Meytal Landau

2009

Molecular mechanisms for protein-encoded inheritance

Wiltzius, J. J. W., Landau, M., Nelson, R., Sawaya, M. R., Apostol, M. I., Goldschmidt, L., Soriaga, A. B., Cascio, D., Rajashankar, K. & Eisenberg, D., Sep 2009, In: Nature Structural and Molecular Biology. 16, 9, p. 973-978 6 p.

Research output: Contribution to journal › Article › peer-review

Open Access

Three residues at the interface of factor.XI (FXI) monomers augment covalent dimerization of FXI

Zucker, M., Zivelin, A., Landau, M., Rosenberg, N. & Seligsohn, U., 2009, In: Journal of Thrombosis and Haemostasis. 7, 6, p. 970-975 6 p.

Research output: Contribution to journal › Article › peer-review

Open Access

2008

Dynamic equilibrium between multiple active and inactive conformations explains regulation and oncogenic mutations in ErbB receptors

Landau, M. & Ben-Tal, N., Jan 2008, In: Biochimica et Biophysica Acta - Reviews on Cancer. 1785, 1, p. 12-31 20 p.

Research output: Contribution to journal › Review article › peer-review

Specific cysteines in β3 are involved in disulfide bond exchange-dependent and -independent activation of αIIbβ3

Mor-Cohen, R., Rosenberg, N., Landau, M., Lahav, J. & Seligsohn, U., 11 Jul 2008, In: Journal of Biological Chemistry. 283, 28, p. 19235-19244 10 p.

Research output: Contribution to journal › Article › peer-review

Open Access

2007

A novel factor XI missense mutation (Val371Ile) in the activation loop is responsible for a case of mild type II factor XI deficiency

Bozzao, C., Rimoldi, V., Asselta, R., Landau, M., Ghiotto, R., Tenchini, M. L., De Cristofaro, R., Castaman, G. & Duga, S., Dec 2007, In: FEBS Journal. 274, 23, p. 6128-6138 11 p.

Research output: Contribution to journal › Article › peer-review

Open Access

Disulfide bond disruption by a β3-Cys549Arg mutation in six Jordanian families with Glanzmann thrombasthenia causes diminished production of constitutively active αIIbβ3

Mor-Cohen, R., Rosenberg, N., Peretz, H., Landau, M., Coller, B. S., Awidi, A. & Seligsohn, U., Dec 2007, In: Thrombosis and Haemostasis. 98, 6, p. 1257-1265 9 p.

Research output: Contribution to journal › Article › peer-review

Model structure of the Na⁺/H⁺ exchanger 1 (NHE1): Functional and clinical implications

Landau, M., Herz, K., Padan, E. & Ben-Tal, N., 28 Dec 2007, In: Journal of Biological Chemistry. 282, 52, p. 37854-37863 10 p.

Research output: Contribution to journal › Article › peer-review

Open Access

Trp207Gly in platelet glycoprotein Ib α is a novel mutation that disrupts the connection between the leucine-rich repeat domain and the disulfide loop structure and causes Bernard-Soulier syndrome

Rosenberg, N., Lalezari, S., Landau, M., Shenkman, B., Seligsohn, U. & Izraeli, S., Feb 2007, In: Journal of Thrombosis and Haemostasis. 5, 2, p. 378-386 9 p.

Research output: Contribution to journal › Article › peer-review

Open Access

2006

Molecular diversity of Glanzmann thrombasthenia in Southern India: New insights into mRNA splicing and structure-function correlations of αIIbβ3 integrin (ITGA2B, ITGB3)

Peretz, H., Rosenberg, N., Landau, M., Usher, S., Nelson, E. J. R., Mor-Cohen, R., French, D. L., Mitchell, B. W., Nair, S. C., Chandy, M., Coller, B. S., Srivastava, A. & Seligsohn, U., Apr 2006, In: Human Mutation. 27, 4, p. 359-369 11 p.

