VIAF

Virtual International Authority File

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Leader 00000nz a2200037n 45 0
001 WKP|Q63127925 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241121000119.0
008 241121nneanz||abbn n and d
035 ‎‡a (WKP)Q63127925‏
024 ‎‡a 0000-0001-9485-1428‏ ‎‡2 orcid‏
024 ‎‡a 6507319250‏ ‎‡2 scopus‏
035 ‎‡a (OCoLC)Q63127925‏
100 0 ‎‡a Andrew J Sutherland-Smith‏ ‎‡c researcher‏ ‎‡9 en‏
375 ‎‡a 1‏ ‎‡2 iso5218‏
400 0 ‎‡a Andrew J Sutherland-Smith‏ ‎‡c wetenschapper‏ ‎‡9 nl‏
670 ‎‡a Author's An open or closed case for the conformation of calponin homology domains on F-actin?‏
670 ‎‡a Author's Beyond BLASTing: tertiary and quaternary structure analysis helps identify major vault proteins.‏
670 ‎‡a Author's Biallelic mutations in CYP26B1: A differential diagnosis for Pfeiffer and Antley-Bixler syndromes‏
670 ‎‡a Author's Characterization of a dual-function domain that mediates membrane insertion and excision of Ff filamentous bacteriophage.‏
670 ‎‡a Author's Crystal structure of a human embryonic haemoglobin: the carbonmonoxy form of gower II‏
670 ‎‡a Author's 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
670 ‎‡a Author's Cytotoxic aggregation and amyloid formation by the myostatin precursor protein‏
670 ‎‡a Author's Developing a video tracking method to study interactions between close pairs of optically trapped particles in three dimensions‏
670 ‎‡a Author's Diverse phenotypic consequences of mutations affecting the C-terminus of FLNA.‏
670 ‎‡a Author's Expression and role in glycolysis of human ADP-dependent glucokinase‏
670 ‎‡a Author's Filamin structure, function and mechanics: are altered filamin-mediated force responses associated with human disease?‏
670 ‎‡a Author's Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans.‏
670 ‎‡a Author's Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development‏
670 ‎‡a Author's Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal Dysplasia‏
670 ‎‡a Author's Skeletal dysplasias due to filamin A mutations result from a gain-of-function mechanism distinct from allelic neurological disorders‏
670 ‎‡a Author's 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
670 ‎‡a Author's Structure and Evolution of the Archaeal Lipid Synthesis Enzyme sn-Glycerol-1-phosphate Dehydrogenase‏
670 ‎‡a Author's The C313Y Piedmontese mutation decreases myostatin covalent dimerisation and stability.‏
670 ‎‡a Author's The Emery-Dreifuss muscular dystrophy associated-protein emerin is phosphorylated on serine 49 by protein kinase A.‏
670 ‎‡a Author's The Structural and Functional Characterization of Mammalian ADP-dependent Glucokinase.‏
670 ‎‡a Author's 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
670 ‎‡a Author's X-ray crystallographic analyses of the structures of two heme proteins‏
909 ‎‡a (orcid) 0000000194851428‏ ‎‡9 1‏
909 ‎‡a (scopus) 6507319250‏ ‎‡9 1‏
919 ‎‡a c313ypiedmontesemutationdecreasesmyostatincovalentdimerisationandstability‏ ‎‡A The C313Y Piedmontese mutation decreases myostatin covalent dimerisation and stability.‏ ‎‡9 1‏
919 ‎‡a 10raycrystallographicanalysesofthestructuresof2hemeproteins‏ ‎‡A X-ray crystallographic analyses of the structures of two heme proteins‏ ‎‡9 1‏
919 ‎‡a structureofthenterminalactinbindingdomainofhumandystrophinandhowmutationsinthisdomainmaycauseduchenneorbeckermusculardystrophy‏ ‎‡A 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 ‎‡9 1‏
919 ‎‡a structuralandfunctionalcharacterizationofmammalianadpdependentglucokinase‏ ‎‡A The Structural and Functional Characterization of Mammalian ADP-dependent Glucokinase.‏ ‎‡9 1‏
