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Multiplex Ligation-Dependent Probe Amplification Versus Multiprobe Fluorescence in Situ Hybridization To Detect Genomic Aberrations in Chronic Lymphocytic Leukemia

The Journal of molecular diagnostics : JMD, 2010-03, Vol.12 (2), p.197-203

2010

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CANTRK: A Canadian Ring Study to Optimize Detection of NTRK Gene Fusions by Next-Generation RNA Sequencing

The Journal of molecular diagnostics : JMD, 2023-03, Vol.25 (3), p.168-174

2023

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Abstract B21: Investigating targeted driver mutations and PD-L1 expression for improved therapy of non-small cell lung cancer

Clinical cancer research, 2018-09, Vol.24 (17_Supplement), p.B21-B21

2018

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ALK+ lung adenocarcinoma in never smokers and long-term ex-smokers: prevalence and detection by immunohistochemistry and fluorescence in situ hybridization

Virchows Archiv : an international journal of pathology, 2016-11, Vol.469 (5), p.533-540

2016

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CANTRK

The Journal of molecular diagnostics : JMD, 2023-03, Vol.25 (3), p.168-174

2023

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Role of Allogeneic Hematopoietic Cell Transplant in Patients with Myelofibrosis in the JAK Inhibitor Era

Blood, 2020-11, Vol.136 (Supplement 1), p.52-53

2020

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Significant Discrepancy In Peripheral Blood Compared to Bone Marrow BCR-ABL Transcript Levels In Chronic Phase Chronic Myeloid Leukemia (CML)

Blood, 2010-11, Vol.116 (21), p.4471-4471

2010

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Novel splice‐site mutation in ATP8B1 results in atypical P rogressive F amilial I ntrahepatic C holestasis T ype 1

Journal of gastroenterology and hepatology, 2013-03, Vol.28 (3), p.560-564

2013

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Canadian ALK (CALK): A pan-Canadian multicenter study to optimize and standardize ALK immunohistochemistry (IHC) and fluorescence in situ hybridization (FISH) for ALK gene rearrangements

Journal of clinical oncology, 2013-05, Vol.31 (15_suppl), p.8096-8096

2013

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Do the SLC25A38 or ALAS2 Genes Play a Role In the Phenotypic Expression of Ringed Sideroblasts In Acquired Myelodysplastic Syndrome?

Blood, 2010-11, Vol.116 (21), p.4954-4954

2010

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Hemophilia a Carriers Experience Errors and Deficiencies in Care Leading to Emotional and Behavioral Responses That Could Further Compromise Their Care

Blood, 2008-11, Vol.112 (11), p.4502-4502

2008

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Familial Essential Thrombocythemia Showing Spontaneous Megakaryocyte Colony Formation and Acquired JAK2 Mutations without a Germline Mutation in C-MPL or TPO

Blood, 2007-11, Vol.110 (11), p.4655-4655

2007

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A Rare Case of JAK2 V617F Positive Polycythemia Vera in a Child with Neurofibromatosis Type I

Blood, 2007-11, Vol.110 (11), p.4661-4661

2007

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Acute promyelocytic leukemia: a novel PML/RARalpha fusion that generates a frameshift in the RARalpha transcript and ATRA resistance

Leukemia & lymphoma, 2007-03, Vol.48 (3), p.489-496

2007

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Altered expression of leucocyte sialoglycoprotein in Wiskott-Aldrich syndrome is associated with a specific defect in O-glycosylation

Biochemistry and cell biology, 1989-09, Vol.67 (9), p.503

1989

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X-Chromosome inactivation in the Wiskott-Aldrich syndrome: A marker for detection of the carrier state and identfication of cell lineages expressing the gene defect

Genomics (San Diego, Calif.), 1989, Vol.4 (1), p.60-67

1989

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Early nuclear events in lymphocyte proliferation

Experimental cell research, 1986-10, Vol.166 (2), p.399-415

1986

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Linkage of Wiskott-Aldrich syndrome with three marker loci, DXS426, SYP and TFE3, which map to the Xp11.3-p11.22 region

Human genetics, 1993-10, Vol.92 (3), p.250-253

1993

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Regulation of Lymphocyte Proliferation by a Continuous Production and Repair of DNA Strand Breaks

ADP-Ribosylation of Proteins, p.417-423

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Guanosine metabolism in Neurospora crassa

Greer, Wenda Louise

1981

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ProQuest

Molecular characterization of the X-linked immunodeficiency diseases

Clinical immunology newsletter, 1994, Vol.14 (2), p.17-25

1994

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Genetic Analysis of Familial Myelodysplastic Syndrome

Cancer genetics and cytogenetics, 1998-09, Vol.105 (2), p.113-118

1998

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Multiplex Ligation-Dependent Probe Amplification Versus Multiprobe Fluorescence in Situ Hybridization To Detect Genomic Aberrations in Chronic Lymphocytic Leukemia

CANTRK: A Canadian Ring Study to Optimize Detection of NTRK Gene Fusions by Next-Generation RNA Sequencing

Abstract B21: Investigating targeted driver mutations and PD-L1 expression for improved therapy of non-small cell lung cancer

ALK+ lung adenocarcinoma in never smokers and long-term ex-smokers: prevalence and detection by immunohistochemistry and fluorescence in situ hybridization

CANTRK

Role of Allogeneic Hematopoietic Cell Transplant in Patients with Myelofibrosis in the JAK Inhibitor Era

Significant Discrepancy In Peripheral Blood Compared to Bone Marrow BCR-ABL Transcript Levels In Chronic Phase Chronic Myeloid Leukemia (CML)

Germline Mutations in MAP3K6 Are Associated with Familial Gastric Cancer: e1004669

Novel splice‐site mutation in ATP8B1 results in atypical P rogressive F amilial I ntrahepatic C holestasis T ype 1

Canadian ALK (CALK): A pan-Canadian multicenter study to optimize and standardize ALK immunohistochemistry (IHC) and fluorescence in situ hybridization (FISH) for ALK gene rearrangements

Do the SLC25A38 or ALAS2 Genes Play a Role In the Phenotypic Expression of Ringed Sideroblasts In Acquired Myelodysplastic Syndrome?

Hemophilia a Carriers Experience Errors and Deficiencies in Care Leading to Emotional and Behavioral Responses That Could Further Compromise Their Care

Familial Essential Thrombocythemia Showing Spontaneous Megakaryocyte Colony Formation and Acquired JAK2 Mutations without a Germline Mutation in C-MPL or TPO

A Rare Case of JAK2 V617F Positive Polycythemia Vera in a Child with Neurofibromatosis Type I

Acute promyelocytic leukemia: a novel PML/RARalpha fusion that generates a frameshift in the RARalpha transcript and ATRA resistance

Altered expression of leucocyte sialoglycoprotein in Wiskott-Aldrich syndrome is associated with a specific defect in O-glycosylation

X-Chromosome inactivation in the Wiskott-Aldrich syndrome: A marker for detection of the carrier state and identfication of cell lineages expressing the gene defect

Early nuclear events in lymphocyte proliferation

Linkage of Wiskott-Aldrich syndrome with three marker loci, DXS426, SYP and TFE3, which map to the Xp11.3-p11.22 region

Regulation of Lymphocyte Proliferation by a Continuous Production and Repair of DNA Strand Breaks

Guanosine metabolism in Neurospora crassa

Molecular characterization of the X-linked immunodeficiency diseases

Genetic Analysis of Familial Myelodysplastic Syndrome

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