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Journal Articles

Phenotypes of Hb Okayama Mutation

Rudra Ray, PhD MSc, Ankita Biswas, Msc, Sunistha Bhattacharjee, Msc, Maitreyee Bhattacharyya, DM

Blood (2018) 132 (Supplement 1): 4898.

https://doi.org/10.1182/blood-2018-99-118079

Published: 2018

Journal Articles

IGHV-D-J Repertoire Analysis Obtained By High-Throughput Sequencing of CD5+ B-Cells in CLL Patients: Prognostic Markers and Disease Development Implications

Davide Bagnara, PhD, Stefano Vergani, PhD, Andrea Nicola Mazzarello, PhD, Gerardo Ferrer, PhD, Franco Fais, PhD, Nicholas Chiorazzi, MD

Blood (2017) 130 (Supplement 1): 54.

https://doi.org/10.1182/blood.V130.Suppl_1.54.54

Published: 2017

Journal Articles

Cluster Regulation of RUNX Family By "Gene Switch" Triggers a Profound Tumor Regression of Diverse Origins

Ken Morita, MD, PhD, Kensho Suzuki, Shintaro Maeda, Yoshihide Mitsuda, Ayaka Yano, Yoshimi Yamada, Hiroki Kiyose, Chieko Tokushige, Paul P. Liu, MD PhD, Souichi Adachi, MD, PhD, Hiroshi Sugiyama, PhD, Yasuhiko Kamikubo, MD, PhD

Blood (2016) 128 (22): 443.

https://doi.org/10.1182/blood.V128.22.443.443

Published: 2016

Journal Articles

CD4 Treg and CD4 Tcon Utilize Distinct TCR Vbeta Repertoires in Response to Alloantigen

Anandharaman Veerapathran, PhD, Micheal Schell, PhD, Francisca Beato, B.S, TzuHua Juan, MPH, Sean Yoder, M.S, Brian C Betts, MD, Joseph A Pidala, MD, PhD, Claudio Anasetti, MD

Blood (2015) 126 (23): 4286.

https://doi.org/10.1182/blood.V126.23.4286.4286

Published: 2015

Journal Articles

Repair Of DNA Double Strand Breaks By Insertion Of Nucleotide Sequences Derived From Distant Regions Of The Genome

Masahiro Onozawa, MD, PhD., Zhenhua Zhang, Yoo Jung Kim, Liat Goldberg, PhD, Tamas Varga, PhD, Leif Bergsagel, M.D., Michael Kuehl, MD, Peter D Aplan, MD

Blood (2013) 122 (21): 1243.

https://doi.org/10.1182/blood.V122.21.1243.1243

Published: 2013

Journal Articles

Evidence for Allelic Exclusion of p53 within Single Sorted Human B Cells

Shabirul Haque, Ph.D., Jennifer Nieto, Hyunjoo Lee, Nicholas Chiorazzi, M.D., Patricia Mongini, Ph.D.

Blood (2011) 118 (21): 1122.

https://doi.org/10.1182/blood.V118.21.1122.1122

Published: 2011

Journal Articles

Unmutated IGHV1-69/D3-16/J3 Stereotyped HCDR3 Rearrangements (Subset 6) Are Associated with Indolent Disease Course and Have Outcome Independent of Mutational Status In Early Stage CLL (Rai 0)

Blood (2010) 116 (21): 1371.

https://doi.org/10.1182/blood.V116.21.1371.1371

Published: 2010

Journal Articles

Molecular Basis for A Thrombophilic Patient's Combined Deficiencies in Proteins C and S.

Tyler W Smith, MD, Isis S. R Carter, BSc, PGDipSci, Cedric John Carter, MD, Ross T.A MacGillivray, PhD

Blood (2009) 114 (22): 4198.

https://doi.org/10.1182/blood.V114.22.4198.4198

Published: 2009

Journal Articles

Pathogenetic Role of Impaired Telomere Repair in Myelodysplastic Syndrome.