919 ‎‡a emerydreifussmusculardystrophyassociatedproteinemerinisphosphorylatedonserine49byproteinkinasea‏ ‎‡A The Emery-Dreifuss muscular dystrophy associated-protein emerin is phosphorylated on serine 49 by protein kinase A.‏ ‎‡9 1‏
919 ‎‡a openorclosedcasefortheconformationofcalponinhomologydomainsonfactin‏ ‎‡A An open or closed case for the conformation of calponin homology domains on F-actin?‏ ‎‡9 1‏
919 ‎‡a beyondblastingtertiaryandquaternarystructureanalysishelpsidentifymajorvaultproteins‏ ‎‡A Beyond BLASTing: tertiary and quaternary structure analysis helps identify major vault proteins.‏ ‎‡9 1‏
919 ‎‡a biallelicmutationsincyp26b1adifferentialdiagnosisforpfeifferandantleybixlersyndromes‏ ‎‡A Biallelic mutations in CYP26B1: A differential diagnosis for Pfeiffer and Antley-Bixler syndromes‏ ‎‡9 1‏
919 ‎‡a characterizationofadualfunctiondomainthatmediatesmembraneinsertionandexcisionoffffilamentousbacteriophage‏ ‎‡A Characterization of a dual-function domain that mediates membrane insertion and excision of Ff filamentous bacteriophage.‏ ‎‡9 1‏
919 ‎‡a crystalstructureofahumanembryonichaemoglobinthecarbonmonoxyformofgower2‏ ‎‡A Crystal structure of a human embryonic haemoglobin: the carbonmonoxy form of gower II‏ ‎‡9 1‏
919 ‎‡a crystalstructureofahumanembryonichaemoglobinthecarbonmonoxyformofgower2α2ε2haemoglobinat29aresolution11editedbyknagai‏ ‎‡A 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 ‎‡9 1‏
919 ‎‡a cytotoxicaggregationandamyloidformationbythemyostatinprecursorprotein‏ ‎‡A Cytotoxic aggregation and amyloid formation by the myostatin precursor protein‏ ‎‡9 1‏
919 ‎‡a developingavideotrackingmethodtostudyinteractionsbetweenclosepairsofopticallytrappedparticlesin3dimensions‏ ‎‡A Developing a video tracking method to study interactions between close pairs of optically trapped particles in three dimensions‏ ‎‡9 1‏
919 ‎‡a diversephenotypicconsequencesofmutationsaffectingthe100terminusofflna‏ ‎‡A Diverse phenotypic consequences of mutations affecting the C-terminus of FLNA.‏ ‎‡9 1‏
919 ‎‡a expressionandroleinglycolysisofhumanadpdependentglucokinase‏ ‎‡A Expression and role in glycolysis of human ADP-dependent glucokinase‏ ‎‡9 1‏
919 ‎‡a filaminstructurefunctionandmechanicsarealteredfilaminmediatedforceresponsesassociatedwithhumandisease‏ ‎‡A Filamin structure, function and mechanics: are altered filamin-mediated force responses associated with human disease?‏ ‎‡9 1‏
919 ‎‡a localizedmutationsinthegeneencodingthecytoskeletalproteinfilaminacausediversemalformationsinhumans‏ ‎‡A Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans.‏ ‎‡9 1‏
919 ‎‡a mutationsingenesencodingthecadherinreceptorligandpairdchs1andfat4disruptcerebralcorticaldevelopment‏ ‎‡A Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development‏ ‎‡9 1‏
919 ‎‡a mutationsinmap3k7thataltertheactivityofthetak1signalingcomplexcausefrontometaphysealdysplasia‏ ‎‡A Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal Dysplasia‏ ‎‡9 1‏
919 ‎‡a skeletaldysplasiasduetofilaminamutationsresultfromagainoffunctionmechanismdistinctfromallelicneurologicaldisorders‏ ‎‡A Skeletal dysplasias due to filamin A mutations result from a gain-of-function mechanism distinct from allelic neurological disorders‏ ‎‡9 1‏
919 ‎‡a structuraldeterminationofarchaealudpnacetylglucosamine4epimerasefrommethanobrevibacterruminantiumm1incomplexwiththebacterialcellwallintermediateudpnacetylmuramicacid‏ ‎‡A 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 ‎‡9 1‏
919 ‎‡a structureandevolutionofthearchaeallipidsynthesisenzymesnglycerol1phosphatedehydrogenase‏ ‎‡A Structure and Evolution of the Archaeal Lipid Synthesis Enzyme sn-Glycerol-1-phosphate Dehydrogenase‏ ‎‡9 1‏
946 ‎‡a b‏ ‎‡9 1‏
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