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Determination of the Functionality of Common APOA5 Polymorphisms

The Journal of biological chemistry, 2005-08, Vol.280 (31), p.28215-28220

2005

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Effects of six APOA5 variants, identified in patients with severe hypertriglyceridemia, on in vitro lipoprotein lipase activity and receptor binding

Arteriosclerosis, thrombosis, and vascular biology, 2008-10, Vol.28 (10), p.1866-1871

2008

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FUNCTIONAL ANALYSIS OF REGULATORY LPL SNPS

Atherosclerosis, 2009, Vol.207 (1), p.e3-e4

2009

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Cloning and chromosome assignment of the human CDX2 gene

Annals of human genetics, 1997-09, Vol.61 (5), p.393-400, Article S0003480097006465

1997

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The human homolog T of the mouse T(Brachyury) gene; gene structure, cDNA sequence, and assignment to chromosome 6q27

Genome research, 1996-03, Vol.6 (3), p.226-233

1996

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Application of statistical and functional methodologies for the investigation of genetic determinants of coronary heart disease biomarkers: lipoprotein lipase genotype and plasma triglycerides as an exemplar

Human molecular genetics, 2010-10, Vol.19 (20), p.3936-3947

2010

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Variation in USF1 shows haplotype effects, gene : gene and gene : environment associations with glucose and lipid parameters in the European Atherosclerosis Research Study II

Human molecular genetics, 2004-08, Vol.13 (15), p.1587-1597

2004

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The embryonic RNA helicase gene (ERH): a new member of the DEAD box family of RNA helicases

Biochemical journal, 1995-06, Vol.308 ( Pt 3) (3), p.839-846

1995

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A Novel Human Phosphoglucomutase (PGM5) Maps to the Centromeric Region of Chromosome 9

Genomics (San Diego, Calif.), 1995-11, Vol.30 (2), p.350-353

1995

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Alternative splicing of the neural cell adhesion molecule gene generates variant extracellular domain structure in skeletal muscle and brain

Genes & development, 1989-03, Vol.3 (3), p.348-357

1989

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Cloning and chromosome assignment of the human CDX2 gene

Annals of human genetics, 1997-09, Vol.61 (5), p.393-400

1997

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Phosphoglucomutase 1 : a gene with two promoters and a duplicated first exon

Biochemical journal, 1993-12, Vol.296 (2), p.417-422

1993

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The Classical Human Phosphoglucomutase (PGM1) Isozyme Polymorphism is Generated by Intragenic Recombination

Proceedings of the National Academy of Sciences - PNAS, 1993-11, Vol.90 (22), p.10730-10733

1993

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Complete sequence and in vitro expression of a tissue-specific phosphatidylinositol-linked N-CAM isoform from skeletal muscle

Development (Cambridge), 1988-09, Vol.104 (1), p.165-173

1988

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Identification and characterisation of polymorphisms in human phosphoglucomutase (PGM1)

Annals of human genetics, 1999-03, Vol.63 (2), p.129-140

1999

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The identification of novel sequences expressed in the mouse notochord

Mammalian genome, 1997-01, Vol.8 (1), p.42-44

1997

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Canine homolog of the T-box transcription factor T; failure of the protein to bind to its DNA target leads to a short-tail phenotype

Mammalian genome, 2001-03, Vol.12 (3), p.212-218

2001

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Phosphoglucomutase 1: Complete Human and Rabbit mRNA Sequences and Direct Mapping of this Highly Polymorphic Marker on Human Chromosome 1

Proceedings of the National Academy of Sciences - PNAS, 1992-01, Vol.89 (1), p.411-415

1992

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Up71 and Up140, Two Novel Transcripts of Utrophin That Are Homologues of Short Forms of Dystrophin

Human molecular genetics, 1999-07, Vol.8 (7), p.1271-1278

1999

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Canine TCOF1; cloning, chromosome assignment and genetic analysis in dogs with different head types

Mammalian genome, 2001-08, Vol.12 (8), p.622-629

2001

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Immunological detection of the sixth complement component (C6) following flat bed polyacrylamide gel isoelectric focusing and electrophoretic transfer to nitrocellulose filters

Annals of human genetics, 1983-01, Vol.47 (1), p.1-8

1983

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Enhanced bridging function and augmented monocyte adhesion by lipoprotein lipase N9: insights into increased risk of coronary artery disease in N9 carriers

Atherosclerosis, 2003-02, Vol.166 (2), p.243-251

2003

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A study of short utrophin isoforms in mice deficient for full-length utrophin

Mammalian genome, 2003-01, Vol.14 (1), p.47-60

2003

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The human TBX6 gene : Cloning and assignment to chromosome 16p11.2

Genomics (San Diego, Calif.), 1999-01, Vol.55 (2), p.238-241

1999

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Genetics of four plasma protein loci in Equus przewalskii: new alleles at the prealbumin, postalbumin and transferrin loci

Animal Blood Groups and Biochemical Genetics, 1983-01, Vol.14 (1), p.7-16

1983

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Determination of the Functionality of Common APOA5 Polymorphisms

Effects of six APOA5 variants, identified in patients with severe hypertriglyceridemia, on in vitro lipoprotein lipase activity and receptor binding

FUNCTIONAL ANALYSIS OF REGULATORY LPL SNPS

Cloning and chromosome assignment of the human CDX2 gene

The human homolog T of the mouse T(Brachyury) gene; gene structure, cDNA sequence, and assignment to chromosome 6q27

Application of statistical and functional methodologies for the investigation of genetic determinants of coronary heart disease biomarkers: lipoprotein lipase genotype and plasma triglycerides as an exemplar

Variation in USF1 shows haplotype effects, gene : gene and gene : environment associations with glucose and lipid parameters in the European Atherosclerosis Research Study II

The embryonic RNA helicase gene (ERH): a new member of the DEAD box family of RNA helicases

A Novel Human Phosphoglucomutase (PGM5) Maps to the Centromeric Region of Chromosome 9

Alternative splicing of the neural cell adhesion molecule gene generates variant extracellular domain structure in skeletal muscle and brain

Cloning and chromosome assignment of the human CDX2 gene

Phosphoglucomutase 1 : a gene with two promoters and a duplicated first exon

The Classical Human Phosphoglucomutase (PGM1) Isozyme Polymorphism is Generated by Intragenic Recombination

Complete sequence and in vitro expression of a tissue-specific phosphatidylinositol-linked N-CAM isoform from skeletal muscle

Identification and characterisation of polymorphisms in human phosphoglucomutase (PGM1)

The identification of novel sequences expressed in the mouse notochord

Canine homolog of the T-box transcription factor T; failure of the protein to bind to its DNA target leads to a short-tail phenotype

Phosphoglucomutase 1: Complete Human and Rabbit mRNA Sequences and Direct Mapping of this Highly Polymorphic Marker on Human Chromosome 1

Up71 and Up140, Two Novel Transcripts of Utrophin That Are Homologues of Short Forms of Dystrophin

Canine TCOF1; cloning, chromosome assignment and genetic analysis in dogs with different head types

Immunological detection of the sixth complement component (C6) following flat bed polyacrylamide gel isoelectric focusing and electrophoretic transfer to nitrocellulose filters

Enhanced bridging function and augmented monocyte adhesion by lipoprotein lipase N9: insights into increased risk of coronary artery disease in N9 carriers

A study of short utrophin isoforms in mice deficient for full-length utrophin

The human TBX6 gene : Cloning and assignment to chromosome 16p11.2

Genetics of four plasma protein loci in Equus przewalskii: new alleles at the prealbumin, postalbumin and transferrin loci

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