Founder mutation for Huntington disease in Caucasus Jews
Melamed, O., Behar, D. M., Bram, C., Magal, N., Pras, E., Reznik-Wolf, H., Borochowitz, Z. U., Davidov, B., Mor-Cohen, R., Baris, H. N.
Published in Clinical genetics (01.02.2015)
Published in Clinical genetics (01.02.2015)
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A 13‐bp deletion in αIIb 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.
Published in Journal of thrombosis and haemostasis (01.12.2005)
Published in Journal of thrombosis and haemostasis (01.12.2005)
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ADP-coupled integrin regulation by the extracellular redox system
Lahav, J, Hess, O, Calo, D, Kehrel, B, Jurk, K, Seligsohn, U, Mor-Cohen, R, Rosenberg, N
Published in Pathophysiology of haemostasis and thrombosis (01.01.2006)
Published in Pathophysiology of haemostasis and thrombosis (01.01.2006)
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Identification and Functional Analysis of Two Novel Mutations in the Multidrug Resistance Protein 2 Gene in Israeli Patients with Dubin-Johnson Syndrome
Mor-Cohen, Ronit, Zivelin, Ariella, Rosenberg, Nurit, Shani, Mordechai, Muallem, Shmuel, Seligsohn, Uri
Published in The Journal of biological chemistry (05.10.2001)
Published in The Journal of biological chemistry (05.10.2001)
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A 13-bp deletion in alpha(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
Published in Journal of thrombosis and haemostasis (01.12.2005)
Published in Journal of thrombosis and haemostasis (01.12.2005)
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Molecular diversity of Glanzmann thrombasthenia in southern India: new insights into mRNA splicing and structure-function correlations of α IIb β 3 integrin ( ITGA2B, ITGB3 )
Peretz, Hava, Rosenberg, Nurit, Landau, Meytal, Usher, Saly, Nelson, Everette J.R., Mor-Cohen, Ronit, French, Deborah L., Mitchell, Beau W., Nair, Sukesh C., Chandy, Mammen, Coller, Barry S., Srivastava, Alok, Seligsohn, Uri
Published in Human mutation (01.04.2006)
Published in Human mutation (01.04.2006)
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ORIGINAL ARTICLE: A 13-bp deletion in alpha sub(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
Published in Journal of thrombosis and haemostasis (01.12.2005)
Published in Journal of thrombosis and haemostasis (01.12.2005)
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Journal Article
A novel ancestral splicing mutation in the multidrug resistance protein 2 gene causes Dubin-Johnson syndrome in Ashkenazi Jewish patients
Mor-Cohen, Ronit, Zivelin, Ariella, Rosenberg, Nurit, Goldberg, Iris, Seligsohn, Uri
Published in Hepatology research (01.02.2005)
Published in Hepatology research (01.02.2005)
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The lower incidence of myotonic dystrophy in Ashkenazic Jews compared to North African Jews is associated with a significantly lower number of CTG trinucleotide repeats
Mor-Cohen, R, Magal, N, Gadoth, N, Achiron, A, Shohat, T, Shohat, M
Published in Israel journal of medical sciences (01.03.1997)
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Published in Israel journal of medical sciences (01.03.1997)
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Correlation between the incidence of myotonic dystrophy in different groups in Israel and the number of CTG trinucleotide repeats in the myotonin gene
Mor-Cohen, R, Magal, N, Gadoth, N, Shohat, T, Shohat, M
Published in American journal of medical genetics (08.08.1997)
Published in American journal of medical genetics (08.08.1997)
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