Ngā hua rapu kaituhi :: APM

1

Immunologic aspects of preeclampsia mā Henri Boulanger, S. Bounan, Amel Mahdhi, Dominique Drouin, Salima Ahriz-Saksi, Fabien Guimiot, Nathalie Rouas‐Freiss

I whakaputaina 2024

Whiwhi kuputuhi katoa
Artigo

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2

Negative Fetal FSH/LH Regulation in Late Pregnancy Is Associated with Declined Kisspeptin/KISS1R Expression in the Tuberal Hypothalamus mā Fabien Guimiot, L. Chevrier, Sophie Dreux, Didier Chevenne, Alain Caraty, Anne Lise Delezoïde, Nicolás de Roux

I whakaputaina 2012

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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3

Defective migration of neuroendocrine GnRH cells in human arrhinencephalic conditions mā Luís Teixeira, Fabien Guimiot, Catherine Dodé, Catherine Fallet‐Bianco, Robert P. Millar, Anne‐Lise Delezoide, Jean‐Pierre Hardelin

I whakaputaina 2010

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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4

Diffusion‐weighted magnetic resonance imaging of the fetal brain in intrauterine growth restriction mā Owen J. Arthurs, A. Rega, Fabien Guimiot, N. Belarbi, Jonathan Rosenblatt, Valérie Biran, Monique Elmaleh, G. Sebag, Marianne Alison

I whakaputaina 2016

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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5

Fetal urine biochemistry at 13-23 weeks of gestation in lower urinary tract obstruction: criteria for<i>in-utero</i>treatment mā W. Abdennadher, G. E. Chalouhi, Sophie Dreux, Jonathan Rosenblatt, R. Favre, Fabien Guimiot, Laurent Salomon, J.-F. Oury, Y. Ville, Françoise Müller

I whakaputaina 2014

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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6

Single-Cell Transcriptomic Analyses of the Developing Meninges Reveal Meningeal Fibroblast Diversity and Function mā John DeSisto, Rebecca O’Rourke, Hannah E. Jones, Bradley Pawlikowski, Alexandra D. Malek, Stephanie Bonney, Fabien Guimiot, Kenneth L. Jones, Julie A. Siegenthaler

I whakaputaina 2020

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Artigo

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7

Phenotypic outcomes in Mouse and Human Foxc1 dependent Dandy-Walker cerebellar malformation suggest shared mechanisms mā Parthiv Haldipur, Derek Dang, Kimberly A. Aldinger, Olivia K Janson, Fabien Guimiot, Homa Adle-Biasette, William B. Dobyns, Joseph R. Siebert, Rosa Russo, Kathleen J. Millen

I whakaputaina 2017

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Artigo

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8

Sodium/Iodide Symporter (NIS) Gene Expression Is the Limiting Step for the Onset of Thyroid Function in the Human Fetus mā Gabor Szinnai, Ludovic Lacroix, Aurore Carré, Fabien Guimiot, Monique Talbot, Jéléna Martinovic, Anne‐Lise Delezoide, Michel Vekemans, Stefan Michiels, Bernard Caillou, Martin Schlumberger, Jean‐Michel Bidart, Michel Polak

I whakaputaina 2006

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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9

Dynamics of Thymus-Colonizing Cells during Human Development mā Rima Haddad, Fabien Guimiot, Emmanuelle Six, Frédéric Jourquin, Niclas Setterblad, Edmond Kahn, Micaël Yagello, Cécile Schiffer, Isabelle André‐Schmutz, Marina Cavazzana, Jean Claude Gluckman, Anne‐Lise Delezoide, Françoise Pflumio, Bruno Canque

I whakaputaina 2006

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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10

Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ gene mā Pascale Saugier‐Veber, Florent Marguet, François Lecoquierre, Homa Adle‐Biassette, Fabien Guimiot, Sara Cipriani, Sophie Patrier, M. Brasseur‐Daudruy, Alice Goldenberg, Valérie Layet, Yline Capri, Marion Gérard, Thierry Frébourg, Annie Laquerrière

