Search Results - Annette Schenck
- Showing 1 - 20 results of 28
- Go to Next Page
-
1
-
2
-
3
A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P by Annette Schenck, Barbara Bardoni, Annamaria Moro, Claudia Bagni, Jean‐Louis Mandel
Published 2001Artigo -
4
-
5
-
6
-
7
Protein complexes containing CYFIP/Sra/PIR121 coordinate Arf1 and Rac1 signalling during clathrin–AP-1-coated carrier biogenesis at the TGN by Mihaela Anitei, Christoph Stange, Irina Parshina, Thorsten Baust, Annette Schenck, Graça Raposo, Tomas Kirchhausen, Bernard Hoflack
Published 2010Artigo -
8
-
9
-
10
-
11
FMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts by Marie Castets, Céline Schaeffer, Elías Bechara, Annette Schenck, E.W. Khandjian, Sylvie Luche, Hervé Moine, Thierry Rabilloud, Jean‐Louis Mandel, Barbara Bardoni
Published 2005Artigo -
12
A New Fiji-Based Algorithm That Systematically Quantifies Nine Synaptic Parameters Provides Insights into Drosophila NMJ Morphometry by Bonnie Nijhof, Anna Castells‐Nobau, Louis Wolf, Jolanda M. Scheffer-de Gooyert, Ignacio Cobeta, Laura Torroja, Lluís Coromina, Jeroen van der Laak, Annette Schenck
Published 2016Artigo -
13
Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules by Korinna Kochinke, Christiane Zweier, Bonnie Nijhof, Michaela Fencková, Pavel Čížek, Frank Honti, Shivakumar Keerthikumar, Merel A.W. Oortveld, Tjitske Kleefstra, Jamie M. Kramer, Caleb Webber, Martijn A. Huynen, Annette Schenck
Published 2016Artigo -
14
CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila by Christiane Zweier, Eiko K. de Jong, Markus Zweier, Alfredo Orrico, Lilian Bomme Ousager, Amanda Collins, Emilia K. Bijlsma, Merel A.W. Oortveld, Arif B. Ekici, André Reis, Annette Schenck, Anita Rauch
Published 2009Artigo -
15
Habituation Learning Is a Widely Affected Mechanism in Drosophila Models of Intellectual Disability and Autism Spectrum Disorders by Michaela Fencková, Laura E.R. Blok, Lenke Asztalos, David P. Goodman, Pavel Čížek, Euginia L. Singgih, Jeffrey Glennon, Joanna IntHout, Christiane Zweier, Evan E. Eichler, Catherine R. von Reyn, Raphael Bernier, Zoltán Asztalos, Annette Schenck
Published 2019Artigo -
16
Epigenetic Regulation of Learning and Memory by Drosophila EHMT/G9a by Jamie M. Kramer, Korinna Kochinke, Merel A.W. Oortveld, Hendrik Marks, Daniela Kramer, Eiko K. de Jong, Zoltán Asztalos, J. Timothy Westwood, Hendrik G. Stunnenberg, Marla B. Sokolowski, Krystyna Keleman, Huiqing Zhou, Hans van Bokhoven, Annette Schenck
Published 2011Artigo -
17
CDK19 is disrupted in a female patient with bilateral congenital retinal folds, microcephaly and mild mental retardation by Arijit Mukhopadhyay, Jamie M. Kramer, Gerard Merkx, Dorien Lugtenberg, Dominique Smeets, Merel A.W. Oortveld, Ellen A.W. Blokland, Jyoti Agrawal, Annette Schenck, Hans van Bokhoven, Erik Huys, Eric Schoenmakers, Ad Geurts van Kessel, C. E. van Nouhuys, Frans P.M. Cremers
Published 2010Artigo -
18
Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegeneration by Aline Dubos, Anna Castells‐Nobau, Hamid Méziane, Merel A.W. Oortveld, Xander Houbaert, Giovanni Iacono, Christelle Martin, Christophe Mittelhaeuser, Valérie Lalanne, Jamie M. Kramer, Anuradha Bhukel, Christine Quentin, Jan Slabbert, Patrik Verstreken, Stefan J. Sigrist, Nadia Messaddeq, Marie‐Christine Birling, Mohammed Selloum, Henk G. Stunnenberg, Yann Humeau, Annette Schenck, Yann Hérault
Published 2015Artigo -
19
SLC29A3 gene is mutated in pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome and interacts with the insulin signaling pathway by Simon T. Cliffe, Jamie M. Kramer, Khalid Hussain, Joris H. Robben, Eiko K. de Jong, Arjan Pm de Brouwer, Esther Nibbeling, Erik‐Jan Kamsteeg, Melanie Wong, Julie Prendiville, Chela James, Raja Padidela, Charlie Becknell, Hans van Bokhoven, Peter M.T. Deen, Raoul C. M. Hennekam, Robert Lindeman, Annette Schenck, Tony Roscioli, Michael F. Buckley
Published 2009Artigo -
20
Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorder by Tom S. Koemans, Tjitske Kleefstra, Melissa C. Chubak, Max H. Stone, Margot R.F. Reijnders, Sonja de Munnik, Marjolein H. Willemsen, Michaela Fencková, Connie T. R. M. Stumpel, Levinus A. Bok, Margarita Sáenz, Kyna A. Byerly, Linda B. Baughn, Alexander P.A. Stegmann, Rolph Pfundt, Huiqing Zhou, Hans van Bokhoven, Annette Schenck, Jamie M. Kramer
Published 2017Artigo
Search Tools:
Related Subjects
Biology
Genetics
Gene
Neuroscience
Phenotype
Intellectual disability
Cell biology
Medicine
Psychology
Autism
Psychiatry
Drosophila (subgenus)
Drosophila melanogaster
Cell
Computational biology
Histone
Signal transduction
Actin cytoskeleton
Candidate gene
Computer science
Cytoskeleton
Developmental psychology
Disease
Epigenetics
Exome sequencing
FMR1
Fragile x
Gene knockdown
Haploinsufficiency
Microcephaly