Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 118

1.

Expression of Cntnap2 (Caspr2) in multiple levels of sensory systems.

Gordon A, Salomon D, Barak N, Pen Y, Tsoory M, Kimchi T, Peles E.

Mol Cell Neurosci. 2016 Jan;70:42-53. doi: 10.1016/j.mcn.2015.11.012. Epub 2015 Dec 2.

PMID:
26647347
2.

Genetic variants in autism-related CNTNAP2 impair axonal growth of cortical neurons.

Canali G, Garcia M, Hivert B, Pinatel D, Goullancourt A, Oguievetskaia K, Saint-Martin M, Girault JA, Faivre-Sarrailh C, Goutebroze L.

Hum Mol Genet. 2018 Jun 1;27(11):1941-1954. doi: 10.1093/hmg/ddy102.

PMID:
29788201
3.

Learning delays in a mouse model of Autism Spectrum Disorder.

Rendall AR, Truong DT, Fitch RH.

Behav Brain Res. 2016 Apr 15;303:201-7. doi: 10.1016/j.bbr.2016.02.006. Epub 2016 Feb 9.

4.

Caspr2-reactive antibody cloned from a mother of an ASD child mediates an ASD-like phenotype in mice.

Brimberg L, Mader S, Jeganathan V, Berlin R, Coleman TR, Gregersen PK, Huerta PT, Volpe BT, Diamond B.

Mol Psychiatry. 2016 Dec;21(12):1663-1671. doi: 10.1038/mp.2016.165. Epub 2016 Oct 4.

5.

Interaction proteomics of canonical Caspr2 (CNTNAP2) reveals the presence of two Caspr2 isoforms with overlapping interactomes.

Chen N, Koopmans F, Gordon A, Paliukhovich I, Klaassen RV, van der Schors RC, Peles E, Verhage M, Smit AB, Li KW.

Biochim Biophys Acta. 2015 Jul;1854(7):827-33. doi: 10.1016/j.bbapap.2015.02.008. Epub 2015 Feb 21.

PMID:
25707359
6.

CASPR2 forms a complex with GPR37 via MUPP1 but not with GPR37(R558Q), an autism spectrum disorder-related mutation.

Tanabe Y, Fujita-Jimbo E, Momoi MY, Momoi T.

J Neurochem. 2015 Aug;134(4):783-93. doi: 10.1111/jnc.13168. Epub 2015 Jun 3.

7.

Variants of the CNTNAP2 5' promoter as risk factors for autism spectrum disorders: a genetic and functional approach.

Chiocchetti AG, Kopp M, Waltes R, Haslinger D, Duketis E, Jarczok TA, Poustka F, Voran A, Graab U, Meyer J, Klauck SM, Fulda S, Freitag CM.

Mol Psychiatry. 2015 Jul;20(7):839-49. doi: 10.1038/mp.2014.103. Epub 2014 Sep 16.

PMID:
25224256
8.

Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development.

Anderson GR, Galfin T, Xu W, Aoto J, Malenka RC, Südhof TC.

Proc Natl Acad Sci U S A. 2012 Oct 30;109(44):18120-5. doi: 10.1073/pnas.1216398109. Epub 2012 Oct 16.

9.

Synaptic abnormalities and cytoplasmic glutamate receptor aggregates in contactin associated protein-like 2/Caspr2 knockout neurons.

Varea O, Martin-de-Saavedra MD, Kopeikina KJ, Schürmann B, Fleming HJ, Fawcett-Patel JM, Bach A, Jang S, Peles E, Kim E, Penzes P.

Proc Natl Acad Sci U S A. 2015 May 12;112(19):6176-81. doi: 10.1073/pnas.1423205112. Epub 2015 Apr 27.

10.

Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.

Peñagarikano O, Abrahams BS, Herman EI, Winden KD, Gdalyahu A, Dong H, Sonnenblick LI, Gruver R, Almajano J, Bragin A, Golshani P, Trachtenberg JT, Peles E, Geschwind DH.

Cell. 2011 Sep 30;147(1):235-46. doi: 10.1016/j.cell.2011.08.040.

11.

Selective Dysregulation of Hippocampal Inhibition in the Mouse Lacking Autism Candidate Gene CNTNAP2.

Jurgensen S, Castillo PE.

J Neurosci. 2015 Oct 28;35(43):14681-7. doi: 10.1523/JNEUROSCI.1666-15.2015.

