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Results: 1 to 20 of 40

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1.

VAV1 and BAFF, via NFκB pathway, are genetic risk factors for myasthenia gravis.

Avidan N, Le Panse R, Harbo HF, Bernasconi P, Poulas K, Ginzburg E, Cavalcante P, Colleoni L, Baggi F, Antozzi C, Truffault F, Horn-Saban S, Pöschel S, Zagoriti Z, Maniaol A, Lie BA, Bernard I, Saoudi A, Illes Z, Casasnovas Pons C, Melms A, Tzartos S, Willcox N, Kostera-Pruszczyk A, Tallaksen C, Mantegazza R, Berrih-Aknin S, Miller A.

Ann Clin Transl Neurol. 2014 May;1(5):329-39. doi: 10.1002/acn3.51. Epub 2014 Apr 11.

PMID:
25356403
[PubMed]
Free PMC Article
2.

Gene expression profiling of the response to interferon beta in Epstein-Barr-transformed and primary B cells of patients with multiple sclerosis.

Khsheibun R, Paperna T, Volkowich A, Lejbkowicz I, Avidan N, Miller A.

PLoS One. 2014 Jul 15;9(7):e102331. doi: 10.1371/journal.pone.0102331. eCollection 2014.

PMID:
25025430
[PubMed - in process]
Free PMC Article
3.

Genetic basis of myasthenia gravis - a comprehensive review.

Avidan N, Le Panse R, Berrih-Aknin S, Miller A.

J Autoimmun. 2014 Aug;52:146-53. doi: 10.1016/j.jaut.2013.12.001. Epub 2013 Dec 19.

PMID:
24361103
[PubMed - in process]
4.

Interferon-beta induces distinct gene expression response patterns in human monocytes versus T cells.

Henig N, Avidan N, Mandel I, Staun-Ram E, Ginzburg E, Paperna T, Pinter RY, Miller A.

PLoS One. 2013 Apr 23;8(4):e62366. doi: 10.1371/journal.pone.0062366. Print 2013.

PMID:
23626809
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Exome sequencing identifies SMAD3 mutations as a cause of familial thoracic aortic aneurysm and dissection with intracranial and other arterial aneurysms.

Regalado ES, Guo DC, Villamizar C, Avidan N, Gilchrist D, McGillivray B, Clarke L, Bernier F, Santos-Cortez RL, Leal SM, Bertoli-Avella AM, Shendure J, Rieder MJ, Nickerson DA; NHLBI GO Exome Sequencing Project, Milewicz DM.

Circ Res. 2011 Sep 2;109(6):680-6. doi: 10.1161/CIRCRESAHA.111.248161. Epub 2011 Jul 21.

PMID:
21778426
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

The genetics of colored sequence synesthesia: suggestive evidence of linkage to 16q and genetic heterogeneity for the condition.

Tomson SN, Avidan N, Lee K, Sarma AK, Tushe R, Milewicz DM, Bray M, Leal SM, Eagleman DM.

Behav Brain Res. 2011 Sep 30;223(1):48-52. doi: 10.1016/j.bbr.2011.03.071. Epub 2011 Apr 8. Erratum in: Behav Brain Res. 2013 Apr 15;243:322.

PMID:
21504763
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Opposing effects of the HLA-DRB1*0301-DQB1*0201 haplotype on the risk for multiple sclerosis in diverse Arab populations in Israel.

Benedek G, Paperna T, Avidan N, Lejbkowicz I, Oksenberg JR, Wang J, Brautbar C, Israel S, Miller A; Israeli MS Genetics group.

Genes Immun. 2010 Jul;11(5):423-31. doi: 10.1038/gene.2010.20. Epub 2010 May 13.

PMID:
20463743
[PubMed - indexed for MEDLINE]
8.

Hepatitis C viral kinetics during treatment with peg IFN-alpha-2b in HIV/HCV coinfected patients as a function of baseline CD4+ T-cell counts.

Avidan NU, Goldstein D, Rozenberg L, McLaughlin M, Ferenci P, Masur H, Buti M, Fauci AS, Polis MA, Kottilil S.

J Acquir Immune Defic Syndr. 2009 Dec 1;52(4):452-8. doi: 10.1097/QAI.0b013e3181be7249.

PMID:
19797971
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Insulin-like growth factor-binding protein 7 regulates keratinocyte proliferation, differentiation and apoptosis.

Nousbeck J, Sarig O, Avidan N, Indelman M, Bergman R, Ramon M, Enk CD, Sprecher E.

J Invest Dermatol. 2010 Feb;130(2):378-87. doi: 10.1038/jid.2009.265. Epub 2009 Aug 27.

PMID:
19710688
[PubMed - indexed for MEDLINE]
Free Article
10.

Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease.

Guo DC, Papke CL, Tran-Fadulu V, Regalado ES, Avidan N, Johnson RJ, Kim DH, Pannu H, Willing MC, Sparks E, Pyeritz RE, Singh MN, Dalman RL, Grotta JC, Marian AJ, Boerwinkle EA, Frazier LQ, LeMaire SA, Coselli JS, Estrera AL, Safi HJ, Veeraraghavan S, Muzny DM, Wheeler DA, Willerson JT, Yu RK, Shete SS, Scherer SE, Raman CS, Buja LM, Milewicz DM.

