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Items: 1 to 50 of 161

1.

Smek1/2 is a nuclear chaperone and cofactor for cleaved Wnt receptor Ryk, regulating cortical neurogenesis.

Chang WH, Choi SH, Moon BS, Cai M, Lyu J, Bai J, Gao F, Hajjali I, Zhao Z, Campbell DB, Weiner LP, Lu W.

Proc Natl Acad Sci U S A. 2017 Dec 12;114(50):E10717-E10725. doi: 10.1073/pnas.1715772114. Epub 2017 Nov 27.

2.

Transcriptional Gene Silencing of the Autism-Associated Long Noncoding RNA MSNP1AS in Human Neural Progenitor Cells.

DeWitt JJ, Hecht PM, Grepo N, Wilkinson B, Evgrafov OV, Morris KV, Knowles JA, Campbell DB.

Dev Neurosci. 2016;38(5):375-383. doi: 10.1159/000453258. Epub 2016 Dec 29.

3.

Impact of the Autism-Associated Long Noncoding RNA MSNP1AS on Neuronal Architecture and Gene Expression in Human Neural Progenitor Cells.

DeWitt JJ, Grepo N, Wilkinson B, Evgrafov OV, Knowles JA, Campbell DB.

Genes (Basel). 2016 Sep 28;7(10). pii: E76.

4.

Noncoding RNA in the transcriptional landscape of human neural progenitor cell differentiation.

Hecht PM, Ballesteros-Yanez I, Grepo N, Knowles JA, Campbell DB.

Front Neurosci. 2015 Oct 23;9:392. doi: 10.3389/fnins.2015.00392. eCollection 2015.

5.

The autism-associated gene chromodomain helicase DNA-binding protein 8 (CHD8) regulates noncoding RNAs and autism-related genes.

Wilkinson B, Grepo N, Thompson BL, Kim J, Wang K, Evgrafov OV, Lu W, Knowles JA, Campbell DB.

Transl Psychiatry. 2015 May 19;5:e568. doi: 10.1038/tp.2015.62.

6.

Genetic investigation of autism-related social communication deficits.

Campbell DB.

Am J Psychiatry. 2015 Mar 1;172(3):212-3. doi: 10.1176/appi.ajp.2014.14121503. No abstract available.

PMID:
25727530
7.

Contribution of long noncoding RNAs to autism spectrum disorder risk.

Wilkinson B, Campbell DB.

Int Rev Neurobiol. 2013;113:35-59. doi: 10.1016/B978-0-12-418700-9.00002-2. Review.

PMID:
24290382
8.

Autism spectrum disorder: interaction of air pollution with the MET receptor tyrosine kinase gene.

Volk HE, Kerin T, Lurmann F, Hertz-Picciotto I, McConnell R, Campbell DB.

Epidemiology. 2014 Jan;25(1):44-7. doi: 10.1097/EDE.0000000000000030.

9.

SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs).

Abrahams BS, Arking DE, Campbell DB, Mefford HC, Morrow EM, Weiss LA, Menashe I, Wadkins T, Banerjee-Basu S, Packer A.

Mol Autism. 2013 Oct 3;4(1):36. doi: 10.1186/2040-2392-4-36.

10.

A noncoding RNA antisense to moesin at 5p14.1 in autism.

Kerin T, Ramanathan A, Rivas K, Grepo N, Coetzee GA, Campbell DB.

Sci Transl Med. 2012 Apr 4;4(128):128ra40. doi: 10.1126/scitranslmed.3003479.

11.

Isolated cardiac metastasis from papillary thyroid cancer: prolonged survival with late diagnosis related to inadequate positron emission tomography preparation.

Kaul S, Tulchinsky M, Campbell DB, Crist HS, Manni A.

Thyroid. 2012 Apr;22(4):443-4. doi: 10.1089/thy.2011.0295. Epub 2012 Feb 29. No abstract available.

PMID:
22376168
12.

Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorder.

Campbell DB, Datta D, Jones ST, Batey Lee E, Sutcliffe JS, Hammock EA, Levitt P.

J Neurodev Disord. 2011 Jun;3(2):101-12. doi: 10.1007/s11689-010-9071-2. Epub 2011 Jan 6.

13.

The autism risk genes MET and PLAUR differentially impact cortical development.

Eagleson KL, Campbell DB, Thompson BL, Bergman MY, Levitt P.

Autism Res. 2011 Feb;4(1):68-83. doi: 10.1002/aur.172. Epub 2010 Dec 3.

14.

Association of a MET genetic variant with autism-associated maternal autoantibodies to fetal brain proteins and cytokine expression.

Heuer L, Braunschweig D, Ashwood P, Van de Water J, Campbell DB.

Transl Psychiatry. 2011 Oct 18;1:e48. doi: 10.1038/tp.2011.48.

15.

Echocardiographic recognition of mitral valve involvement in primary aortic valve endocarditis.

