissue, Adrien Morel, Karen Marcela Jiménez, Thierry Fournier, Laurence Stouvenel, Céline Méhats, Francisco Miralles, Daniel Vaiman

    Diterbitkan 2024-03-01
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  11. 11
    Structural Modelling of KCNQ1 and KCNH2 Double Mutant Proteins, Identified in Two Severe Long QT Syndrome Cases, Reveals New Insights into Cardiac Channelopathies

    Structural Modelling of KCNQ1 and KCNH2 Double Mutant Proteins, Identified in Two Severe Long QT Syndrome Cases, Reveals New Insights into Cardiac Channelopathies oleh William A. Agudelo, Sebastian Ramiro Gil-Quiñones, Alejandra Fonseca, Alvaro Arenas, Laura Castro, Diana Carolina Sierra-Díaz, Manuel A. Patarroyo, Paul Laissue, Carlos F. Suárez, Rodrigo Cabrera

    Diterbitkan 2021-11-01
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  12. 12
    Copy number variation profiling in pharmacogenetics CYP-450 and GST genes in Colombian population

    Copy number variation profiling in pharmacogenetics CYP-450 and GST genes in Colombian population oleh Brian Ramírez, María José Niño-Orrego, Daniel Cárdenas, Kevin Enrique Ariza, Karol Quintero, Nora Constanza Contreras Bravo, Caroll Tamayo-Agudelo, María Alejandra González, Paul Laissue, Dora Janeth Fonseca Mendoza

    Diterbitkan 2019-07-01
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  13. 13
    Whole-exome sequencing enables rapid determination of xeroderma pigmentosum molecular etiology.

    Whole-exome sequencing enables rapid determination of xeroderma pigmentosum molecular etiology. oleh Oscar Ortega-Recalde, Jéssica Inés Vergara, Dora Janeth Fonseca, Xiomara Ríos, Hernando Mosquera, Olga María Bermúdez, Claudia Liliana Medina, Clara Inés Vargas, Argemiro Enrique Pallares, Carlos Martín Restrepo, Paul Laissue

    Diterbitkan 2014-01-01
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  14. 14
    Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure.

    Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure. oleh Sandrine Caburet, Petra Zavadakova, Ziva Ben-Neriah, Kamal Bouhali, Aurélie Dipietromaria, Céline Charon, Céline Besse, Paul Laissue, Vered Chalifa-Caspi, Sophie Christin-Maitre, Daniel Vaiman, Giovanni Levi, Reiner A Veitia, Marc Fellous

    Diterbitkan 2012-01-01
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  15. 15
    FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia

    FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia oleh Paula Quintero-Ronderos, Karen Marcela Jiménez, Clara Esteban-Pérez, Diego A. Ojeda, Sandra Bello, Dora Janeth Fonseca, María Alejandra Coronel, Harold Moreno-Ortiz, Diana Carolina Sierra-Díaz, Elkin Lucena, Sandrine Barbaux, Daniel Vaiman, Paul Laissue

    Diterbitkan 2019-08-01
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  16. 16
    Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans

    Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans oleh Paul Laissue, Besma Lakhal, Magalie Vatin, Frank Batista, Gaëtan Burgio, Eric Mercier, Esther Dos Santos, Christophe Buffat, Diana Carolina Sierra-Diaz, Gilles Renault, Xavier Montagutelli, Jane Salmon, Philippe Monget, Reiner A. Veitia, Céline Méhats, Marc Fellous, Jean-Christophe Gris, Julie Cocquet, Daniel Vaiman

    Diterbitkan 2016-01-01
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  17. 17
    Molecular Mechanisms of Trophoblast Dysfunction Mediated by Imbalance between STOX1 Isoforms

    Molecular Mechanisms of Trophoblast Dysfunction Mediated by Imbalance between STOX1 Isoforms oleh Aurélien Ducat, Betty Couderc, Anthony Bouter, Louise Biquard, Rajaa Aouache, Bruno Passet, Ludivine Doridot, Marie-Benoîte Cohen, Pascale Ribaux, Clara Apicella, Irène Gaillard, Sophia Palfray, Yulian Chen, Alexandra Vargas, Amélie Julé, Léo Frelin, Julie Cocquet, Camino Ruano San Martin, Sébastien Jacques, Florence Busato, Jorg Tost, Céline Méhats, Paul Laissue, Jean-Luc Vilotte, Francisco Miralles, Daniel Vaiman

    Diterbitkan 2020-05-01
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