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Bio-Protocol
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August 28, 2023
T Cell Clonal Analysis Using Single-cell RNA Sequencing and Reference Maps
Massimo Andreatta, Paul Gueguen, Nicholas Borcherding, et al.
Annales De Biologie Clinique
|
August 6, 2016
Next generation sequencing with a semi-conductor technology (Ion Torrent PGM™) for HLA typing: overall workflow performance and debate
Virginie Moalic-Allain, Bernard Mercier, Paul Gueguen, et al.
Nature Communications
|
January 29, 2024
Semi-supervised integration of single-cell transcriptomics data
Massimo Andreatta, Léonard Hérault, Paul Gueguen, et al.
British Journal of Haematology
|
May 27, 2015
A new point mutation in EPOR inducing a short deletion in congenital erythrocytosis
Aurélie Chauveau, Damien Luque Paz, Lydie Lecucq, et al.
Applied Immunohistochemistry & Molecular Morphology : AIMM
|
May 7, 2016
Is SP174 Immunohistochemistry an Interesting Ancillary Tool to Determine RAS Mutational Status in Colorectal Carcinoma?
Arnaud Uguen, Paul Gueguen, Briac Guibourg, et al.
Molecular Genetics & Genomic Medicine
|
May 15, 2025
A new syndromic case of hearing loss and ectodermal anomalies associated with a recurrent missense variation in GJB6 gene
Badreddine Elmakhzen, Paul Rollier, Clémence Saillard, et al.
Nature Communications
|
July 4, 2018
Human in vivo-generated monocyte-derived dendritic cells and macrophages cross-present antigens through a vacuolar pathway
Tsing-Lee Tang-Huau, Paul Gueguen, Christel Goudot, et al.
Stem Cells (Dayton, Ohio)
|
November 26, 2025
Stem cell specification and niche formation in developing incisor requires actomyosin forces
Yasmin Mohtadi Hamadani, Laura Evers, Satu-Marja Myllymaki, et al.
Science (New York, N.Y.)
|
January 13, 2018
The epigenetic control of stemness in CD8<sup>+</sup> T cell fate commitment
Luigia Pace, Christel Goudot, Elina Zueva, et al.
Clinical Genetics
|
November 10, 2024
Identification of a Rare Branch Point Variant in the SMS Gene in a Large Family With a Severe Form of Snyder-Robinson Syndrome
Antoine Civit, Nathalie Ronce, Benjamin Cogné, et al.
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of 5
Search research articles
Search
Showing results (1-10 of 44) with videos related to
Sort By:
Page
of 5
Bio-Protocol
|
August 28, 2023
T Cell Clonal Analysis Using Single-cell RNA Sequencing and Reference Maps
Massimo Andreatta, Paul Gueguen, Nicholas Borcherding, et al.
Annales De Biologie Clinique
|
August 6, 2016
Next generation sequencing with a semi-conductor technology (Ion Torrent PGM™) for HLA typing: overall workflow performance and debate
Virginie Moalic-Allain, Bernard Mercier, Paul Gueguen, et al.
Nature Communications
|
January 29, 2024
Semi-supervised integration of single-cell transcriptomics data
Massimo Andreatta, Léonard Hérault, Paul Gueguen, et al.
British Journal of Haematology
|
May 27, 2015
A new point mutation in EPOR inducing a short deletion in congenital erythrocytosis
Aurélie Chauveau, Damien Luque Paz, Lydie Lecucq, et al.
Applied Immunohistochemistry & Molecular Morphology : AIMM
|
May 7, 2016
Is SP174 Immunohistochemistry an Interesting Ancillary Tool to Determine RAS Mutational Status in Colorectal Carcinoma?
Arnaud Uguen, Paul Gueguen, Briac Guibourg, et al.
Molecular Genetics & Genomic Medicine
|
May 15, 2025
A new syndromic case of hearing loss and ectodermal anomalies associated with a recurrent missense variation in GJB6 gene
Badreddine Elmakhzen, Paul Rollier, Clémence Saillard, et al.
Nature Communications
|
July 4, 2018
Human in vivo-generated monocyte-derived dendritic cells and macrophages cross-present antigens through a vacuolar pathway
Tsing-Lee Tang-Huau, Paul Gueguen, Christel Goudot, et al.
Stem Cells (Dayton, Ohio)
|
November 26, 2025
Stem cell specification and niche formation in developing incisor requires actomyosin forces
Yasmin Mohtadi Hamadani, Laura Evers, Satu-Marja Myllymaki, et al.
Science (New York, N.Y.)
|
January 13, 2018
The epigenetic control of stemness in CD8<sup>+</sup> T cell fate commitment
Luigia Pace, Christel Goudot, Elina Zueva, et al.
Clinical Genetics
|
November 10, 2024
Identification of a Rare Branch Point Variant in the SMS Gene in a Large Family With a Severe Form of Snyder-Robinson Syndrome
Antoine Civit, Nathalie Ronce, Benjamin Cogné, et al.
Page
of 5