The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

Rudolph E. Tanzi, Konstantin Petrukhin, Jean‐Luc Pellequer, +18

Nature Genetics

Mendelian DisorderDisease MechanismWilson Disease GeneGeneticsPathogenesis +9

ClpB is the Escherichia coli heat shock protein F84.1

Catherine L. Squires, Steen B. Pedersen, B. Ross, +1

Journal of Bacteriology

Systems BiologyProtein ExpressionClpa SubunitProtein FoldingMedicine +11

Cognitive performance of <i>GBA</i> mutation carriers with early-onset PD

Roy N. Alcalay, Elise Caccappolo, Helen Mejia‐Santana, +35

Neurology

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

Lorraine N. Clark, B. Ross, Y. Wang, +11

Neurology

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

Olesia Buiakova, J. Xu, Svetlana Lutsenko, +7

Human Molecular Genetics

GeneticsPathologyMolecular BiologyMolecular GeneticsOxidative Stress +15

AAC-11, a novel cDNA that inhibits apoptosis after growth factor withdrawal.

Manu Tewari, M Yu, B. Ross, +3

PubMed

Cancer ResearchLeucine Zipper DomainCell RegulationGrowth Factor WithdrawalMedicine +13

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

T. A. Carter, Carsten G. Bönnemann, C. H. Wang, +9

Human Molecular Genetics

GeneticsGene CharacterizationMolecular GeneticsDisease Gene IdentificationMendelian Disorder +18

Construction of a yeast artificial chromosome contig spanning the spinal muscular atrophy disease gene region.

Patrick W. Kleyn, C H Wang, L L Lien, +7

Proceedings of the National Academy of Sciences

Genetic AnalysisPcr AmplificationGenetic DisorderSma LocusGenetics +12

Olfaction in <i>Parkin</i> heterozygotes and compound heterozygotes

Roy N. Alcalay, Andrew Siderowf, Ruth Ottman, +31

Neurology

The relation between depression and parkin genotype: The CORE-PD study

Abhilekh Srivastava, Ming Tang, Helen Mejia‐Santana, +31

Parkinsonism & Related Disorders

Parkin GenotypePsychiatryMood SymptomGenetic EpidemiologyDepression +9