Tabib A - Search Results

1

The Thr224Asn mutation in the VPS45 gene is associated with the congenital neutropenia and primary myelofibrosis of infancy.

Stepensky P, Saada A, Cowan M, Tabib A, Fischer U, Berkun Y, Saleh H, Simanovsky N, Kogot-Levin A, Weintraub M, Ganaiem H, Shaag A, Zenvirt S, Borkhardt A, Elpeleg O, Bryant NJ, Mevorach D. Stepensky P, et al. Among authors: tabib a. Blood. 2013 Jun 20;121(25):5078-87. doi: 10.1182/blood-2012-12-475566. Epub 2013 Apr 18. Blood. 2013. PMID: 23599270 Free article.

2

Thrombospondin-1-N-terminal domain induces a phagocytic state and thrombospondin-1-C-terminal domain induces a tolerizing phenotype in dendritic cells.

Tabib A, Krispin A, Trahtemberg U, Verbovetski I, Lebendiker M, Danieli T, Mevorach D. Tabib A, et al. PLoS One. 2009 Aug 31;4(8):e6840. doi: 10.1371/journal.pone.0006840. PLoS One. 2009. PMID: 19721725 Free PMC article.

3

What do we mean when we write "senescence," "apoptosis," "necrosis," or "clearance of dying cells"?

Mevorach D, Trahtemberg U, Krispin A, Attalah M, Zazoun J, Tabib A, Grau A, Verbovetski-Reiner I. Mevorach D, et al. Among authors: tabib a. Ann N Y Acad Sci. 2010 Oct;1209:1-9. doi: 10.1111/j.1749-6632.2010.05774.x. Ann N Y Acad Sci. 2010. PMID: 20958309

4

Role of class A human thrombospondins in the clearance of dying cells and tolerance induction.

Tabib A, Krispin A, Mevorach D. Tabib A, et al. Ann N Y Acad Sci. 2010 Oct;1209:43-8. doi: 10.1111/j.1749-6632.2010.05773.x. Ann N Y Acad Sci. 2010. PMID: 20958315

5

CD59 deficiency is associated with chronic hemolysis and childhood relapsing immune-mediated polyneuropathy.

Nevo Y, Ben-Zeev B, Tabib A, Straussberg R, Anikster Y, Shorer Z, Fattal-Valevski A, Ta-Shma A, Aharoni S, Rabie M, Zenvirt S, Goldshmidt H, Fellig Y, Shaag A, Mevorach D, Elpeleg O. Nevo Y, et al. Among authors: tabib a. Blood. 2013 Jan 3;121(1):129-35. doi: 10.1182/blood-2012-07-441857. Epub 2012 Nov 13. Blood. 2013. PMID: 23149847 Free article.

6

Apoptotic cells induce NF-κB and inflammasome negative signaling.

Grau A, Tabib A, Grau I, Reiner I, Mevorach D. Grau A, et al. Among authors: tabib a. PLoS One. 2015 Mar 30;10(3):e0122440. doi: 10.1371/journal.pone.0122440. eCollection 2015. PLoS One. 2015. PMID: 25822487 Free PMC article.

7

Devastating recurrent brain ischemic infarctions and retinal disease in pediatric patients with CD59 deficiency.

Ben-Zeev B, Tabib A, Nissenkorn A, Garti BZ, Gomori JM, Nass D, Goldshmidt H, Fellig Y, Anikster Y, Nevo Y, Elpeleg O, Mevorach D. Ben-Zeev B, et al. Among authors: tabib a. Eur J Paediatr Neurol. 2015 Nov;19(6):688-93. doi: 10.1016/j.ejpn.2015.07.001. Epub 2015 Jul 20. Eur J Paediatr Neurol. 2015. PMID: 26233519

8

Therapy with eculizumab for patients with CD59 p.Cys89Tyr mutation.

Mevorach D, Reiner I, Grau A, Ilan U, Berkun Y, Ta-Shma A, Elpeleg O, Shorer Z, Edvardson S, Tabib A. Mevorach D, et al. Among authors: tabib a. Ann Neurol. 2016 Nov;80(5):708-717. doi: 10.1002/ana.24770. Epub 2016 Sep 19. Ann Neurol. 2016. PMID: 27568864 Clinical Trial.

9

Identification and Characterization of Two Human Monocyte-Derived Dendritic Cell Subpopulations with Different Functions in Dying Cell Clearance and Different Patterns of Cell Death.

Trahtemberg U, Grau A, Tabib A, Atallah M, Krispin A, Mevorach D. Trahtemberg U, et al. Among authors: tabib a. PLoS One. 2016 Sep 30;11(9):e0162984. doi: 10.1371/journal.pone.0162984. eCollection 2016. PLoS One. 2016. PMID: 27690130 Free PMC article.

10

Demyelination, strokes, and eculizumab: Lessons from the congenital CD59 gene mutations.

Tabib A, Karbian N, Mevorach D. Tabib A, et al. Mol Immunol. 2017 Sep;89:69-72. doi: 10.1016/j.molimm.2017.05.024. Epub 2017 Jun 13. Mol Immunol. 2017. PMID: 28622911 Review.

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