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Reduction of antibiotic‐induced biofilm accumulation of Pseudomonas aeruginosa by quaternized phytoglycogen

Letters in applied microbiology, 2021-11, Vol.73 (5), p.544-552

2021

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Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data

Prenatal diagnosis, 2002-07, Vol.22 (7), p.609-615

2002

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Enduring the chaos. Psychoanalytical psychotherapy in Poland

Psychoanalytic psychotherapy, 2021-04, Vol.35 (2), p.141-159

2021

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Staging nature in twentieth-century teacher education and classrooms

Paedagogica historica, 2020-03, Vol.56 (1-2), p.121-149

2020

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Nitrite Formation at a Diiron Dinitrosyl Complex

Journal of the American Chemical Society, 2023-10, Vol.145 (42), p.22993-22999

2023

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PCR quantitation of fetal cells in maternal blood in normal and aneuploid pregnancies

American journal of human genetics, 1997-10, Vol.61 (4), p.822-829

1997

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Germline mutations in the ribonuclease L gene in families showing linkage with HPC1

Nature genetics, 2002-02, Vol.30 (2), p.181-184

2002

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Strong homophilic interactions of the Ig-like domains of polycystin-1, the protein product of an autosomal dominant polycystic kidney disease gene, PKD1

Human molecular genetics, 2000-07, Vol.9 (11), p.1641-1649

2000

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Transcriptional response to GAA deficiency (Pompe disease) in infantile-onset patients

Molecular genetics and metabolism, 2012-07, Vol.106 (3), p.287-300

2012

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Mutation Detection of PKD1 Identifies a Novel Mutation Common to Three Families with Aneurysms and/or Very-Early-Onset Disease

American journal of human genetics, 1999-12, Vol.65 (6), p.1561-1571

1999

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Multiplex PCR amplification from the CFTR gene using DNA prepared from buccal brushes/swabs

Human molecular genetics, 1993-02, Vol.2 (2), p.159-163

1993

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CNS-targeted gene therapy improves survival and motor function in a mouse model of spinal muscular atrophy

The Journal of clinical investigation, 2010-04, Vol.120 (4), p.1253-1264

2010

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Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells

Nature (London), 1990-09, Vol.347 (6291), p.358-363

1990

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INFLUENCE OF SPATIOTEMPORAL SCALE ON THE INTERPRETATION OF PALEOCOMMUNITY STRUCTURE: LATERAL VARIATION IN THE IMPERIAL FORMATION OF CALIFORNIA

Palaios, 2007-11, Vol.22 (6), p.630-641

2007

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Transcriptional Response to GAA Deficiency in Mice and Humans

Clinical therapeutics, 2011-06, Vol.33 (6), p.S25-S25

2011

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The Importance of Job Autonomy, Cognitive Ability, and Job-Related Skill for Predicting Role Breadth and Job Performance

Journal of applied psychology, 2005-03, Vol.90 (2), p.399-406

2005

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Somatic Mutation in Individual Liver Cysts Supports a Two-Hit Model of Cystogenesis in Autosomal Dominant Polycystic Kidney Disease

Molecular cell, 1998-08, Vol.2 (2), p.247-251

1998

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Significant fetal-maternal hemorrhage after termination of pregnancy: Implications for development of fetal cell microchimerism

American journal of obstetrics and gynecology, 2001-03, Vol.184 (4), p.703-706

2001

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Inhibition of Glycogen Biosynthesis via mTORC1 Suppression as an Adjunct Therapy for Pompe Disease

Clinical therapeutics, 2011-06, Vol.33 (6), p.S31-S31

2011

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Expression and characterization of the cystic fibrosis transmembrane conductance regulator

Nature (London), 1990-09, Vol.347 (6291), p.382-386

1990

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P4.52 Transcriptional response to GAA deficiency in mice and humans

Neuromuscular disorders : NMD, 2010-10, Vol.20 (9), p.674-674

2010

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Alternative Splicing of Exon 3 of the Human Growth Hormone Receptor is the Result of an Unusual Genetic Polymorphism

Proceedings of the National Academy of Sciences - PNAS, 1996-10, Vol.93 (22), p.12394-12399

1996

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Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization : clinical experience with 4,500 specimens

American journal of human genetics, 1993-05, Vol.52 (5), p.854-865

1993

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High Throughput Parallel Analysis of Hundreds of Patient Samples for More Than 100 Mutations in Multiple Disease Genes

Human molecular genetics, 1997-03, Vol.6 (3), p.337-347

1997

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A simplified procedure for developing multiplex PCRs

Genome research, 1995-12, Vol.5 (5), p.488-493

1995

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Reduction of antibiotic‐induced biofilm accumulation of Pseudomonas aeruginosa by quaternized phytoglycogen

Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data

Enduring the chaos. Psychoanalytical psychotherapy in Poland

Staging nature in twentieth-century teacher education and classrooms

Nitrite Formation at a Diiron Dinitrosyl Complex

PCR quantitation of fetal cells in maternal blood in normal and aneuploid pregnancies

Germline mutations in the ribonuclease L gene in families showing linkage with HPC1

Strong homophilic interactions of the Ig-like domains of polycystin-1, the protein product of an autosomal dominant polycystic kidney disease gene, PKD1

Transcriptional response to GAA deficiency (Pompe disease) in infantile-onset patients

Mutation Detection of PKD1 Identifies a Novel Mutation Common to Three Families with Aneurysms and/or Very-Early-Onset Disease

Multiplex PCR amplification from the CFTR gene using DNA prepared from buccal brushes/swabs

CNS-targeted gene therapy improves survival and motor function in a mouse model of spinal muscular atrophy

Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells

INFLUENCE OF SPATIOTEMPORAL SCALE ON THE INTERPRETATION OF PALEOCOMMUNITY STRUCTURE: LATERAL VARIATION IN THE IMPERIAL FORMATION OF CALIFORNIA

Transcriptional Response to GAA Deficiency in Mice and Humans

The Importance of Job Autonomy, Cognitive Ability, and Job-Related Skill for Predicting Role Breadth and Job Performance

Somatic Mutation in Individual Liver Cysts Supports a Two-Hit Model of Cystogenesis in Autosomal Dominant Polycystic Kidney Disease

Significant fetal-maternal hemorrhage after termination of pregnancy: Implications for development of fetal cell microchimerism

Inhibition of Glycogen Biosynthesis via mTORC1 Suppression as an Adjunct Therapy for Pompe Disease

Expression and characterization of the cystic fibrosis transmembrane conductance regulator

P4.52 Transcriptional response to GAA deficiency in mice and humans

Alternative Splicing of Exon 3 of the Human Growth Hormone Receptor is the Result of an Unusual Genetic Polymorphism

Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization : clinical experience with 4,500 specimens

High Throughput Parallel Analysis of Hundreds of Patient Samples for More Than 100 Mutations in Multiple Disease Genes

A simplified procedure for developing multiplex PCRs

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