Rao SL, Campbell DB, Haouzi-Judenherc AR.

Anesth Analg. 2011 Jan;112(1):59-61. doi: 10.1213/ANE.0b013e3181fe756b. Epub 2010 Oct 21. No abstract available.

PMID:
20966435
16.

Evaluation, diagnosis, and treatment of gastrointestinal disorders in individuals with ASDs: a consensus report.

Buie T, Campbell DB, Fuchs GJ 3rd, Furuta GT, Levy J, Vandewater J, Whitaker AH, Atkins D, Bauman ML, Beaudet AL, Carr EG, Gershon MD, Hyman SL, Jirapinyo P, Jyonouchi H, Kooros K, Kushak R, Levitt P, Levy SE, Lewis JD, Murray KF, Natowicz MR, Sabra A, Wershil BK, Weston SC, Zeltzer L, Winter H.

Pediatrics. 2010 Jan;125 Suppl 1:S1-18. doi: 10.1542/peds.2009-1878C.

PMID:
20048083
17.

Association of MET with social and communication phenotypes in individuals with autism spectrum disorder.

Campbell DB, Warren D, Sutcliffe JS, Lee EB, Levitt P.

Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):438-446. doi: 10.1002/ajmg.b.30998.

PMID:
19548256
18.

Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder.

Campbell DB, Li C, Sutcliffe JS, Persico AM, Levitt P.

Autism Res. 2008 Jun;1(3):159-68. doi: 10.1002/aur.27.

19.

The genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disorders.

Levitt P, Campbell DB.

J Clin Invest. 2009 Apr;119(4):747-54. doi: 10.1172/JCI37934. Epub 2009 Apr 1. Review.

20.

Distinct genetic risk based on association of MET in families with co-occurring autism and gastrointestinal conditions.

Campbell DB, Buie TM, Winter H, Bauman M, Sutcliffe JS, Perrin JM, Levitt P.

Pediatrics. 2009 Mar;123(3):1018-24. doi: 10.1542/peds.2008-0819. Erratum in: Pediatrics. 2009 Apr;123(4):1255.

PMID:
19255034
21.

Dynamic gene and protein expression patterns of the autism-associated met receptor tyrosine kinase in the developing mouse forebrain.

Judson MC, Bergman MY, Campbell DB, Eagleson KL, Levitt P.

J Comp Neurol. 2009 Apr 10;513(5):511-31. doi: 10.1002/cne.21969.

22.

When linkage signal for autism MET candidate gene.

Campbell DB.

Eur J Hum Genet. 2009 Jun;17(6):699-700. doi: 10.1038/ejhg.2008.217. Epub 2008 Nov 12. No abstract available.

23.

Future of individualized psychiatric treatment.

Campbell DB, Levitt P.

Pharmacogenomics. 2008 May;9(5):493-5. doi: 10.2217/14622416.9.5.493. No abstract available.

24.

Association of RGS2 and RGS5 variants with schizophrenia symptom severity.

Campbell DB, Lange LA, Skelly T, Lieberman J, Levitt P, Sullivan PF.

Schizophr Res. 2008 Apr;101(1-3):67-75. doi: 10.1016/j.schres.2008.01.006. Epub 2008 Feb 11.

25.

Disruption of cerebral cortex MET signaling in autism spectrum disorder.

Campbell DB, D'Oronzio R, Garbett K, Ebert PJ, Mirnics K, Levitt P, Persico AM.

Ann Neurol. 2007 Sep;62(3):243-50.

PMID:
17696172
26.

Ethnic stratification of the association of RGS4 variants with antipsychotic treatment response in schizophrenia.

Campbell DB, Ebert PJ, Skelly T, Stroup TS, Lieberman J, Levitt P, Sullivan PF.

Biol Psychiatry. 2008 Jan 1;63(1):32-41. Epub 2007 Jun 22.

27.

Return of collective rotation in 157Er and 158Er at ultrahigh spin.

Paul ES, Twin PJ, Evans AO, Pipidis A, Riley MA, Simpson J, Appelbe DE, Campbell DB, Choy PT, Clark RM, Cromaz M, Fallon P, Görgen A, Joss DT, Lee IY, Macchiavelli AO, Nolan PJ, Ward D, Ragnarsson I.

Phys Rev Lett. 2007 Jan 5;98(1):012501. Epub 2007 Jan 5.

PMID:
17358470
28.

A genetic variant that disrupts MET transcription is associated with autism.

Campbell DB, Sutcliffe JS, Ebert PJ, Militerni R, Bravaccio C, Trillo S, Elia M, Schneider C, Melmed R, Sacco R, Persico AM, Levitt P.

Proc Natl Acad Sci U S A. 2006 Nov 7;103(45):16834-9. Epub 2006 Oct 19.

29.

No evidence for thick deposits of ice at the lunar south pole.

Campbell DB, Campbell BA, Carter LM, Margot JL, Stacy NJ.

