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Allelic association and deletions in autosomal recessive proximal spinal muscular atrophy: association of marker genotype with disease severity and candidate cDNAs

Human molecular genetics, 1995-08, Vol.4 (8), p.1273-1284

1995

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Survival motor neuron (SMN) protein: role in neurite outgrowth and neuromuscular maturation during neuronal differentiation and development

Human molecular genetics, 2002-07, Vol.11 (14), p.1605-1614

2002

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Regulation of murine survival motor neuron (Smn) protein levels by modifying Smn exon 7 splicing

Human molecular genetics, 2001-11, Vol.10 (23), p.2727-2736

2001

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Monitoring Orthosia hibisci (Lepidoptera: Noctuidae) with Pherocon IC and Hara traps

Journal of economic entomology, 1986-12, Vol.79 (6), p.1497-1500

1986

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Two 5q13 simple tandem repeat loci are in linkage disequilibrium with Type 1 spinal muscular atrophy

Human molecular genetics, 1994-11, Vol.3 (11), p.1951-1956

1994

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Linkage disequilibrium analysis of childhoot-onset spinal muscular atrophy (SMA) in the French-Canadian population

Human molecular genetics, 1994, Vol.3 (3), p.459-463

1994

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Incidence of Genital Warts in Sweden Before and After Quadrivalent Human Papillomavirus Vaccine Availability

The Journal of infectious diseases, 2012-09, Vol.206 (6), p.860-866

2012

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Quadrivalent Human Papillomavirus Vaccine Effectiveness: A Swedish National Cohort Study

JNCI : Journal of the National Cancer Institute, 2013-04, Vol.105 (7), p.469-474

2013

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Effects of Maternal Surgical Weight Loss in Mothers on Intergenerational Transmission of Obesity

The journal of clinical endocrinology and metabolism, 2009-11, Vol.94 (11), p.4275-4283

2009

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Effect of nitrogen source on the solubilization of different inorganic phosphates by an isolate of Penicillium rugulosum and two UV-induced mutants

FEMS microbiology ecology, 1999-03, Vol.28 (3), p.281-290

1999

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Two Different Corticosteroid-Binding Globulin Variants that Lack Cortisol-Binding Activity in a Greek Woman

The journal of clinical endocrinology and metabolism, 2012-11, Vol.97 (11), p.4260-4267

2012

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COMPARATIVE STUDY OF DECOMPRESSIVE CRANIECTOMY AFTER MASS LESION EVACUATION IN SEVERE HEAD INJURY

Neurosurgery, 2009-05, Vol.64 (5), p.927-940

2009

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Prospective Cost-Effectiveness Analysis of Cetuximab in Metastatic Colorectal Cancer: Evaluation of National Cancer Institute of Canada Clinical Trials Group CO.17 Trial

JNCI : Journal of the National Cancer Institute, 2009-09, Vol.101 (17), p.1182-1192

2009

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Effects of concentrations of cyanocobalamin in the gestation diet on some criteria of vitamin B12 metabolism in first-parity sows

Journal of animal science, 2007-12, Vol.85 (12), p.3294

2007

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New insight into the molecular basis of 3β-hydroxysteroid dehydrogenase deficiency: Identification of eight mutations in the HSD3B2 gene in eleven patients from seven new families and comparison of the functional properties of twenty-five mutant enzymes

The journal of clinical endocrinology and metabolism, 1999, Vol.84 (12), p.4410-4425

1999

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A novel A10E homozygous mutation in the HSD3B2 gene causing severe salt-wasting 3β-hydroxysteroid dehydrogenase deficiency in 46,XX and 46,XY French-Canadians : Evaluation of gonadal function after puberty

The journal of clinical endocrinology and metabolism, 2000-05, Vol.85 (5), p.1968-1974

2000

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Microtitre plate hybridization system for detection of thermophilic Campylobacter rRNA

Journal of applied microbiology, 1997-02, Vol.82 (2), p.259-266

1997

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Comparison of behavior and vector efficiency of Anopheles gambiae and An. arabiensis (Diptera: Culicidae) in Barkedji, a Sahelian area of Senegal

Journal of medical entomology, 1997-07, Vol.34 (4), p.396-403

1997

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Characteristics of phosphate solubilization by an isolate of a tropical Penicillium rugulosum and two UV-induced mutants

FEMS microbiology ecology, 1999-03, Vol.28 (3), p.291-295

1999

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Detection and functional characterization of the novel missense mutation Y254D in type II 3β-hydroxysteroid dehydrogenase (3βHSD) gene of a female patient with nonsalt-losing 3βHSD deficiency

The journal of clinical endocrinology and metabolism, 1994-03, Vol.78 (3), p.561-567

