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Accumulated Chromosomal Instability in Murine Bone Marrow Mesenchymal Stem Cells Leads to Malignant Transformation

Stem cells (Dayton, Ohio), 2006-04, Vol.24 (4), p.1095-1103

2006

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Establishment of Papillomavirus Infection Is Enhanced by Promyelocytic Leukemia Protein (PML) Expression

Proceedings of the National Academy of Sciences - PNAS, 2004-09, Vol.101 (39), p.14252-14257

2004

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Control of the Papillomavirus Early-to-Late Switch by Differentially Expressed SRp20

Journal of Virology, 2009-01, Vol.83 (1), p.167-180

2009

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A Mechanism for Controlled Access to GWAS Data: Experience of the GAIN Data Access Committee

American journal of human genetics, 2013-04, Vol.92 (4), p.479-488

2013

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The E6AP Ubiquitin Ligase Is Required for Transactivation of the hTERT Promoter by the Human Papillomavirus E6 Oncoprotein

The Journal of biological chemistry, 2005-03, Vol.280 (11), p.10807-10816

2005

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Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome

Human mutation, 2006-11, Vol.27 (11), p.1092-1103

2006

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Papillomavirus genome structure, expression, and post-transcriptional regulation

Frontiers in bioscience, 2006-09, Vol.11, p.2286

2006

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A pyrimidine-rich exonic splicing suppressor binds multiple RNA splicing factors and inhibits spliceosome assembly

Proceedings of the National Academy of Sciences - PNAS, 1998-11, Vol.95 (24), p.14088-14093

1998

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Xeroderma Pigmentosum-Variant Patients from America, Europe, and Asia

Journal of investigative dermatology, 2008-08, Vol.128 (8), p.2055-2068

2008

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The human XPC DNA repair gene: arrangement, splice site information content and influence of a single nucleotide polymorphism in a splice acceptor site on alternative splicing and function

Nucleic acids research, 2002-08, Vol.30 (16), p.3624

2002

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Keratinocyte growth conditions modulate telomerase expression, senescence, and immortalization by human papillomavirus type 16 E6 and E7 oncogenes

Cancer research (Chicago, Ill.), 2003-11, Vol.63 (22), p.7815-7824

2003

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Repression of HPV16 early region transcription by the E2 protein

Virology (New York, N.Y.), 2006-07, Vol.351 (1), p.29-41

2006

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Codon optimization of the HPV-16 E5 gene enhances protein expression

Virology (New York, N.Y.), 2003-06, Vol.311 (1), p.105-114

2003

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Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients

Carcinogenesis (New York), 2006-01, Vol.27 (1), p.84-94

2006

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Increased expression of VEGF121/VEGF165–189 ratio results in a significant enhancement of human prostate tumor angiogenesis

International journal of cancer, 2007-05, Vol.120 (10), p.2096-2109

2007

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Production of Infectious Bovine Papillomavirus from Cloned Viral DNA by Using an Organotypic Raft/Xenograft Technique

Proceedings of the National Academy of Sciences - PNAS, 2000-05, Vol.97 (10), p.5534-5539

2000

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XPC initiation codon mutation in xeroderma pigmentosum patients with and without neurological symptoms

DNA repair, 2009-01, Vol.8 (1), p.114-125

2009

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XPC branch-point sequence mutations disrupt U2 snRNP binding, resulting in abnormal pre-mRNA splicing in xeroderma pigmentosum patients

Human mutation, 2010-02, Vol.31 (2), p.167-175

2010

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Two essential splice lariat branchpoint sequences in one intron in a xeroderma pigmentosum DNA repair gene: mutations result in reduced XPC mRNA levels that correlate with cancer risk

Human molecular genetics, 2004-02, Vol.13 (3), p.343-352

2004

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Structure, function and diversity of the healthy human microbiome

Nature (London), 2012-06, Vol.486 (7402), p.207-214

2012

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A framework for human microbiome research

Nature (London), 2012-06, Vol.486 (7402), p.215-221

2012

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Cervical Tissue Collection Methods for RNA Preservation: Comparison of Snap-frozen, Ethanol-fixed, and RNAlater-fixation

Diagnostic molecular pathology, 2006-09, Vol.15 (3), p.144-148

2006

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Messenger RNA Repair and Restoration of Protein Function by Spliceosome-Mediated RNA Trans-Splicing

Molecular therapy, 2001-08, Vol.4 (2), p.105-114

2001

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A Transcriptional Initiator Overlaps with a Conserved YY1 Binding Site in the Long Control Region of Human Papillomavirus Type 16

Virology (New York, N.Y.), 2003-01, Vol.305 (2), p.486-501

2003

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Accumulated Chromosomal Instability in Murine Bone Marrow Mesenchymal Stem Cells Leads to Malignant Transformation

Establishment of Papillomavirus Infection Is Enhanced by Promyelocytic Leukemia Protein (PML) Expression

Control of the Papillomavirus Early-to-Late Switch by Differentially Expressed SRp20

A Mechanism for Controlled Access to GWAS Data: Experience of the GAIN Data Access Committee

The E6AP Ubiquitin Ligase Is Required for Transactivation of the hTERT Promoter by the Human Papillomavirus E6 Oncoprotein

The NIH Human Microbiome Project

Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome

Papillomavirus genome structure, expression, and post-transcriptional regulation

A pyrimidine-rich exonic splicing suppressor binds multiple RNA splicing factors and inhibits spliceosome assembly

Xeroderma Pigmentosum-Variant Patients from America, Europe, and Asia

The human XPC DNA repair gene: arrangement, splice site information content and influence of a single nucleotide polymorphism in a splice acceptor site on alternative splicing and function

Keratinocyte growth conditions modulate telomerase expression, senescence, and immortalization by human papillomavirus type 16 E6 and E7 oncogenes

Repression of HPV16 early region transcription by the E2 protein

Codon optimization of the HPV-16 E5 gene enhances protein expression

Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients

Increased expression of VEGF121/VEGF165–189 ratio results in a significant enhancement of human prostate tumor angiogenesis

Production of Infectious Bovine Papillomavirus from Cloned Viral DNA by Using an Organotypic Raft/Xenograft Technique

XPC initiation codon mutation in xeroderma pigmentosum patients with and without neurological symptoms

XPC branch-point sequence mutations disrupt U2 snRNP binding, resulting in abnormal pre-mRNA splicing in xeroderma pigmentosum patients

Two essential splice lariat branchpoint sequences in one intron in a xeroderma pigmentosum DNA repair gene: mutations result in reduced XPC mRNA levels that correlate with cancer risk

Structure, function and diversity of the healthy human microbiome

A framework for human microbiome research

Cervical Tissue Collection Methods for RNA Preservation: Comparison of Snap-frozen, Ethanol-fixed, and RNAlater-fixation

Messenger RNA Repair and Restoration of Protein Function by Spliceosome-Mediated RNA Trans-Splicing

A Transcriptional Initiator Overlaps with a Conserved YY1 Binding Site in the Long Control Region of Human Papillomavirus Type 16

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