Zohar Keren

发表

Chronic B Cell Deficiency from Birth Prevents Age-Related Alterations in the B Lineage

K. Golan, T. Itkin, T. Lapidot, 2011, The Journal of Immunology.

LineagePrevents Age-Related Alterations in the B Chronic B Cell Deficiency from Birth

K. Golan, T. Itkin, T. Lapidot, 2011 .

Depletion of B lymphocytes in rheumatoid arthritis patients modifies IL-8-anti-IL-8 autoantibody network.

Y. Braun-Moscovici, A. Balbir-Gurman, D. Melamed, 2009, Clinical immunology.

Development of ALS-like disease in SOD-1 mice deficient of B lymphocytes

M. Machluf, D. Melamed, Z. Keren, 2009, Journal of Neurology.

Phospholipase A2-activating protein is associated with a novel form of leukoencephalopathy

J. Mullikin, W. Baze, J. Peterson, 2017, Brain : a journal of neurology.

Phospholipase A 2-activating protein is associated with a novel form of 1 leukoencephalopathy 2

J. Mullikin, T. Vilboux, Y. Anikster, 2016 .

Antigen receptor signaling competence and the determination of B cell fate in B-lymphopoiesis.

D. Melamed, Z. Keren, Zohar Keren, 2005, Histology and histopathology.

A Fail-safe Mechanism for Negative Selection of Isotype-switched B Cell Precursors Is Regulated by the Fas/FasL Pathway

M. Machluf, J. Seagal, D. Melamed, 2003, The Journal of experimental medicine.

CD19 regulates positive selection and maturation in B lymphopoiesis: lack of CD19 imposes developmental arrest of immature B cells and consequential stimulation of receptor editing.

D. Melamed, Z. Keren, Eran Diamant, 2005, Blood.

Modification of Ligand-independent B Cell Receptor Tonic Signals Activates Receptor Editing in Immature B Lymphocytes*

O. Ostrovsky, D. Melamed, Z. Keren, 2004, Journal of Biological Chemistry.

B-cell depletion reactivates B lymphopoiesis in the BM and rejuvenates the B lineage in aging.

T. Itkin, T. Lapidot, M. Schmidt-Supprian, 2011, Blood.

the B lineage in aging B-cell depletion reactivates B lymphopoiesis in the BM and rejuvenates

K. Golan, T. Itkin, Y. Sasaki, 2011 .

A novel XPD mutation in a compound heterozygote; the mutation in the second allele is present in three homozygous patients with mild sun sensitivity

P. Hanawalt, G. Spivak, L. Kalfon, 2012, Environmental and molecular mutagenesis.