Lista de obras - Andrew J Sutherland-Smith

An open or closed case for the conformation of calponin homology domains on F-actin?

artículo científico publicado en 2004

Beyond BLASTing: tertiary and quaternary structure analysis helps identify major vault proteins.

artículo científico publicado en 2013

Biallelic mutations in CYP26B1: A differential diagnosis for Pfeiffer and Antley-Bixler syndromes

artículo científico publicado en 2016

Characterization of a dual-function domain that mediates membrane insertion and excision of Ff filamentous bacteriophage.

artículo científico publicado en 2011

Crystal structure of a human embryonic haemoglobin: the carbonmonoxy form of gower II (α 2 ϵ 2 ) haemoglobin at 2.9 å resolution 1 1Edited by K. Nagai

Cytotoxic aggregation and amyloid formation by the myostatin precursor protein

artículo científico publicado en 2010

Developing a video tracking method to study interactions between close pairs of optically trapped particles in three dimensions

artículo científico publicado en 2015

Diverse phenotypic consequences of mutations affecting the C-terminus of FLNA.

artículo científico publicado en 2015

Expression and role in glycolysis of human ADP-dependent glucokinase

artículo científico publicado en 2012

Filamin structure, function and mechanics: are altered filamin-mediated force responses associated with human disease?

artículo científico publicado en 2011

Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans.

artículo científico publicado en 2003

Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal Dysplasia

scientific journal article

Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development

scientific journal article

Skeletal dysplasias due to filamin A mutations result from a gain-of-function mechanism distinct from allelic neurological disorders

artículo científico publicado en 2009

Structural determination of archaeal UDP-N-acetylglucosamine 4-epimerase from Methanobrevibacter ruminantium M1 in complex with the bacterial cell wall intermediate UDP-N-acetylmuramic acid

scientific article published on 05 October 2018

Structure and Evolution of the Archaeal Lipid Synthesis Enzyme sn-Glycerol-1-phosphate Dehydrogenase

artículo científico publicado en 2015

The C313Y Piedmontese mutation decreases myostatin covalent dimerisation and stability.

artículo científico publicado en 2011

The Emery-Dreifuss muscular dystrophy associated-protein emerin is phosphorylated on serine 49 by protein kinase A.

artículo científico publicado en 2006

The Structural and Functional Characterization of Mammalian ADP-dependent Glucokinase.

artículo científico publicado en 2015

The structure of the N-terminal actin-binding domain of human dystrophin and how mutations in this domain may cause Duchenne or Becker muscular dystrophy

artículo científico publicado en 2000

X-ray crystallographic analyses of the structures of two heme proteins

1998 doctoral thesis by Andrew John Sutherland-Smith at Massey University

Lista de obras de Andrew J Sutherland-Smith

An open or closed case for the conformation of calponin homology domains on F-actin?

Beyond BLASTing: tertiary and quaternary structure analysis helps identify major vault proteins.

Biallelic mutations in CYP26B1: A differential diagnosis for Pfeiffer and Antley-Bixler syndromes

Characterization of a dual-function domain that mediates membrane insertion and excision of Ff filamentous bacteriophage.

Crystal structure of a human embryonic haemoglobin: the carbonmonoxy form of gower II (α 2 ϵ 2 ) haemoglobin at 2.9 å resolution 1 1Edited by K. Nagai

Cytotoxic aggregation and amyloid formation by the myostatin precursor protein

Developing a video tracking method to study interactions between close pairs of optically trapped particles in three dimensions

Diverse phenotypic consequences of mutations affecting the C-terminus of FLNA.

Expression and role in glycolysis of human ADP-dependent glucokinase

Filamin structure, function and mechanics: are altered filamin-mediated force responses associated with human disease?

Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans.

Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal Dysplasia

Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development

Skeletal dysplasias due to filamin A mutations result from a gain-of-function mechanism distinct from allelic neurological disorders

Structural determination of archaeal UDP-N-acetylglucosamine 4-epimerase from Methanobrevibacter ruminantium M1 in complex with the bacterial cell wall intermediate UDP-N-acetylmuramic acid

Structure and Evolution of the Archaeal Lipid Synthesis Enzyme sn-Glycerol-1-phosphate Dehydrogenase

The C313Y Piedmontese mutation decreases myostatin covalent dimerisation and stability.

The Emery-Dreifuss muscular dystrophy associated-protein emerin is phosphorylated on serine 49 by protein kinase A.

The Structural and Functional Characterization of Mammalian ADP-dependent Glucokinase.

The structure of the N-terminal actin-binding domain of human dystrophin and how mutations in this domain may cause Duchenne or Becker muscular dystrophy

X-ray crystallographic analyses of the structures of two heme proteins