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Golzio, Christelle
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1

Improving laboratory animal genetic reporting: LAG-R guidel..:

Teboul, Lydia ; Amos-Landgraf, James ; Benavides, Fernando J....
Nature Communications.  15 (2024)  1 - p. , 2024
Link: https://doi.org/10.1038/..
 
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2

Loss of autism-candidate CHD8 perturbs neural crest develop..:

Hayot, Gaëlle ; Massonot, Mathieu ; Keime, Céline..
Life Science Alliance.  6 (2022)  1 - p. e202201456 , 2022
Link: https://doi.org/10.26508..
 
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3

Regulation of autism-relevant behaviors by cerebellar–prefr..:

Kelly, Elyza ; Meng, Fantao ; Fujita, Hirofumi...
Nature Neuroscience.  23 (2020)  9 - p. 1102-1110 , 2020
Link: https://doi.org/10.1038/..
 
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4

Mutations in the KIF21B kinesin gene cause neurodevelopment..:

Asselin, Laure ; Rivera Alvarez, José ; Heide, Solveig...
Nature Communications.  11 (2020)  1 - p. , 2020
Link: https://doi.org/10.1038/..
 
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5

A dominant vimentin variant causes a rare syndrome with pre..:

Cogné, Benjamin ; Bouameur, Jamal-Eddine ; Hayot, Gaëlle...
European Journal of Human Genetics.  28 (2020)  9 - p. 1218-1230 , 2020
Link: https://doi.org/10.1038/..
 
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6

International meeting on Wolf‐Hirschhorn syndrome: Update o..:

Nevado, Julián ; Ho, Karen S. ; Zollino, Marcella...
American Journal of Medical Genetics Part A.  182 (2019)  1 - p. 257-267 , 2019
Link: https://doi.org/10.1002/..
 
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7

Small molecule inhibition of RAS/MAPK signaling ameliorates..:

Tsai, I-Chun ; McKnight, Kelly ; McKinstry, Spencer U....
Scientific Reports.  8 (2018)  1 - p. , 2018
Link: https://doi.org/10.1038/..
 
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8

Kctd13-deficient mice display short-term memory impairment ..:

Arbogast, Thomas ; Razaz, Parisa ; Ellegood, Jacob...
Human Molecular Genetics.  28 (2018)  9 - p. 1474-1486 , 2018
Link: https://doi.org/10.1093/..
 
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9

Endoglin interacts with VEGFR2 to promote angiogenesis:

Tian, Hongyu ; Huang, Jennifer J. ; Golzio, Christelle...
The FASEB Journal.  32 (2018)  6 - p. 2934-2949 , 2018
Link: https://doi.org/10.1096/..
 
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10

Partial uniparental isodisomy of chromosome 16 unmasks a de..:

Helm, Benjamin M. ; Willer, Jason R. ; Sadeghpour, Azita...
Human Genomics.  11 (2017)  1 - p. , 2017
Link: https://doi.org/10.1186/..
 
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11

Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autos..:

Bolar, Nikhita Ajit ; Golzio, Christelle ; Živná, Martina...
The American Journal of Human Genetics.  99 (2016)  1 - p. 174-187 , 2016
Link: https://doi.org/10.1016/..
 
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12

Identification of cis-suppression of human disease mutation..:

Task Force for Neonatal Genomics ; Jordan, Daniel M. ; Frangakis, Stephan G....
Nature.  524 (2015)  7564 - p. 225-229 , 2015
Link: https://doi.org/10.1038/..
 
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13

Rbm8aHaploinsufficiency Disrupts Embryonic Cortical Develop..:

Mao, Hanqian ; Pilaz, Louis-Jan ; McMahon, John J....
The Journal of Neuroscience.  35 (2015)  18 - p. 7003-7018 , 2015
Link: https://doi.org/10.1523/..
 
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14

Phosphorylation of Threonine 794 on Tie1 by Rac1/PAK1 Revea..:

Reinardy, Jessica L. ; Corey, Daniel M. ; Golzio, Christelle...
PLOS ONE.  10 (2015)  10 - p. e0139614 , 2015
Link: https://doi.org/10.1371/..
 
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15

A Novel Ribosomopathy Caused by Dysfunction of RPL10 Disrup..:

Brooks, Susan S ; Wall, Alissa L ; Golzio, Christelle...
Genetics.  198 (2014)  2 - p. 723-733 , 2014
Link: https://doi.org/10.1534/..
 
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