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

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

2007

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Null Mutation of the Murine ATP7B (Wilson Disease) Gene Results in Intracellular Copper Accumulation and Late-Onset Hepatic Nodular Transformation

Human molecular genetics, 1999-09, Vol.8 (9), p.1665-1671

1999

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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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ClpB is the Escherichia coli heat shock protein F84.1

Journal of Bacteriology, 1991-07, Vol.173 (14), p.4254-4262

1991

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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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A portable, submersible, MR sensor – The Proteus magnet

Journal of magnetic resonance (1997), 2021-05, Vol.326, p.106964-106964, Article 106964

2021

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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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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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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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One type of gamma-turn, rather than the other gives rise to chain-reversal in proteins

Journal of molecular biology, 1988-12, Vol.204 (3), p.777-782

1988

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

Null Mutation of the Murine ATP7B (Wilson Disease) Gene Results in Intracellular Copper Accumulation and Late-Onset Hepatic Nodular Transformation

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

ClpB is the Escherichia coli heat shock protein F84.1

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

A portable, submersible, MR sensor – The Proteus magnet

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

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

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

One type of gamma-turn, rather than the other gives rise to chain-reversal in proteins

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

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

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