Výsledky vyhledávání - Suzanne Vercauteren

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  1. 1
    Alkaline Phosphatase-Positive Colony Formation Is a Sensitive, Specific, and Quantitative Indicator of Undifferentiated Human Embryonic Stem Cells

    Alkaline Phosphatase-Positive Colony Formation Is a Sensitive, Specific, and Quantitative Indicator of Undifferentiated Human Embryonic Stem Cells Autor Michael D. O’Connor, Melanie Kardel, Ioulia Iosfina, David Youssef, Min Lu, Michael Li, Suzanne Vercauteren, András Nagy, Connie J. Eaves

    Vydáno 2008
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    Artigo
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  2. 2
    Genetic Hemoglobin Disorders Rather Than Iron Deficiency Are a Major Predictor of Hemoglobin Concentration in Women of Reproductive Age in Rural Prey Veng, Cambodia,

    Genetic Hemoglobin Disorders Rather Than Iron Deficiency Are a Major Predictor of Hemoglobin Concentration in Women of Reproductive Age in Rural Prey Veng, Cambodia, Autor Crystal D Karakochuk, Kyly C. Whitfield, Susan I. Barr, Yvonne Lamers, Angela M. Devlin, Suzanne Vercauteren, Hou Kroeun, Aminuzzaman Talukder, Judy McLean, Tim Green

    Vydáno 2014
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  3. 3
    High-resolution whole genome tiling path array CGH analysis of CD34+ cells from patients with low-risk myelodysplastic syndromes reveals cryptic copy number alterations and predicts overall and leukemia-free survival

    High-resolution whole genome tiling path array CGH analysis of CD34+ cells from patients with low-risk myelodysplastic syndromes reveals cryptic copy number alterations and predict... Autor Daniel T. Starczynowski, Suzanne Vercauteren, Adèle Telenius, Sandy Sung, Kaoru Tohyama, Angela Brooks‐Wilson, John J. Spinelli, Connie J. Eaves, Allen Eaves, Douglas E. Horsman, Wan L. Lam, Aly Karsan

    Vydáno 2008
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  4. 4
    A longitudinal single-cell atlas of treatment response in pediatric AML

    A longitudinal single-cell atlas of treatment response in pediatric AML Autor Sander Lambo, Diane L. Trinh, Rhonda E. Ries, Dan Jin, Audi Setiadi, Michelle Ng, Véronique G. LeBlanc, Michael R. Loken, Lisa Eidenschink Brodersen, Fangyan Dai, Laura Pardo, Xiaotu Ma, Suzanne Vercauteren, Soheil Meshinchi, Marco A. Marra

    Vydáno 2023
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  5. 5
    JAK1 gain-of-function causes an autosomal dominant immune dysregulatory and hypereosinophilic syndrome

    JAK1 gain-of-function causes an autosomal dominant immune dysregulatory and hypereosinophilic syndrome Autor Kate L. Del Bel, Robert J. Ragotte, Aabida Saferali, Susan Lee, Suzanne Vercauteren, Sara Mostafavi, Richard A. Schreiber, Julie Prendiville, Min Phang, Jessica Halparin, Nicholas Au, John Mark Dean, John J. Priatel, Emily Jewels, Anne Junker, Paul Rogers, Michael Seear, Margaret L. McKinnon, Stuart E. Turvey

    Vydáno 2017
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    Carta
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  6. 6
    De Novo Mutations in YWHAG Cause Early-Onset Epilepsy

    De Novo Mutations in YWHAG Cause Early-Onset Epilepsy Autor Ilaria Guella, Marna B. McKenzie, Daniel M. Evans, Sarah E. Buerki, Eric Toyota, Margot I. Van Allen, Mohnish Suri, Frances Elmslie, Marleen Simon, Koen L.I. van Gassen, Delphine Héron, Boris Keren, Caroline Nava, Mary Connolly, Michelle Demos, Matthew J. Farrer, Shelin Adam, Cyrus Boelman, Corneliu Bolbocean, Tara Candido, Patrice Eydoux, Gabriella Horváth, Linda Huh, Tanya N. Nelson, Graham Sinclair, Clara van Karnebeek, Suzanne Vercauteren

    Vydáno 2017
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  7. 7
    Metabolomic in severe traumatic brain injury: exploring primary, secondary injuries, diagnosis, and severity

    Metabolomic in severe traumatic brain injury: exploring primary, secondary injuries, diagnosis, and severity Autor Mohammad Mehdi Banoei, James S. Hutchison, William J. Panenka, Andy Kin On Wong, David S. Wishart, Brent W. Winston, Cheryl L. Wellington, Noah D. Silverberg, Sanjay K. Murthy, Keith R. Walley, Quynh Doan, Ivan J. Torres, Prescilla Carrion, Suzanne Vercauteren, Angela Aquino, Keith Owen Yeates, Michael J. Esser, Karen Barlow, Josee Wong, Anne‐Marie Guerguerian, Adrienne L. Davis, Robin Green, Anne L. Wheeler, Katia J. Sinopoli, Shannon E. Scratch, Angela Colantonio, Lili‐Naz Hazrati, Elizabeth Wilson, Arash Khosroawshahi, Grace Zhang, Leanne Fernandes, Katie Hutchison, J. Lacroix, Catherine Farrell, Laurence Ducharme‐Crevier, Miriam H. Beauchamp, Mindy French, David B. Clarke, Lorelei Audas, Kathleen A. Martin, Lynne Fenerty, Patricia C. Liaw, Alexis F. Turgeon

    Vydáno 2025
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  8. 8
    Loss-of-Function and Gain-of-Function Mutations in KCNQ5 Cause Intellectual Disability or Epileptic Encephalopathy

    Loss-of-Function and Gain-of-Function Mutations in KCNQ5 Cause Intellectual Disability or Epileptic Encephalopathy Autor Anna Lehman, Samrat Thouta, Grazia M.S. Mancini, Sakkubai Naidu, Marjon van Slegtenhorst, Kirsty McWalter, Richard Person, Jill Mwenifumbo, Ramona Salvarinova, Ilaria Guella, Marna B. McKenzie, Anita Datta, Mary Connolly, Somayeh Mojard Kalkhoran, Damon Poburko, Jan M. Friedman, Matthew J. Farrer, Michelle Demos, Sonal Desai, Tom W. Claydon, Shelin Adam, Christèle du Souich, Alison M. Elliott, Anna Lehman, Jill Mwenifumbo, Tanya N. Nelson, Clara van Karnebeek, Jan M. Friedman, Shelin Adam, Cyrus Boelman, Corneliu Bolbocean, Sarah E. Buerki, Tara Candido, Patrice Eydoux, Daniel M. Evans, William T. Gibson, Gabriella Horváth, Linda Huh, Tanya N. Nelson, Graham Sinclair, Tamsin Tarling, Eric Toyota, Katelin N. Townsend, Margot I. Van Allen, Clara van Karnebeek, Suzanne Vercauteren

    Vydáno 2017
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