Search Results - "LOCKHART, P. J"
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Investigating the Association Reactions of HOCH 2 CO and HOCHCHO with O 2 : A Quantum Computational and Master Equation Study
Published in The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory (18-05-2023)“…Glycolaldehyde, HOCH CHO, is an important multifunctional atmospheric trace gas formed in the oxidation of ethylene and isoprene and emitted directly from…”
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Investigating the Association Reactions of HOCH2CO and HOCHCHO with O2: A Quantum Computational and Master Equation Study
Published in The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory (18-05-2023)“…Glycolaldehyde, HOCH2CHO, is an important multifunctional atmospheric trace gas formed in the oxidation of ethylene and isoprene and emitted directly from…”
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3
Mutant torsinA interacts with tyrosine hydroxylase in cultured cells
Published in Neuroscience (15-12-2009)“…Abstract A specific mutation (ΔE302/303) in the torsinA gene underlies most cases of dominantly inherited early-onset torsion dystonia. This mutation causes…”
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Recovering evolutionary trees under a more realistic model of sequence evolution
Published in Molecular biology and evolution (01-07-1994)“…We report a new transformation, the LogDet, that is consistent for sequences with differing nucleotide composition and that have arisen under simple but…”
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Implementation of ironXS: a study of the acceptability and feasibility of genetic screening for hereditary hemochromatosis in high schools
Published in Clinical genetics (01-03-2010)“…Delatycki MB, Wolthuizen M, Collins V, Varley E, Craven J, Allen KJ, Aitken MA, Bond L, Lockhart PJ, Wilson GR, Macciocca I, Metcalfe SA. Implementation of…”
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Evolution of chlorophyll and bacteriochlorophyll: the problem of invariant sites in sequence analysis
Published in Proceedings of the National Academy of Sciences - PNAS (05-03-1996)“…Competing hypotheses seek to explain the evolution of oxygenic and anoxygenic processes of photosynthesis. Since chlorophyll is less reduced and precedes…”
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DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein function
Published in Journal of medical genetics (01-03-2004)Get full text
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Spinocerebellar ataxia type 14: study of a family with an exon 5 mutation in the PRKCG gene
Published in Journal of neurology, neurosurgery and psychiatry (01-12-2005)“…We report our observations in an Australian family with spinocerebellar ataxia type 14 (SCA 14). We describe a novel mutation in exon 5 of the PRKCG gene,…”
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Confidence in evolutionary trees from biological sequence data
Published in Nature (London) (29-07-1993)“…The reliable construction of evolutionary trees from nucleotide sequences often depends on randomization tests such as the bootstrap and PTP (cladistic…”
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The origin of plastids
Published in Philosophical transactions of the Royal Society of London. Series B. Biological sciences (27-08-2008)“…It is generally accepted that plastids first arose by acquisition of photosynthetic prokaryotic endosymbionts by non-photosynthetic eukaryotic hosts. It is…”
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A covariotide model explains apparent phylogenetic structure of oxygenic photosynthetic lineages
Published in Molecular biology and evolution (01-09-1998)“…The aims of the work were (1) to develop statistical tests to identify whether substitution takes place under a covariotide model in sequences used for…”
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Trees for bees
Published in Trends in ecology & evolution (Amsterdam) (01-02-2001)“…Controversy over the origins and evolution of social behaviour in the major groups of social bees (the corbiculate bees) has fuelled arguments over different…”
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The kinetics of the gas-phase reactions of selected monoterpenes and cyclo-alkenes with ozone and the NO3 radical
Published in Atmospheric environment (1994) (01-05-2013)“…The relative rate method has been used to measure the room-temperature rate constants for the gas-phase reactions of ozone and NO3 with selected monoterpenes…”
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Unclassified white matter disorders: A diagnostic journey requiring close collaboration between clinical and laboratory services
Published in European journal of medical genetics (01-09-2022)“…Next generation sequencing studies have revealed an ever-increasing number of causes for genetic disorders of central nervous system white matter. A…”
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Use of ISSR profiles and ITS-sequences to study the biogeography of alpine cushion plants in the genus Raoulia (Asteraceae)
Published in Plant systematics and evolution (01-06-2003)“…Nuclear ITS sequences and ISSR profiles provide evidence that Raoulia rubra is endemic to the Tararua Range in the southern part of the North Island of New…”
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Markers derived from amplified fragment length polymorphism gels for plant ecology and evolution studies
Published in Molecular ecology (01-11-2000)“…We describe the types of polymerase chain reaction (PCR) markers that we have isolated using amplified fragment length polymorphisms (AFLP) in closely related…”
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Functional Analysis and Intracellular Localization of the Human Menkes Protein (MNK) Stably Expressed from a cDNA Construct in Chinese Hamster Ovary Cells (CHO-K1)
Published in Human molecular genetics (01-08-1998)“…The Menkes protein (MNK or ATP7A) is an important component of the mammalian copper transport pathway and is defective in Menkes disease, a fatal X-linked…”
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Evidence for the recent dispersal of Sophora (Leguminosae) around the Southern Oceans: molecular data
Published in Journal of biogeography (01-05-1999)“…Aim The aim is to use DNA sequence data to test between vicariance and long range dispersal (by floating seed-pods) explanations for the origin and range of…”
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Parkin Protects against the Toxicity Associated with Mutant α-Synuclein: Proteasome Dysfunction Selectively Affects Catecholaminergic Neurons
Published in Neuron (Cambridge, Mass.) (19-12-2002)“…One hypothesis for the etiology of Parkinson's disease (PD) is that subsets of neurons are vulnerable to a failure in proteasome-mediated protein turnover…”
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Deletion of the Parkin co-regulated gene causes defects in ependymal ciliary motility and hydrocephalus in the quakingviable mutant mouse
Published in Human molecular genetics (15-04-2010)“…The quakingviable mouse (qkv) is a spontaneous recessive mouse mutant with a deletion of ∼1.1 Mb in the proximal region of chromosome 17. The deletion affects…”
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