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Bone morphogenetic protein signaling and growth suppression in colon cancer

American journal of physiology: Gastrointestinal and liver physiology, 2006-07, Vol.291 (1), p.G135-G145

2006

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Evidence for an hMSH3 defect in familial hamartomatous polyps

Cancer, 2011-02, Vol.117 (3), p.492-500

2011

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Mutation rates of TGFBR2 and ACVR2 coding microsatellites in human cells with defective DNA mismatch repair

PloS one, 2008-10, Vol.3 (10), p.e3463

2008

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Lynch Syndrome: A Pediatric Perspective

Journal of pediatric gastroenterology and nutrition, 2014-02, Vol.58 (2), p.144-152

2014

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Biallelic Mismatch Repair Deficiency in an Adolescent Female

Case reports in genetics, 2018, Vol.2018 (2018), p.1-5

2018

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Pediatric juvenile polyposis syndromes: An update

Current gastroenterology reports, 2009-06, Vol.11 (3), p.211-219

2009

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Large intron 14 rearrangement in APC results in splice defect and attenuated FAP

Human genetics, 2010-03, Vol.127 (3), p.359-369

2010

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Cyclooxygenase‐2 Expression in Polyps From a Patient With Juvenile Polyposis Syndrome With Mutant BMPR1A

Journal of pediatric gastroenterology and nutrition, 2007-03, Vol.44 (3), p.318-325

2007

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Genetic heterogeneity in familial juvenile polyposis

Cancer research (Chicago, Ill.), 2000-12, Vol.60 (24), p.6882-6885

2000

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Lynch Syndrome

Journal of pediatric gastroenterology and nutrition, 2014-02, Vol.58 (2), p.144-152

2014

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Germline characterization of early-aged onset of hereditary non-polyposis colorectal cancer

The Journal of pediatrics, 2001-05, Vol.138 (5), p.629-635

2001

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PTEN and Cancer

Reference Module in Life Sciences, 2017

Huang, Sherry C.

2017

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The mismatch repair (MMR) protein hMSH3 is lost from polyp epithelium of patients with PTEN germline hamartomatous syndromes

Gastroenterology (New York, N.Y. 1943), 2003-04, Vol.124 (4), p.A42-A42

2003

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Loss of PTEN and hMSH3 protein expression from familial jevenile polyp epithelium

Gastroenterology (New York, N.Y. 1943), 2001-04, Vol.120 (5), p.A210-A210

2001

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Dinucleotide, but not mononucleotide microsatellite instability, is present in familial juvenile polyps

Gastroenterology (New York, N.Y. 1943), 2000-04, Vol.118 (4), p.A57-A57

2000

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Germline characterization of early-aged onset of HNPCC

Gastroenterology (New York, N.Y. 1943), 2000-04, Vol.118 (4), p.A178-A178

2000

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True association of germline PTEN mutation with juvenile polyposis syndrome

Gastroenterology (New York, N.Y. 1943), 2000-04, Vol.118 (4), p.A43-A43

2000

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Biallelic Mismatch Repair Deficiency in an Adolescent Female

Case reports in genetics, 2018, Vol.2018, p.8657823-8657823

2018

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H0LiCOW – III. Quantifying the effect of mass along the line of sight to the gravitational lens HE 0435−1223 through weighted galaxy counts

Monthly notices of the Royal Astronomical Society, 2017-06, Vol.467 (4), p.4220-4242

2017

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Crystallography of a Lewis-binding norovirus, elucidation of strain-specificity to the polymorphic human histo-blood group antigens

PLoS pathogens, 2011-07, Vol.7 (7), p.e1002152-e1002152

2011

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Neuronal uptake transporters contribute to oxaliplatin neurotoxicity in mice

The Journal of clinical investigation, 2020-09, Vol.130 (9), p.4601-4606

2020

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ALS-associated mutation FUS-R521C causes DNA damage and RNA splicing defects

The Journal of clinical investigation, 2014-03, Vol.124 (3), p.981-999

2014

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Adoptive Cell Therapy for Patients With Metastatic Melanoma: Evaluation of Intensive Myeloablative Chemoradiation Preparative Regimens

Journal of clinical oncology, 2008-11, Vol.26 (32), p.5233-5239

2008

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Orthogonal Mass Spectrometry-Based Footprinting for Epitope Mapping and Structural Characterization: The IL‑6 Receptor upon Binding of Protein Therapeutics

Analytical chemistry (Washington), 2017-07, Vol.89 (14), p.7742-7749

2017

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Proliferation of cells with HIV integrated into cancer genes contributes to persistent infection

Science (American Association for the Advancement of Science), 2014-08, Vol.345 (6196), p.570-573

2014

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Bone morphogenetic protein signaling and growth suppression in colon cancer

Evidence for an hMSH3 defect in familial hamartomatous polyps

Mutation rates of TGFBR2 and ACVR2 coding microsatellites in human cells with defective DNA mismatch repair

Lynch Syndrome: A Pediatric Perspective

Biallelic Mismatch Repair Deficiency in an Adolescent Female

Pediatric juvenile polyposis syndromes: An update

Large intron 14 rearrangement in APC results in splice defect and attenuated FAP

Cyclooxygenase‐2 Expression in Polyps From a Patient With Juvenile Polyposis Syndrome With Mutant BMPR1A

Genetic heterogeneity in familial juvenile polyposis

Lynch Syndrome

Germline characterization of early-aged onset of hereditary non-polyposis colorectal cancer

PTEN and Cancer

The mismatch repair (MMR) protein hMSH3 is lost from polyp epithelium of patients with PTEN germline hamartomatous syndromes

Loss of PTEN and hMSH3 protein expression from familial jevenile polyp epithelium

Dinucleotide, but not mononucleotide microsatellite instability, is present in familial juvenile polyps

Germline characterization of early-aged onset of HNPCC

True association of germline PTEN mutation with juvenile polyposis syndrome

Biallelic Mismatch Repair Deficiency in an Adolescent Female

H0LiCOW – III. Quantifying the effect of mass along the line of sight to the gravitational lens HE 0435−1223 through weighted galaxy counts

Crystallography of a Lewis-binding norovirus, elucidation of strain-specificity to the polymorphic human histo-blood group antigens

Neuronal uptake transporters contribute to oxaliplatin neurotoxicity in mice

ALS-associated mutation FUS-R521C causes DNA damage and RNA splicing defects

Adoptive Cell Therapy for Patients With Metastatic Melanoma: Evaluation of Intensive Myeloablative Chemoradiation Preparative Regimens

Orthogonal Mass Spectrometry-Based Footprinting for Epitope Mapping and Structural Characterization: The IL‑6 Receptor upon Binding of Protein Therapeutics

Proliferation of cells with HIV integrated into cancer genes contributes to persistent infection

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