Nature. 2006 Oct 19;443(7113):835-7.

PMID:
17051213
30.
31.
32.
33.

p-sd Shell gap reduction in neutron-rich systems and cross-shell excitations in 20 O.

Wiedeking M, Tabor SL, Pavan J, Volya A, Aguilar AL, Calderin IJ, Campbell DB, Cluff WT, Diffenderfer E, Fridmann J, Hoffman CR, Kemper KW, Lee S, Riley MA, Roeder BT, Teal C, Tripathi V, Wiedenhöver I.

Phys Rev Lett. 2005 Apr 8;94(13):132501. Epub 2005 Apr 7.

PMID:
15903988
34.

High-spin structure beyond band termination in 157Er.

Evans AO, Paul ES, Simpson J, Riley MA, Appelbe DE, Campbell DB, Choy PT, Clark RM, Cromaz M, Fallon P, Görgen A, Joss DT, Lee IY, Macchiavelli AO, Nolan PJ, Pipidis A, Ward D, Ragnarsson I, Sarić F.

Phys Rev Lett. 2004 Jun 25;92(25 Pt 1):252502. Epub 2004 Jun 25.

PMID:
15245000
35.

Radar detection of Iapetus.

Black GJ, Campbell DB, Carter LM, Ostro SJ.

Science. 2004 Apr 23;304(5670):553. No abstract available.

36.

Endoscopic clip application as an adjunct to closure of mature esophageal perforation with fistulae.

Raymer GS, Sadana A, Campbell DB, Rowe WA.

Clin Gastroenterol Hepatol. 2003 Jan;1(1):44-50.

PMID:
15017516
37.

Regulation of tyrosine hydroxylase expression in tottering mouse Purkinje cells.

Fureman BE, Campbell DB, Hess EJ.

Neurotox Res. 2003;5(7):521-8.

PMID:
14715436
38.
39.

Radar imaging of the lunar poles.

Campbell BA, Campbell DB, Chandler JF, Hine AA, Nolan MC, Perillat PJ.

Nature. 2003 Nov 13;426(6963):137-8. No abstract available.

PMID:
14614491
40.

Radar evidence for liquid surfaces on Titan.

Campbell DB, Black GJ, Carter LM, Ostro SJ.

Science. 2003 Oct 17;302(5644):431-4. Epub 2003 Oct 2.

41.

Genetic disruption of cortical interneuron development causes region- and GABA cell type-specific deficits, epilepsy, and behavioral dysfunction.

Powell EM, Campbell DB, Stanwood GD, Davis C, Noebels JL, Levitt P.

J Neurosci. 2003 Jan 15;23(2):622-31.

42.

Binary asteroids in the near-Earth object population.

Margot JL, Nolan MC, Benner LA, Ostro SJ, Jurgens RF, Giorgini JD, Slade MA, Campbell DB.

Science. 2002 May 24;296(5572):1445-8. Epub 2002 Apr 11.

43.

Clinical-pathologic conference in thoracic surgery: basaloid squamous carcinoma of the trachea.

Patterson GA, Campbell DB.

J Thorac Cardiovasc Surg. 2000 Jul;120(1):187-93. No abstract available.

44.

Radar observations of asteroid 216 kleopatra

Ostro SJ, Hudson RS, Nolan MC, Margot JL, Scheeres DJ, Campbell DB, Magri C, Giorgini JD, Yeomans DK.

Science. 2000 May 5;288(5467):836-9.

45.

Setting behavioral limits.

Campbell DB, Anderson BJ.

Am J Nurs. 1999 Dec;99(12):40-2. No abstract available.

PMID:
10738383
46.

Clinical-pathologic conference in thoracic surgery: Masaoka stage 2-a thymoma.

Patterson GA, Campbell DB.

J Thorac Cardiovasc Surg. 2000 Mar;119(3):624-9. No abstract available.

PMID:
10694628
47.

Tottering mouse motor dysfunction is abolished on the Purkinje cell degeneration (pcd) mutant background.

Campbell DB, North JB, Hess EJ.

Exp Neurol. 1999 Nov;160(1):268-78.

PMID:
10630211
48.

Clinical-Pathologic Conference in Thoracic Surgery: T1 N1 stage IIA adenocarcinoma.

Patterson GA, Campbell DB.

J Thorac Cardiovasc Surg. 1999 Jul;118(1):201-6. No abstract available.

PMID:
10419377
49.

L-type calcium channel regulation of abnormal tyrosine hydroxylase expression in cerebella of tottering mice.

Fureman BE, Campbell DB, Hess EJ.

Ann N Y Acad Sci. 1999 Apr 30;868:217-9. No abstract available.

PMID:
10414297
50.

Topography of the lunar poles from radar interferometry: a survey of cold trap locations.

Margot JL, Campbell DB, Jurgens RF, Slade MA.

Science. 1999 Jun 4;284(5420):1658-60.

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