(Q48029963)

7 February 2018

title

Absent CNKSR2 causes seizures and intellectual, attention, and language deficits. (English)

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7 February 2018

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7 February 2018

Brigitte Gilbert-Dussardier

object named as

Brigitte Gilbert-Dussardier

4

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Stephen W. Scherer

16

object named as

Stephen W Scherer

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7 February 2018

Andrea K Vaags

1

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7 February 2018

Sarah Bowdin

2

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7 February 2018

Mary-Lou Smith

3

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7 February 2018

Katja S Brocke-Holmefjord

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7 February 2018

Katia Sinopoli

6

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7 February 2018

Cindy Gilles

7

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7 February 2018

Tove B Haaland

8

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7 February 2018

Catherine Vincent-Delorme

9

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7 February 2018

Emmanuelle Lagrue

10

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7 February 2018

Radu Harbuz

11

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7 February 2018

Susan Walker

12

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7 February 2018

Christian R Marshall

13

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7 February 2018

Gunnar Houge

14

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7 February 2018

Berge A Minassian

17

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7 February 2018

publication date

4 October 2014

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7 February 2018

published in

Annals of Neurology

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7 February 2018

volume

76

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7 February 2018

issue

5

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7 February 2018

page(s)

758-764

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7 February 2018

Characterization of the proteome, diseases and evolution of the human postsynaptic density.

cites work

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Organization and dynamics of PDZ-domain-related supramodules in the postsynaptic density

21 January 2018

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CNK2 couples NGF signal propagation to multiple regulatory cascades driving cell differentiation.

21 January 2018

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Proteomic characterization of the dynamic KSR-2 interactome, a signaling scaffold complex in MAPK pathway

21 January 2018

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Densin-180, a synaptic protein, links to PSD-95 through its direct interaction with MAGUIN-1

21 January 2018

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CNK and HYP form a discrete dimer by their SAM domains to mediate RAF kinase signaling

21 January 2018

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Association of membrane-associated guanylate kinase-interacting protein-1 with Raf-1.

21 January 2018

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Human homologue of Drosophila CNK interacts with Ras effector proteins Raf and Rlf

21 January 2018

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Defining mechanisms of actin polymerization and depolymerization during dendritic spine morphogenesis

21 January 2018

1 reference

The Database of Genomic Variants: a curated collection of structural variation in the human genome.

21 January 2018

1 reference

Prediction of the coding sequences of unidentified human genes. IX. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro

21 January 2018

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Uncovering quantitative protein interaction networks for mouse PDZ domains using protein microarrays

21 January 2018

1 reference

Clinical genetic study of the epilepsy-aphasia spectrum

21 January 2018

1 reference

What causes attention deficit hyperactivity disorder?

21 January 2018

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Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

21 January 2018

1 reference

Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.

21 January 2018

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Attention deficit disorder: a review of the past 10 years

21 January 2018

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eXclusion: toward integrating the X chromosome in genome-wide association analyses

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/ANA.24274

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7 February 2018

PubMed ID

25223753

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7 February 2018