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Catheter failure rates and time course with epidural versus combined spinal-epidural analgesia in labor

International journal of obstetric anesthesia, 2016-05, Vol.26, p.4-7

2016

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Caspase cleavage of the APC tumor suppressor and release of an amino-terminal domain is required for the transcription-independent function of APC in apoptosis

Oncogene, 2007-07, Vol.26 (33), p.4872-4876

2007

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Mutator Phenotypes in Human Colorectal Carcinoma Cell Lines

Proceedings of the National Academy of Sciences - PNAS, 1994-07, Vol.91 (14), p.6319-6323

1994

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Prostaglandin H Synthase 2 is Expressed Abnormally in Human Colon Cancer: Evidence for a Transcriptional Effect

Proceedings of the National Academy of Sciences - PNAS, 1996-05, Vol.93 (10), p.4816-4820

1996

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Touch and go: Mediating cell-to-cell interactions and Wnt signaling in gastrointestinal tumor formation

Gastroenterology (New York, N.Y. 1943), 2000-10, Vol.119 (4), p.1161-1164

Groden, Joanna

2000

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The Werner and Bloom Syndrome Proteins Catalyze Regression of a Model Replication Fork

Biochemistry (Easton), 2006-11, Vol.45 (47), p.13939-13946

2006

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Pathology of mouse models of intestinal cancer: Consensus report and recommendations

Gastroenterology (New York, N.Y. 1943), 2003-03, Vol.124 (3), p.762-777

2003

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Biology of the Adenomatous Polyposis Coli Tumor Suppressor

Journal of clinical oncology, 2000-05, Vol.18 (9), p.1967-1979

2000

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β-Catenin mutation is a frequent cause of Wnt pathway activation in gastric cancer

Cancer research (Chicago, Ill.), 2002-06, Vol.62 (12), p.3503-3506

2002

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RecQ Family Members Combine Strand Pairing and Unwinding Activities to Catalyze Strand Exchange

The Journal of biological chemistry, 2005-06, Vol.280 (24), p.23397-23407

2005

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The identical 5' splice-site acceptor mutation in five attenuated APC families from Newfoundland demonstrates a founder effect

Human genetics, 1999-11, Vol.105 (5), p.388-398

1999

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Crosslinks and crosstalk: Human cancer syndromes and DNA repair defects

Cancer Cell, 2004-12, Vol.6 (6), p.539-545

2004

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Germ-line mutations in the first 14 exons of the adenomatous polyposis coli (APC) gene

American journal of human genetics, 1993-02, Vol.52 (2), p.273-279

1993

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Mutational analysis of patients with adenomatous polyposis : identical inactivating mutations in unrelated individuals

American journal of human genetics, 1993-02, Vol.52 (2), p.263-272

1993

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Human melanocortin 1 receptor variants, receptor function and melanocyte response to UV radiation

Journal of cell science, 2002-06, Vol.115 (Pt 11), p.2349-2355

2002

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Linkage disequilibrium predicts physical distance in the adenomatous polyposis coli region

American journal of human genetics, 1994-05, Vol.54 (5), p.884-898

1994

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Enhanced Tumor Formation in Mice Heterozygous for Blm Mutation

Science (American Association for the Advancement of Science), 2002-09, Vol.297 (5589), p.2051-2053

2002

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The Bloom's syndrome gene product is homologous to RecQ helicases

Cell, 1995-11, Vol.83 (4), p.655-666

1995

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Molecular Evidence that Homologous Recombination Occurs in Proliferating Human Somatic Cells

Proceedings of the National Academy of Sciences - PNAS, 1990-06, Vol.87 (11), p.4315-4319

1990

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Transcriptional profiles of intestinal tumors in Apc(Min) mice are unique from those of embryonic intestine and identify novel gene targets dysregulated in human colorectal tumors

Cancer research (Chicago, Ill.), 2005-01, Vol.65 (1), p.166-176

2005

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Crosslinks and crosstalkHuman cancer syndromes and DNA repair defects

Cancer cell, 2004-12, Vol.6 (6), p.539-545

2004

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The Bloom's Syndrome Protein (BLM) Interacts with MLH1 but Is Not Required for DNA Mismatch Repair

The Journal of biological chemistry, 2001-08, Vol.276 (32), p.30031-30035

2001

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Identification of APC gene mutations in Italian adenomatous polyposis coli patients by PCR-SSCP analysis

American journal of human genetics, 1993-02, Vol.52 (2), p.280-285

1993

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Identification and characterization of the familial adenomatous polyposis coli gene

Cell, 1991-08, Vol.66 (3), p.589-600

1991

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BLM helicase complements disrupted type II telomere lengthening in telomerase-negative sgs1 yeast

Cancer research (Chicago, Ill.), 2005-07, Vol.65 (13), p.5520-5522

2005

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Catheter failure rates and time course with epidural versus combined spinal-epidural analgesia in labor

Caspase cleavage of the APC tumor suppressor and release of an amino-terminal domain is required for the transcription-independent function of APC in apoptosis

Mutator Phenotypes in Human Colorectal Carcinoma Cell Lines

Prostaglandin H Synthase 2 is Expressed Abnormally in Human Colon Cancer: Evidence for a Transcriptional Effect

Touch and go: Mediating cell-to-cell interactions and Wnt signaling in gastrointestinal tumor formation

The Werner and Bloom Syndrome Proteins Catalyze Regression of a Model Replication Fork

Pathology of mouse models of intestinal cancer: Consensus report and recommendations

Biology of the Adenomatous Polyposis Coli Tumor Suppressor

β-Catenin mutation is a frequent cause of Wnt pathway activation in gastric cancer

RecQ Family Members Combine Strand Pairing and Unwinding Activities to Catalyze Strand Exchange

The identical 5' splice-site acceptor mutation in five attenuated APC families from Newfoundland demonstrates a founder effect

Crosslinks and crosstalk: Human cancer syndromes and DNA repair defects

Germ-line mutations in the first 14 exons of the adenomatous polyposis coli (APC) gene

Mutational analysis of patients with adenomatous polyposis : identical inactivating mutations in unrelated individuals

Human melanocortin 1 receptor variants, receptor function and melanocyte response to UV radiation

Linkage disequilibrium predicts physical distance in the adenomatous polyposis coli region

Enhanced Tumor Formation in Mice Heterozygous for Blm Mutation

The Bloom's syndrome gene product is homologous to RecQ helicases

Molecular Evidence that Homologous Recombination Occurs in Proliferating Human Somatic Cells

Transcriptional profiles of intestinal tumors in Apc(Min) mice are unique from those of embryonic intestine and identify novel gene targets dysregulated in human colorectal tumors

Crosslinks and crosstalkHuman cancer syndromes and DNA repair defects

The Bloom's Syndrome Protein (BLM) Interacts with MLH1 but Is Not Required for DNA Mismatch Repair

Identification of APC gene mutations in Italian adenomatous polyposis coli patients by PCR-SSCP analysis

Identification and characterization of the familial adenomatous polyposis coli gene

BLM helicase complements disrupted type II telomere lengthening in telomerase-negative sgs1 yeast

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