Search Results - Mali Gana‐Weisz

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  1. 1
    Imatinib binding and cKIT inhibition is abrogated by the cKIT kinase domain I missense mutation Val654Ala

    Imatinib binding and cKIT inhibition is abrogated by the cKIT kinase domain I missense mutation Val654Ala by Sean R. McLean, Mali Gana‐Weisz, Basil Hartzoulakis, Richard Frow, Jeremy Whelan, David L. Selwood, Chris Boshoff

    Published 2005
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  2. 2
    <i>OPTN</i> 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes

    <i>OPTN</i> 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes by Orly Goldstein, Omri Nayshool, Beatrice Nefussy, Bryan J. Traynor, Alan E. Renton, Mali Gana‐Weisz, Vivian E. Drory, Avi Orr‐Urtreger

    Published 2016
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  3. 3
    Differential effects of severe vs mild <i>GBA</i> mutations on Parkinson disease

    Differential effects of severe vs mild <i>GBA</i> mutations on Parkinson disease by Ziv Gan‐Or, Idan Amshalom, Laura L. Kilarski, Anat Bar‐Shira, Mali Gana‐Weisz, Anat Mirelman, Karen Marder, Susan Bressman, Nir Giladi, Avi Orr‐Urtreger

    Published 2015
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  4. 4
    A homozygous mutation in <i><scp>SLC1A4</scp></i> in siblings with severe intellectual disability and microcephaly

    A homozygous mutation in <i><scp>SLC1A4</scp></i> in siblings with severe intellectual disability and microcephaly by Myriam Srour, Fadi F. Hamdan, Ziv Gan‐Or, D. Labuda, Christina Nassif, Maryam Oskoui, Mali Gana‐Weisz, Avi Orr‐Urtreger, Guy A. Rouleau, Jacques L. Michaud

    Published 2015
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  5. 5
    High Frequency of <i>GBA</i> Gene Mutations in Dementia With Lewy Bodies Among Ashkenazi Jews

    High Frequency of <i>GBA</i> Gene Mutations in Dementia With Lewy Bodies Among Ashkenazi Jews by Tamara Shiner, Anat Mirelman, Mali Gana Weisz, Anat Bar‐Shira, Elissa L. Ash, Ron Cialic, Naomi Nevler, Tanya Gurevich, Noa Bregman, Avi Orr‐Urtreger, Nir Giladi

    Published 2016
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  6. 6
    Novel Ras antagonist blocks human melanoma growth

    Novel Ras antagonist blocks human melanoma growth by Burkhard Jansen, Hermine Schlagbauer‐Wadl, Heike Kahr, Elisabeth Heere‐Ress, Balázs Mayer, H.-G. Eichler, Hubert Pehamberger, Mali Gana‐Weisz, Eitan Ben‐David, Yoel Kloog, K. Wolff

    Published 1999
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  7. 7
    The effect of polygenic risk score on PD risk and phenotype in <i>LRRK2</i> G2019S and <i>GBA1</i> carriers

    The effect of polygenic risk score on PD risk and phenotype in <i>LRRK2</i> G2019S and <i>GBA1</i> carriers by Orly Goldstein, Shachar Shani, Mali Gana‐Weisz, Nadav Elkoshi, Fergal Casey, Yu Sun, Khyati Chandratre, Jesse M. Cedarbaum, Cornelis Blauwendraat, Anat Bar‐Shira, Avner Thaler, Tanya Gurevich, Anat Mirelman, Nir Giladi, Avi Orr‐Urtreger, Roy N. Alcalay

    Published 2025
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  8. 8
    The p.L302P mutation in the lysosomal enzyme gene <i>SMPD1</i> is a risk factor for Parkinson disease

    The p.L302P mutation in the lysosomal enzyme gene <i>SMPD1</i> is a risk factor for Parkinson disease by Ziv Gan‐Or, Laurie J. Ozelius, Anat Bar‐Shira, Rachel Saunders‐Pullman, Anat Mirelman, Ruth Kornreich, Mali Gana‐Weisz, Deborah Raymond, Liron Rozenkrantz, Andres Deik, Tanya Gurevich, Susan J. Gross, Nicole Schreiber‐Agus, Nir Giladi, Susan Bressman, Avi Orr‐Urtreger

    Published 2013
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  9. 9
    Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the <i>LRRK2</i> gene

    Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the <i>LRRK2</i> gene by Anat Mirelman, Roy N. Alcalay, Rachel Saunders‐Pullman, Kira Yasinovsky, Avner Thaler, Tanya Gurevich, Helen Mejia‐Santana, Deborah Raymond, Mali Gana‐Weisz, Anat Bar‐Shira, Laurie J. Ozelius, Lorraine N. Clark, Avi Orr‐Urtreger, Susan Bressman, Karen Marder, Nir Giladi

    Published 2015
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  10. 10
    The histone H2B-specific ubiquitin ligase RNF20/hBRE1 acts as a putative tumor suppressor through selective regulation of gene expression

    The histone H2B-specific ubiquitin ligase RNF20/hBRE1 acts as a putative tumor suppressor through selective regulation of gene expression by Efrat Shema, Itay Tirosh, Yael Aylon, Jing Huang, Chaoyang Ye, Neta Moskovits, Nina Raver-Shapira, Neri Minsky, Judith Pirngruber, Gabi Tarcic, Pavla Hublarová, Lilach Moyal, Mali Gana‐Weisz, Yosef Shiloh, Yossef Yarden, Steven A. Johnsen, Bořivoj Vojtěšek, Shelley L. Berger, Moshe Oren

    Published 2008
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  11. 11
    Application of the Movement Disorder Society prodromal criteria in healthy <i>G2019S</i>‐<i>LRRK2</i> carriers

    Application of the Movement Disorder Society prodromal criteria in healthy <i>G2019S</i>‐<i>LRRK2</i> carriers by Anat Mirelman, Rachel Saunders‐Pullman, Roy N. Alcalay, Shiran Shustak, Avner Thaler, Tanya Gurevich, Deborah Raymond, Helen Mejia‐Santana, Martha Orbe Reilly, Laurie J. Ozelius, Lorraine N. Clark, Mali Gana‐Weisz, Anat Bar‐Shira, Avi Orr‐Utreger, Susan Bressman, Karen Marder, Nir Giladi

    Published 2018
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  12. 12
    Radiological markers of CSF α-synuclein aggregation in Parkinson’s disease patients

    Radiological markers of CSF α-synuclein aggregation in Parkinson’s disease patients by Amgad Droby, Avital Yoffe-Vasiliev, Dikla Atias, Kyle Fraser, Omar S. Mabrouk, Nurit Omer, Anat Bar‐Shira, Mali Gana‐Weisz, Orly Goldstein, Moran Artzi, Dafna Ben Bashat, Roy N. Alcalay, Avi Orr‐Urtreger, Julia Shirvan, Jesse M. Cedarbaum, Nir Giladi, Anat Mirelman, Avner Thaler

    Published 2025
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  13. 13
    Requirement of ATM-Dependent Monoubiquitylation of Histone H2B for Timely Repair of DNA Double-Strand Breaks

    Requirement of ATM-Dependent Monoubiquitylation of Histone H2B for Timely Repair of DNA Double-Strand Breaks by Lilach Moyal, Yaniv Lerenthal, Mali Gana‐Weisz, Gilad Mass, Sairei So, Shih-Ya Wang, Berina Eppink, Young‐Min Chung, Gil Shalev, Efrat Shema, Dganit Shkedy, Nechama I. Smorodinsky, Nicole van Vliet, Bernhard Küster, Matthias Mann, Aaron Ciechanover, Jochen Dahm‐Daphi, Roland Kanaar, Mickey C.‐T. Hu, David J. Chen, Moshe Oren, Yosef Shiloh

    Published 2011
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  14. 14
    Arm swing as a potential new prodromal marker of Parkinson's disease

    Arm swing as a potential new prodromal marker of Parkinson's disease by Anat Mirelman, Hagar Bernad‐Elazari, Avner Thaler, Eytan Giladi‐Yacobi, Tanya Gurevich, Mali Gana‐Weisz, Rachel Saunders‐Pullman, Deborah Raymond, Nancy Doan, Susan Bressman, Karen Marder, Roy N. Alcalay, Ashwini K. Rao, Daniela Berg, Kathrin Brockmann, Jan Aasly, Bjørg Warø, Eduardo Tolosa, Dolores Vilas, Claustre Pont‐Sunyer, Avi Orr‐Urtreger, Jeffrey M. Hausdorff, Nir Giladi

