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Experiences of donors enrolled in a randomized study of allogeneic bone marrow or peripheral blood stem cell transplantation
Neutrophil-specific granule deficiency: homozygous recessive inheritance of a frameshift mutation in the gene encoding transcription factor CCAAT/enhancer binding protein–ε
High response rate in refractory and poor-risk multiple myeloma after allotransplantation using a nonmyeloablative conditioning regimen and donor lymphocyte infusions
Influence of the hematopoietic stem cell source on early immunohematologic reconstitution after allogeneic transplantation
Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B–severe combined immune deficiency or Omenn syndrome
T-cell lines from 2 patients with adenosine deaminase (ADA) deficiency showed the restoration of ADA activity resulted from the reversion of an inherited mutation
Issue Archive
May 1 2001
Table of Contents
INSIDE BLOOD
REVIEW ARTICLES
CLINICAL OBSERVATIONS, INTERVENTIONS, AND THERAPEUTIC TRIALS
Experiences of donors enrolled in a randomized study of allogeneic bone marrow or peripheral blood stem cell transplantation
Clinical Trials & Observations
Neutrophil-specific granule deficiency: homozygous recessive inheritance of a frameshift mutation in the gene encoding transcription factor CCAAT/enhancer binding protein–ε
Clinical Trials & Observations
Adrian F. Gombart,Masaaki Shiohara,Scott H. Kwok,Kazunaga Agematsu,Atsushi Komiyama,H. Phillip Koeffler
High response rate in refractory and poor-risk multiple myeloma after allotransplantation using a nonmyeloablative conditioning regimen and donor lymphocyte infusions
Clinical Trials & Observations
Ashraf Badros,Bart Barlogie,Christopher Morris,Raman Desikan,Sara R. Martin,Nikhil Munshi,Maurizio Zangari,Jayesh Mehta,Amir Toor,Michele Cottler-Fox,Athanasios Fassas,Elias Anaissie,Steven Schichman,Guido Tricot
Influence of the hematopoietic stem cell source on early immunohematologic reconstitution after allogeneic transplantation
Clinical Trials & Observations
Valérie Lapierre,Nadia Oubouzar,Anne Aupérin,Dominique Tramalloni,Hakim Tayebi,Eric Robinet,Matthieu Kuentz,Didier Blaise,Olivier Hartmann,Patrick Hervé,Pierre Tiberghien,for the Société Française de Greffe de Moelle
HEMATOPOIESIS
Ionizing radiation sensitizes erythroleukemic cells but not normal erythroblasts to tumor necrosis factor–related apoptosis-inducing ligand (TRAIL)–mediated cytotoxicity by selective up-regulation of TRAIL-R1
Roberta Di Pietro,Paola Secchiero,Rosalba Rana,Davide Gibellini,Giuseppe Visani,Kristi Bemis,Loris Zamai,Sebastiano Miscia,Giorgio Zauli
HEMOSTASIS, THROMBOSIS, AND VASCULAR BIOLOGY
IMMUNOBIOLOGY
Localization of recombination activating gene 1/green fluorescent protein (RAG1/GFP) expression in secondary lymphoid organs after immunization with T-dependent antigens in rag1/gfpknockin mice
Hideya Igarashi,Naomi Kuwata,Kumiko Kiyota,Kiminobu Sumita,Toshio Suda,Shiro Ono,Steven R. Bauer,Nobuo Sakaguchi
Immunoglobulin heavy-chain gene rearrangement in adult acute lymphoblastic leukemia reveals preferential usage of JH-proximal variable gene segments
Forida Y. Mortuza,Ilidia M. Moreira,Maria Papaioannou,Paula Gameiro,Luke A. Coyle,Clair S. Gricks,Peter Amlot,Hugh Grant Prentice,Alejandro Madrigal,Alan Victor Hoffbrand,Letizia Foroni
Signal-regulatory protein α (SIRPα) but not SIRPβ is involved in T-cell activation, binds to CD47 with high affinity, and is expressed on immature CD34+CD38−hematopoietic cells
Martina Seiffert,Peter Brossart,Charles Cant,Marina Cella,Marco Colonna,Wolfram Brugger,Lothar Kanz,Axel Ullrich,Hans-Jörg Bühring
Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B–severe combined immune deficiency or Omenn syndrome
Clinical Trials & Observations
Barbara Corneo,Despina Moshous,Tayfun Güngör,Nicolas Wulffraat,Pierre Philippet,Françoise Le Deist,Alain Fischer,Jean-Pierre de Villartay
NEOPLASIA
PHAGOCYTES
RED CELLS
TRANSFUSION MEDICINE
Molecular identification of Knops blood group polymorphisms found in long homologous region D of complement receptor 1
Joann M. Moulds,Peter A. Zimmerman,Ogobara K. Doumbo,Lalla Kassambara,Issaka Sagara,Dapa A. Diallo,John P. Atkinson,Malgorzata Krych-Goldberg,Richard E. Hauhart,Dennis E. Hourcade,David T. McNamara,Daniel J. Birmingham,J. Alexandra Rowe,John J. Moulds,Louis H. Miller
TRANSPLANTATION
Differential use of Fas ligand and perforin cytotoxic pathways by donor T cells in graft-versus-host disease and graft-versus-leukemia effect
Cornelius Schmaltz,Onder Alpdogan,Kirsten J. Horndasch,Stephanie J. Muriglan,Barry J. Kappel,Takanori Teshima,James L. M. Ferrara,Steven J. Burakoff,Marcel R. M. van den Brink
BRIEF REPORTS
T-cell lines from 2 patients with adenosine deaminase (ADA) deficiency showed the restoration of ADA activity resulted from the reversion of an inherited mutation
Brief Report
Tadashi Ariga,Noriko Oda,Koji Yamaguchi,Nobuaki Kawamura,Hideaki Kikuta,Shoichiro Taniuchi,Yohnosuke Kobayashi,Kihei Terada,Hisami Ikeda,Michael S. Hershfield,Kunihiko Kobayashi,Yukio Sakiyama
CORRESPONDENCE
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