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You search for a phrase ""Paul Laissue"" according to the criterion: Author

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    Showing 1-18 from 18 results
    Title:
    Linking genotype to trophoblast phenotype in preeclampsia and HELLP syndrome associated with STOX1 genetic variants
    Authors:
    Lorenzo Costa
    Luis Bermudez-Guzman
    Ikram Benouda
    Paul Laissue
    Adrien Morel
    Karen Marcela Jiménez
    Thierry Fournier
    Laurence Stouvenel
    Céline Méhats
    Francisco Miralles
    Daniel Vaiman
    Show more
    Subject Terms:
    Pregnancy
    Human Genetics
    Phenotyping
    Cell biology
    Transcriptomics
    Science
    Source:
    iScience, Vol 27, Iss 3, Pp 109260- (2024)
    File Description:
    electronic resource
    Relation:
    http://www.sciencedirect.com/science/article/pii/S2589004224004814; https://doaj.org/toc/2589-0042
    Access URL:
    https://doaj.org/article/b911a702ca1a4fb291a95d0fd611069d  Link opens in a new window
    Academic Journal
    Details
    Title:
    The forkhead-box family of transcription factors: key molecular players in colorectal cancer pathogenesis
    Authors:
    Paul Laissue
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    Subject Terms:
    Colorectal cancer
    Forkhead transcription factors
    Molecular aetiology
    Neoplasms. Tumors. Oncology. Including cancer and carcinogens
    RC254-282
    Source:
    Molecular Cancer, Vol 18, Iss 1, Pp 1-13 (2019)
    File Description:
    electronic resource
    Relation:
    http://link.springer.com/article/10.1186/s12943-019-0938-x; https://doaj.org/toc/1476-4598
    Access URL:
    https://doaj.org/article/3fea0f710be34451b8e22431beb7c649  Link opens in a new window
    Academic Journal
    Full Text  Link opens in a new window Full TextDetails
    Title:
    Structural Modelling of KCNQ1 and KCNH2 Double Mutant Proteins, Identified in Two Severe Long QT Syndrome Cases, Reveals New Insights into Cardiac Channelopathies
    Authors:
    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
    Show more
    Subject Terms:
    long QT syndrome
    KCNQ1
    KCNH2
    cardiac channelopathies-computational modelling
    Biology (General)
    QH301-705.5
    Chemistry
    QD1-999
    Source:
    International Journal of Molecular Sciences, Vol 22, Iss 23, p 12861 (2021)
    File Description:
    electronic resource
    Relation:
    https://www.mdpi.com/1422-0067/22/23/12861; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067
    Access URL:
    https://doaj.org/article/e73a5706d8984af78fe301c64f6d4aa5  Link opens in a new window
    Academic Journal
    Full Text  Link opens in a new windowDetails
    Title:
    Novel genes and mutations in patients affected by recurrent pregnancy loss.
    Authors:
    Paula Quintero-Ronderos
    Eric Mercier
    Michiko Fukuda
    Ronald González
    Carlos Fernando Suárez
    Manuel Alfonso Patarroyo
    Daniel Vaiman
    Jean-Christophe Gris
    Paul Laissue
    Show more
    Subject Terms:
    Medicine
    Science
    Source:
    PLoS ONE, Vol 12, Iss 10, p e0186149 (2017)
    File Description:
    electronic resource
    Relation:
    http://europepmc.org/articles/PMC5634651?pdf=render; https://doaj.org/toc/1932-6203
    Access URL:
    https://doaj.org/article/75387b41be224ec28540989547e13ec5  Link opens in a new window
    Academic Journal
    Full Text  Link opens in a new windowDetails
    Title:
    Exome sequencing is an efficient tool for variant late-infantile neuronal ceroid lipofuscinosis molecular diagnosis.
    Authors:
    Liliana Catherine Patiño
    Rajani Battu
    Oscar Ortega-Recalde
    Jeyabalan Nallathambi
    Venkata Ramana Anandula
    Umashankar Renukaradhya
    Paul Laissue
    Show more
    Subject Terms:
    Medicine
    Science
    Source:
    PLoS ONE, Vol 9, Iss 10, p e109576 (2014)
    File Description:
    electronic resource
    Relation:
    http://europepmc.org/articles/PMC4198115?pdf=render; https://doaj.org/toc/1932-6203
    Access URL:
    https://doaj.org/article/10d9951d115b4fce98d1f082ff924fd6  Link opens in a new window
    Academic Journal
    Full Text  Link opens in a new windowDetails
    Title:
    Refined mapping of a quantitative trait locus on chromosome 1 responsible for mouse embryonic death.
    Authors:
    Magalie Vatin
    Gaetan Burgio
    Gilles Renault
    Paul Laissue
    Virginie Firlej
    Françoise Mondon
    Xavier Montagutelli
    Daniel Vaiman
    Catherine Serres
    Ahmed Ziyyat
    Show more
    Subject Terms:
    Medicine
    Science
    Source:
    PLoS ONE, Vol 7, Iss 8, p e43356 (2012)
    File Description:
    electronic resource
    Relation:
    https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22916247/pdf/?tool=EBI; https://doaj.org/toc/1932-6203
    Access URL:
    https://doaj.org/article/3c85b1fbc93948ed8d34f85be915745b  Link opens in a new window
    Academic Journal
    Full Text  Link opens in a new windowDetails
    Title:
    Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure.
    Authors:
    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
    Show more
    Subject Terms:
    Medicine
    Science
    Source:
    PLoS ONE, Vol 7, Iss 3, p e33412 (2012)
    File Description:
    electronic resource
    Relation:
    http://europepmc.org/articles/PMC3302824?pdf=render; https://doaj.org/toc/1932-6203
    Access URL:
    https://doaj.org/article/06c5913e0dc14403ac36ee9c837b2c4d  Link opens in a new window
    Academic Journal
    Full Text  Link opens in a new windowDetails
    Title:
    Ausencia de mutaciones en HPGD en una familia colombiana afectada por osteoartropatía hipertrófica primaria sugiere un nuevo locus de la enfermedad
    Authors:
    Carolina Rivera Nieto
    Carlos M. Restrepo
    Chae Bong Whang
    David Bonthron
    Paul Laissue
    Show more
    Subject Terms:
    Medicine
    Medicine (General)
    R5-920
    Source:
    Iatreia, Vol 23, Iss 4-S (2010)
    File Description:
    electronic resource
    Relation:
    https://revistas.udea.edu.co/index.php/iatreia/article/view/8178; https://doaj.org/toc/2011-7965
    Access URL:
    https://doaj.org/article/5c24ce9717e742139a950d07d1a1ce40  Link opens in a new window
    Academic Journal
    Details
    Title:
    Agammaglobulinemia ligada A X Y onicodistrofia: dos nuevas mutaciones en el gen BTK y exclusión de mutaciones en el gen SOX9
    Authors:
    Carolina Rivera Nieto
    Taryn Castro
    Carlos Olmos
    Carlos M. Restrepo
    Paul Laissue
    Show more
    Subject Terms:
    Medicine
    Medicine (General)
    R5-920
    Source:
    Iatreia, Vol 23, Iss 4-S (2010)
    File Description:
    electronic resource
    Relation:
    https://revistas.udea.edu.co/index.php/iatreia/article/view/8175; https://doaj.org/toc/2011-7965
    Access URL:
    https://doaj.org/article/9bd173e5556b4b19af9f7be1f07a16bf  Link opens in a new window
    Academic Journal
    Details
      Showing 1-18 from 18 results

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