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There are 42404 results for: content related to: GPI-anchored protein-deficient T cells in patients with aplastic anemia and low-risk myelodysplastic syndrome: implications for the immunopathophysiology of bone marrow failure

  1. Whole transcriptome sequencing identifies increased CXCR2 expression in PNH granulocytes

    British Journal of Haematology

    Kohei Hosokawa, Sachiko Kajigaya, Keyvan Keyvanfar, Wangmin Qiao, Yanling Xie, Angelique Biancotto, Danielle M. Townsley, Xingmin Feng and Neal S. Young

    Version of Record online : 1 FEB 2017, DOI: 10.1111/bjh.14502

  2. You have free access to this content
    Molecular Basis of Paroxysmal Nocturnal Hemoglobinuria

    STEM CELLS

    Volume 14, Issue 4, July 1996, Pages: 396–411, Dr. Charles J. Parker

    Version of Record online : 1 JUL 1996, DOI: 10.1002/stem.140396

  3. Paroxysmal Nocturnal Hemoglobinuria— the Selection of a Clone

    Reviews in Clinical and Experimental Hematology

    Volume 4, Issue 3, September 2000, Pages: 216–235, Peter Hillmen and Stephen Richards

    Version of Record online : 25 DEC 2001, DOI: 10.1046/j.1468-0734.2000.00016.x

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    IMPLICATIONS OF RECENT INSIGHTS INTO THE PATHOPHYSIOLOGY OF PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA

    British Journal of Haematology

    Volume 108, Issue 3, March 2000, Pages: 470–479, Peter Hillmen and Stephen J. Richards

    Version of Record online : 24 DEC 2001, DOI: 10.1046/j.1365-2141.2000.01802.x

  5. Increased glycosylphosphatidylinositol-anchored protein-deficient granulocytes define a benign subset of bone marrow failures in patients with trisomy 8

    European Journal of Haematology

    Volume 95, Issue 3, September 2015, Pages: 230–238, Kohei Hosokawa, Naomi Sugimori, Takamasa Katagiri, Yumi Sasaki, Chizuru Saito, Yu Seiki, Kanako Mochizuki, Hirohito Yamazaki, Akiyoshi Takami and Shinji Nakao

    Version of Record online : 4 FEB 2015, DOI: 10.1111/ejh.12484

  6. Diagnostic screening of paroxysmal nocturnal hemoglobinuria: Prospective multicentric evaluation of the current medical indications

    Cytometry Part B: Clinical Cytometry

    Marta Morado, Alex Freire Sandes, Enrique Colado, Dolores Subirá, Paloma Isusi, María Soledad Noya, María Belén Vidriales, Amparo Sempere, José Ángel Díaz, Alfredo Minguela, Beatriz Álvarez, Cristina Serrano, Teresa Caballero, Mercedes Rey, Ana Pérez Corral, María Cristina Fernández Jiménez, Elena Magro, Angelina Lemes, Celina Benavente, Helena Bañas, Juana Merino, Celine Castejon, Olivier Gutierrez, Pilar Rabasa, Matheus Vescosi Gonçalves, Martin Perez-Andres, Alberto Orfao and on behalf of the PNH working group of the Iberian Society of Cytometry (SIC)

    Version of Record online : 1 OCT 2016, DOI: 10.1002/cyto.b.21480

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    Historical aspects of paroxysmal nocturnal haemoglobinuria: ‘defining the disease’

    British Journal of Haematology

    Volume 117, Issue 1, April 2002, Pages: 3–22,

    Version of Record online : 25 MAR 2002, DOI: 10.1046/j.1365-2141.2002.03374.x

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    Guidelines for the diagnosis and monitoring of paroxysmal nocturnal hemoglobinuria and related disorders by flow cytometry

    Cytometry Part B: Clinical Cytometry

    Volume 78B, Issue 4, July 2010, Pages: 211–230, Michael J. Borowitz, Fiona E. Craig, Joseph A. DiGiuseppe, Andrea J. Illingworth, Wendell Rosse, D. Robert Sutherland, Carl T. Wittwer and Stephen J. Richards

    Version of Record online : 28 APR 2010, DOI: 10.1002/cyto.b.20525

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    Relationship between bone marrow failure syndromes and the presence of glycophosphatidyl inositol-anchored protein-deficient clones

    British Journal of Haematology

    Volume 115, Issue 4, December 2001, Pages: 1015–1022, Jaroslaw P. Maciejewski, Candido Rivera, Hoon Kook, Daniel Dunn and Neal S. Young

    Version of Record online : 20 DEC 2001, DOI: 10.1046/j.1365-2141.2001.03191.x

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    Application of flow cytometry to the diagnosis of paroxysmal nocturnal hemoglobinuria

    Cytometry

    Volume 42, Issue 4, 15 August 2000, Pages: 223–233, Stephen J. Richards, Andrew C. Rawstron and Peter Hillmen