Am J Hum Genet. 2009 May;84(5):617-27. doi: 10.1016/j.ajhg.2009.04.007. Epub 2009 Apr 30.

PMID:
19409525
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Translation towards personalized medicine in Multiple Sclerosis.

Miller A, Avidan N, Tzunz-Henig N, Glass-Marmor L, Lejbkowicz I, Pinter RY, Paperna T.

J Neurol Sci. 2008 Nov 15;274(1-2):68-75. doi: 10.1016/j.jns.2008.07.028. Epub 2008 Sep 12. Review.

PMID:
18789804
[PubMed - indexed for MEDLINE]
12.

Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections.

Guo DC, Pannu H, Tran-Fadulu V, Papke CL, Yu RK, Avidan N, Bourgeois S, Estrera AL, Safi HJ, Sparks E, Amor D, Ades L, McConnell V, Willoughby CE, Abuelo D, Willing M, Lewis RA, Kim DH, Scherer S, Tung PP, Ahn C, Buja LM, Raman CS, Shete SS, Milewicz DM.

Nat Genet. 2007 Dec;39(12):1488-93. Epub 2007 Nov 11. Erratum in: Nat Genet. 2008 Feb;40(2):255.

PMID:
17994018
[PubMed - indexed for MEDLINE]
13.

Pharmacogenetics of glatiramer acetate therapy for multiple sclerosis reveals drug-response markers.

Grossman I, Avidan N, Singer C, Goldstaub D, Hayardeny L, Eyal E, Ben-Asher E, Paperna T, Pe'er I, Lancet D, Beckmann JS, Miller A.

Pharmacogenet Genomics. 2007 Aug;17(8):657-66.

PMID:
17622942
[PubMed - indexed for MEDLINE]
14.

Genetic basis of thoracic aortic aneurysms and dissections: potential relevance to abdominal aortic aneurysms.

Pannu H, Avidan N, Tran-Fadulu V, Milewicz DM.

Ann N Y Acad Sci. 2006 Nov;1085:242-55.

PMID:
17182941
[PubMed - indexed for MEDLINE]
15.

Mutations in olfactory signal transduction genes are not a major cause of human congenital general anosmia.

Feldmesser E, Bercovich D, Avidan N, Halbertal S, Haim L, Gross-Isseroff R, Goshen S, Lancet D.

Chem Senses. 2007 Jan;32(1):21-30. Epub 2006 Sep 28.

PMID:
17008420
[PubMed - indexed for MEDLINE]
Free Article
16.

AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia.

Amann-Zalcenstein D, Avidan N, Kanyas K, Ebstein RP, Kohn Y, Hamdan A, Ben-Asher E, Karni O, Mujaheed M, Segman RH, Maier W, Macciardi F, Beckmann JS, Lancet D, Lerer B.

Eur J Hum Genet. 2006 Oct;14(10):1111-9. Epub 2006 Jun 14. Erratum in: Eur J Hum Genet. 2007 Mar;15(3):387.

PMID:
16773125
[PubMed - indexed for MEDLINE]
Free Article
17.

Linkage and mutational analysis of the CDAN1 gene reveals genetic heterogeneity in congenital dyserythropoietic anemia type I.

Ahmed MR, Chehal A, Zahed L, Taher A, Haidar J, Shamseddine A, O'Hea AM, Bienz N, Dgany O, Avidan N, Beckmann JS, Tamary H, Higgs D, Vyas P, Wood WG, Wickramasinghe SN.

Blood. 2006 Jun 15;107(12):4968-9. No abstract available.

PMID:
16754775
[PubMed - indexed for MEDLINE]
Free Article
18.

The trace amine receptor 4 gene is not associated with schizophrenia in a sample linked to chromosome 6q23.

Amann D, Avidan N, Kanyas K, Kohn Y, Hamdan A, Ben-Asher E, Macciardi F, Beckmann JS, Lancet D, Lerer B.

Mol Psychiatry. 2006 Feb;11(2):119-21. No abstract available.

PMID:
16189505
[PubMed - indexed for MEDLINE]
19.

Clinical and molecular variability in congenital dyserythropoietic anaemia type I.

Tamary H, Dgany O, Proust A, Krasnov T, Avidan N, Eidelitz-Markus T, Tchernia G, Geneviève D, Cormier-Daire V, Bader-Meunier B, Ferrero-Vacher C, Munzer M, Gruppo R, Fibach E, Konen O, Yaniv I, Delaunay J.

Br J Haematol. 2005 Aug;130(4):628-34.

PMID:
16098079
[PubMed - indexed for MEDLINE]
20.

Analysis of genetic polymorphisms in acetylcholinesterase as reflected in different populations.

Hasin Y, Avidan N, Bercovich D, Korczyn AD, Silman I, Beckmann JS, Sussman JL.

Curr Alzheimer Res. 2005 Apr;2(2):207-18.

PMID:
15974920
[PubMed - indexed for MEDLINE]
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