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Linaclotide, through activation of guanylate cyclase C, acts locally in the gastrointestinal tract to elicit enhanced intestinal secretion and transit

European journal of pharmacology, 2010-12, Vol.649 (1), p.328-335

2010

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Linaclotide activates guanylate cyclase‐C/cGMP/protein kinase‐II‐dependent trafficking of CFTR in the intestine

Physiological reports, 2017-06, Vol.5 (11), p.e13299-n/a

2017

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Differential Bile Acid Detection in Refractory GERD Patient Saliva Using a Simple and Sensitive Liquid Chromatography Tandem Mass Spectrometry Approach

Journal of clinical gastroenterology, 2022-03, Vol.56 (3), p.218-223

2022

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Guanylate cyclase 2C agonism corrects CFTR mutants

JCI insight, 2017-10, Vol.2 (19)

2017

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Pharmacologic properties, metabolism, and disposition of linaclotide, a novel therapeutic peptide approved for the treatment of irritable bowel syndrome with constipation and chronic idiopathic constipation

The Journal of pharmacology and experimental therapeutics, 2013-01, Vol.344 (1), p.196-206

2013

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The Soluble Guanylate Cyclase Stimulator IWP-953 Increases Conventional Outflow Facility in Mouse Eyes

Investigative ophthalmology & visual science, 2016-03, Vol.57 (3), p.1317-1326

2016

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Linaclotide is a potent and selective guanylate cyclase C agonist that elicits pharmacological effects locally in the gastrointestinal tract

Life sciences (1973), 2010-05, Vol.86 (19), p.760-765

2010

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Systematic discovery of new genes in the Saccharomyces cerevisiae genome

Genome research, 2003-02, Vol.13 (2), p.264-271

2003

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The Natriuretic Peptide Uroguanylin Elicits Physiologic Actions Through 2 Distinct Topoisomers

Hypertension (Dallas, Tex. 1979), 2009-05, Vol.53 (5), p.867-876

2009

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Gastrointestinal pain: Unraveling a novel endogenous pathway through uroguanylin/guanylate cyclase-C/cGMP activation

Pain (Amsterdam), 2013-09, Vol.154 (9), p.1820-1830

2013

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MRP4 Modulation of the Guanylate Cyclase-C/cGMP Pathway: Effects on Linaclotide-Induced Electrolyte Secretion and cGMP Efflux

The Journal of pharmacology and experimental therapeutics, 2015-10, Vol.355 (1), p.48-56

2015

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Identification of potential cell‐surface proteins in Candida albicans and investigation of the role of a putative cell‐surface glycosidase in adhesion and virulence

Yeast (Chichester, England), 2004-03, Vol.21 (4), p.285-302

2004

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The use of direct cDNA selection to rapidly and effectively identify genes in the fungus Aspergillus fumigatus

Fungal genetics and biology, 2002-06, Vol.36 (1), p.59-70

2002

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Cleavage Factor II of Saccharomyces cerevisiaeContains Homologues to Subunits of the Mammalian Cleavage/ Polyadenylation Specificity Factor and Exhibits Sequence-specific, ATP-dependent Interaction with Precursor RNA

The Journal of biological chemistry, 1997-04, Vol.272 (16), p.10831-10838

1997

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Monoclonal antibodies to yeast poly(A) polymerase (PAP) provide evidence for association of PAP with cleavage factor I

Biochemistry (Easton), 1995-02, Vol.34 (5), p.1750-1759

1995

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Hrp1, a sequence-specific RNA-binding protein that shuttles between the nucleus and the cytoplasm, is required for mRNA 3'-end formation in yeast

Genes & development, 1997-10, Vol.11 (19), p.2545-2556

1997

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Purification of the Saccharomyces cerevisiae Cleavage/Polyadenylation Factor I

The Journal of biological chemistry, 1996-10, Vol.271 (43), p.27167-27175

1996

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Structure-Function Relationships in the Saccharomyces cerevisiae Poly(A) Polymerase

The Journal of biological chemistry, 1995-11, Vol.270 (44), p.26715-26720

1995

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THE NATRIURETIC PEPTIDE UROGUANYLIN ELICITS PHYSIOLOGIC ACTIONS THROUGH TWO DISTINCT TOPOISOMERS

Hypertension (Dallas, Tex. 1979), 2009-03, Vol.53 (5), p.867-876

2009

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Purification of the Saccharomyces cerevisiae cleavage/polyadenylation factor I: separation into two components that are required for both cleavage and polyadenylation of mRNA 3' ends

