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Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease

Neurology, 2007-09, Vol.69 (12), p.1270-1277

2007

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Biomarkers of oxidative stress in schizophrenic and control subjects

Prostaglandins, leukotrienes and essential fatty acids, 2007-02, Vol.76 (2), p.73-85

2007

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Transgenic mice expressing the human heat shock protein 70 have improved post-ischemic myocardial recovery

The Journal of clinical investigation, 1995-04, Vol.95 (4), p.1854-60

1995

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The analysis of oral air using selected ion flow tube mass spectrometry in persons with and without a history of oral malodour

International journal of dental hygiene, 2009-05, Vol.7 (2), p.136-143

2009

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Identification and Analysis of Mutations in the Wilson Disease Gene ( ATP7B): Population Frequencies, Genotype-Phenotype Correlation, and Functional Analyses

American journal of human genetics, 1997-08, Vol.61 (2), p.317-328

1997

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Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictions

Human molecular genetics, 1994-09, Vol.3 (9), p.1647-1656

1994

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Elevated activity of phospholipid biosynthetic enzymes in substantia nigra of patients with Parkinson's disease

Neuroscience, 2001-01, Vol.102 (4), p.899-904

2001

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TULP1 mutation in two extended Dominican kindreds with autosomal recessive Retinitis pigmentosa

Nature genetics, 1998-02, Vol.18 (2), p.177-179

1998

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Low activity of key phospholipid catabolic and anabolic enzymes in human substantia nigra: possible implications for Parkinson's disease

Neuroscience, 1998-04, Vol.83 (3), p.791-798

1998

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Application packs

British dental journal, 2005-03, Vol.198 (6), p.321-321

Ross, M B

2005

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A Multicopy Transcription-Repair Gene, BTF2p44, Maps to the SMA Region and Demonstrates SMA Associated Deletions

Human molecular genetics, 1997-02, Vol.6 (2), p.229-236

1997

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Cisplatin, Etoposide, and Paclitaxel in the Treatment of Patients With Extensive Small-Cell Lung Carcinoma

Journal of clinical oncology, 1999-08, Vol.17 (8), p.2309-2315

1999

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Characterization of Survival Motor Neuron (SMNT) Gene Deletions in Asymptomatic Carriers of Spinal Muscular Atrophy

Human molecular genetics, 1996-03, Vol.5 (3), p.359-365

1996

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Differential alteration of phospholipase A2 activities in brain of patients with schizophrenia

Brain research, 1999-03, Vol.821 (2), p.407-413

1999

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Phospholipid‐Metabolizing Enzymes in Alzheimer's Disease: Increased Lysophospholipid Acyltransferase Activity and Decreased Phospholipase A2 Activity

Journal of neurochemistry, 1998-02, Vol.70 (2), p.786-793

1998

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Construction of a Yeast Artificial Chromosome Contig Spanning the Spinal Muscular Atrophy Disease Gene Region

Proceedings of the National Academy of Sciences - PNAS, 1993-07, Vol.90 (14), p.6801-6805

1993

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Phosphatidylcholine and phosphatidylethanolamine metabolites may regulate brain phospholipid catabolism via inhibition of lysophospholipase activity

Brain research, 1999-07, Vol.834 (1), p.207-210

1999

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On the Stability of Messenger RNA and Ribosomal RNA in the Brains of Control Human Subjects and Patients with Alzheimer's Disease

Journal of neurochemistry, 1992-05, Vol.58 (5), p.1810-1819

1992

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An assessment of patients' attitudes to day-case general anaesthesia for removal of mandibular third molars

British journal of oral & maxillofacial surgery, 1998-02, Vol.36 (1), p.27-29

Ross, M.B.