12.

Comprehensive Analysis of the 16p11.2 Deletion and Null Cntnap2 Mouse Models of Autism Spectrum Disorder.

Brunner D, Kabitzke P, He D, Cox K, Thiede L, Hanania T, Sabath E, Alexandrov V, Saxe M, Peles E, Mills A, Spooren W, Ghosh A, Feliciano P, Benedetti M, Luo Clayton A, Biemans B.

PLoS One. 2015 Aug 14;10(8):e0134572. doi: 10.1371/journal.pone.0134572. eCollection 2015.

13.

Inherited genetic variants in autism-related CNTNAP2 show perturbed trafficking and ATF6 activation.

Falivelli G, De Jaco A, Favaloro FL, Kim H, Wilson J, Dubi N, Ellisman MH, Abrahams BS, Taylor P, Comoletti D.

Hum Mol Genet. 2012 Nov 1;21(21):4761-73. doi: 10.1093/hmg/dds320. Epub 2012 Aug 7.

14.

Auditory processing and morphological anomalies in medial geniculate nucleus of Cntnap2 mutant mice.

Truong DT, Rendall AR, Castelluccio BC, Eigsti IM, Fitch RH.

Behav Neurosci. 2015 Dec;129(6):731-43. doi: 10.1037/bne0000096. Epub 2015 Oct 26.

PMID:
26501174
15.

Homozygous Loss of Autism-Risk Gene CNTNAP2 Results in Reduced Local and Long-Range Prefrontal Functional Connectivity.

Liska A, Bertero A, Gomolka R, Sabbioni M, Galbusera A, Barsotti N, Panzeri S, Scattoni ML, Pasqualetti M, Gozzi A.

Cereb Cortex. 2018 Apr 1;28(4):1141-1153. doi: 10.1093/cercor/bhx022.

PMID:
28184409
16.

Multiple molecular interactions determine the clustering of Caspr2 and Kv1 channels in myelinated axons.

Horresh I, Poliak S, Grant S, Bredt D, Rasband MN, Peles E.

J Neurosci. 2008 Dec 24;28(52):14213-22. doi: 10.1523/JNEUROSCI.3398-08.2008.

17.

Immune or Genetic-Mediated Disruption of CASPR2 Causes Pain Hypersensitivity Due to Enhanced Primary Afferent Excitability.

Dawes JM, Weir GA, Middleton SJ, Patel R, Chisholm KI, Pettingill P, Peck LJ, Sheridan J, Shakir A, Jacobson L, Gutierrez-Mecinas M, Galino J, Walcher J, Kühnemund J, Kuehn H, Sanna MD, Lang B, Clark AJ, Themistocleous AC, Iwagaki N, West SJ, Werynska K, Carroll L, Trendafilova T, Menassa DA, Giannoccaro MP, Coutinho E, Cervellini I, Tewari D, Buckley C, Leite MI, Wildner H, Zeilhofer HU, Peles E, Todd AJ, McMahon SB, Dickenson AH, Lewin GR, Vincent A, Bennett DL.

Neuron. 2018 Feb 21;97(4):806-822.e10. doi: 10.1016/j.neuron.2018.01.033. Epub 2018 Feb 8.

18.

Single nucleotide polymorphisms in the CNTNAP2 gene in Brazilian patients with autistic spectrum disorder.

Nascimento PP, Bossolani-Martins AL, Rosan DB, Mattos LC, Brandão-Mattos C, Fett-Conte AC.

Genet Mol Res. 2016 Feb 5;15(1). doi: 10.4238/gmr.15017422.

19.

Haploinsufficiency of autism causative gene Tbr1 impairs olfactory discrimination and neuronal activation of the olfactory system in mice.

Huang TN, Yen TL, Qiu LR, Chuang HC, Lerch JP, Hsueh YP.

Mol Autism. 2019 Feb 11;10:5. doi: 10.1186/s13229-019-0257-5. eCollection 2019.

20.

Cntnap2 Knockout Rats and Mice Exhibit Epileptiform Activity and Abnormal Sleep-Wake Physiology.

Thomas AM, Schwartz MD, Saxe MD, Kilduff TS.

Sleep. 2017 Jan 1;40(1). doi: 10.1093/sleep/zsw026.

PMID:
28364455

Supplemental Content

Support Center