Publications by authors named "Debbie Ang"

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A recurrent de novo variant is associated with hypomyelinating leukodystrophy.
Cagla Cömert, Lauren Brick, Debbie Ang, Johan Palmfeldt, Brandon F Meaney

Cold Spring Harb Mol Case Stud· June 2020

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An ORFan no more: the bacteriophage T4 39.2 gene product, NwgI, modulates GroEL chaperone function.
Debbie Ang, Costa Georgopoulos

Genetics· March 2012

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Mitochondrial hsp60 chaperonopathy causes an autosomal-recessive neurodegenerative disorder linked to brain hypomyelination and leukodystrophy.
Daniella Magen, Costa Georgopoulos, Peter Bross, Debbie Ang, Yardena Segev

Am J Hum Genet· July 2008

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The Hsp60-(p.V98I) mutation associated with hereditary spastic paraplegia SPG13 compromises chaperonin function both in vitro and in vivo.
Peter Bross, Søren Naundrup, Jakob Hansen, Marit Nyholm Nielsen, Jane Hvarregaard Christensen, Debbie Ang

J Biol Chem· June 2008

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A novel mutation in the HSPD1 gene in a patient with hereditary spastic paraplegia.
Jakob Hansen, Kirsten Svenstrup, Debbie Ang, Marit N Nielsen, Jane H Christensen

J Neurol· July 2007

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Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potential.
Peter Bross, Zhijie Li, Jakob Hansen, Jens Jacob Hansen, Marit Nyholm Nielsen, Debbie Ang, Huanming Yang

J Hum Genet· March 2007

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Trigger Factor can antagonize both SecB and DnaK/DnaJ chaperone functions in Escherichia coli.
Ronald S Ullers, Debbie Ang, Françoise Schwager, Costa Georgopoulos, Pierre Genevaux

Proc Natl Acad Sci U S A· February 2007

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Functional characterization of an archaeal GroEL/GroES chaperonin system: significance of substrate encapsulation.
Luis Figueiredo, Daniel Klunker, Debbie Ang, Dean J Naylor, Michael J Kerner

J Biol Chem· January 2004

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The OmpL porin does not modulate redox potential in the periplasmic space of Escherichia coli.
Abhijit A Sardesai, Pierre Genevaux, Françoise Schwager, Debbie Ang, Costa Georgopoulos

EMBO J· April 2003

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Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60.
Jens Jacob Hansen, Alexandra Dürr, Isabelle Cournu-Rebeix, Costa Georgopoulos, Debbie Ang

Am J Hum Genet· May 2002

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