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Alternative mechanisms associated with silencing of CDKN1C in Beckwith–Wiedemann syndrome

Journal of medical genetics, 2005-08, Vol.42 (8), p.648-655

2005

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NUP98-HOXD13 gene fusion in therapy-related acute myelogenous leukemia

Cancer research (Chicago, Ill.), 1998-10, Vol.58 (19), p.4269-4273

1998

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Chromosomal localization of a human mucin gene (MUC8) and cloning of the cDNA corresponding to the carboxy terminus

American journal of respiratory cell and molecular biology, 1997-03, Vol.16 (3), p.232-241

1997

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Association of Germline p53 Mutation With MLL Segmental Jumping Translocation in Treatment-Related Leukemia

Blood, 1998-06, Vol.91 (12), p.4451-4456

1998

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The pericentromeric region of human chromosome 11: evidence for a chromosome-specific duplication

Cytogenetic and genome research, 2001-01, Vol.94 (3-4), p.137-141

2001

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The t(14;21)(q11.2;q22) Chromosomal Translocation Associated with T-Cell Acute Lymphoblastic Leukemia Activates the BHLHB1 Gene

Proceedings of the National Academy of Sciences - PNAS, 2000-03, Vol.97 (7), p.3497-3502

2000

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Demonstration of Urokinase Expression in Cancer Cells of Colon Adenocarcinomas by Immunohistochemistry and in Situ Hybridization

The American journal of pathology, 1999-10, Vol.155 (4), p.1115-1120

1999

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Mechanisms of MLL gene rearrangement: site-specific DNA cleavage within the breakpoint cluster region is independent of chromosomal context

Human molecular genetics, 2001-10, Vol.10 (22), p.2481-2491

2001

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T-Cell activation by t(9;22) acute lymphoblastic leukemia-derived dendritic-like cells is associated with increased tapasin expression

Cancer Immunology, Immunotherapy, 2006-02, Vol.55 (2), p.160-165

2006

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A 1-Mb Physical Map and PAC Contig of the Imprinted Domain in 11p15.5 That Contains TAPA1 and the BWSCR1/WT2 Region

Genomics (San Diego, Calif.), 1997-08, Vol.43 (3), p.366-375

1997

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Structure and Chromosomal Localization of the Human Salivary Mucin Gene, MUC7

Genomics (San Diego, Calif.), 1996-02, Vol.31 (3), p.277-282

1996

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A High-Resolution Physical Map of Human Chromosome 11

Proceedings of the National Academy of Sciences - PNAS, 1996-04, Vol.93 (7), p.3149-3154

1996

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Chromosome mapping and organization of the human beta-galactoside alpha 2,6-sialyltransferase gene. Differential and cell-type specific usage of upstream exon sequences in B-lymphoblastoid cells

The Journal of biological chemistry, 1993-02, Vol.268 (6), p.4355-4361

1993

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A Chromosome 11 YAC Library

Genomics (San Diego, Calif.), 1993-06, Vol.16 (3), p.580-585

1993

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Association of IDH1 mutations in normal karyotype acute myeloid leukemia samples with higher HIF-1α and VEGF-A expression

Journal of clinical oncology, 2011-05, Vol.29 (15_suppl), p.6530-6530

2011

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Chromosomal localization of the gene encoding the human DNA helicase RECQL and its mouse homologue

Genomics (San Diego, Calif.), 1995-04, Vol.26 (3), p.595-598

1995

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The Human HNP36 Gene Is Localized to Chromosome 11q13 and Produces Alternative Transcripts That Are Not Mutated in Multiple Endocrine Neoplasia, Type 1 (MEN I) Syndrome

Genomics (San Diego, Calif.), 1997-06, Vol.42 (2), p.325-330

1997

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The role of FLT3 in sole trisomy 8 acute myeloid leukemia

Journal of clinical oncology, 2010-05, Vol.28 (15_suppl), p.6562-6562

2010

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Mapping of ribosomal protein S3 and internally nested snoRNA U15A gene to human chromosome 11q13.3–q13.5