1994

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Down-regulation of estrogen receptors by androgens in the ZR-75-1 human breast cancer cell line

Endocrinology (Philadelphia), 1989-07, Vol.125 (1), p.392-399

1989

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Genetic mapping of the breast-ovarian cancer syndrome to a small interval on chromosome 17q12–21: exclusion of candidate genes EDH17B2 and RARA

Human molecular genetics, 1993-08, Vol.2 (8), p.1193-1199

1993

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Binding of a member of the NF1 family of transcription factors to two distinct cis-acting elements in the promoter and 5'-flanking region of the human cellular retinol binding protein 1 gene

Molecular endocrinology (Baltimore, Md.), 1994-06, Vol.8 (6), p.732-745

1994

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Detection of a novel mutation (stop 468) in exon 10 of the low-density lipoprotein receptor gene causing familial hypercholesterolemia among French Canadians

Human molecular genetics, 1994-09, Vol.3 (9), p.1689-1691

1994

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Ovarian 3β-hydroxysteroid dehydrogenase and sulfated glycoprotein-2 gene expression are differentially regulated by the induction of ovulation, pseudopregnancy, and luteolysis in the immature rat

Endocrinology (Philadelphia), 1992-04, Vol.130 (4), p.2192-2200

1992

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Allelic association and deletions in autosomal recessive proximal spinal muscular atrophy: association of marker genotype with disease severity and candidate cDNAs

Survival motor neuron (SMN) protein: role in neurite outgrowth and neuromuscular maturation during neuronal differentiation and development

Regulation of murine survival motor neuron (Smn) protein levels by modifying Smn exon 7 splicing

Monitoring Orthosia hibisci (Lepidoptera: Noctuidae) with Pherocon IC and Hara traps

Two 5q13 simple tandem repeat loci are in linkage disequilibrium with Type 1 spinal muscular atrophy

Linkage disequilibrium analysis of childhoot-onset spinal muscular atrophy (SMA) in the French-Canadian population

Incidence of Genital Warts in Sweden Before and After Quadrivalent Human Papillomavirus Vaccine Availability

Quadrivalent Human Papillomavirus Vaccine Effectiveness: A Swedish National Cohort Study

Effects of Maternal Surgical Weight Loss in Mothers on Intergenerational Transmission of Obesity

Effect of nitrogen source on the solubilization of different inorganic phosphates by an isolate of Penicillium rugulosum and two UV-induced mutants

Two Different Corticosteroid-Binding Globulin Variants that Lack Cortisol-Binding Activity in a Greek Woman

COMPARATIVE STUDY OF DECOMPRESSIVE CRANIECTOMY AFTER MASS LESION EVACUATION IN SEVERE HEAD INJURY

Prospective Cost-Effectiveness Analysis of Cetuximab in Metastatic Colorectal Cancer: Evaluation of National Cancer Institute of Canada Clinical Trials Group CO.17 Trial

Effects of concentrations of cyanocobalamin in the gestation diet on some criteria of vitamin B12 metabolism in first-parity sows

New insight into the molecular basis of 3β-hydroxysteroid dehydrogenase deficiency: Identification of eight mutations in the HSD3B2 gene in eleven patients from seven new families and comparison of the functional properties of twenty-five mutant enzymes

A novel A10E homozygous mutation in the HSD3B2 gene causing severe salt-wasting 3β-hydroxysteroid dehydrogenase deficiency in 46,XX and 46,XY French-Canadians : Evaluation of gonadal function after puberty

Microtitre plate hybridization system for detection of thermophilic Campylobacter rRNA

Comparison of behavior and vector efficiency of Anopheles gambiae and An. arabiensis (Diptera: Culicidae) in Barkedji, a Sahelian area of Senegal

Characteristics of phosphate solubilization by an isolate of a tropical Penicillium rugulosum and two UV-induced mutants

Detection and functional characterization of the novel missense mutation Y254D in type II 3β-hydroxysteroid dehydrogenase (3βHSD) gene of a female patient with nonsalt-losing 3βHSD deficiency

Down-regulation of estrogen receptors by androgens in the ZR-75-1 human breast cancer cell line

Genetic mapping of the breast-ovarian cancer syndrome to a small interval on chromosome 17q12–21: exclusion of candidate genes EDH17B2 and RARA

Binding of a member of the NF1 family of transcription factors to two distinct cis-acting elements in the promoter and 5'-flanking region of the human cellular retinol binding protein 1 gene

Detection of a novel mutation (stop 468) in exon 10 of the low-density lipoprotein receptor gene causing familial hypercholesterolemia among French Canadians

Ovarian 3β-hydroxysteroid dehydrogenase and sulfated glycoprotein-2 gene expression are differentially regulated by the induction of ovulation, pseudopregnancy, and luteolysis in the immature rat

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