Megan Maxwell | Researchain

Archive Network Publication Hotspot Collaboration

Network

Latest external collaboration on country level. Dive into details by clicking on the dots.

Explore More

Hotspot

Dive into the research topics where Megan Maxwell is active.

Explore More

Publication

Featured researches published by Megan Maxwell.

Human Genetics | 1999

A common PEX1 frameshift mutation in patients with disorders of peroxisome biogenesis correlates with the severe Zellweger syndrome phenotype.

Megan Maxwell; Paul V. Nelson; Sharon J. Chin; Barbara C. Paton; William F. Carey; Denis I. Crane

Human Mutation | 2002

Novel PEX1 mutations and genotype-phenotype correlations in Australasian peroxisome biogenesis disorder patients.

Megan Maxwell; Tamara Louise Allen; P. B. Solly; Terje Svingen; Barbara C. Paton; Denis I. Crane

Human Mutation | 2005

PEX1 mutations in the Zellweger spectrum of the peroxisome biogenesis disorders.

Denis I. Crane; Megan Maxwell; Barbara C. Paton

Genesis | 2002

Conditional inactivation of the peroxisome biogenesis Pex13 gene by Cre-loxP excision.

Jonas Carl-Otto Bjorkman; Ian D. Tonks; Megan Maxwell; Carol Paterson; Graham F. Kay; Denis I. Crane

Human Mutation | 2005

Novel PEX1 coding mutations and 5' UTR regulatory polymorphisms

Megan Maxwell; Pamela B. Leane; Barbara C. Paton; Denis I. Crane

ComBio 2003 | 2003

Pex13 conditional inactivation in the mouse: A model for the peroxisome biogenesis disorders.

Denis I. Crane; Megan Maxwell; Jonas Carl-Otto Bjorkman; Tam Nguyen; Phillip A. Sharp; Ian D. Tonks; Carol Paterson; John Finnie; Barbara C. Paton; Graham F. Kay

Archive | 2002

Mouse models of the peroxisome biogenesis disorders through conditional inactivation of Pex13

Denis I. Crane; Megan Maxwell; Jonas Carl-Otto Bjorkman; Ian D. Tonks; Carol Paterson; John Finnie; Barbara C. Paton; Graham F. Kay

26th Annual Scientific Meeting of the Human Genetics Society of Australasia Inc | 2002

Genetic characterisation of patients with peroxisomal biogenesis and oxidation defects: A progress report on findings from a largely Australasian population.

Barbara C. Paton; Megan Maxwell; G.A. Joseph; A.N. Pollard; N.R. Bockmann; P. B. Solly; Michael Fietz; Denis I. Crane

2002 Symposium on Peroxisome Biogenesis | 2002

Pex13 inactivation in the mouse disrupts peroxisome biogenesis and leads to a Zellweger syndrome phenotype

Denis I. Crane; Megan Maxwell; Jonas Carl-Otto Bjorkman; Tam Nguyen; Phillip A. Sharp; Ian D. Tonks; Carol Paterson; John Finnie; Barbara C. Paton; Graham F. Kay

2002 Symposium on Peroxisome Biogenesis | 2002

Genetic characterisation of patients with peroxisomal biogenesis and oxidation defects: the Australasian experience.

Barbara C. Paton; Megan Maxwell; Jonas Carl-Otto Bjorkman; G.A. Joseph; A.N. Pollard; M.R. Bockman; P. B. Solly; S.M. Kerin; Michael Fietz; Denis I. Crane

Explore More