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Risk of recurrent venous thrombosis in children with combined prothrombotic risk factors
Rising pp65 antigenemia during preemptive anticytomegalovirus therapy after allogeneic hematopoietic stem cell transplantation: risk factors, correlation with DNA load, and outcomes
The Kozak sequence polymorphism of platelet glycoprotein Ibα and risk of nonfatal myocardial infarction and nonfatal stroke in young women
Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome)
Issue Archive
Table of Contents
PLENARY PAPERS
RETRACTIONS
CHEMOKINES
CLINICAL OBSERVATIONS, INTERVENTIONS, AND THERAPEUTIC TRIALS
Risk of recurrent venous thrombosis in children with combined prothrombotic risk factors
Clinical Trials & Observations
Ulrike Nowak-Göttl,Ralf Junker,Wolfhart Kreuz,Arnold von Eckardstein,Andrea Kosch,Natascha Nohe,Rosemarie Schobess,Silke Ehrenforth,for the Childhood Thrombophilia Study Group
Rising pp65 antigenemia during preemptive anticytomegalovirus therapy after allogeneic hematopoietic stem cell transplantation: risk factors, correlation with DNA load, and outcomes
Clinical Trials & Observations
W. Garrett Nichols,Lawrence Corey,Ted Gooley,W. Lawrence Drew,Richard Miner,Meei-Li Huang,Chris Davis,Michael Boeckh
The Kozak sequence polymorphism of platelet glycoprotein Ibα and risk of nonfatal myocardial infarction and nonfatal stroke in young women
Clinical Trials & Observations
Michele B. Frank,Alexander P. Reiner,Stephen M. Schwartz,Prasanna N. Kumar,Rachel M. Pearce,Patrick G. Arbogast,W. T. Longstreth, Jr,Frits R. Rosendaal,Bruce M. Psaty,David S. Siscovick
GENE THERAPY
HEMATOPOIESIS
mDYRK3 kinase is expressed selectively in late erythroid progenitor cells and attenuates colony-forming unit–erythroid development
Justin N. Geiger,Geoffry T. Knudsen,Leigh Panek,Ajay K. Pandit,Michael D. Yoder,Kenneth A. Lord,Caretha L. Creasy,Brian M. Burns,Peter Gaines,Susan B. Dillon,Don M. Wojchowski
HEMOSTASIS, THROMBOSIS, AND VASCULAR BIOLOGY
The arginine-552-cysteine (R1315C) mutation within the A1 loop of von Willebrand factor induces an abnormal folding with a loss of function resulting in type 2A–like phenotype of von Willebrand disease: study of 10 patients and mutated recombinant von Willebrand factor
Anne-Sophie Ribba,Lysiane Hilbert,Jean-Maurice Lavergne,Edith Fressinaud,Catherine Boyer-Neumann,Catherine Ternisien,Irène Juhan-Vague,Jenny Goudemand,Jean-Pierre Girma,Claudine Mazurier,Dominique Meyer
Abnormal secretion and function of recombinant human factor VII as the result of modification to a calcium binding site caused by a 15–base pair insertion in the F7 gene
Flora Peyvandi,Josephine A. Carew,David J. Perry,Mathilde Hunault,Uma Khanduri,Stephen J. Perkins,Pier M. Mannucci,Kenneth A. Bauer
Aberrant fibrin formation and cross-linking of fibrinogen Nieuwegein, a variant with a shortened Aα-chain, alters endothelial capillary tube formation
Annemie Collen,Annemarie Maas,Teake Kooistra,Florea Lupu,Jos Grimbergen,Fred J. L. M. Haas,Douwe H. Biesma,Pieter Koolwijk,Jaap Koopman,Victor W. M. van Hinsbergh
IMMUNOBIOLOGY
Selective down-regulation of high-affinity IgE receptor (FcεRI) α-chain messenger RNA among transcriptome in cord blood–derived versus adult peripheral blood–derived cultured human mast cells
Makoto Iida,Kenji Matsumoto,Hisashi Tomita,Toshiharu Nakajima,Akira Akasawa,Noriko Yuyama Ohtani,Ning Lu Yoshida,Keiko Matsui,Akiko Nakada,Yuji Sugita,Yuji Shimizu,Shunichi Wakahara,Toru Nakao,Yasuyuki Fujii,Chisei Ra,Hirohisa Saito
NEOPLASIA
Expression of the c-met proto-oncogene and its ligand, hepatocyte growth factor, in Hodgkin disease
Luciana Teofili,Anna Laura Di Febo,Francesco Pierconti,Nicola Maggiano,Maurizio Bendandi,Sergio Rutella,Antonella Cingolani,Nicola Di Renzo,Pellegrino Musto,Stefano Pileri,Giuseppe Leone,Luigi Maria Larocca
PHAGOCYTES
RED CELLS
TRANSPLANTATION
Prevention of lethal acute graft-versus-host disease in mice by oral administration of T helper 1 inhibitor, TAK-603
Yue Lu,Sumio Sakamaki,Hiroyuki Kuroda,Toshiro Kusakabe,Yuichi Konuma,Takehide Akiyama,Akihito Fujimi,Naofumi Takemoto,Kyokusen Nishiie,Takuya Matsunaga,Yasuo Hirayama,Junji Kato,Shinichiro Kon,Katsuhisa Kogawa,Yoshiro Niitsu
BRIEF REPORTS
Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome)
Brief Report
Shinji Kunishima,Tetsuhito Kojima,Tadashi Matsushita,Toshihiro Tanaka,Masahito Tsurusawa,Yoshio Furukawa,Yukitsugu Nakamura,Takashi Okamura,Norihiko Amemiya,Takayuki Nakayama,Tadashi Kamiya,Hidehiko Saito
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