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Fabien Guimiot

Showing results (71-80 of 92) with videos related to

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Neuron|March 17, 2026
Two translocation mechanisms drive neural stem cell dissemination into the human fetal cortexRyszard Wimmer, Clarisse Brunet Avalos, Pauline Lestienne, et al.
Haematologica|June 29, 2019
CD117<sup>hi</sup> expression identifies a human fetal hematopoietic stem cell population with high proliferation and self-renewal potentialLoïc Maillard, Sandra Sanfilippo, Carine Domenech, et al.
American Journal of Medical Genetics. Part A|May 19, 2009
Giant diencephalic harmartoma and related anomalies: a newly recognized entity distinct from the Pallister-Hall syndromeFabien Guimiot, Pascale Marcorelles, Azzedine Aboura, et al.
Prenatal Diagnosis|November 22, 2012
Application of a new molecular technique for the genetic evaluation of products of conceptionFrancesca R Grati, Denise Molina Gomes, Devika Ganesamoorthy, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 19, 2019
Sostdc1 is expressed in all major compartments of developing and adult mammalian eyesMaud Valensi, Gabrielle Goldman, Dominique Marchant, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 18, 2025
Mapping the developmental profile of ventricular zone-derived neurons in the human cerebellumAnders W Erickson, Henry Tan, Liam D Hendrikse, et al.
Cell Reports|June 9, 2023
Distinct subsets of multi-lymphoid progenitors support ontogeny-related changes in human lymphopoiesisSeydou Keita, Samuel Diop, Shalva Lekiashvili, et al.
Immunity|October 19, 2017
Molecular and Functional Characterization of Lymphoid Progenitor Subsets Reveals a Bipartite Architecture of Human LymphopoiesisKutaiba Alhaj Hussen, Thien-Phong Vu Manh, Fabien Guimiot, et al.
Acta Neuropathologica Communications|July 26, 2014
Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephalyCatherine Fallet-Bianco, Annie Laquerrière, Karine Poirier, et al.
Prenatal Diagnosis|November 19, 2016
Fraser syndrome: features suggestive of prenatal diagnosis in a review of 38 casesAude Tessier, Mélie Sarreau, Fanny Pelluard, et al.
Pageof 10

Showing results (71-80 of 92) with videos related to

Sort By:
Pageof 10
Neuron|March 17, 2026
Two translocation mechanisms drive neural stem cell dissemination into the human fetal cortexRyszard Wimmer, Clarisse Brunet Avalos, Pauline Lestienne, et al.
Haematologica|June 29, 2019
CD117<sup>hi</sup> expression identifies a human fetal hematopoietic stem cell population with high proliferation and self-renewal potentialLoïc Maillard, Sandra Sanfilippo, Carine Domenech, et al.
American Journal of Medical Genetics. Part A|May 19, 2009
Giant diencephalic harmartoma and related anomalies: a newly recognized entity distinct from the Pallister-Hall syndromeFabien Guimiot, Pascale Marcorelles, Azzedine Aboura, et al.
Prenatal Diagnosis|November 22, 2012
Application of a new molecular technique for the genetic evaluation of products of conceptionFrancesca R Grati, Denise Molina Gomes, Devika Ganesamoorthy, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 19, 2019
Sostdc1 is expressed in all major compartments of developing and adult mammalian eyesMaud Valensi, Gabrielle Goldman, Dominique Marchant, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 18, 2025
Mapping the developmental profile of ventricular zone-derived neurons in the human cerebellumAnders W Erickson, Henry Tan, Liam D Hendrikse, et al.
Cell Reports|June 9, 2023
Distinct subsets of multi-lymphoid progenitors support ontogeny-related changes in human lymphopoiesisSeydou Keita, Samuel Diop, Shalva Lekiashvili, et al.
Immunity|October 19, 2017
Molecular and Functional Characterization of Lymphoid Progenitor Subsets Reveals a Bipartite Architecture of Human LymphopoiesisKutaiba Alhaj Hussen, Thien-Phong Vu Manh, Fabien Guimiot, et al.
Acta Neuropathologica Communications|July 26, 2014
Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephalyCatherine Fallet-Bianco, Annie Laquerrière, Karine Poirier, et al.
Prenatal Diagnosis|November 19, 2016
Fraser syndrome: features suggestive of prenatal diagnosis in a review of 38 casesAude Tessier, Mélie Sarreau, Fanny Pelluard, et al.
Pageof 10