I whakaputaina 2017

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Artigo

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11

A cell fate decision map reveals abundant direct neurogenesis bypassing intermediate progenitors in the human developing neocortex mā Laure Coquand, Clarisse Brunet Avalos, Anne‐Sophie Macé, Sarah Farcy, Amandine Di Cicco, Maruša Lampič, Ryszard Wimmer, B. Bessières, Tania Attié‐Bitach, Vincent Fraisier, Pierre Sens, Fabien Guimiot, Jean‐Baptiste Brault, Alexandre D. Baffet

I whakaputaina 2024

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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12

Mutations in GLDN , Encoding Gliomedin, a Critical Component of the Nodes of Ranvier, Are Responsible for Lethal Arthrogryposis mā Jérôme Maluenda, Constance Manso, Loïc Quevarec, Alexandre Vivanti, Florent Marguet, Marie Gonzalès, Fabien Guimiot, Florence Petit, Annick Toutain, Sandra Whalen, R Grigorescu, Anne Dieux Coeslier, Marta Gut, Marta Gut, Annie Laquerrière, Jérôme Devaux, Judith Melki

I whakaputaina 2016

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Artigo

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13

Molecular and Functional Characterization of Lymphoid Progenitor Subsets Reveals a Bipartite Architecture of Human Lymphopoiesis mā Kutaiba Alhaj Hussen, Thien‐Phong Vu Manh, Fabien Guimiot, Elisabeth Nelson, Emna Chabaane, Marc Delord, Maxime Barbier, Claire Berthault, Nicolas Dulphy, A. Alberdi, Odile Burlen‐Defranoux, Gèrard Socié, Jean Christophe Bories, Jérôme Larghero, Valérie Vanneaux, Els Verhoeyen, Thierry Wirth, Marc Dalod, Jean Claude Gluckman, Ana Cumano, Bruno Canque

I whakaputaina 2017

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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14

Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly mā Catherine Fallet‐Bianco, Annie Laquerrière, Karine Poirier, Ferechté Razavi, Fabien Guimiot, Patrícia Dias, Laurence Lœuillet, Karine Lascelles, Chérif Beldjord, Nathalie Carion, Aurélie Toussaint, Nicole Revençu, Marie‐Claude Addor, Benoît Lhermitte, Marie Gonzalès, Jelena Martinovich, Bettina Bessières, Maryse Marcy-Bonnière, Frédérique Jossic, Pascale Marcorelles, Philippe Loget, Jamel Chelly, Nadia Bahi‐Buisson

I whakaputaina 2014

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Artigo

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15

Spatiotemporal expansion of primary progenitor zones in the developing human cerebellum mā Parthiv Haldipur, Kimberly A. Aldinger, Silvia Bernardo, Mei Deng, Andrew E. Timms, Lynne M. Overman, Conrad Winter, Steven Lisgo, Razavi, Evelina Silvestri, Lucia Manganaro, Homa Adle‐Biassette, Fabien Guimiot, Rosa Russo, Debora Kidron, Patrick R. Hof, Dianne Gerrelli, Susan Lindsay, William B. Dobyns, Ian Glass, Paula Alexandre, Kathleen J. Millen

I whakaputaina 2019

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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16

Identification of Mutations in TMEM5 and ISPD as a Cause of Severe Cobblestone Lissencephaly mā Sandrine Vuillaumier‐Barrot, C. Bouchet-Séraphin, M. Chelbi, Louise Devisme, Samuel Quentin, Steven Gazal, Annie Laquerrière, Catherine Fallet‐Bianco, Philippe Loget, Sylvie Odent, Dominique Carles, Anne Bazin, Jacqueline Aziza, Alix Clémenson, Fabien Guimiot, Maryse Bonnière, Sophie Monnot, Christine Bôle‐Feysot, Jean‐Pierre Bernard, Laurence Lœuillet, Marie Gonzalès, Koryna Socha, Bernard Grandchamp, Tania Attié‐Bitach, Férechté Encha‐Razavi, Nathalie Seta