    Published 2016
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  15. 15
    Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes

    Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes by Vladimir Vacic, Laurie J. Ozelius, Lorraine N. Clark, Anat Bar‐Shira, Mali Gana‐Weisz, Tanya Gurevich, Alexander Gusev, Merav Kedmi, Eimear E. Kenny, X. Liu, Helen Mejia‐Santana, Anat Mirelman, Deborah Raymond, Rachel Saunders‐Pullman, Robert J. Desnick, Gil Atzmon, E. Robert Burns, Harry Ostrer, Hákon Hákonarson, Aviv Bergman, Nir Barzilai, Ariel Darvasi, Inga Peter, Saurav Guha, Todd Lencz, Nir Giladi, K. Marder, I. Pe'er, Susan Bressman, Avi Orr‐Urtreger

    Published 2014
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  16. 16
    Parkinson disease phenotype in Ashkenazi jews with and without <i>LRRK2</i> G2019S mutations

    Parkinson disease phenotype in Ashkenazi jews with and without <i>LRRK2</i> G2019S mutations by Roy N. Alcalay, Anat Mirelman, Rachel Saunders‐Pullman, Ming‐X Tang, Helen Mejia Santana, Deborah Raymond, Ernest Roos, Martha Orbe‐Reilly, Tanya Gurevich, Anat Bar Shira, Mali Gana Weisz, Kira Yasinovsky, Maayan Zalis, Avner Thaler, Andres Deik, Matthew J. Barrett, Jose Cabassa, Mark Groves, Ann Hunt, Naomi Lubarr, Marta San Luciano, Joan Miravite, Christina A. Palmese, Rivka Sachdev, Harini Sarva, Lawrence Severt, Vicki Shanker, Matthew Swan, Jeannie Soto‐Valencia, Brooke Johannes, Robert Ortega, Stanley Fahn, Lucien Côté, Cheryl Waters, Pietro Mazzoni, Blair Ford, Elan D. Louis, Oren Levy, Llency Rosado, Dylanis Lopez Ruiz, Tsvyatko Dorovski, Michael W. Pauciulo, William C. Nichols, Avi Orr‐Urtreger, Laurie J. Ozelius, Lorraine N. Clark, Nir Giladi, Susan Bressman, Karen Marder

    Published 2013
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  17. 17
    Age-specific penetrance of<i>LRRK2</i>G2019S in the Michael J. Fox Ashkenazi Jewish LRRK2 Consortium

    Age-specific penetrance of<i>LRRK2</i>G2019S in the Michael J. Fox Ashkenazi Jewish LRRK2 Consortium by Karen Marder, Yuanjia Wang, Roy N. Alcalay, Helen Mejia‐Santana, Ming‐Xin Tang, Annie Lee, Deborah Raymond, Anat Mirelman, Rachel Saunders‐Pullman, Lorraine N. Clark, Laurie J. Ozelius, Avi Orr‐Urtreger, Nir Giladi, Susan Bressman, Roy N. Alcalay, Ming-X Tang, Helen Mejia Santana, Ernest Roos, Martha Orbe‐Reilly, Stanley Fahn, Lucien Côté, Cheryl Waters, Pietro Mazzoni, Blair Ford, Elan D. Louis, Oren Levy, Llency Rosado, Dylanis Lopez Ruiz, Tsvyatko Dorovski, Paul Greene, Lorraine N. Clark, Karen Marder, Tanya Gurevich, Anat Bar Shira, Mali Gana Weisz, Kira Yasinovsky, Maayan Zalis, Avner Thaler, Yaacov Balash, Shabtai Hertzel, Ziv Gan‐Or, Hila Kobo, Ariella Hillel, Anat Shkedy, Avi Orr‐Urtreger, Nir Giladi, Andres Deik, Matthew J. Barrett, Jose Cabassa, Mark Groves, Ann Hunt, Naomi Lubarr, Marta San Luciano, Joan Miravite, Christina A. Palmese, Rivka Sachdev, Harini Sarva, Lawrence Severt, Vicki Shanker, Matthew Swan, Jeannie Soto‐Valencia, Brooke Johannes, Robert Ortega, Laurie J. Ozelius, Rachel Saunders‐Pullman, Deborah Raymond, Susan Bressman

    Published 2015
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