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Expressed antibody repertoires in human cord blood cells: 454 sequencing and IMGT/HighV-QUEST analysis of germline gene usage, junctional diversity, and somatic mutations

Immunogenetics (New York), 2012-05, Vol.64 (5), p.337-350

2012

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Lens epithelium-derived growth factor fusion proteins redirect HIV-1 DNA integration

Proceedings of the National Academy of Sciences - PNAS, 2010-02, Vol.107 (7), p.3135-3140

2010

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Human T-Cell Leukemia Virus Type 1 Integration Target Sites in the Human Genome: Comparison with Those of Other Retroviruses

Journal of Virology, 2007-06, Vol.81 (12), p.6731-6741

2007

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Analysis of 454 sequencing error rate, error sources, and artifact recombination for detection of Low-frequency drug resistance mutations in HIV-1 DNA

Retrovirology, 2013-02, Vol.10 (1), p.18-18, Article 18

2013

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Detailed DNA methylation profiles of the E-cadherin promoter in the NCI-60 cancer cells

Molecular cancer therapeutics, 2007-02, Vol.6 (2), p.391-403

2007

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A comprehensive SNP-based genetic analysis of inbred mouse strains

Mammalian genome, 2005-07, Vol.16 (7), p.476-480

2005

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Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients

Cell, 1990-06, Vol.61 (5), p.863-870

1990

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Effect of Vitamin Intervention on the Relationship between GSTM1, Smoking, and Lung Cancer Risk Among Male Smokers

Cancer epidemiology, biomarkers & prevention, 1999-11, Vol.8 (11), p.965-970

1999

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Common Sites of Retroviral Integration in Mouse Hematopoietic Tumors Identified by High-Throughput, Single Nucleotide Polymorphism-Based Mapping and Bacterial Artificial Chromosome Hybridization

Journal of Virology, 2003-01, Vol.77 (2), p.1584-1588

2003

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Genes affected by mouse mammary tumor virus (MMTV) proviral insertions in mouse mammary tumors are deregulated or mutated in primary human mammary tumors

Oncotarget, 2012-11, Vol.3 (11), p.1320-1334

2012

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Efficacy of Cobalt Chelates in the Rabbit Eye Model for Epithelial Herpetic Keratitis

Cornea, 1998-09, Vol.17 (5), p.550-557

1998

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Cytokine-independent growth and clonal expansion of a primary human CD8+ T-cell clone following retroviral transduction with the IL-15 gene

Blood, 2007-06, Vol.109 (12), p.5168-5177

2007

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Candidate genes and cerebral palsy: a population-based study

Pediatrics (Evanston), 2008-11, Vol.122 (5), p.1079

2008

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Genetic polymorphisms and spontaneous preterm birth

Obstetrics and gynecology (New York. 1953), 2007-02, Vol.109 (2), p.384-391

2007

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Abstract 1147: High-throughput nanofluidic PCR-based preparation of 454 sequencing libraries for identifying mutations in EGFR and MET

Cancer research (Chicago, Ill.), 2010-04, Vol.70 (8_Supplement), p.1147-1147

2010

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Abstract 2198: Exome and transcriptome sequencing of human tumors and tumor-derived cell lines

Cancer research (Chicago, Ill.), 2010-04, Vol.70 (8_Supplement), p.2198-2198

2010

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Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosis

JAMA : the journal of the American Medical Association, 1992-04, Vol.267 (13), p.1794

1992

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Candidate Genes and Cerebral Palsy: A Population-Based Study

Obstetrical & gynecological survey, 2009-03, Vol.64 (3), p.154-155

2009

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Unravelling Dietary Acculturation in the 21st Century

Social Science Perspectives on Global Public Health, 2023, p.169-178

1, 2023

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Development of multiplex DNA electronic microarrays using a universal adaptor system for detection of single nucleotide polymorphisms

BioTechniques, 2004-04, Vol.36 (4), p.682-688

2004

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Detection of three rare frameshift mutations in the cystic fibrosis gene in an African-American (CF444delA), an Italian (CF2522insC), and a Soviet (CF3821delT) 1

Genomics (San Diego, Calif.), 1991-05, Vol.10 (1), p.266-269

1991

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XIIXVI. Yeast sequencing reports. Mapping and sequencing of two yeast genes belonging to the ATP‐binding cassette superfamily

Yeast (Chichester, England), 1994-03, Vol.10 (3), p.377-383

1994

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Analysis of Mdr50: A Drosophila P-Glycoprotein/Multidrug Resistance Gene Homolog

Genomics (San Diego, Calif.), 1993-07, Vol.17 (1), p.83-88

1993

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Polymorphic admixture typing in human ethnic populations

American journal of human genetics, 1994-10, Vol.55 (4), p.788-808

1994

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Localization of the gene for the nevoid basal cell carcinoma syndrome

American journal of human genetics, 1994-05, Vol.54 (5), p.765-773

1994

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Expressed antibody repertoires in human cord blood cells: 454 sequencing and IMGT/HighV-QUEST analysis of germline gene usage, junctional diversity, and somatic mutations

Lens epithelium-derived growth factor fusion proteins redirect HIV-1 DNA integration

Human T-Cell Leukemia Virus Type 1 Integration Target Sites in the Human Genome: Comparison with Those of Other Retroviruses

Analysis of 454 sequencing error rate, error sources, and artifact recombination for detection of Low-frequency drug resistance mutations in HIV-1 DNA

Detailed DNA methylation profiles of the E-cadherin promoter in the NCI-60 cancer cells

A comprehensive SNP-based genetic analysis of inbred mouse strains

Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients

Effect of Vitamin Intervention on the Relationship between GSTM1, Smoking, and Lung Cancer Risk Among Male Smokers

Common Sites of Retroviral Integration in Mouse Hematopoietic Tumors Identified by High-Throughput, Single Nucleotide Polymorphism-Based Mapping and Bacterial Artificial Chromosome Hybridization

Genes affected by mouse mammary tumor virus (MMTV) proviral insertions in mouse mammary tumors are deregulated or mutated in primary human mammary tumors

Efficacy of Cobalt Chelates in the Rabbit Eye Model for Epithelial Herpetic Keratitis

Cytokine-independent growth and clonal expansion of a primary human CD8+ T-cell clone following retroviral transduction with the IL-15 gene

Candidate genes and cerebral palsy: a population-based study

Genetic polymorphisms and spontaneous preterm birth

Abstract 1147: High-throughput nanofluidic PCR-based preparation of 454 sequencing libraries for identifying mutations in EGFR and MET

Abstract 2198: Exome and transcriptome sequencing of human tumors and tumor-derived cell lines

Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosis

Candidate Genes and Cerebral Palsy: A Population-Based Study

Unravelling Dietary Acculturation in the 21st Century

Development of multiplex DNA electronic microarrays using a universal adaptor system for detection of single nucleotide polymorphisms

Detection of three rare frameshift mutations in the cystic fibrosis gene in an African-American (CF444delA), an Italian (CF2522insC), and a Soviet (CF3821delT) 1

XIIXVI. Yeast sequencing reports. Mapping and sequencing of two yeast genes belonging to the ATP‐binding cassette superfamily

Analysis of Mdr50: A Drosophila P-Glycoprotein/Multidrug Resistance Gene Homolog

Polymorphic admixture typing in human ethnic populations

Localization of the gene for the nevoid basal cell carcinoma syndrome

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