Research output: Contribution to journal › Article › peer-review

Open Access

2005

A 13-bp deletion in α_IIb gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia

Rosenberg, N., Hauschner, H., Peretz, H., Mor-Cohen, R., Landau, M., Shenkman, B., Kenet, G., Coller, B. S., Awidi, A. A. & Seligsohn, U., Dec 2005, In: Journal of Thrombosis and Haemostasis. 3, 12, p. 2764-2772 9 p.

Research output: Contribution to journal › Article › peer-review

Open Access

ConSurf 2005: The projection of evolutionary conservation scores of residues on protein structures

Landau, M., Mayrose, I., Rosenberg, Y., Glaser, F., Martz, E., Pupko, T. & Ben-Tal, N., Jul 2005, In: Nucleic Acids Research. 33, SUPPL. 2, p. W299-W302

Research output: Contribution to journal › Article › peer-review

Open Access

Of four mutations in the factor VII gene in Tunisian patients, one novel mutation (Ser339Phe) in three unrelated families abrogates factor X activation

Fromovich-Amit, Y., Zivelin, A., Rosenberg, N., Landau, M., Rosa, J. P. & Seligsohn, U., Jul 2005, In: Blood Coagulation and Fibrinolysis. 16, 5, p. 369-374 6 p.

Research output: Contribution to journal › Article › peer-review

Single point mutations in the zinc finger motifs of the human immunodeficiency virus type 1 nucleocapsid alter RNA binding specificities of the Gag protein and enhance packaging and infectivity

Mark-Danieli, M., Laham, N., Kenan-Eichler, M., Castiel, A., Melamed, D., Landau, M., Bouvier, N. M., Evans, M. J. & Bacharach, E., Jun 2005, In: Journal of Virology. 79, 12, p. 7756-7767 12 p.

Research output: Contribution to journal › Article › peer-review

Open Access

2004

A novel Phe171Cys mutation in integrin α_IIb causes Glanzmann thrombasthenia by abrogating α_IIbβ₃ complex formation

Rosenberg, N., Landau, M., Luboshitz, J., Rechavi, G. & Seligsohn, U., Jul 2004, In: Journal of Thrombosis and Haemostasis. 2, 7, p. 1167-1175 9 p.

Research output: Contribution to journal › Article › peer-review

Open Access

Characterization of mutations causing factor VII deficiency in 61 unrelated Israeli patients

Fromovich-Amit, Y., Zivelin, A., Rosenberg, N., Tamary, H., Landau, M. & Seligsohn, U., Oct 2004, In: Journal of Thrombosis and Haemostasis. 2, 10, p. 1774-1781 8 p.

Research output: Contribution to journal › Article › peer-review

Open Access

Evolution of p53 in hypoxia-stressed Spalax mimics human tumor mutation

Ashur-Fabian, C., Avivi, A., Trakhtenbrot, L., Adamsky, K., Cohen, M., Kajakaro, G., Joel, A., Amariglio, N., Nevo, E. & Rechavi, G., 17 Aug 2004, In: Proceedings of the National Academy of Sciences of the United States of America. 101, 33, p. 12236-12241

Research output: Contribution to journal › Article › peer-review

Seven novel mutations in the factor XIII A-subunit gene causing hereditary factor XIII deficiency in 10 unrelated families

Vysokovsky, A., Saxena, R., Landau, M., Zivelin, A., Eskaraev, R., Rosenberg, N., Seligsohn, U. & Inbal, A., Oct 2004, In: Journal of Thrombosis and Haemostasis. 2, 10, p. 1790-1797 8 p.

Research output: Contribution to journal › Article › peer-review

Open Access

Severe factor XI deficiency caused by a Gly555 to Glu mutation (factor XI-Glu555): A cross-reactive material positive variant defective in factor IX activation

Zivelin, A., Ogawa, T., Bulvik, S., Landau, M., Toomey, J. R., Lane, J., Seligsohn, U. & Gailani, D., Oct 2004, In: Journal of Thrombosis and Haemostasis. 2, 10, p. 1782-1789 8 p.

Research output: Contribution to journal › Article › peer-review

Open Access

Meytal Landau

Research output

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