Torthaí cuardaigh - Debbie Ang
- 1 - 5 toradh as 5 á dtaispeáint
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1
Trigger Factor can antagonize both SecB and DnaK/DnaJ chaperone functions in <i>Escherichia coli</i> de réir Ronald S. Ullers, Debbie Ang, Françoise Schwager, Costa Georgopoulos, Pierre Genevaux
Foilsithe / Cruthaithe 2007Artigo -
2
Polypeptide Flux through Bacterial Hsp70 de réir Sarah Teter, Walid A. Houry, Debbie Ang, Thomas Tradler, David Rockabrand, Gunter Fischer, Paul Blum, Costa Georgopoulos, F.Ulrich Hartl
Foilsithe / Cruthaithe 1999Artigo -
3
Hereditary Spastic Paraplegia SPG13 Is Associated with a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60 de réir Jens Jacob Hansen, Alexandra Dürr, Isabelle Cournu‐Rebeix, Costa Georgopoulos, Debbie Ang, Marit N. Nielsen, Claire‐Sophie Davoine, Alexis Brice, Bertrand Fontaine, Niels Gregersen, Peter Bross
Foilsithe / Cruthaithe 2002Artigo -
4
The Hsp60-(p.V98I) Mutation Associated with Hereditary Spastic Paraplegia SPG13 Compromises Chaperonin Function Both in Vitro and in Vivo de réir Peter Bross, Søren Naundrup, Jakob Hansen, Marit N. Nielsen, Jane Christensen, Mogens Kruhøffer, Johan Palmfeldt, Thomas J. Corydon, Niels Gregersen, Debbie Ang, Costa Georgopoulos, Kåre Lehmann Nielsen
Foilsithe / Cruthaithe 2008Artigo -
5
Mitochondrial Hsp60 Chaperonopathy Causes an Autosomal-Recessive Neurodegenerative Disorder Linked to Brain Hypomyelination and Leukodystrophy de réir Daniella Magen, Costa Georgopoulos, Peter Bross, Debbie Ang, Yardena Segev, Dorit Goldsher, Alexandra Nemirovski, Eli Shahar, Sarit Ravid, Anthony Luder, Bayan Heno, Ruth Gershoni‐Baruch, Karl Skorecki, Hanna Mandel
Foilsithe / Cruthaithe 2008Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Gene
Genetics
Cell biology
Escherichia coli
Heat shock protein
Hsp70
Medicine
Molecular biology
Mutant
Pathology
Biochemistry
Chaperone (clinical)
Chaperonin
HSP60
Mutation
Phenotype
RNA
Ribosome
Ataxia
Complementation
Disease
GroEL
Hereditary spastic paraplegia
Inner membrane
Leukodystrophy
Membrane
Membrane protein
Missense mutation
Neurodegeneration