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Age-Gender Influence on the Rate-Corrected QT Interval and the QT-Heart Rate Relation in Families With Genotypically Characterized Long QT Syndrome

Journal of the American College of Cardiology, 1997-01, Vol.29 (1), p.93-99

1997

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Filtered Technetium-99m-Sulfur Colloid Evaluated for Lymphoscintigraphy

The Journal of nuclear medicine (1978), 1995-10, Vol.36 (10), p.1895-1901

1995

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T wave “humps” as a potential electrocardiographic marker of the long QT syndrome

Journal of the American College of Cardiology, 1994-09, Vol.24 (3), p.746-754

1994

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Human gastric cathepsin E. Predicted sequence, localization to chromosome 1, and sequence homology with other aspartic proteinases

The Journal of biological chemistry, 1989-10, Vol.264 (28), p.16748-16753

1989

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Evidence of genetic heterogeneity in Romano-Ward long QT syndrome : analysis of 23 families

Circulation (New York, N.Y.), 1994-12, Vol.90 (6), p.2635-2644

1994

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Cloning and expression of steroid sulfatase cDNA and the frequent occurrence of deletions in STS deficiency: Implications for X-Y interchange

Cell, 1987-05, Vol.49 (4), p.443-454

1987

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Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: a clinically and genetically distinct syndrome

Surgery, 1990-12, Vol.108 (6), p.1006-1013

1990

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Isolation and characterization of recombinant human cathepsin E expressed in Chinese hamster ovary cells

The Journal of biological chemistry, 1993-04, Vol.268 (10), p.7276-7282

1993

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Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland

American journal of human genetics, 1994-06, Vol.54 (6), p.1060-1066

1994

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Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity

Nature genetics, 1994-10, Vol.8 (2), p.141-147

1994

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Human gastric cathepsin E gene. Multiple transcripts result from alternative polyadenylation of the primary transcripts of a single gene locus at 1q31-q32

The Journal of biological chemistry, 1992-01, Vol.267 (3), p.1609-1614

1992

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Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of μ-calpain as the multiple endocrine neoplasia type 1 gene

Human genetics, 1996-06, Vol.97 (6), p.732-741

1996

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Slow moving proteinase: isolation, characterization, and immunohistochemical localization in gastric mucosa

Gastroenterology (New York, N.Y. 1943), 1987-07, Vol.93 (1), p.77-84

1987

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Variable Numbers of Pepsinogen Genes are Located in the Centromeric Region of Human Chromosome 11 and Determine the High-Frequency Electrophoretic Polymorphism

Proceedings of the National Academy of Sciences - PNAS, 1985-09, Vol.82 (18), p.6240-6244

1985

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Novel mutations associated with carnitine palmitoyltransferase II deficiency

Human mutation, 1999, Vol.13 (3), p.210-220

1999

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Human pepsinogen C (progastricsin). Isolation of cDNA clones, localization to chromosome 6, and sequence homology with pepsinogen A

The Journal of biological chemistry, 1989-01, Vol.264 (1), p.375

1989

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Pepsinogen C gene polymorphisms associated with gastric body ulcer

Gut, 1993-04, Vol.34 (4), p.450-455

1993

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A Variable Myopathy Associated with Heterozygosity for the R503C Mutation in the Carnitine Palmitoyltransferase II Gene

Molecular genetics and metabolism, 2000-06, Vol.70 (2), p.134-141

2000

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Genetic variation of human aspartic proteinases

Scandinavian journal of clinical & laboratory investigation. Supplement, 1992, Vol.210, p.111-119

Taggart, R T

1992

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Effects of bombesin on the release of glycine-extended progastrin (gastrin G) in rat antral tissue culture

Gastroenterology (New York, N.Y. 1943), 1987-08, Vol.93 (2), p.322-329

1987

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Comparative Gene Mapping: Order of Loci on the X Chromosome is Different in Mice and Humans

Proceedings of the National Academy of Sciences - PNAS, 1980-06, Vol.77 (6), p.3595-3599

1980

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Assignment of the Gene for Cytoplasmic Superoxide Dismutase (Sod-1) to a Region of Chromosome 16 and of Hprt to a Region of the X Chromosome in the Mouse

Proceedings of the National Academy of Sciences - PNAS, 1979-10, Vol.76 (10), p.5230-5233

1979

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D11S971 CATT polymorphism (RC27) located near the MEN1 locus at 11q13

Human molecular genetics, 1993-06, Vol.2 (6), p.825-825

1993

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Radiochemical purity testing for 99Tcm-exametazime: a comparison study for three-paper chromatography

Nuclear medicine communications, 1994-07, Vol.15 (7), p.569-573

1994

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The human loci DNF15S2 and D3S94 have a high degree of sequence similarity to acyl-peptide hydrolase and are located at 3p21.3

American journal of human genetics, 1992-04, Vol.50 (4), p.826-833

1992

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Age-Gender Influence on the Rate-Corrected QT Interval and the QT-Heart Rate Relation in Families With Genotypically Characterized Long QT Syndrome

Filtered Technetium-99m-Sulfur Colloid Evaluated for Lymphoscintigraphy

T wave “humps” as a potential electrocardiographic marker of the long QT syndrome

Human gastric cathepsin E. Predicted sequence, localization to chromosome 1, and sequence homology with other aspartic proteinases

Evidence of genetic heterogeneity in Romano-Ward long QT syndrome : analysis of 23 families

Cloning and expression of steroid sulfatase cDNA and the frequent occurrence of deletions in STS deficiency: Implications for X-Y interchange

Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: a clinically and genetically distinct syndrome

Isolation and characterization of recombinant human cathepsin E expressed in Chinese hamster ovary cells

Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland

Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity

Human gastric cathepsin E gene. Multiple transcripts result from alternative polyadenylation of the primary transcripts of a single gene locus at 1q31-q32

Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of μ-calpain as the multiple endocrine neoplasia type 1 gene

Slow moving proteinase: isolation, characterization, and immunohistochemical localization in gastric mucosa

Variable Numbers of Pepsinogen Genes are Located in the Centromeric Region of Human Chromosome 11 and Determine the High-Frequency Electrophoretic Polymorphism

Novel mutations associated with carnitine palmitoyltransferase II deficiency

Human pepsinogen C (progastricsin). Isolation of cDNA clones, localization to chromosome 6, and sequence homology with pepsinogen A

Pepsinogen C gene polymorphisms associated with gastric body ulcer

A Variable Myopathy Associated with Heterozygosity for the R503C Mutation in the Carnitine Palmitoyltransferase II Gene

Genetic variation of human aspartic proteinases

Effects of bombesin on the release of glycine-extended progastrin (gastrin G) in rat antral tissue culture

Comparative Gene Mapping: Order of Loci on the X Chromosome is Different in Mice and Humans

Assignment of the Gene for Cytoplasmic Superoxide Dismutase (Sod-1) to a Region of Chromosome 16 and of Hprt to a Region of the X Chromosome in the Mouse

D11S971 CATT polymorphism (RC27) located near the MEN1 locus at 11q13

Radiochemical purity testing for 99Tcm-exametazime: a comparison study for three-paper chromatography

The human loci DNF15S2 and D3S94 have a high degree of sequence similarity to acyl-peptide hydrolase and are located at 3p21.3

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