P.K. Epling-Burnette, PhD, Alan F List, MD, Justine Clark, MS, Ji-Hyun Lee, Kristen A. Jonathan, William Fulp, Xiaohong Li, Weipeng Zheng, Jeffrey S. Painter, B.S., JianXiang Zou, MD, Rami S. Komrokji, MD, Sheng Wei, MD, Jong Park, Amber Schmidt, Undergraduate, student, Chiharu Sugimori, MD, Ashley Cole, Dana E Rollison, PhD

Blood (2009) 114 (22): 2777.

https://doi.org/10.1182/blood.V114.22.2777.2777

Published: 2009

Journal Articles

Double CEBPA mutations, but not single CEBPA mutations, define a subgroup of acute myeloid leukemia with a distinctive gene expression profile that is uniquely associated with a favorable outcome

Bas J. Wouters, Bob Löwenberg, Claudia A. J. Erpelinck-Verschueren, Wim L. J. van Putten, Peter J. M. Valk, Ruud Delwel

Blood (2009) 113 (13): 3088–3091.

https://doi.org/10.1182/blood-2008-09-179895

Published: 2009

Includes: Supplemental data

Journal Articles

The Feature of CD3-zeta Chain Gene Expression in Mononuclear Cells without and with Stimulation by Different Factors from Umbilical Cord Blood.

Shaohua Chen, BA, Yangqiu Li, MD, Lijian Yang, Si Chen, BA

Blood (2007) 110 (11): 3870.

https://doi.org/10.1182/blood.V110.11.3870.3870

Published: 2007

Journal Articles

Molecular Serotype Analysis of Adenoviruses: Clinical Implications.

Thomas Lion, MD, PhD, Karin Ebner, MS, Susanne Matthes-Martin, MD, Franz Watzinger, PhD

Blood (2004) 104 (11): 2237.

https://doi.org/10.1182/blood.V104.11.2237.2237

Published: 2004

Journal Articles

Human Monoclonal Cryocrystalglobulinemia: First Complete Heavy and Light Chain Variable Region Nucleotide Sequences.

Vittorio Perfetti, MD, Valentina Navazza, PhD, Sofia Giorgietti, PhD, Loredana Marchese, PhD, Giovanni Palladini, MD, Roberto Caporali, MD, Claudio Montecucco, MD, Giampaolo Merlini, MD

Blood (2004) 104 (11): 1381.

https://doi.org/10.1182/blood.V104.11.1381.1381

Published: 2004

Journal Articles

Prognostic Impact of V H Gene Mutational Status and CD38 Expression in Japanese CLL Patients.

Hiromi Koiso, MD, Masamitsu Karasawa, MD, Arito Yamane, MD, Takeki Mitsui, MD, Takafumi Matsushima, MD, Norifumi Tsukamoto, MD, Hirokazu Murakami, MD, Syuichi Miyawaki, MD, Yoshihisa NOjima, MD

Blood (2004) 104 (11): 4783.

https://doi.org/10.1182/blood.V104.11.4783.4783

Published: 2004

Journal Articles

A Novel Mechanism of ADAMTS13 Deficiency in Mice.

Wenhua Zhou, Ph.D., Lingli Dong, M.D., Eric E. Bouhassira, Ph.D., Han-Mou Tsai, M.D.

Blood (2004) 104 (11): 3668.

https://doi.org/10.1182/blood.V104.11.3668.3668

Published: 2004

Journal Articles

Identification of a 4-base deletion in the gene in inherited intrinsic factor deficiency

Fawwaz Yassin, Sheldon P. Rothenberg, Sreedhar Rao, Marilyn M. Gordon, David H. Alpers, Edward V. Quadros

Blood (2004) 103 (4): 1515–1517.

https://doi.org/10.1182/blood-2003-07-2239

Published: 2004

Journal Articles

Nucleotide sequence, transcription map, and mutation analysis of the 13q14 chromosomal region deleted in B-cell chronic lymphocytic leukemia

