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Journal Articles

Systematic Analyses of Clinically Relevant Single Nucleotide Polymorphisms (SNPs) of NR3C1 in Patients from the Italian Registry of Diamond Blackfan Anemia

Jiawen Li, Mayte Suarez-Farinas, Stuart Scott, PhD, Lilian Varricchio, Carolyn F. Whitsett, MD, Ugo Ramenghi, MD, Irma Dianzani, Anna Rita Migliaccio, PhD

Blood (2017) 130 (Supplement 1): 2200.

https://doi.org/10.1182/blood.V130.Suppl_1.2200.2200

Published: 2017

Journal Articles

Novel Mutations of the JAK2 Gene and Erythropoietin Receptor Gene in Japanese Chronic Myeloproliferative Diseases.

Mitsuharu Inami, MD, PhD, Hiroki Yamaguchi, MD, PhD, Setsuo Hasegawa, MD, PhD, Seiji Gomi, MD, PhD, Ayako Watanabe, MD, PhD, Fumiko Kosaka, Yoshio Mitamura, Ai Kobayashi, Sayaka Kimura, Kazuo Dan, MD, Koiti Inokuchi, MD, PhD

Blood (2007) 110 (11): 2535.

https://doi.org/10.1182/blood.V110.11.2535.2535

Published: 2007

Journal Articles

Distinct Profile of FLT3 Mutations in Brazil.

Danielle L.C.F. Souza, Ana Silvia G. Lima, Guilherme A.A. Santos, Lidiane C. Melato, Adriana I. Dore, Dirceu E. Silva, Sebastião Ismael, Wilson A. Silva, Junior, Eduardo M. Rego

Blood (2005) 106 (11): 4532.

https://doi.org/10.1182/blood.V106.11.4532.4532

Published: 2005

Journal Articles

Biochemical Characterization of Recombinant Von Willebrand Factor (VWF) with a Type 2B Mutation (P1337L) Coexpressed with a Type 1 VWF Defect (C275R): A Complex Molecular Defect in a Patient Previously Diagnosed with Type 2A Von Willebrand Disease (VWD).

Luciano Baronciani, PhD, Augusto B. Federici, MD, Matteo Beretta, PhD, Giovanna Cozzi, PhD, Maria T. Canciani, PhD, Pier M. Mannucci, MD

Blood (2004) 104 (11): 1025.

https://doi.org/10.1182/blood.V104.11.1025.1025

Published: 2004

Journal Articles

Mutations in the AML1 Gene Define an Unfavorable Subgroup in Acute Myeloid Leukemia with FAB M0.

Frank Dicker, PhD, Mirjam Klaus, MD, Torsten Haferlach, MD, Wolfgang Kern, MD, Wolfgang Hiddemann, MD, Claudia Schoch, MD, Susanne Schnittger, MD

Blood (2004) 104 (11): 4340.

https://doi.org/10.1182/blood.V104.11.4340.4340

Published: 2004

Journal Articles

Presence of the BCR-ABL mutation Glu255Lys prior to STI571 (imatinib) treatment in patients with Ph + acute lymphoblastic leukemia

Wolf-Karsten Hofmann, Martina Komor, Barbara Wassmann, Letetia C. Jones, Harald Gschaidmeier, Dieter Hoelzer, H. Phillip Koeffler, Oliver G. Ottmann

Blood (2003) 102 (2): 659–661.

https://doi.org/10.1182/blood-2002-06-1756

Published: 2003

Journal Articles

Germinal center phenotype and bcl-2 expression combined with the International Prognostic Index improves patient risk stratification in diffuse large B-cell lymphoma

Sharon L. Barrans, Ian Carter, Roger G. Owen, Faith E. Davies, Russell D. Patmore, Andrew P. Haynes, Gareth J. Morgan, Andrew S. Jack

Blood (2002) 99 (4): 1136–1143.

https://doi.org/10.1182/blood.V99.4.1136

Published: 2002

Journal Articles

Single-tube multiplex PCR-SSCP analysis distinguishes 7 common ABO alleles and readily identifies new alleles

Shea Ping Yip

Blood (2000) 95 (4): 1487–1492.

https://doi.org/10.1182/blood.V95.4.1487.004k53_1487_1492

Published: 2000

Journal Articles

The IVS4 + 4 A to T mutation of the Fanconi anemia gene FANCC is not associated with a severe phenotype in Japanese patients

Makoto Futaki, Takayuki Yamashita, Hiroshi Yagasaki, Tatsushi Toda, Miharu Yabe, Shunichi Kato, Shigetaka Asano, Tatsutoshi Nakahata

Blood (2000) 95 (4): 1493–1498.

https://doi.org/10.1182/blood.V95.4.1493.004k35_1493_1498

Published: 2000

Journal Articles

Clonal Expansion of β-T Lymphocytes With Inverted Jβ1 Bias in Familial Hemophagocytic Lymphohistiocytosis

