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Saillour, Yoann
92  Ergebnisse:
Personensuche X
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1

Repurposing of the multiciliation gene regulatory network i..:

Moreau, Matthieu X. ; Saillour, Yoann ; Elorriaga, Vicente...
Developmental Cell.  58 (2023)  15 - p. 1365-1382.e6 , 2023
Link: https://doi.org/10.1016/..
 
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CROSSTALK BETWEEN PROTOCADHERIN 8 AND TRANSCRIPTION FACTOR ..:

Cwetsch, Andrzej W ; Gilabert-Juan, Javier ; Ferreira, Sofia...
IBRO Neuroscience Reports.  15 (2023)  - p. S85 , 2023
Link: https://doi.org/10.1016/..
 
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3

Severe and progressive neuronal loss in myelomeningocele be..:

Ben Miled, Selima ; Loeuillet, Laurence ; Duong Van Huyen, Jean-Paul...
American Journal of Obstetrics and Gynecology.  223 (2020)  2 - p. 256.e1-256.e9 , 2020
Link: https://doi.org/10.1016/..
 
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4

The intellectual disability protein Oligophrenin‐1 controls..:

Pillet, Laure‐Elise ; Cresto, Noémie ; Saillour, Yoann...
Glia.  68 (2020)  9 - p. 1729-1742 , 2020
Link: https://doi.org/10.1002/..
 
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5

Evolutionary Gain of Dbx1 Expression Drives Subplate Identi..:

Arai, Yoko ; Cwetsch, Andrzej W. ; Coppola, Eva...
Cell Reports.  29 (2019)  3 - p. 645-658.e5 , 2019
Link: https://doi.org/10.1016/..
 
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6

Ciliogenesis and cell cycle alterations contribute to KIF2A..:

Broix, Loïc ; Asselin, Laure ; Silva, Carla G...
Human Molecular Genetics.  27 (2017)  2 - p. 224-238 , 2017
Link: https://doi.org/10.1093/..
 
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7

Mutations in the HECT domain of NEDD4L lead to AKT–mTOR pat..:

Deciphering Developmental Disorders study ; Broix, Loïc ; Jagline, Hélène...
Nature Genetics.  48 (2016)  11 - p. 1349-1358 , 2016
Link: https://doi.org/10.1038/..
 
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8

List of Contributors:

, In: Neuronal and Synaptic Dysfunction in Autism Spectrum Disorder and Intellectual Disability,
Barnes, Stephanie A. ; Bassani, Silvia ; Bayés, Àlex... - p. ix-x , 2016
Link: https://doi.org/10.1016/..
 
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9

Genetic Causes of Intellectual Disability: The Genes Contro..:

, In: Neuronal and Synaptic Dysfunction in Autism Spectrum Disorder and Intellectual Disability,
Saillour, Yoann ; Chelly, Jamel - p. 43-64 , 2016
Link: https://doi.org/10.1016/..
 
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10

De novo TUBB2B mutation causes fetal akinesia deformation s..:

Laquerriere, Annie ; Gonzales, Marie ; Saillour, Yoann...
European Journal of Medical Genetics.  59 (2016)  4 - p. 249-256 , 2016
Link: https://doi.org/10.1016/..
 
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11

Altered microtubule dynamics and vesicular transport in mou..:

Delépine, Chloé ; Meziane, Hamid ; Nectoux, Juliette...
Human Molecular Genetics.  25 (2015)  1 - p. 146-157 , 2015
Link: https://doi.org/10.1093/..
 
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12

The wide spectrum of tubulinopathies: what are the key feat..:

Bahi-Buisson, Nadia ; Poirier, Karine ; Fourniol, Franck...
Brain.  137 (2014)  6 - p. 1676-1700 , 2014
Link: https://doi.org/10.1093/..
 
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13

Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malforma..:

Poirier, Karine ; Lebrun, Nicolas ; Broix, Loic...
Nature Genetics.  45 (2013)  6 - p. 639-647 , 2013
Link: https://doi.org/10.1038/..
 
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14

Homozygous truncating mutation of the KBP gene, encoding a ..:

Valence, Stéphanie ; Poirier, Karine ; Lebrun, Nicolas...
neurogenetics.  14 (2013)  3-4 - p. 215-224 , 2013
Link: https://doi.org/10.1007/..
 
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15

Erratum: Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause..:

Poirier, Karine ; Lebrun, Nicolas ; Broix, Loic...
Nature Genetics.  45 (2013)  8 - p. 962-962 , 2013
Link: https://doi.org/10.1038/..
 
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