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Complete sequence and genomic analysis of murine gammaherpesvirus 68

Journal of Virology, 1997-08, Vol.71 (8), p.5894-5904

1997

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Mature B cells are required for acute splenic infection, but not for establishment of latency, by murine gammaherpesvirus 68

Journal of Virology, 1996-10, Vol.70 (10), p.6775-6780

1996

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A flawed challenge but valid recommendation: a response to Takoudes and Hamar

Ultrasound in obstetrics & gynecology, 2015-01, Vol.45 (1), p.117-117

2015

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Macrophages Are the Major Reservoir of Latent Murine Gammaherpesvirus 68 in Peritoneal Cells

Journal of Virology, 1999-04, Vol.73 (4), p.3273-3283

1999

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Activation of the human immunodeficiency virus by herpes simplex virus type 1

Journal of Virology, 1987-12, Vol.61 (12), p.3726-3732

1987

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B Cells Regulate Murine Gammaherpesvirus 68 Latency

Journal of Virology, 1999-06, Vol.73 (6), p.4651-4661

1999

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Murine γ-herpesvirus 68 causes severe large-vessel arteritis in mice lacking interferon-γ responsiveness: A new model for virus-induced vascular disease

Nature medicine, 1997-12, Vol.3 (12), p.1346-1353

1997

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Estimation of the Warfarin Dose with Clinical and Pharmacogenetic Data

The New England journal of medicine, 2009-02, Vol.360 (8), p.753-764

2009

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Hepatitis C Virus Quantitation: Optimization of Strategies for Detecting Low-Level Viremia

Journal of Clinical Microbiology, 2000-02, Vol.38 (2), p.888-891

2000

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Podocyte-associated gene mutation screening in a heterogeneous cohort of patients with sporadic focal segmental glomerulosclerosis

Nephrology, dialysis, transplantation, 2014-11, Vol.29 (11), p.2062-2069

2014

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C50 CYSTIC FIBROSIS AND UNCOMMON PEDIATRIC DISEASES: Primary Ciliary Dyskinesia In Children With Cri-Du-Chat Syndrome: A Genetic Connection

American journal of respiratory and critical care medicine, 2014-01, Vol.189, p.1

2014

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Molecular genetic testing for fragile X syndrome: laboratory performance on the College of American Pathologists proficiency surveys (2001–2009)

Genetics in medicine, 2012-03, Vol.14 (3), p.306-312

2012

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Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in primary ciliary dyskinesia: Implications for application to clinical testing

Genetics in medicine, 2011-03, Vol.13 (3), p.218-229

2011

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Hepatitis C Virus Genotyping: Interrogation of the 5′ Untranslated Region Cannot Accurately Distinguish Genotypes 1a and 1b

Journal of Clinical Microbiology, 2002-09, Vol.40 (9), p.3127-3134

2002

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Phenotypic Heterogeneity in Females with X-Linked Alport Syndrome

Journal of nephrology & therapeutics, 2014, Vol.4 (4)

KE Weck, SC Allred

2014

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Abstract P1-05-20: Comparing the frequency and types of genetic aberrations between older and younger women with metastatic breast cancer at the University of North Carolina at Chapel Hill

Cancer research (Chicago, Ill.), 2017-02, Vol.77 (4_Supplement), p.P1-P1-05-20

2017

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Abstract PD6-07: Genomic sequencing in metastatic breast cancer patients to inform clinical practice at the University of North Carolina at Chapel Hill

Cancer research (Chicago, Ill.), 2016-02, Vol.76 (4_Supplement), p.PD6-07-PD6-07

2016

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Estimation of the Warfarin Dose with Clinical and Pharmacogenetic Data

The New England journal of medicine, 2009-10, Vol.361 (16), p.1613-1613

2009

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Comprehensive CYP2D6 genotyping in a multiracial population shows differences in allele frequencies between races

Journal of clinical oncology, 2011-05, Vol.29 (15_suppl), p.e11095-e11095

2011

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Comprehensive CYP2D6 genotyping in a multiracial U.S. breast cancer population