Mitsuyuki Nagano, Nobuhiro Kimura, Eiichi Ishii, Nobuyuki Yoshida, Tetsuya Yoshida, Masahiro Sako, Shigeyoshi Hibi, Shinsaku Imashuku, Sumio Miyazaki, Toshiro Hara, Shuki Mizutani

Blood (1999) 94 (7): 2374–2382.

https://doi.org/10.1182/blood.V94.7.2374.419k06_2374_2382

Published: 1999

Journal Articles

Loss of p73 Gene Expression in Leukemias/Lymphomas Due to Hypermethylation

Seiji Kawano, Carl W. Miller, Adrian F. Gombart, Claus R. Bartram, Yoshinobu Matsuo, Hiroya Asou, Akiko Sakashita, Jonathan Said, Eiji Tatsumi, H. Phillip Koeffler

Blood (1999) 94 (3): 1113–1120.

https://doi.org/10.1182/blood.V94.3.1113.415k33_1113_1120

Published: 1999

Journal Articles

PTEN Gene Alterations in Lymphoid Neoplasms

Akira Sakai, Catherine Thieblemont, Axel Wellmann, Elaine S. Jaffe, Mark Raffeld

Blood (1998) 92 (9): 3410–3415.

https://doi.org/10.1182/blood.V92.9.3410

Published: 1998

Journal Articles

Ig Heavy Chain Third Complementarity Determining Regions (H CDR3s) After Stem Cell Transplantation Do Not Resemble the Developing Human Fetal H CDR3s in Size Distribution and Ig Gene Utilization

Erhan Gokmen, Frank M. Raaphorst, David H. Boldt, Judy M. Teale

Blood (1998) 92 (8): 2802–2814.

https://doi.org/10.1182/blood.V92.8.2802

Published: 1998

Journal Articles

Frequent Hypermethylation of p16 and p15 Genes in Multiple Myeloma

M.H.L. Ng, Y.F. Chung, K.W. Lo, N.W.R. Wickham, J.C.K. Lee, D.P. Huang

Blood (1997) 89 (7): 2500–2506.

https://doi.org/10.1182/blood.V89.7.2500

Published: 1997

Journal Articles

HPA-10w b (La a ): Genetic Determination of a New Platelet-Specific Alloantigen on Glycoprotein IIIa and Its Expression in COS-7 Cells

O. Peyruchaud, F. Bourre, M.-C. Morel-Kopp, D. Reviron, P. Mercier, A. Nurden, C. Kaplan

Blood (1997) 89 (7): 2422–2428.

https://doi.org/10.1182/blood.V89.7.2422

Published: 1997

NARROW

Systematic Analyses of Clinically Relevant Single Nucleotide Polymorphisms (SNPs) of NR3C1 in Patients from the Italian Registry of Diamond Blackfan Anemia

Novel Mutations of the JAK2 Gene and Erythropoietin Receptor Gene in Japanese Chronic Myeloproliferative Diseases.

Distinct Profile of FLT3 Mutations in Brazil.

Biochemical Characterization of Recombinant Von Willebrand Factor (VWF) with a Type 2B Mutation (P1337L) Coexpressed with a Type 1 VWF Defect (C275R): A Complex Molecular Defect in a Patient Previously Diagnosed with Type 2A Von Willebrand Disease (VWD).

Mutations in the AML1 Gene Define an Unfavorable Subgroup in Acute Myeloid Leukemia with FAB M0.

Presence of the BCR-ABL mutation Glu255Lys prior to STI571 (imatinib) treatment in patients with Ph + acute lymphoblastic leukemia

Germinal center phenotype and bcl-2 expression combined with the International Prognostic Index improves patient risk stratification in diffuse large B-cell lymphoma

Single-tube multiplex PCR-SSCP analysis distinguishes 7 common ABO alleles and readily identifies new alleles

The IVS4 + 4 A to T mutation of the Fanconi anemia gene FANCC is not associated with a severe phenotype in Japanese patients

Clonal Expansion of β-T Lymphocytes With Inverted Jβ1 Bias in Familial Hemophagocytic Lymphohistiocytosis

Loss of p73 Gene Expression in Leukemias/Lymphomas Due to Hypermethylation

PTEN Gene Alterations in Lymphoid Neoplasms

Ig Heavy Chain Third Complementarity Determining Regions (H CDR3s) After Stem Cell Transplantation Do Not Resemble the Developing Human Fetal H CDR3s in Size Distribution and Ig Gene Utilization

Frequent Hypermethylation of p16 and p15 Genes in Multiple Myeloma

HPA-10w b (La a ): Genetic Determination of a New Platelet-Specific Alloantigen on Glycoprotein IIIa and Its Expression in COS-7 Cells

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American Society of Hematology

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American Society of Hematology

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