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SMN gene duplication and the emergence of the SMN2 gene occurred in distinct hominids : SMN2 is unique to Homo sapiens

Human genetics, 2001-03, Vol.108 (3), p.255-266

2001

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Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy number

American journal of human genetics, 1997-06, Vol.60 (6), p.1411-1422

1997

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Fast Identification of Echinacea purpurea Dried Roots Using Near-Infrared Spectroscopy

Analytical chemistry (Washington), 2002-06, Vol.74 (11), p.2493-2499

2002

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Pulmonary Recruitment Protocol For Organ Donors: A New Strategy to Improve the Rate of Lung Utilization

Transplantation proceedings, 2009-10, Vol.41 (8), p.3284-3289

2009

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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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The Δ>15 Kb deletion French Canadian founder mutation in familial hypercholesterolemia: rapid polymerase chain reaction-based diagnostic assay and prevalence in Quebec

Clinical genetics, 2004-03, Vol.65 (3), p.202-208

2004

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Induction of IL-1 during hemodialysis: Transmembrane passage of intact endotoxins (LPS)

Kidney international, 1990-12, Vol.38 (6), p.1089-1094

1990

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Intragenic complementation at the argininosuccinate lyase locus: Reconstruction of the active site

Journal of inherited metabolic disease, 1998-06, Vol.21 (S1), p.72-85

1998

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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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Natalizumab effects on immune cell responses in multiple sclerosis

Annals of neurology, 2006-05, Vol.59 (5), p.748-754

2006

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Linkage study of chronic childhood-onset spinal muscular atrophy (SMA): Confirmation of close linkage to D5S39 in French Canadian families

Genomics (San Diego, Calif.), 1992-09, Vol.14 (1), p.188-190

1992

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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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Direct analysis of amniotic fluid cells by multiplex PCR provides rapid prenatal diagnosis for Duchenne muscular dystrophy

Nucleic acids research, 1991-05, Vol.19 (9), p.2501-2501

1991

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A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patients

Nature genetics, 1995-01, Vol.9 (1), p.56-62

1995

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Preclinical and Clinical Performance of the Efoora Test, a Rapid Test for Detection of Human Immunodeficiency Virus-Specific Antibodies

Journal of Clinical Microbiology, 2005-05, Vol.43 (5), p.2399-2406

2005

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Genetic amniocentesis: a six-years experience in an isolated region of northeastern Quebec (Canada)

Genetic counseling, 1993, Vol.4 (2), p.103

1993

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Ingestion of Flouride from Dentrifices by Children Aged 12 to 24 Months

Clinical pediatrics, 1991-11, Vol.30 (11), p.614-617

1991

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SMNT and NAIP mutations in Canadian families with spinal muscular atrophy (SMA): Genotype/phenotype correlations with disease severity

American journal of medical genetics, 1997-10, Vol.72 (1), p.51-58

1997

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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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Carrier status diagnosis in Duchenne muscular dystrophy with conformtional DNA polymorphism

The Lancet (British edition), 1992, Vol.339 (8785)

1992

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Deletions in the dystrophin gene : analysis of Duchenne and Becker muscular dystrophy pateints in Quebec

Human genetics, 1992, Vol.89 (4), p.419-424

1992

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Association between AgI-CA alleles and severity of autosomal recessive proximal spinal muscular atrophy

American journal of human genetics, 1994, Vol.55 (6), p.1218-1229

1994

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Argininosuccinate lyase deficiency: evidence for heterogeneous structural gene mutations by immunoblotting

American journal of human genetics, 1986-07, Vol.39 (1), p.38-51

1986

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Linkage relationship between incontinentia pigmenti (IP2) and mine terminal X long arm markers

Human genetics, 1991, Vol.86 (3), p.297-299

1991

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SMN gene duplication and the emergence of the SMN2 gene occurred in distinct hominids : SMN2 is unique to Homo sapiens

Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy number

Fast Identification of Echinacea purpurea Dried Roots Using Near-Infrared Spectroscopy

Pulmonary Recruitment Protocol For Organ Donors: A New Strategy to Improve the Rate of Lung Utilization

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

The Δ>15 Kb deletion French Canadian founder mutation in familial hypercholesterolemia: rapid polymerase chain reaction-based diagnostic assay and prevalence in Quebec

Induction of IL-1 during hemodialysis: Transmembrane passage of intact endotoxins (LPS)

Intragenic complementation at the argininosuccinate lyase locus: Reconstruction of the active site

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

Natalizumab effects on immune cell responses in multiple sclerosis

Linkage study of chronic childhood-onset spinal muscular atrophy (SMA): Confirmation of close linkage to D5S39 in French Canadian families

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

Direct analysis of amniotic fluid cells by multiplex PCR provides rapid prenatal diagnosis for Duchenne muscular dystrophy

A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patients

Preclinical and Clinical Performance of the Efoora Test, a Rapid Test for Detection of Human Immunodeficiency Virus-Specific Antibodies

Genetic amniocentesis: a six-years experience in an isolated region of northeastern Quebec (Canada)

Ingestion of Flouride from Dentrifices by Children Aged 12 to 24 Months

SMNT and NAIP mutations in Canadian families with spinal muscular atrophy (SMA): Genotype/phenotype correlations with disease severity

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

Carrier status diagnosis in Duchenne muscular dystrophy with conformtional DNA polymorphism

Deletions in the dystrophin gene : analysis of Duchenne and Becker muscular dystrophy pateints in Quebec

Association between AgI-CA alleles and severity of autosomal recessive proximal spinal muscular atrophy

Argininosuccinate lyase deficiency: evidence for heterogeneous structural gene mutations by immunoblotting

Linkage relationship between incontinentia pigmenti (IP2) and mine terminal X long arm markers

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