Journal of clinical oncology, 2009-05, Vol.27 (15_suppl), p.553-553

2009

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Depletion of pulmonary EC-SOD after exposure to hyperoxia

American journal of physiology. Lung cellular and molecular physiology, 2002-10, Vol.283 (4), p.777-L784

2002

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Impact of human herpesvirus-6 on the frequency and severity of recurrent hepatitis C virus hepatitis in liver transplant recipients

Clinical transplantation, 2002-04, Vol.16 (2), p.92-96

2002

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New cytogenetic variant, insertion (15;17)(q22;q12q21), in an adolescent with acute promyelocytic leukemia

Cancer genetics and cytogenetics, 2002-04, Vol.134 (1), p.55-59

2002

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College of American Pathologists' laboratory standards for next-generation sequencing clinical tests

Archives of pathology & laboratory medicine (1976), 2015-04, Vol.139 (4), p.481-493

2015

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Hypersensitivity to nonsteroidal anti-inflammatory drugs (NSAIDs) ― classification, diagnosis and management: review of the EAACI/ENDA and GA2LEN/HANNA

Allergy (Copenhagen), 2011-07, Vol.66 (7), p.818-829

2011

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Complete sequence and genomic analysis of murine gammaherpesvirus 68

Mature B cells are required for acute splenic infection, but not for establishment of latency, by murine gammaherpesvirus 68

A flawed challenge but valid recommendation: a response to Takoudes and Hamar

Macrophages Are the Major Reservoir of Latent Murine Gammaherpesvirus 68 in Peritoneal Cells

Activation of the human immunodeficiency virus by herpes simplex virus type 1

B Cells Regulate Murine Gammaherpesvirus 68 Latency

Murine γ-herpesvirus 68 causes severe large-vessel arteritis in mice lacking interferon-γ responsiveness: A new model for virus-induced vascular disease

Estimation of the Warfarin Dose with Clinical and Pharmacogenetic Data

Hepatitis C Virus Quantitation: Optimization of Strategies for Detecting Low-Level Viremia

Podocyte-associated gene mutation screening in a heterogeneous cohort of patients with sporadic focal segmental glomerulosclerosis

C50 CYSTIC FIBROSIS AND UNCOMMON PEDIATRIC DISEASES: Primary Ciliary Dyskinesia In Children With Cri-Du-Chat Syndrome: A Genetic Connection

Molecular genetic testing for fragile X syndrome: laboratory performance on the College of American Pathologists proficiency surveys (2001–2009)

Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in primary ciliary dyskinesia: Implications for application to clinical testing

Hepatitis C Virus Genotyping: Interrogation of the 5′ Untranslated Region Cannot Accurately Distinguish Genotypes 1a and 1b

Phenotypic Heterogeneity in Females with X-Linked Alport Syndrome

Abstract P1-05-20: Comparing the frequency and types of genetic aberrations between older and younger women with metastatic breast cancer at the University of North Carolina at Chapel Hill

Abstract PD6-07: Genomic sequencing in metastatic breast cancer patients to inform clinical practice at the University of North Carolina at Chapel Hill

Estimation of the Warfarin Dose with Clinical and Pharmacogenetic Data

Comprehensive CYP2D6 genotyping in a multiracial population shows differences in allele frequencies between races

Comprehensive CYP2D6 genotyping in a multiracial U.S. breast cancer population

Depletion of pulmonary EC-SOD after exposure to hyperoxia

Impact of human herpesvirus-6 on the frequency and severity of recurrent hepatitis C virus hepatitis in liver transplant recipients

New cytogenetic variant, insertion (15;17)(q22;q12q21), in an adolescent with acute promyelocytic leukemia

College of American Pathologists' laboratory standards for next-generation sequencing clinical tests

Hypersensitivity to nonsteroidal anti-inflammatory drugs (NSAIDs) ― classification, diagnosis and management: review of the EAACI/ENDA and GA2LEN/HANNA

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