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Dario Acampora

Showing results (31-40 of 40) with videos related to

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Peerj|September 7, 2013
The homeodomain factor Gbx1 is required for locomotion and cell specification in the dorsal spinal cordHamid Meziane, Valérie Fraulob, Fabrice Riet, et al.
Human Molecular Genetics|September 6, 2011
Combined deficiency of alpha and epsilon sarcoglycan disrupts the cardiac dystrophin complexAlessio Lancioni, Ida Luisa Rotundo, Yvonne Monique Kobayashi, et al.
The American Journal of Pathology|November 7, 2009
Expression of the brain transcription factor OTX1 occurs in a subset of normal germinal-center B cells and in aggressive Non-Hodgkin LymphomaDaniela Omodei, Dario Acampora, Filippo Russo, et al.
Cell Reports|August 16, 2014
Sox6 and Otx2 control the specification of substantia nigra and ventral tegmental area dopamine neuronsLia Panman, Maria Papathanou, Ariadna Laguna, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 23, 2003
Unsuspected role of the brain morphogenetic gene Otx1 in hematopoiesisElena Levantini, Alessandra Giorgetti, Francesco Cerisoli, et al.
Human Molecular Genetics|November 16, 2013
Graded Otx2 activities demonstrate dose-sensitive eye and retina phenotypesClémence Bernard, Hyoung-Tai Kim, Raoul Torero Ibad, et al.
Nature Communications|September 3, 2016
Cripto is essential to capture mouse epiblast stem cell and human embryonic stem cell pluripotencyAlessandro Fiorenzano, Emilia Pascale, Cristina D'Aniello, et al.
Genes & Development|March 7, 2024
A maternal-effect <i>Padi6</i> variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryosCarlo Giaccari, Francesco Cecere, Lucia Argenziano, et al.
Molecular Neurodegeneration|June 21, 2021
Identification of sixteen novel candidate genes for late onset Parkinson's diseaseAlessandro Gialluisi, Mafalda Giovanna Reccia, Nicola Modugno, et al.
EMBO Molecular Medicine|January 17, 2012
Mutant p63 causes defective expansion of ectodermal progenitor cells and impaired FGF signalling in AEC syndromeGiustina Ferone, Helen A Thomason, Dario Antonini, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Peerj|September 7, 2013
The homeodomain factor Gbx1 is required for locomotion and cell specification in the dorsal spinal cordHamid Meziane, Valérie Fraulob, Fabrice Riet, et al.
Human Molecular Genetics|September 6, 2011
Combined deficiency of alpha and epsilon sarcoglycan disrupts the cardiac dystrophin complexAlessio Lancioni, Ida Luisa Rotundo, Yvonne Monique Kobayashi, et al.
The American Journal of Pathology|November 7, 2009
Expression of the brain transcription factor OTX1 occurs in a subset of normal germinal-center B cells and in aggressive Non-Hodgkin LymphomaDaniela Omodei, Dario Acampora, Filippo Russo, et al.
Cell Reports|August 16, 2014
Sox6 and Otx2 control the specification of substantia nigra and ventral tegmental area dopamine neuronsLia Panman, Maria Papathanou, Ariadna Laguna, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 23, 2003
Unsuspected role of the brain morphogenetic gene Otx1 in hematopoiesisElena Levantini, Alessandra Giorgetti, Francesco Cerisoli, et al.
Human Molecular Genetics|November 16, 2013
Graded Otx2 activities demonstrate dose-sensitive eye and retina phenotypesClémence Bernard, Hyoung-Tai Kim, Raoul Torero Ibad, et al.
Nature Communications|September 3, 2016
Cripto is essential to capture mouse epiblast stem cell and human embryonic stem cell pluripotencyAlessandro Fiorenzano, Emilia Pascale, Cristina D'Aniello, et al.
Genes & Development|March 7, 2024
A maternal-effect <i>Padi6</i> variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryosCarlo Giaccari, Francesco Cecere, Lucia Argenziano, et al.
Molecular Neurodegeneration|June 21, 2021
Identification of sixteen novel candidate genes for late onset Parkinson's diseaseAlessandro Gialluisi, Mafalda Giovanna Reccia, Nicola Modugno, et al.
EMBO Molecular Medicine|January 17, 2012
Mutant p63 causes defective expansion of ectodermal progenitor cells and impaired FGF signalling in AEC syndromeGiustina Ferone, Helen A Thomason, Dario Antonini, et al.
Pageof 4