Genomics (San Diego, Calif.), 1995-01, Vol.25 (2), p.577-580

1995

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The kinase insert domain receptor gene (KDR) has been relocated to chromosome 4q11-->q12

Cytogenetic and genome research, 1995-01, Vol.70 (1-2), p.145-146

1995

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The role of minimal residual disease (MRD) by flow cytometry (FC) in predicting outcome in similarly treated acute lymphoblastic leukemia (ALL) patients

Journal of clinical oncology, 2011-05, Vol.29 (15_suppl), p.6592-6592

2011

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The human T-cell leukemia virus-related endogenous sequence ( HRES1) is located on chromosome 1 at q42

Genomics (San Diego, Calif.), 1991-12, Vol.11 (4), p.1172-1173

1991

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Erythropoietin-dependent transformation of myelodysplastic syndrome to acute monoblastic leukemia

Blood, 2001-12, Vol.98 (12), p.3492-3494

2001

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Therapy-related myelodysplastic syndrome (t-MDS) following treatment of acute myeloid leukemia (AML)

Journal of clinical oncology, 2007-06, Vol.25 (18_suppl), p.17509-17509

2007

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Acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS) following treatment for ovarian cancer

Journal of clinical oncology, 2007-06, Vol.25 (18_suppl), p.17506-17506

2007

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Alternative mechanisms associated with silencing of CDKN1C in Beckwith–Wiedemann syndrome

NUP98-HOXD13 gene fusion in therapy-related acute myelogenous leukemia

Chromosomal localization of a human mucin gene (MUC8) and cloning of the cDNA corresponding to the carboxy terminus

Association of Germline p53 Mutation With MLL Segmental Jumping Translocation in Treatment-Related Leukemia

The pericentromeric region of human chromosome 11: evidence for a chromosome-specific duplication

The t(14;21)(q11.2;q22) Chromosomal Translocation Associated with T-Cell Acute Lymphoblastic Leukemia Activates the BHLHB1 Gene

Demonstration of Urokinase Expression in Cancer Cells of Colon Adenocarcinomas by Immunohistochemistry and in Situ Hybridization

Mechanisms of MLL gene rearrangement: site-specific DNA cleavage within the breakpoint cluster region is independent of chromosomal context

T-Cell activation by t(9;22) acute lymphoblastic leukemia-derived dendritic-like cells is associated with increased tapasin expression

A 1-Mb Physical Map and PAC Contig of the Imprinted Domain in 11p15.5 That Contains TAPA1 and the BWSCR1/WT2 Region

Structure and Chromosomal Localization of the Human Salivary Mucin Gene, MUC7

A High-Resolution Physical Map of Human Chromosome 11

Chromosome mapping and organization of the human beta-galactoside alpha 2,6-sialyltransferase gene. Differential and cell-type specific usage of upstream exon sequences in B-lymphoblastoid cells

A Chromosome 11 YAC Library

Association of IDH1 mutations in normal karyotype acute myeloid leukemia samples with higher HIF-1α and VEGF-A expression

Chromosomal localization of the gene encoding the human DNA helicase RECQL and its mouse homologue

The Human HNP36 Gene Is Localized to Chromosome 11q13 and Produces Alternative Transcripts That Are Not Mutated in Multiple Endocrine Neoplasia, Type 1 (MEN I) Syndrome

The role of FLT3 in sole trisomy 8 acute myeloid leukemia

Mapping of ribosomal protein S3 and internally nested snoRNA U15A gene to human chromosome 11q13.3–q13.5

The kinase insert domain receptor gene (KDR) has been relocated to chromosome 4q11-->q12

The role of minimal residual disease (MRD) by flow cytometry (FC) in predicting outcome in similarly treated acute lymphoblastic leukemia (ALL) patients

The human T-cell leukemia virus-related endogenous sequence ( HRES1) is located on chromosome 1 at q42

Erythropoietin-dependent transformation of myelodysplastic syndrome to acute monoblastic leukemia

Therapy-related myelodysplastic syndrome (t-MDS) following treatment of acute myeloid leukemia (AML)

Acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS) following treatment for ovarian cancer

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