Search Results - "Vecsler, Manuela"

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    Using standard optical flow cytometry for synchronizing proliferating cells in the G1 phase by Vecsler, Manuela, Lazar, Itay, Tzur, Amit

    Published in PloS one (31-12-2013)
    “…Cell cycle research greatly relies on synchronization of proliferating cells. However, effective synchronization of mammalian cells is commonly achieved by…”
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    Journal Article
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    A coding VKORC1 Asp36Tyr polymorphism predisposes to warfarin resistance by Loebstein, Ronen, Dvoskin, Ilana, Halkin, Hillel, Vecsler, Manuela, Lubetsky, Aharon, Rechavi, Gideon, Amariglio, Ninette, Cohen, Yoram, Ken-Dror, Gie, Almog, Shlomo, Gak, Eva

    Published in Blood (15-03-2007)
    “…CYP2C9 and VKORC1 genetic variants are associated with low and intermediate warfarin dose requirements, but markers of high doses are less well characterized…”
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    Unbiased transcriptome signature of in vivo cell proliferation reveals pro- and antiproliferative gene networks by Cohen, Meital, Vecsler, Manuela, Liberzon, Arthur, Noach, Meirav, Zlotorynski, Eitan, Tzur, Amit

    Published in Cell cycle (Georgetown, Tex.) (15-09-2013)
    “…Different types of mature B-cell lymphocytes are overall highly similar. Nevertheless, some B cells proliferate intensively, while others rarely do. Here, we…”
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    Ex vivo treatment with a novel synthetic aminoglycoside NB54 in primary fibroblasts from Rett syndrome patients suppresses MECP2 nonsense mutations by Vecsler, Manuela, Ben Zeev, Bruria, Nudelman, Igor, Anikster, Yair, Simon, Amos J, Amariglio, Ninette, Rechavi, Gideon, Baasov, Timor, Gak, Eva

    Published in PloS one (13-06-2011)
    “…Nonsense mutations in the X-linked methyl CpG-binding protein 2 (MECP2) comprise a significant proportion of causative MECP2 mutations in Rett syndrome (RTT)…”
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    Journal Article
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    Gas2l3, a novel constriction site-associated protein whose regulation is mediated by the APC/C Cdh1 complex by Pe'er, Tal, Lahmi, Roxane, Sharaby, Yaara, Chorni, Evelin, Noach, Meirav, Vecsler, Manuela, Zlotorynski, Eitan, Steen, Hanno, Steen, Judith A, Tzur, Amit

    Published in PloS one (2013)
    “…Growth arrest-specific 2-like protein 3 (Gas2l3) was recently identified as an Actin/Tubulin cross-linker protein that regulates cytokinesis. Using cell-free…”
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    Journal Article
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    MeCP2 deficiency down-regulates specific nuclear proteins that could be partially recovered by valproic acid in vitro by Vecsler, Manuela, Simon, Amos J., Amariglio, Ninette, Rechavi, Gideon, Gak, Eva

    Published in Epigenetics (01-01-2010)
    “…MeCP2, the major causative factor of Rett syndrome and related phenotypes including autism, is a two-face nuclear modulator acting via transcriptional and…”
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    Validation of prostate and breast cancer detection artificial intelligence algorithms for accurate histopathological diagnosis and grading: a retrospective study with a Japanese cohort by Lami, Kris, Yoon, Han-Seung, Parwani, Anil V., Pham, Hoa Hoang Ngoc, Tachibana, Yuri, Linhart, Chaim, Grinwald, Maya, Vecsler, Manuela, Fukuoka, Junya

    Published in Pathology (01-08-2024)
    “…Prostate and breast cancer incidence rates have been on the rise in Japan, emphasising the need for precise histopathological diagnosis to determine patient…”
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    Journal Article
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    Epilepsy in Rett syndrome—The experience of a National Rett Center by Nissenkorn, Andreea, Gak, Eva, Vecsler, Manuela, Reznik, Haia, Menascu, Shay, Ben Zeev, Bruria

    Published in Epilepsia (Copenhagen) (01-07-2010)
    “…Summary Purpose:  Rett syndrome (RTT), an X‐linked, dominant neurodevelopmental disorder caused by mutations in the methyl‐CpG‐binding protein 2 (MECP2) gene,…”
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    Journal Article
  13. 13

    Combined genetic profiles of components and regulators of the vitamin K-dependent gamma-carboxylation system affect individual sensitivity to warfarin by Vecsler, Manuela, Loebstein, Ronen, Almog, Shlomo, Kurnik, Daniel, Goldman, Boleslav, Halkin, Hillel, Gak, Eva

    Published in Thrombosis and haemostasis (01-02-2006)
    “…We examined the influence of combined genotypes on interindividual variability in warfarin dose-response. In 100 anticoagulated patients we quantified the…”
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    Journal Article
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    Abstract P6-04-07: Primary Diagnosis of Breast Biopsies supported by AI versus Microscope: Multi-Site Clinical Reader Study by Salomon, Anne, Nudelman, Alona, Cyrta, Joanna, Maklakovski, Marina, Shach, Anat Albrecht, Sebag, Geraldine, Mallel, Giuseppe, Krasnitsky, Ira, Feinberg, Tali, Vecsler, Manuela, Sandbank, Judith

    Published in Cancer research (Chicago, Ill.) (01-03-2023)
    “…Objective This study aimed to clinically validate the use of an AI-based solution by pathologists for the primary diagnosis of breast core needle biopsies as…”
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    Journal Article
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    MeCP2 deficiency downregulates specific nuclear proteins that could be partially recovered by valproic acid in vitro by Vecsler, Manuela, Simon, Amos J, Amariglio, Ninette, Rechavi, Gideon, Gak, Eva

    Published in Epigenetics (01-01-2010)
    “…MeCP2, the major causative factor of Rett syndrome and related phenotypes including autism, is a two-face nuclear modulator acting via transcriptional and…”
    Get full text
    Journal Article
  17. 17

    Using Standard Optical Flow Cytometry for Synchronizing Proliferating Cells in the G1 Phase: e83935 by Vecsler, Manuela, Lazar, Itay, Tzur, Amit

    Published in PloS one (01-12-2013)
    “…Cell cycle research greatly relies on synchronization of proliferating cells. However, effective synchronization of mammalian cells is commonly achieved by…”
    Get full text
    Journal Article
  18. 18

    Gas2l3, a Novel Constriction Site-Associated Protein Whose Regulation Is Mediated by the APC/CCdh1 Complex by Pe’er, Tal, Lahmi, Roxane, Sharaby, Yaara, Chorni, Evelin, Noach, Meirav, Vecsler, Manuela, Zlotorynski, Eitan, Steen, Hanno, Steen, Judith A., Tzur, Amit

    Published in PloS one (28-02-2013)
    “…Growth arrest-specific 2-like protein 3 (Gas2l3) was recently identified as an Actin/Tubulin cross-linker protein that regulates cytokinesis. Using cell-free…”
    Get full text
    Journal Article
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    Common Genetic Variants of Microsomal Epoxide Hydrolase Affect Warfarin Dose Requirements Beyond the Effect of Cytochrome P450 2C9 by Loebstein, Ronen, Vecsler, Manuela, Kurnik, Daniel, Austerweil, Naomi, Gak, Eva, Halkin, Hillel, Almog, Shlomo

    Published in Clinical pharmacology and therapeutics (01-05-2005)
    “…Background Warfarin dose response is partially explained by the polymorphisms in the cytochrome P450 (CYP) 2C9 gene, affecting S‐warfarin clearance, as well as…”
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    Journal Article