The Journal of biological chemistry, 1996-10, Vol.271 (43), p.27167-27175

1996

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Cleavage factor II of Saccharomyces cerevisiae contains homologues to subunits of the mammalian cleavage/polyadenylation specificity factor and exhibits sequence-specific, ATP-dependent interaction with precursor RNA

The Journal of biological chemistry, 1997-04, Vol.272 (16), p.10831-10838

1997

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Structure-function relationships in the Saccharomyces cerevisiae poly(A) polymerase. Identification of a novel RNA binding site and a domain that interacts with specificity factor(s)

The Journal of biological chemistry, 1995-11, Vol.270 (44), p.26715-26720

1995

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Requirement of A-A-U-A-A-A and adjacent downstream sequences for SV40 early potyadenylation

Nucleic acids research, 1986-06, Vol.14 (12), p.4939-4952

1986

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Polyadenylylation of Sea Urchin Histone RNA Sequences in Transfected COS Cells

Proceedings of the National Academy of Sciences - PNAS, 1985-02, Vol.82 (4), p.1094-1098

1985

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Polyadenylation at a cryptic site in the pBR322 portion of pSV2-neo: prevention of its utilization by the SV40 late poly(A) signal

Nucleic acids research, 1987-01, Vol.15 (2), p.631-642

1987

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Linaclotide, through activation of guanylate cyclase C, acts locally in the gastrointestinal tract to elicit enhanced intestinal secretion and transit

Linaclotide activates guanylate cyclase‐C/cGMP/protein kinase‐II‐dependent trafficking of CFTR in the intestine

Differential Bile Acid Detection in Refractory GERD Patient Saliva Using a Simple and Sensitive Liquid Chromatography Tandem Mass Spectrometry Approach

Guanylate cyclase 2C agonism corrects CFTR mutants

Pharmacologic properties, metabolism, and disposition of linaclotide, a novel therapeutic peptide approved for the treatment of irritable bowel syndrome with constipation and chronic idiopathic constipation

The Soluble Guanylate Cyclase Stimulator IWP-953 Increases Conventional Outflow Facility in Mouse Eyes

Linaclotide is a potent and selective guanylate cyclase C agonist that elicits pharmacological effects locally in the gastrointestinal tract

Systematic discovery of new genes in the Saccharomyces cerevisiae genome

The Natriuretic Peptide Uroguanylin Elicits Physiologic Actions Through 2 Distinct Topoisomers

Gastrointestinal pain: Unraveling a novel endogenous pathway through uroguanylin/guanylate cyclase-C/cGMP activation

MRP4 Modulation of the Guanylate Cyclase-C/cGMP Pathway: Effects on Linaclotide-Induced Electrolyte Secretion and cGMP Efflux

Identification of potential cell‐surface proteins in Candida albicans and investigation of the role of a putative cell‐surface glycosidase in adhesion and virulence

The use of direct cDNA selection to rapidly and effectively identify genes in the fungus Aspergillus fumigatus

Cleavage Factor II of Saccharomyces cerevisiaeContains Homologues to Subunits of the Mammalian Cleavage/ Polyadenylation Specificity Factor and Exhibits Sequence-specific, ATP-dependent Interaction with Precursor RNA

Monoclonal antibodies to yeast poly(A) polymerase (PAP) provide evidence for association of PAP with cleavage factor I

Hrp1, a sequence-specific RNA-binding protein that shuttles between the nucleus and the cytoplasm, is required for mRNA 3'-end formation in yeast

Purification of the Saccharomyces cerevisiae Cleavage/Polyadenylation Factor I

Structure-Function Relationships in the Saccharomyces cerevisiae Poly(A) Polymerase

THE NATRIURETIC PEPTIDE UROGUANYLIN ELICITS PHYSIOLOGIC ACTIONS THROUGH TWO DISTINCT TOPOISOMERS

Purification of the Saccharomyces cerevisiae cleavage/polyadenylation factor I: separation into two components that are required for both cleavage and polyadenylation of mRNA 3' ends

Cleavage factor II of Saccharomyces cerevisiae contains homologues to subunits of the mammalian cleavage/polyadenylation specificity factor and exhibits sequence-specific, ATP-dependent interaction with precursor RNA

Structure-function relationships in the Saccharomyces cerevisiae poly(A) polymerase. Identification of a novel RNA binding site and a domain that interacts with specificity factor(s)

Requirement of A-A-U-A-A-A and adjacent downstream sequences for SV40 early potyadenylation

Polyadenylylation of Sea Urchin Histone RNA Sequences in Transfected COS Cells

Polyadenylation at a cryptic site in the pBR322 portion of pSV2-neo: prevention of its utilization by the SV40 late poly(A) signal

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