Anna Migliazza, Francesc Bosch, Hirokazu Komatsu, Eftihia Cayanis, Stefano Martinotti, Elena Toniato, Ernesto Guccione, Xiaoyan Qu, Minchen Chien, V. V. V. Murty, Gianluca Gaidano, Giorgio Inghirami, Peisen Zhang, Stuart Fischer, Sergey M. Kalachikov, James Russo, Isidore Edelman, Argiris Efstratiadis, Riccardo Dalla-Favera

Blood (2001) 97 (7): 2098–2104.

https://doi.org/10.1182/blood.V97.7.2098

Published: 2001

Journal Articles

Clonal evolution in Waldenstrom macroglobulinemia highlights functional role of B-cell receptor

Bogoljub Ciric, Virginia VanKeulen, Moses Rodriguez, Robert A. Kyle, Morie A. Gertz, Larry R. Pease

Blood (2001) 97 (1): 321–323.

https://doi.org/10.1182/blood.V97.1.321

Published: 2001

Journal Articles

Detection of clonotypic IGH and TCR rearrangements in the neonatal blood spots of infants and children with B-cell precursor acute lymphoblastic leukemia

Tomohito Yagi, Shigeyoshi Hibi, Yasuhiro Tabata, Kikuko Kuriyama, Tomoko Teramura, Tetsuo Hashida, Yoshitaka Shimizu, Tetsuya Takimoto, Shinjiro Todo, Tadashi Sawada, Shinsaku Imashuku

Blood (2000) 96 (1): 264–268.

https://doi.org/10.1182/blood.V96.1.264

Published: 2000

Journal Articles

RHD gene deletion occurred in the Rhesus box

Franz F. Wagner, Willy A. Flegel

Blood (2000) 95 (12): 3662–3668.

https://doi.org/10.1182/blood.V95.12.3662

Published: 2000

NARROW

Phenotypes of Hb Okayama Mutation

IGHV-D-J Repertoire Analysis Obtained By High-Throughput Sequencing of CD5+ B-Cells in CLL Patients: Prognostic Markers and Disease Development Implications

Cluster Regulation of RUNX Family By "Gene Switch" Triggers a Profound Tumor Regression of Diverse Origins

CD4 Treg and CD4 Tcon Utilize Distinct TCR Vbeta Repertoires in Response to Alloantigen

Repair Of DNA Double Strand Breaks By Insertion Of Nucleotide Sequences Derived From Distant Regions Of The Genome

Evidence for Allelic Exclusion of p53 within Single Sorted Human B Cells

Unmutated IGHV1-69/D3-16/J3 Stereotyped HCDR3 Rearrangements (Subset 6) Are Associated with Indolent Disease Course and Have Outcome Independent of Mutational Status In Early Stage CLL (Rai 0)

Molecular Basis for A Thrombophilic Patient's Combined Deficiencies in Proteins C and S.

Pathogenetic Role of Impaired Telomere Repair in Myelodysplastic Syndrome.

Double CEBPA mutations, but not single CEBPA mutations, define a subgroup of acute myeloid leukemia with a distinctive gene expression profile that is uniquely associated with a favorable outcome

The Feature of CD3-zeta Chain Gene Expression in Mononuclear Cells without and with Stimulation by Different Factors from Umbilical Cord Blood.

Molecular Serotype Analysis of Adenoviruses: Clinical Implications.

Human Monoclonal Cryocrystalglobulinemia: First Complete Heavy and Light Chain Variable Region Nucleotide Sequences.

Prognostic Impact of V H Gene Mutational Status and CD38 Expression in Japanese CLL Patients.

A Novel Mechanism of ADAMTS13 Deficiency in Mice.

Identification of a 4-base deletion in the gene in inherited intrinsic factor deficiency

Nucleotide sequence, transcription map, and mutation analysis of the 13q14 chromosomal region deleted in B-cell chronic lymphocytic leukemia

Clonal evolution in Waldenstrom macroglobulinemia highlights functional role of B-cell receptor

Detection of clonotypic IGH and TCR rearrangements in the neonatal blood spots of infants and children with B-cell precursor acute lymphoblastic leukemia

RHD gene deletion occurred in the Rhesus box

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American Society of Hematology

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American Society of Hematology

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