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In Vivo Selection of Aptamers Targeting Pancreatic Cancer

The Journal of surgical research, 2012, Vol.172 (2), p.341-341

2012

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Myotilin is mutated in limb girdle muscular dystrophy 1A

Human molecular genetics, 2000-09, Vol.9 (14), p.2141-2147

2000

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In-vivo SELEX Against Pancreatic Cancer Xenografts

The Journal of surgical research, 2011, Vol.165 (2), p.307-307

2011

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Effect of ketoprofen treatment on the uterine inflammatory response after AI of jennies with frozen semen

Theriogenology, 2013-04, Vol.79 (7), p.1019-1026

2013

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Influence of seminal plasma on leucocyte migration and amount of COX-2 protein in the jenny endometrium after insemination with frozen–thawed semen

Animal reproduction science, 2013-12, Vol.143 (1-4), p.57-63

2013

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Color Doppler provides a reliable and rapid means of monitoring luteolysis in female donkeys

Theriogenology, 2015-03, Vol.83 (4), p.485-490

2015

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Identification of a New Autosomal Dominant Limb-Girdle Muscular Dystrophy Locus on Chromosome 7

American journal of human genetics, 1999-02, Vol.64 (2), p.556-562

1999

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54: Development of a Gene Expression Profile for Predicting Gemcitabine Response in Pancreatic Cancer

The Journal of surgical research, 2009, Vol.151 (2), p.195-195

2009

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Possible interaction of genotypes at cystathionine β-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects

Clinical genetics, 1999-08, Vol.56 (2), p.142-144

1999

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Evidence for Locus Heterogeneity in the Bethlem Myopathy and Linkage to 2q37

Human molecular genetics, 1996-07, Vol.5 (7), p.1043-1046

1996

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Use of a CEPH Meiotic Breakpoint Panel to Refine the Locus of Limb-Girdle Muscular Dystrophy Type 1A (LGMD1A) to a 2-Mb Interval on 5q31

Genomics (San Diego, Calif.), 1998-12, Vol.54 (2), p.250-255

1998

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Exclusion of Identified LGMD1 Loci from Four Dominant Limb-Girdle Muscular Dystrophy Families

Human heredity, 1998-07, Vol.48 (4), p.179-184

1998

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Missense Mutation in a Von Willebrand Factor Type a Domain of the α3(VI) Collagen Gene (COL6A3) in a Family with Bethlem Myopathy

Human molecular genetics, 1998-05, Vol.7 (5), p.807-812

1998

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Missense mutation in a von Willebrand factor type A domain of the alpha 3(VI) collagen gene (COL6A3) in a family with Bethlem myopathy

Human molecular genetics, 1998-05, Vol.7 (5), p.807-812

1998

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Genetic Studies in Neural Tube Defects

Pediatric neurosurgery, 2000-01, Vol.32 (1), p.1-9

2000

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Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular Dystrophy

Journal of clinical neuromuscular disease, 2001-09, Vol.3 (1), p.1-7

2001

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Possible interaction of genotypes at cystathionine beta-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects. NTD Collaborative Group

Clinical genetics, 1999-08, Vol.56 (2), p.142-144

1999

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Heterogeneity in Paget disease of the bone

American journal of medical genetics, 2000-06, Vol.92 (5), p.303-307

2000

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Genetic studies in neural tube defects. NTD Collaborative Group

Pediatric neurosurgery, 2000-01, Vol.32 (1), p.1-9

2000

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Cryoballoon versus Radiofrequency Catheter Ablation in Atrial Fibrillation: A Meta-Analysis

Journal of cardiovascular electrophysiology, 2016-10, Vol.27 (10), p.1151-1159

2016

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T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families

American journal of medical genetics, 2002-07, Vol.110 (3), p.215-218

2002

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Litter decomposition: what controls it and how can we alter it to sequester more carbon in forest soils

Biogeochemistry, 2010-12, Vol.101 (1-3), p.133-149

Prescott, Cindy E

2010

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Metabolomic profiles of cartilage and bone reflect tissue type, radiography-confirmed osteoarthritis, and spatial location within the joint

Biochemical and biophysical research communications, 2024-04, Vol.703, p.149683-149683, Article 149683

2024

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Surface hardness as a proxy for weathering behaviour of limestone heritage: a case study on dated headstones on the Isle of Portland, UK

Environmental earth sciences, 2016-05, Vol.75 (10), p.1, Article 931

2016

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Effect of darapladib on major coronary events after an acute coronary syndrome: the SOLID-TIMI 52 randomized clinical trial

JAMA : the journal of the American Medical Association, 2014-09, Vol.312 (10), p.1006

2014

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In Vivo Selection of Aptamers Targeting Pancreatic Cancer

Myotilin is mutated in limb girdle muscular dystrophy 1A

In-vivo SELEX Against Pancreatic Cancer Xenografts

Effect of ketoprofen treatment on the uterine inflammatory response after AI of jennies with frozen semen

Influence of seminal plasma on leucocyte migration and amount of COX-2 protein in the jenny endometrium after insemination with frozen–thawed semen

Color Doppler provides a reliable and rapid means of monitoring luteolysis in female donkeys

Identification of a New Autosomal Dominant Limb-Girdle Muscular Dystrophy Locus on Chromosome 7

54: Development of a Gene Expression Profile for Predicting Gemcitabine Response in Pancreatic Cancer

Possible interaction of genotypes at cystathionine β-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects

Evidence for Locus Heterogeneity in the Bethlem Myopathy and Linkage to 2q37

Use of a CEPH Meiotic Breakpoint Panel to Refine the Locus of Limb-Girdle Muscular Dystrophy Type 1A (LGMD1A) to a 2-Mb Interval on 5q31

Exclusion of Identified LGMD1 Loci from Four Dominant Limb-Girdle Muscular Dystrophy Families

Missense Mutation in a Von Willebrand Factor Type a Domain of the α3(VI) Collagen Gene (COL6A3) in a Family with Bethlem Myopathy

Missense mutation in a von Willebrand factor type A domain of the alpha 3(VI) collagen gene (COL6A3) in a family with Bethlem myopathy

Genetic Studies in Neural Tube Defects

Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular Dystrophy

Possible interaction of genotypes at cystathionine beta-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects. NTD Collaborative Group

Heterogeneity in Paget disease of the bone

Genetic studies in neural tube defects. NTD Collaborative Group

Cryoballoon versus Radiofrequency Catheter Ablation in Atrial Fibrillation: A Meta-Analysis

T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families

Litter decomposition: what controls it and how can we alter it to sequester more carbon in forest soils

Metabolomic profiles of cartilage and bone reflect tissue type, radiography-confirmed osteoarthritis, and spatial location within the joint

Surface hardness as a proxy for weathering behaviour of limestone heritage: a case study on dated headstones on the Isle of Portland, UK

Effect of darapladib on major coronary events after an acute coronary syndrome: the SOLID-TIMI 52 randomized clinical trial

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