    Version of Record online : 3 AUG 2000, DOI: 10.1002/1097-0320(20000815)42:4<223::AID-CYTO2>3.0.CO;2-D

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    Altered lipid raft composition and defective cell death signal transduction in glycosylphosphatidylinositol anchor-deficient PIG-A mutant cells

    British Journal of Haematology

    Volume 142, Issue 3, August 2008, Pages: 413–422, Hadrian Szpurka, Andrew E. Schade, Anna M. Jankowska and Jaroslaw P. Maciejewski

    Version of Record online : 9 JUN 2008, DOI: 10.1111/j.1365-2141.2008.07203.x

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    Development and evaluation of a stabilized whole-blood preparation as a process control material for screening of paroxysmal nocturnal hemoglobinuria by flow cytometry

    Cytometry Part B: Clinical Cytometry

    Volume 76B, Issue 1, January 2009, Pages: 47–55, Stephen J. Richards, Liam Whitby, Matthew J. Cullen, Anita J. Dickinson, Viv Granger, John T. Reilly, Peter Hillmen and David Barnett

    Version of Record online : 5 SEP 2008, DOI: 10.1002/cyto.b.20438

  13. High-Sensitivity Detection of PNH Red Blood Cells, Red Cell Precursors, and White Blood Cells

    Unit

    Current Protocols in Cytometry

    6:6.37.1–6.37.29

    D. Robert Sutherland, Andrea Illingworth, Michael Keeney and Stephen J. Richards

    Published Online : 1 APR 2015, DOI: 10.1002/0471142956.cy0637s72

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    Flow cytometric analysis of glycosylphosphatidyl-inositol–anchored proteins to assess paroxysmal nocturnal hemoglobinuria clone size

    Cytometry

    Volume 42, Issue 4, 15 August 2000, Pages: 234–238, Josefa Piedras and Xavier López-Karpovitch

    Version of Record online : 3 AUG 2000, DOI: 10.1002/1097-0320(20000815)42:4<234::AID-CYTO3>3.0.CO;2-6

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    Diagnosing PNH with FLAER and multiparameter flow cytometry

    Cytometry Part B: Clinical Cytometry

    Volume 72B, Issue 3, May 2007, Pages: 167–177, D. Robert Sutherland, Nancy Kuek, Jeff Davidson, David Barth, Hong Chang, Erik Yeo, Sylvia Bamford, Ian Chin-Yee and Michael Keeney

    Version of Record online : 6 FEB 2007, DOI: 10.1002/cyto.b.20151

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    Individual Hematopoietic Stem Cells in Human Bone Marrow of Patients with Aplastic Anemia or Myelodysplastic Syndrome Stably Give Rise to Limited Cell Lineages

    STEM CELLS

    Volume 31, Issue 3, March 2013, Pages: 536–546, Takamasa Katagiri, Hiroshi Kawamoto, Takashi Nakakuki, Ken Ishiyama, Mariko Okada-Hatakeyama, Shigeki Ohtake, Yu Seiki, Kohei Hosokawa and Shinji Nakao

    Version of Record online : 25 FEB 2013, DOI: 10.1002/stem.1301

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    Glycosylphosphatidylinositol (GPI)-deficient Jurkat T cells as a model to study functions of GPI-anchored proteins

    Clinical & Experimental Immunology

    Volume 122, Issue 1, October 2000, Pages: 49–54, I. Bastisch, A. Tiede, M. Deckert, A. Ziolek, R. E. Schmidt and J. Schubert

    Version of Record online : 24 DEC 2001, DOI: 10.1046/j.1365-2249.2000.01350.x

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    Multilineage glycosylphosphatidylinositol anchor-deficient haematopoiesis in untreated aplastic anaemia

    British Journal of Haematology

    Volume 115, Issue 2, November 2001, Pages: 476–482, Galina L. Mukhina, J. Thomas Buckley, James P. Barber, Richard J. Jones and Robert A. Brodsky

    Version of Record online : 20 DEC 2001, DOI: 10.1046/j.1365-2141.2001.03127.x

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    Paroxysmal Nocturnal Haemoglobinuria: the Disease and a Hypothesis for a New Treatment

    Scandinavian Journal of Immunology

    Volume 49, Issue 2, February 1999, Pages: 119–125, JARVA and MERI

    Version of Record online : 5 JAN 2002, DOI: 10.1046/j.1365-3083.1999.00489.x

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    Frequent HPRT mutations in paroxysmal nocturnal haemoglobinuria reflect T cell clonal expansion, not genomic instability

    British Journal of Haematology

    Volume 125, Issue 3, May 2004, Pages: 383–391, Guibin Chen, Weihua Zeng, Spencer Green and Neal S. Young

    Version of Record online : 1 APR 2004, DOI: 10.1111/j.1365-2141.2004.04912.x