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Signaling impairments in maternal T cells engrafted in an infant with a novel IL-2 receptor γ mutation

Journal of allergy and clinical immunology, 2015-04, Vol.135 (4), p.1093-1096.e8

2015

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Post-transplant lymphoproliferative disorder subtypes correlate with different recurring chromosomal abnormalities

Genes chromosomes & cancer, 2006-03, Vol.45 (3), p.313-318

2006

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Single Missense Mutation in the Tyrosine Kinase Catalytic Domain of the RET Protooncogene is Associated with Multiple Endocrine Neoplasia Type 2B

Proceedings of the National Academy of Sciences - PNAS, 1994-02, Vol.91 (4), p.1579-1583

1994

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eP353: Testing for Y chromosome in Turner syndrome

Genetics in medicine, 2022-03, Vol.24 (3), p.S221-S222

2022

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OP034: Evaluation of the 2019 ACMG-ClinGen guidelines for interpretation of copy-number variants with borderline classifications at an academic clinical diagnostics laboratory

Genetics in medicine, 2022-03, Vol.24 (3), p.S362-S362

2022

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Identification of new translocations involving ETV6 in hematologic malignancies by fluorescence in situ hybridization and spectral karyotyping

Genes chromosomes & cancer, 2001-06, Vol.31 (2), p.134-142

2001

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Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC

Human molecular genetics, 1993-07, Vol.2 (7), p.851-856

1993

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Mitoxantrone and Etoposide with or without Intermediate-Dose Cytarabine for the Treatment of Patients with Primary Induction Failure or Relapsed Acute Myeloid Leukemia

Blood, 2010-11, Vol.116 (21), p.2174-2174

2010

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Parent-of-origin effects in multiple endocrine neoplasia type 2B

American journal of human genetics, 1994-12, Vol.55 (6), p.1076-1082

1994

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Signaling impairments in maternal T cells engrafted in an infant with a novel IL-2 receptor [gamma] mutation

Journal of allergy and clinical immunology, 2015-04, Vol.135 (4), p.1093

2015

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Spectral Karyotype Analysis of T-Cell Acute Leukemia

Blood, 1999-03, Vol.93 (6), p.2038-2042

1999

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Mitoxantrone and etoposide with or without intermediate dose cytarabine for the treatment of primary induction failure or relapsed acute myeloid leukemia

Leukemia research, 2012-04, Vol.36 (4), p.394-396

2012

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Myeloid Malignancies Induced by Alkylating Agents in Nf1 Mice

Blood, 1999-06, Vol.93 (11), p.3617-3623

1999

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Myeloid Malignancies Induced by Alkylating Agents in Nf1 Mice

Blood, 1999-06, Vol.93 (11), p.3617-3623

1999

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Neuroimaging findings in children with rare or novel de novo chromosomal anomalies

Birth defects research. A Clinical and molecular teratology, 2008-04, Vol.82 (4), p.200-210

2008

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Premenstrual dysphoric disorder and the process of diagnostic decision making between psychologists and psychiatrists

Carlson, Katrin Woodworth

2006

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Characterization of Drug-Resistant Cell Lines by Comparative Genomic Hybridization

Cancer genetics and cytogenetics, 1999-05, Vol.111 (1), p.32-36

1999

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A 4-month-old girl with bilious emesis

Pediatric annals, 2006-07, Vol.35 (7), p.470, 473-478

Listernick, Robert

2006

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1p and 3p deletions in meningiomas without detectable aberrations of chromosome 22 identified by comparative genomic hybridization

Genes chromosomes & cancer, 1997-12, Vol.20 (4), p.419-424

1997

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A 1.5-Megabase Yeast Artificial Chromosome Contig from Human Chromosome 10q11.2 Connecting Three Genetic Loci (RET, D10S94, and D10S102) Closely Linked to the MEN2A Locus

Proceedings of the National Academy of Sciences - PNAS, 1993-01, Vol.90 (2), p.492-496

1993

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Genetic and physical characterization of the multiple endocrine neoplasia type 2 locus

Carlson, Katrin Monica

1995

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Molecular cytogenetic characterization of breakpoints in 19 patients with hematologic malignancies and 12p unbalanced translocations

Cancer genetics and cytogenetics, 2003-04, Vol.142 (2), p.115-119

2003

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A General Molecular Affinity Strategy for Global Detection and Proteomic Analysis of Lysine Methylation

Molecular cell, 2013-05, Vol.50 (3), p.444-456

2013

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Induction of an IFN-Mediated Antiviral Response by a Self-Amplifying RNA Vaccine: Implications for Vaccine Design

The Journal of immunology (1950), 2017-05, Vol.198 (10), p.4012-4024

2017

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The epigenetic regulator SIRT7 guards against mammalian cellular senescence induced by ribosomal DNA instability

The Journal of biological chemistry, 2018-07, Vol.293 (28), p.11242-11250

2018

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Signaling impairments in maternal T cells engrafted in an infant with a novel IL-2 receptor γ mutation

Post-transplant lymphoproliferative disorder subtypes correlate with different recurring chromosomal abnormalities

Single Missense Mutation in the Tyrosine Kinase Catalytic Domain of the RET Protooncogene is Associated with Multiple Endocrine Neoplasia Type 2B

eP353: Testing for Y chromosome in Turner syndrome

OP034: Evaluation of the 2019 ACMG-ClinGen guidelines for interpretation of copy-number variants with borderline classifications at an academic clinical diagnostics laboratory

Identification of new translocations involving ETV6 in hematologic malignancies by fluorescence in situ hybridization and spectral karyotyping

Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC

Mitoxantrone and Etoposide with or without Intermediate-Dose Cytarabine for the Treatment of Patients with Primary Induction Failure or Relapsed Acute Myeloid Leukemia

Parent-of-origin effects in multiple endocrine neoplasia type 2B

Signaling impairments in maternal T cells engrafted in an infant with a novel IL-2 receptor [gamma] mutation

Spectral Karyotype Analysis of T-Cell Acute Leukemia

Mitoxantrone and etoposide with or without intermediate dose cytarabine for the treatment of primary induction failure or relapsed acute myeloid leukemia

Myeloid Malignancies Induced by Alkylating Agents in Nf1 Mice

Myeloid Malignancies Induced by Alkylating Agents in Nf1 Mice

Neuroimaging findings in children with rare or novel de novo chromosomal anomalies

Premenstrual dysphoric disorder and the process of diagnostic decision making between psychologists and psychiatrists

Characterization of Drug-Resistant Cell Lines by Comparative Genomic Hybridization

A 4-month-old girl with bilious emesis

1p and 3p deletions in meningiomas without detectable aberrations of chromosome 22 identified by comparative genomic hybridization

A 1.5-Megabase Yeast Artificial Chromosome Contig from Human Chromosome 10q11.2 Connecting Three Genetic Loci (RET, D10S94, and D10S102) Closely Linked to the MEN2A Locus

Genetic and physical characterization of the multiple endocrine neoplasia type 2 locus

Molecular cytogenetic characterization of breakpoints in 19 patients with hematologic malignancies and 12p unbalanced translocations

A General Molecular Affinity Strategy for Global Detection and Proteomic Analysis of Lysine Methylation

Induction of an IFN-Mediated Antiviral Response by a Self-Amplifying RNA Vaccine: Implications for Vaccine Design

The epigenetic regulator SIRT7 guards against mammalian cellular senescence induced by ribosomal DNA instability

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