1998

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Abnormal activity of membrane phospholipid synthetic enzymes in the brain of patients with Friedreich's ataxia and spinocerebellar atrophy type-1

Movement disorders, 2000-03, Vol.15 (2), p.294-300

2000

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Diagnosis, Treatment and Follow Up of Acute Pulmonary Embolism: Consensus Practice from the PERT Consortium

Clinical and Applied Thrombosis/Hemostasis, 2019-01, Vol.25, p.1076029619853037-1076029619853037

2019

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Clinical subtyping reveals significant differences in calcium-dependent phospholipase A2 activity in schizophrenia

Biological psychiatry (1969), 1999-08, Vol.46 (3), p.401-405

1999

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Brain phospholipids and fatty acids in Friedreich's ataxia and spinocerebellar atrophy type-1

Movement disorders, 1998-09, Vol.13 (5), p.813-819

1998

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Increased Levels of Ethane, A Non-invasive Marker of n-3 Fatty Acid Oxidation, in Breath of Children with Attention Deficit Hyperactivity Disorder

Nutritional neuroscience, 2003-10, Vol.6 (5), p.277-281

2003

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Association of extreme blood lipid profile phenotypic variation with 11 reverse cholesterol transport genes and 10 non-genetic cardiovascular disease risk factors

Human molecular genetics, 2003-11, Vol.12 (21), p.2733-2743

2003

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Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease

Biomarkers of oxidative stress in schizophrenic and control subjects

Transgenic mice expressing the human heat shock protein 70 have improved post-ischemic myocardial recovery

The analysis of oral air using selected ion flow tube mass spectrometry in persons with and without a history of oral malodour

Identification and Analysis of Mutations in the Wilson Disease Gene ( ATP7B): Population Frequencies, Genotype-Phenotype Correlation, and Functional Analyses

Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictions

Elevated activity of phospholipid biosynthetic enzymes in substantia nigra of patients with Parkinson's disease

TULP1 mutation in two extended Dominican kindreds with autosomal recessive Retinitis pigmentosa

Low activity of key phospholipid catabolic and anabolic enzymes in human substantia nigra: possible implications for Parkinson's disease

Application packs

A Multicopy Transcription-Repair Gene, BTF2p44, Maps to the SMA Region and Demonstrates SMA Associated Deletions

Cisplatin, Etoposide, and Paclitaxel in the Treatment of Patients With Extensive Small-Cell Lung Carcinoma

Characterization of Survival Motor Neuron (SMNT) Gene Deletions in Asymptomatic Carriers of Spinal Muscular Atrophy

Differential alteration of phospholipase A2 activities in brain of patients with schizophrenia

Phospholipid‐Metabolizing Enzymes in Alzheimer's Disease: Increased Lysophospholipid Acyltransferase Activity and Decreased Phospholipase A2 Activity

Construction of a Yeast Artificial Chromosome Contig Spanning the Spinal Muscular Atrophy Disease Gene Region

Phosphatidylcholine and phosphatidylethanolamine metabolites may regulate brain phospholipid catabolism via inhibition of lysophospholipase activity

On the Stability of Messenger RNA and Ribosomal RNA in the Brains of Control Human Subjects and Patients with Alzheimer's Disease

An assessment of patients' attitudes to day-case general anaesthesia for removal of mandibular third molars

Abnormal activity of membrane phospholipid synthetic enzymes in the brain of patients with Friedreich's ataxia and spinocerebellar atrophy type-1

Diagnosis, Treatment and Follow Up of Acute Pulmonary Embolism: Consensus Practice from the PERT Consortium

Clinical subtyping reveals significant differences in calcium-dependent phospholipase A2 activity in schizophrenia

Brain phospholipids and fatty acids in Friedreich's ataxia and spinocerebellar atrophy type-1

Increased Levels of Ethane, A Non-invasive Marker of n-3 Fatty Acid Oxidation, in Breath of Children with Attention Deficit Hyperactivity Disorder

Association of extreme blood lipid profile phenotypic variation with 11 reverse cholesterol transport genes and 10 non-genetic cardiovascular disease risk factors

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