Concepedia

Bi‐Xia Ke

BK

4

Publications

249

Citations

4

H-Index

2006

Active since

Affiliations

Murdoch Children's Research Institute(Current)

Deakin University

Royal Children's Hospital

Bi‐Xia Ke is an author at Murdoch Children's Research Institute specializing in molecular genetics, genetics, and medicine.

Top concepts

GeneticsMedicineMolecular GeneticsPublic HealthDna ReplicationSystems BiologyNatural SciencesMolecular BiologyGenetic EngineeringGenetic Epidemiology

Publications per year

2006–2013

4

Publications

4

Respiratory chain complex I deficiency caused by mitochondrial DNA mutations

Helen Swalwell, Denise M. Kirby, Emma L. Blakely et al. · European Journal of Human Genetics · 2011 · 125 citations · Full text

Mitochondrial Myopathy, Respiratory Chain Complex, Mendelian Disorder +10

Deficiency in Mitochondrial Complex I Activity Due to <i>Ndufs6</i> Gene Trap Insertion Induces Renal Disease

Josephine M. Forbes, Bi‐Xia Ke, Tuong‐Vi Nguyen et al. · Antioxidants and Redox Signaling · 2013 · 56 citations

Alteration of copper physiology in mice overexpressing the human Menkes protein ATP7A

Bi‐Xia Ke, Roxana M. Llanos, Magali Wright et al. · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · 2006 · 47 citations

Correction of a mouse model of Menkes disease by the human Menkes gene

Roxana M. Llanos, Bi‐Xia Ke, Magali Wright et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 2006 · 21 citations

Knockout Mouse, Mendelian Disorder, Human Menkes Gene +13

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