I whakaputaina 2012

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Artigo

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17

Extracellular LGALS3BP regulates neural progenitor position and relates to human cortical complexity mā Christina Kyrousi, Adam C. O’Neill, Agnieska Brazovskaja, Zhisong He, Pavel Kielkowski, Laure Coquand, Rossella Di Giaimo, Pierpaolo D’ Andrea, Alexander Belka, Andrea Forero Echeverry, Davide Mei, Matteo Lenge, Cristiana Cruceanu, Isabel Y. Buchsbaum, Shahryar Khattak, Fabien Guimiot, Elisabeth B. Binder, Frances Elmslie, Renzo Guerrini, Alexandre D. Baffet, Stephan A. Sieber, Barbara Treutlein, Stephen P. Robertson, Silvia Cappello

I whakaputaina 2021

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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18

Extracellular LGALS3BP regulates neural progenitor position and relates to human cortical complexity mā Kyrousi, Christina, O’Neill, Adam C., Brazovskaja, Agnieska, He, Zhisong, Kielkowski, Pavel, Coquand, Laure, Di Giaimo, Rossella, D’ Andrea, Pierpaolo, Belka, Alexander, Forero Echeverry, Andrea, Mei, Davide, Lenge, Matteo, Cruceanu, Cristiana, Buchsbaum, Isabel Y., Khattak, Shahryar, Fabien, Guimiot, Binder, Elisabeth, Elmslie, Frances, Guerrini, Renzo, Baffet, Alexandre D., Sieber, Stephan A., Treutlein, Barbara, Robertson, Stephen P., Cappello, Silvia

I whakaputaina 2021

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19

Molecular heterogeneity in fetal forms of type II lissencephaly mā C Bouchet, M. Gonzalés, Sandrine Vuillaumier‐Barrot, Louise Devisme, C. Lebizec, Elisabeth Alanio, Anne Bazin, B. Bessières-Grattagliano, Nicole Bigi, Patricia Blanchet, Dominique Bonneau, Maryse Bonnières, Dominique Carles, Sophie Delahaye, Catherine Fallet‐Bianco, Dominique Figarella‐Branger, Dominique Gaillard, B. Gasser, Fabien Guimiot, Madeleine Joubert, Nicole Laurent, Agnès Liprandi, Philippe Loget, Pascale Marcorelles, Jéléna Martinovic, F. Menez, Sophie Patrier, Fanny Pelluard-Nehmé, Marie-José Perez, C. Rouleau-Dubois, Stéphane Triau, A. Laquérrière, Férechté Encha‐Razavi, Nathalie Seta

I whakaputaina 2007

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Artigo

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20

Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies mā Louise Devisme, C Bouchet, Marie Gonzalès, Elisabeth Alanio, Anne Bazin, Bettina Bessières, Nicole Bigi, Patricia Blanchet, Dominique Bonneau, Maryse Bonnières, Martine Bucourt, Dominique Carles, Bénédicte Clarisse, S. Delahaye, Catherine Fallet‐Bianco, Dominique Figarella‐Branger, Dominique Gaillard, Bernard Gasser, Anne‐Lise Delezoide, Fabien Guimiot, Madeleine Joubert, Nicole Laurent, Annie Laquerrière, Agnès Liprandi, Philippe Loget, Pascale Marcorelles, Jéléna Martinovic, Françoise Ménez, Sophie Patrier, Fanny Pelluard, Marie-José Perez, Caroline Rouleau, Stéphane Triau, Tania Attié‐Bitach, Sandrine Vuillaumier‐Barrot, Nathalie Seta, Férechté Encha‐Razavi

I whakaputaina 2012

Whiwhi kuputuhi katoa
Artigo

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